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CGEN Compugen Ltd

1.41
-0.08 (-5.37%)
16 Nov 2024 - Closed
Delayed by 15 minutes
Share Name Share Symbol Market Type
Compugen Ltd NASDAQ:CGEN NASDAQ Common Stock
  Price Change % Change Share Price Bid Price Offer Price High Price Low Price Open Price Shares Traded Last Trade
  -0.08 -5.37% 1.41 0.30 3.15 1.50 1.35 1.50 441,994 05:00:00

Form 6-K - Report of foreign issuer [Rules 13a-16 and 15d-16]

06/08/2024 12:00pm

Edgar (US Regulatory)


0001119774--12-31falseQ22024-06-30

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
Form 6-K
 
REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
 
For the month of August 2024
Commission File Number 000-30902
 
COMPUGEN LTD.
(Translation of registrant’s name into English)
 
26 Harokmim Street
Holon 5885849, Israel
(Address of Principal Executive Offices)
 
Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F:
 
Form 20-F ☒  Form 40-F ☐
 

Compugen Ltd.
 
On August 6, 2024, Compugen Ltd. (the “Company”) issued a press release reporting the Company’s 2024 second quarter results (the “Press Release”), a copy of which is furnished as Exhibit 99.1 to this Report on Form 6-K. With the exception of the 2nd, 3rd and 4th paragraphs of the Press Release, the information contained in the Press Release is hereby incorporated by reference herein.
 
Second Quarter 2024 Financial Results
 
The unaudited interim consolidated financial statements of the Company and its subsidiary as of June 30, 2024 and December 31, 2023 and for the six months ended June 30, 2024 and 2023 are furnished as Exhibit 99.2 to this Report on Form 6-K and incorporated by reference herein. Management’s Discussion and Analysis of Results of Operations and Financial Condition of the Company as of and for the six months ended June 30, 2024 are furnished as Exhibit 99.3 to this Report on Form 6-K and incorporated by reference herein.
 
The information contained in this Report on Form 6-K is hereby incorporated by reference into the Company’s Registration Statement on Form F-3, File No. 333-270985.
 
Exhibits
Exhibit
Number
Description of Exhibit
99.1
99.2
99.3
101
The following financial information from Compugen Ltd.’s Report on Form 6-K, formatted in Inline XBRL (ieXtensible Business Reporting Language): (i) interim consolidated balance sheets as of June 30, 2024 and December 31, 2023; (ii) interim consolidated statements of comprehensive loss for the six months ended June 30, 2024 and 2023; (iii) interim consolidated statements of changes in shareholders’ equity for the six months ended June 30, 2024 and 2023; (iv) interim consolidated statements of cash flows for the six months ended June 30, 2024 and 2023; and (v) notes to interim consolidated financial statements.
 

Signatures
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
 
COMPUGEN LTD.
 
Date: August 6, 2024
By:
/s/ Eran Ben Dor
 
 
 
Eran Ben Dor
General Counsel
 
 


Exhibit 99.1

 
FOR IMMEDIATE RELEASE  
 
Compugen Reports Second Quarter 2024 Results

FDA clearance of COM503 IND in July 2024 triggered a $30 million milestone payment from Gilead
 
On track to present data from COM701 + COM902 + pembrolizumab, platinum resistant ovarian cancer study in Q4 2024
 
Partner, AstraZeneca, advanced development of rilvegostomig, and provided a non-risk adjusted peak year revenue target of over $5 billion, reflecting the potential of the asset. Compugen is eligible for future milestones and mid-single-digit tiered royalty payments, presenting a significant potential revenue source for the Company
 
Solid balance sheet with cash runway expected to fund operations into 2027
 
HOLON, ISRAEL, August 6, 2024 - Compugen Ltd. (Nasdaq: CGEN) (TASE: CGEN) a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery, today announced financial results for the second quarter ended June 30, 2024, and provided a corporate update.
 
“Continuing our track record in delivering on our plans, we have executed well in the second quarter of 2024,” said Anat Cohen-Dayag, Ph.D., President and Chief Executive Officer of Compugen. “We achieved FDA IND clearance for COM503, a differentiated antibody approach to harness cytokine biology for cancer therapeutics, triggering a right to receive a $30 million milestone payment from our partner Gilead. We are on track to initiate a Phase 1 clinical trial for COM503, as monotherapy and in combination with the anti-PD1 zimberelimab in advanced solid tumors, in the fourth quarter of 2024.”

Dr. Cohen-Dayag continued, “We are also on track to present data from our COM701 + COM902 + pembrolizumab study in platinum resistant ovarian cancer in the fourth quarter of 2024. There is a significant unmet medical need for women with ovarian cancer who could benefit from potentially safe, efficacious and durable alternative treatment options. We previously demonstrated encouraging data in this patient population, including monotherapy activity, overall response rate of 20% and durable responses with some patients benefiting from treatment for over 16 months comparing favorably to standard of care. We believe showing data consistent with what we have previously reported in this indication, will once again confirm that COM701 combinations are active. We plan to share next steps for COM701 combinations at the time of data presentation in the fourth quarter of 2024."

Dr. Cohen-Dayag added, “Our partner, AstraZeneca, is advancing development of rilvegostomig, their PD-1/TIGIT bispecific, and provided a non-risk-adjusted peak year revenue target of more than $5 billion for this asset, reflecting the potential of rilvegostomig. Compugen is eligible for future milestones and mid-single-digit tiered royalty payments, presenting a significant potential revenue source for the Company.”



Upcoming Expected Milestones
COM701 +COM902 + pembrolizumab proof-of-concept study
Platinum resistant ovarian cancer - data presentation in the fourth quarter of 2024

COM503 (licensed to Gilead; Compugen leads through Phase 1 development)
Initiation of COM503 Phase 1 trial in the fourth quarter of 2024

Rilvegostomig (AstraZeneca’s PD-1/TIGIT bispecific, TIGIT component derived from COM902)
AstraZeneca anticipates data from Phase 1/2 ARTEMIDE-01 trial in the second half of 2024; poster presentation from Phase 2 GEMINI-Gastric trial accepted at ESMO 2024

Second Quarter 2024 Financial Highlights
Cash: As of June 30, 2024, Compugen had approximately $92.3 million cash, cash equivalents, short-term bank deposits, restricted cash and short-term bank deposit, and cash investments, compared with approximately $51.1 million as of December 31, 2023. Compugen expects that its cash and cash-related balances together with the additional expected $30 million milestone payment on COM503 IND clearance achieved in July, which is subject to a 15% withholding tax, will be sufficient to fund its operating plans into 2027. The Company has no debt.

Revenues: Compugen reported approximately $6.7 million in revenues for the second quarter ended June 30, 2024, compared to no revenues for the comparable period in 2023. The revenues reported reflect recognition of a portion of the upfront payment from the license agreement with Gilead and the clinical milestone from the license agreement with AstraZeneca in the amount of $5 million.

R&D expenses for the second quarter of 2024 were approximately $6.2 million compared with approximately $7.8 million for the comparable period in 2023.

G&A expenses for the second quarter of 2024 were approximately $2.2 million, compared with approximately $2.4 million for the comparable period in 2023.

Net loss for the second quarter of 2024 was approximately $2.1 million, or $0.02 per basic and diluted share, compared with a net loss of approximately $9.3 million, or $0.11 per basic and diluted share, in the second quarter of 2023.

Full financial tables are included below.
 
Conference Call and Webcast Information
Compugen will hold a conference call today, August 6, 2024, at 8:30 AM ET to review its second quarter 2024 results. To access the live conference call by telephone, please dial 1-866-744-5399 from the U.S., or +972-3-918-0644 internationally. The call will be available via live webcast through Compugen’s website, located at the following link. Following the live webcast, a replay will be available on Compugen’s website.



About Compugen
Compugen is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable predictive computational discovery capabilities to identify new drug targets and biological pathways for developing cancer immunotherapies. Compugen has two proprietary product candidates in Phase 1 development: COM701, a potential first-in-class anti-PVRIG antibody and COM902, a potential best-in-class antibody targeting TIGIT for the treatment of solid tumors. Rilvegostomig, a PD-1/TIGIT bispecific antibody where the TIGIT component is derived from Compugen’s clinical stage anti-TIGIT antibody, COM902, is in Phase 3 development by AstraZeneca through a license agreement for the development of bispecific and multispecific antibodies. In addition, the Company’s therapeutic pipeline of early-stage immuno-oncology programs consists of programs aiming to address various mechanisms of immune resistance, of which the most advanced program, COM503, a potential first-in-class, high affinity anti-IL-18 binding protein antibody, which has been granted IND clearance from the FDA, is licensed to Gilead. Compugen is headquartered in Israel, with offices in San Francisco, CA. Compugen’s shares are listed on Nasdaq and the Tel Aviv Stock Exchange under the ticker symbol CGEN.

Forward-Looking Statement
This press release contains “forward-looking statements” within the meaning of the Securities Act of 1933 and the Securities Exchange Act of 1934, as amended, and the safe-harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements are based on the current beliefs, expectations, and assumptions of Compugen. Forward-looking statements can be identified using terminology such as “will,” “may,” “expects,” “anticipates,” “believes,” “potential,” “plan,” “goal,” “estimate,” “likely,” “should,” “confident,” and “intends,” and similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements include, but are not limited to, statements relating to our expectation to present data from our ongoing trials and the relevant timing thereof; statements relating to potential of rilvegostomig and potential long-term revenue source for Compugen thereof; statements relating to our expectation that our cash is expected to fund operations into 2027; statements relating to receipt of a milestone payment from Gilead; statements regarding our expectation to initiate a Phase 1 study for COM503, as monotherapy and in combination with the anti-PD1 zimberelimab in advanced solid tumors, in fourth quarter of 2024; statements regarding our belief that showing data in platinum resistant ovarian cancer consistent with what we have previously reported in this indication, will once again confirm that COM701 combinations are active; and statements regarding our plans to share next steps for COM701 and timing thereof; and statements relating to data presentations from different rilvegostomig clinical trials. These and other forward-looking statements involve known and unknown risks and uncertainties that may cause the actual results, performance or achievements of Compugen to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Among these risks: Compugen’s business model is substantially dependent on entering into collaboration agreements with third parties, and Compugen may not be successful in generating adequate revenues or commercializing aspects of its business model; Compugen’s approach to the discovery of therapeutic products is based on its proprietary computational target discovery infrastructure, which is unproven clinically; Compugen does not know whether it will be able to discover and develop additional potential product candidates or products of commercial value; the general market, political and economic conditions in the countries in which Compugen operates, including Israel; and the effect of the evolving nature of the recent war in Israel, and the related evolving regional conflicts. These and other risks are more fully discussed in the “Risk Factors” section of Compugen’s most recent Annual Report on Form 20-F as filed with the Securities and Exchange Commission (SEC) as well as other documents that may be subsequently filed by Compugen from time to time with the SEC. While we believe that we have a reasonable basis for each forward-looking statement contained in this press release, we caution you that these statements are based on a combination of facts and factors currently known by us and our projections of the future, about which we cannot be certain. In addition, any forward-looking statements represent Compugen’s views only as of the date of this release and should not be relied upon as representing its views as of any subsequent date. Compugen does not assume any obligation to update any forward-looking statements unless required by law.

Company contact:
Yvonne Naughton, Ph.D.
VP, Head of Investor Relations and Corporate Communications
Email: ir@cgen.com
Tel: +1 (628) 241-0071  



COMPUGEN LTD.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands, except for share and per share amounts)

   
Three Months Ended
   
Six Months Ended,
 
   
June 30,
   
June 30,
 
   
2024
   
2023
   
2024
   
2023
 
   
Unaudited
   
Unaudited
   
Unaudited
   
Unaudited
 
                         
Revenues
   
6,702
     
-
     
9,261
     
-
 
Cost of revenues
   
1,552
     
-
     
3,654
     
-
 
Gross profit
   
5,150
     
-
     
5,607
     
-
 
                                 
Operating expenses
                               
Research and development expenses
   
6,183
     
7,761
     
12,593
     
15,206
 
Marketing and business development expenses
   
157
     
49
     
248
     
165
 
General and administrative expenses
   
2,222
     
2,404
     
4,670
     
4,977
 
Total operating expenses
   
8,562
     
10,214
     
17,511
     
20,348
 
                                 
Operating loss
   
(3,412
)
   
(10,214
)
   
(11,904
)
   
(20,348
)
Financial and other income, net
   
1,300
     
889
     
2,528
     
1,697
 
Loss before taxes on income
   
(2,112
)
   
(9,325
)
   
(9,376
)
   
(18,651
)
Tax benefit (expense)
   
(11
)
   
49
     
(14
)
   
36
 
Net loss
   
(2,123
)
   
(9,276
)
   
(9,390
)
   
(18,615
)
                                 
Basic and diluted net loss per ordinary share
   
(0.02
)
   
(0.11
)
   
(0.10
)
   
(0.21
)
Weighted average number of ordinary shares used in computing basic and diluted net loss per share
   
89,531,937
     
87,182,839
     
89,518,778
     
86,903,741
 


 
COMPUGEN LTD.
CONDENSED CONSOLIDATED BALANCE SHEETS DATA
(U.S. dollars, in thousands)

   
June 30,
   
December 31,
 
   
2024
   
2023
 
   
Unaudited
       
             
ASSETS
           
 
           
Current assets
           
Cash and cash equivalents
   
11,877
     
13,890
 
Restricted cash
   
-
     
365
 
Short-term bank deposits
   
47,439
     
25,053
 
Restricted short-term bank deposit
   
333
     
-
 
Investment in marketable securities
   
32,688
     
11,742
 
Trade receivables
   
5,000
     
61,000
 
Other accounts receivable and prepaid expenses
   
4,796
     
2,529
 
Total current assets
   
102,133
     
114,579
 
                 
Non-current assets
               
Long-term prepaid expenses
   
922
     
1,233
 
Severance pay fund
   
3,023
     
2,977
 
Operating lease right to use asset
   
3,061
     
1,329
 
Property and equipment, net
   
1,028
     
1,216
 
Total non-current assets
   
8,034
     
6,755
 
                 
Total assets
   
110,167
     
121,334
 
                 
LIABILITIES AND SHAREHOLDERS EQUITY
               
                 
Current liabilities
               
Other accounts payable, accrued expenses and trade payables
   
13,068
     
14,485
 
Short-term deferred revenues
   
11,252
     
11,149
 
Current maturity of operating lease liability
   
449
     
632
 
Total current liabilities
   
24,769
     
26,266
 
                 
Non-current liabilities
               
Long-term deferred revenues
   
21,028
     
25,392
 
Long-term operating lease liability
   
2,580
     
719
 
Accrued severance pay
   
3,450
     
3,398
 
Total non-current liabilities
   
27,058
     
29,509
 
 
               
Total shareholders' equity
   
58,340
     
65,559
 
                 
Total liabilities and shareholders' equity
   
110,167
     
121,334
 


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Exhibit 99.2
 
COMPUGEN LTD. AND ITS SUBSIDIARY
 
INTERIM CONSOLIDATED FINANCIAL STATEMENTS
 
AS OF JUNE 30, 2024
 
U.S. DOLLARS IN THOUSANDS
 
UNAUDITED
 
INDEX
 
 
Page
  
F-2 - F-3
  
F-4
  
F-5
  
F-6
  
F-7 - F-18
 
- - - - - - - - - - - - -

COMPUGEN LTD. AND ITS SUBSIDIARY
 
INTERIM CONSOLIDATED BALANCE SHEETS
U.S. dollars in thousands
 
   
June 30,
   
December 31,
 
   
2024
   
2023
 
   
Unaudited
       
ASSETS
           
             
CURRENT ASSETS:
           
Cash and cash equivalents
 
$
11,877
   
$
13,890
 
Restricted cash
   
-
     
365
 
Short-term bank deposits
   
47,439
     
25,053
 
Restricted short-term bank deposit
   
333
     
-
 
Investment in marketable securities
   
32,688
     
11,742
 
Trade receivables
   
5,000
     
61,000
 
Other accounts receivable and prepaid expenses
   
4,796
     
2,529
 
                 
Total current assets
   
102,133
     
114,579
 
                 
NON-CURRENT ASSETS:
               
Long-term prepaid expenses
   
922
     
1,233
 
Severance pay fund
   
3,023
     
2,977
 
Operating lease right to use asset
   
3,061
     
1,329
 
Property and equipment, net
   
1,028
     
1,216
 
                 
Total non-current assets
   
8,034
     
6,755
 
                 
Total assets
 
$
110,167
   
$
121,334
 
 
The accompanying notes are an integral part of the interim consolidated financial statements.
F - 2

COMPUGEN LTD. AND ITS SUBSIDIARY
 
INTERIM CONSOLIDATED BALANCE SHEETS
U.S. dollars in thousands (except share data)
 
   
June 30,
   
December 31,
 
   
2024
   
2023
 
   
Unaudited
       
LIABILITIES AND SHAREHOLDERS' EQUITY
           
             
CURRENT LIABILITIES:
           
Trade payables
 
$
2,378
   
$
3,502
 
Short-term deferred revenues
   
11,252
     
11,149
 
Current maturity of operating lease liability
   
449
     
632
 
Accrued expenses
   
8,218
     
7,858
 
Other accounts payable and accrued expenses
   
2,472
     
3,125
 
                 
Total current liabilities
   
24,769
     
26,266
 
                 
NON- CURRENT LIABILITIES:
               
Long-term deferred revenues
   
21,028
     
25,392
 
Long term operating lease liability
   
2,580
     
719
 
Accrued severance pay
   
3,450
     
3,398
 
                 
Total non-current liabilities
   
27,058
     
29,509
 
                 

COMMITMENTS AND CONTINGENT LIABILITIES (NOTE 6)

           
                 
SHAREHOLDERS' EQUITY:
               
Share capital:
               
   Ordinary shares of NIS 0.01 par value: 200,000,000 shares authorized on June 30, 2024, and December 31, 2023; 89,531,937 and 89,237,465 shares issued and outstanding on June 30, 2024, and December 31, 2023, respectively
   
248
     
247
 
Additional paid-in capital
   
542,032
     
539,837
 
Accumulated other comprehensive income (loss)
   
(23
)
   
2
 
Accumulated deficit
   
(483,917
)
   
(474,527
)
                 
Total shareholders' equity
   
58,340
     
65,559
 
                 
Total liabilities and shareholders' equity
 
$
110,167
   
$
121,334
 
 
The accompanying notes are an integral part of the interim consolidated financial statements.
F - 3

COMPUGEN LTD. AND ITS SUBSIDIARY
 
INTERIM CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
U.S. dollars in thousands (except share and per share data)
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Revenues
 
$
9,261
   
$
-
 
Cost of revenues
   
3,654
     
-
 
                 
Gross profit
   
5,607
     
-
 
                 
Operating expenses:
               
Research and development expenses
   
12,593
     
15,206
 
Marketing and business development expenses
   
248
     
165
 
General and administrative expenses
   
4,670
     
4,977
 
                 
Total operating expenses
   
17,511
     
20,348
 
                 
Operating loss
   
(11,904
)
   
(20,348
)
                 
Financial income, net
   
2,528
     
1,697
 
                 
Loss before taxes on income
   
(9,376
)
   
(18,651
)
Tax benefit (expense)
   
(14
)
   
36
 
                 
Net loss
 
$
(9,390
)
 
$
(18,615
)
                 
Other comprehensive loss:
               
                 
 Change in unrealized gains (losses) on marketable securities:
               
       Unrealized gains (losses) arising during the period, net
 
$
(25
)
 
$
*
 
                 
Total comprehensive loss
 
$
(9,415
)
 
$
(18,615
)
                 
Basic and diluted net loss per share
 
$
(0.10
)
 
$
(0.21
)
                 
Weighted average number of ordinary shares used in computing basic and diluted net loss per share
   
89,518,778
     
86,903,741
 
 
* Represents an amount lower than $1.
 
The accompanying notes are an integral part of the interim consolidated financial statements.
F - 4

COMPUGEN LTD. AND ITS SUBSIDIARY

 

INTERIM STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY
U.S. dollars in thousands (except share data)
 
   
Ordinary shares
   
Additional paid-in
   
Accumulated
other
comprehensive
   
Accumulated
   
Total shareholders’
 
   
Number
   
Amount
   
capital
   
income
   
deficit
   
equity
 
                                     
Balance as of January 1, 2023
   
86,624,643
   
$
240
   
$
533,213
   
$
-
   
$
(455,773
)
 
$
77,680
 
                                                 
Issuance of shares, net
   
1,609,123
     
4
     
1,150
             
-
     
1,154
 
Stock-based compensation issued to employees, directors and non-employees
   
-
     
-
     
1,782
             
-
     
1,782
 
Other comprehensive income (loss) from marketable securities, net
   
-
     
-
     
-
     
*
     
-
     
-
 
Net loss
   
-
     
-
     
-
     
-
     
(18,615
)
   
(18,615
)
                                                 
Balance as of June 30, 2023 (unaudited)
   
88,233,766
   
$
244
   
$
536,145
   
$
*
   
$
(474,388
)
 
$
62,001
 
                                                 
Balance as of January 1, 2024
   
89,237,465
   
$
247
   
$
539,837
   
$
2
   
$
(474,527
)
 
$
65,559
 
                                                 
Options exercised
   
1,744
     
*
     
1
     
-
     
-
     
1
 
Issuance of shares, net
   
292,728
     
1
     
561
     
-
     
-
     
562
 
Stock-based compensation issued to employees, directors and non-employees
   
-
     
-
     
1,633
     
-
     
-
     
1,633
 
Other comprehensive loss from marketable securities, net
   
-
     
-
     
-
     
(25
)
   
-
     
(25
)
Net loss
   
-
     
-
     
-
     
-
     
(9,390
)
   
(9,390
)
                                                 
Balance as of June 30, 2024 (unaudited)
   
89,531,937
   
$
248
   
$
542,032
   
$
(23
)
 
$
(483,917
)
 
$
58,340
 
 
* Represents an amount lower than $1.
 
The accompanying notes are an integral part of the interim consolidated financial statements.
F - 5

COMPUGEN LTD. AND ITS SUBSIDIARY
 
INTERIM CONSOLIDATED STATEMENTS OF CASH FLOWS
U.S. dollars in thousands
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Cash flows from operating activities:
           
Net loss
 
$
(9,390
)
 
$
(18,615
)
                 
Adjustments required to reconcile net loss to net cash used in operating activities:
               
Stock-based compensation
   
1,633
     
1,782
 
Depreciation
   
238
     
237
 
Amortization of discount on marketable securities
   
(796
)
   
(13
)
Realized gain on sale of marketable securities, net
   
-
     
(2
)
Increase in severance pay, net
   
6
     
3
 
Exchange rate differences loss (gain) on cash balances
   
12
     
44
 
Decrease in operating lease right of use asset
   
332
     
290
 
Increase in interest receivables and exchange differences on short-term bank deposits
   
(299
)
   
(140
)
Decrease in trade receivables
   
56,000
     
-
 
Increase in other accounts receivable and prepaid expenses
   
(2,267
)
   
(448
)
Decrease (increase) in long-term prepaid expenses
   
311
     
(13
)
Decrease in trade payables
   
(1,137
)
   
(85
)
Decrease in other accounts payable and accrued expenses
   
(293
)
   
(894
)
Decrease in operating lease liability
   
(386
)
   
(394
)
Decrease in deferred revenues
   
(4,261
)
   
-
 
Decrease in deferred participation in R&D expenses
   
-
     
(325
)
Net cash provided by (used in) operating activities
   
39,703
     
(18,573
)
                 
Cash flows from investing activities:
               
Proceeds from maturity of short-term bank deposits
   
25,011
     
51,350
 
Investment in short-term bank deposits
   
(47,086
)
   
(23,220
)
Proceeds from maturity of marketable securities
   
15,825
     
1,000
 
Investment in marketable securities
   
(36,000
)
   
(5,536
)
Purchase of property and equipment
   
(37
)
   
(63
)
Net cash provided by (used in) investing activities
   
(42,287
)
   
23,531
 
                 
Cash flows from financing activities:
               
Proceeds from issuance of ordinary shares, net
   
562
     
1,351
 
Proceeds from exercise of options
   
1
     
-
 
Net cash provided by financing activities
   
563
     
1,351
 
                 
Effect of exchange rate changes on cash
   
(12
)
   
(44
)
                 
Increase (decrease) in cash, cash equivalents and restricted cash
   
(2,033
)
   
6,265
 
Cash, cash equivalents and restricted cash at the beginning of the period
   
13,910
     
11,421
 
Cash, cash equivalents and restricted cash at the end of the period
 
$
11,877
   
$
17,686
 
                 
Supplemental disclosure of non-cash investing and financing activities:
               
                 
Purchase of property and equipment
 
$
13
   
$
(8
)
Right-of-use asset obtained in exchange for operating lease liability
 
$
2,064
   
$
70
 
Issuance expenses
 
$
-
   
$
197
 
 
The accompanying notes are an integral part of the interim consolidated financial statements.
F - 6

COMPUGEN LTD. AND ITS SUBSIDIARY
 
NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS
U.S. dollars in thousands (except share and per share data)
 
NOTE 1:-
GENERAL
 
  a.
Compugen Ltd. (the “Company”) is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable predictive computational discovery capabilities to identify novel drug targets and new biological pathways to develop therapeutics in the field of cancer immunotherapy. The Company’s innovative immuno-oncology pipeline consists of three clinical stage programs, COM701, COM902 and rilvegostomig, targeting immune checkpoints the Company discovered computationally. Two programs that are pursued internally, COM701, a potential first-in-class anti-PVRIG antibody, and COM902, a potential best-in-class therapeutic anti-TIGIT antibody, are in Phase 1 clinical trials and have been evaluated for the treatment of solid tumors as a monotherapy and in combination of dual (PVRIG/PD-1, PVRIG/TIGIT) and triple (PVRIG/PD-1/TIGIT) blockade. Rilvegostomig, a novel anti PD-1/TIGIT bispecific antibody with a TIGIT specific component that is derived from the Company’s COM902 antibody, is being developed by AstraZeneca pursuant to an exclusive license agreement between the Company and AstraZeneca and is being evaluated in multiple clinical trials, including in Phase 3 clinical trials. The Company’s therapeutic pipeline of early-stage immuno-oncology programs consists of programs aiming to address various mechanisms of immune resistance. The Company’s most advanced early-stage program, COM503, was licensed to Gilead Sciences, Inc. (“Gilead”) in December 2023, see also Note 12. COM503 is a potential first-in-class, high affinity antibody, which blocks the interaction between IL-18 binding protein and IL-18, thereby freeing natural IL-18 in the tumor microenvironment to inhibit cancer growth. The Company’s business model is to selectively enter into collaborations for our novel targets and drug product candidates at various stages of research and development under various revenue-sharing arrangements.
     
  b.
The Company is headquartered in Holon, Israel.
 
  c.
The Company has incurred losses in the amount of $9,390 during the six months ended June 30, 2024, has an accumulated deficit of $483,917 as of June 30, 2024, and has an accumulated negative cash flow from operating activities in the amount of $39,703 for the six months ended June 30, 2024. The Company believes that its existing capital resources will be adequate to satisfy its expected liquidity requirements at the current level of yearly expenditures at least twelve months from the reporting date.
 
  d.
On August 5, 2013, the Company entered into a Research and Development Collaboration and License Agreement (“Bayer Agreement”) with Bayer Pharma AG (“Bayer”) for the research, development, and commercialization of antibody-based therapeutics against two novel Compugen-discovered immune checkpoint regulators.
     

F - 7


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 1:-
GENERAL (Cont.)
 
Under the terms of the Bayer Agreement, the Company received an upfront payment of $10,000, and additional aggregate milestone payments of approximately $23,000.
 
On November 29, 2022, Bayer notified the Company that it had resolved to terminate, effective as of February 27, 2023, the Bayer Agreement.
 
  e.
Effective March 30, 2018, the Company entered into an exclusive license agreement with MedImmune Limited, the global biologics research and development arm of AstraZeneca (“AstraZeneca”) to enable the development of bi-specific and multi-specific immuno-oncology antibody products. Under the terms of the agreement, Compugen provided an exclusive license to AstraZeneca for the development of bi-specific and multi-specific antibody products derived from COM902. AstraZeneca has the right to create multiple products under this license and is solely responsible for all research, development and commercial activities under the agreement. In connection with such license agreement, AstraZeneca developed rilvegostomig, a novel PD-/TIGIT bi-specific antibody with a TIGIT component that is derived from our COM902. Rilvegostomig entered the clinic in September 2021, initiated a Phase 3 with first patient dosing in the first indication Phase 3 study in December 2023, and first patient dosing in the second indication Phase 3 study in May 2024. Compugen received a $10,000 upfront payment and received or accrued $30,500 milestone payments out of up to $200,000 that the Company is eligible to receive in development, regulatory and commercial milestones for the first product as well as tiered royalties on future product sales. If additional products are developed, additional milestones and royalties would be due to Compugen for each product.
 
  f.
On October 10, 2018, the Company entered into a Master Clinical Trial Collaboration Agreement (the “Master Clinical Agreement”) with Bristol Myers Squibb Company (“Bristol Myers Squibb”) to evaluate the safety and tolerability of Compugen’s COM701 in combination with Bristol Myers Squibb’s PD-1 immune checkpoint inhibitor Opdivo® (nivolumab), in patients with advanced solid tumors.
 
Pursuant to the Master Clinical Agreement, as amended from time to time, Compugen sponsored the trials, which included the evaluation of the combination of COM701 and Opdivo® ± Bristol Myers Squibb investigational anti-TIGIT, BMS-986207. Bristol Myers Squibb and Compugen each supplies its own compound(s) for the studies.
 
In conjunction with the signing of the Master Clinical Agreement, Bristol Myers Squibb made a $12,000 investment in Compugen, see Note 7a.
 
Among several amendments to the Master Clinical Agreement, on November 10, 2021, the agreement was further amended and in conjunction with the signing of the amendment to the Agreement, Bristol Myers Squibb made a $20,000 investment in Compugen, see Note 7a.
 
On August 3, 2022, the Company and Bristol Myers Squibb entered into a letter agreement pursuant to which the Master Clinical Agreement, as amended from time to time, was terminated as of such date.
 

F - 8


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 1:-
GENERAL (Cont.)

 

  g.
On December 18, 2023, the Company entered into an exclusive license agreement (the “License Agreement”) with Gilead Sciences, Inc. (“Gilead”), pursuant to which the Company granted Gilead an exclusive license under the Company’s pre-clinical antibody program against IL-18 binding protein and all intellectual property rights subsisting therein, to use, research, develop, manufacture and commercialize products, including the Company’s COM503 product candidate (“COM503 License”), and additional products that may be so developed by Gilead (together with COM503, the “Licensed Products”).
 
Pursuant to the License Agreement, Gilead paid the Company a one-time, upfront payment of $60 million in January 2024. The Company has continued to develop COM503 during the initial development term, which included conducting activities defined within the agreement to advance COM503 through the clearance of an investigational new drug application (“IND”). The Company is eligible to receive from Gilead $30 million in the form of a milestone payment upon clearance of the IND for COM503, see also Note 12. The Company is also eligible to receive up to approximately $758 million in additional milestone payments upon the achievement of certain development, regulatory and commercial milestones. The Company is further eligible to receive single-digit to low double-digit tiered royalties on worldwide net sales of Licensed Products.

The Company will be responsible for conducting a Phase 1 clinical trial for COM503, including handling the regulatory matters in connection therewith, and will bear the costs of such trial (including the COM503 drug supply), with Gilead providing at no cost an anti- PD-1/PD-L1 antibody for such trial. In certain circumstances, Gilead may assume the role of conducting the Phase 1 clinical trial.

Upon completion of the Phase 1 clinical trial for COM503, the Company will initiate the transfer of development activities related to COM503 to Gilead, following which, Gilead will have sole responsibility to develop and commercialize the Licensed Products.
 
During the term of the License Agreement, the Company is prohibited from researching, developing, making, and commercializing any compounds, molecules, products or treatment methods that are directed to IL-18 or any companion diagnostics for an IL-18 product.
 
Unless terminated early by a party pursuant to its terms, the License Agreement will continue in effect on a Licensed Product-by-Licensed Product and country-by-country basis until the expiration of the last royalty term in such country.

Gilead withheld at source 15% from the upfront payment amount paid to the Company in January 2024 and is expected to continue and withhold at source all taxes required by law from all payments payable to the Company under the License Agreement.

The License Agreement contains customary representations, warranties, covenants, and terms governing the prosecution and enforcement of certain intellectual property and issues related to technology transfer, manufacturing transfer, provisions with respect to establishment of joint steering committee and its governance covenants with respect change of control and others.

 

F - 9


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 2:-
SIGNIFICANT ACCOUNTING POLICIES
 
   
These unaudited interim consolidated financial statements should be read in conjunction with the audited consolidated financial statements and accompanying notes for the year ended December 31, 2023. The significant accounting policies applied in the annual consolidated financial statements of the Company as of December 31, 2023, are applied consistently in these interim consolidated financial statements.
 
Recently Accounting Pronouncements
 
In November 2023, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires public entities to disclose information about their reportable segments’ significant expenses and other segment items on an interim and annual basis. Public entities with a single reportable segment are required to apply the disclosure requirements in ASU 2023-07, as well as all existing segment disclosures and reconciliation requirements in ASC 280 on an interim and annual basis. ASU 2023-07 is effective for fiscal years beginning after December 15, 2023, and for interim periods within fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-07.
 
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which requires public entities, on an annual basis, to provide disclosure of specific categories in the rate reconciliation, as well as disclosure of income taxes paid disaggregated by jurisdiction. ASU 2023-09 is effective for fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-09.

 

NOTE 3:-
UNAUDITED INTERIM CONSOLIDATED FINANCIAL STATEMENTS
 
The accompanying unaudited interim consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States for interim financial information. Accordingly, they do not include all the information and footnotes required by accounting principles generally accepted in the United States for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included.
 
Operating results for the six-month period ended June 30, 2024, are not necessarily indicative of the results that may be expected for the year ended December 31, 2024.

 

F - 10


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 4:-
MARKETABLE SECURITIES
 
The following is a summary of available-for-sale marketable securities as of June 30, 2024 and December 31, 2023
 
   
Amortized cost
   
Gross unrealized gains
   
Gross unrealized losses
   
 
 
Fair value
 
As of June 30, 2024:
                       
Available-for-sale – matures within one year:
                       
Governmental bonds
 
$
32,711
   
$
-
   
$
23
   
$
32,688
 
                                 
As of December 31, 2023:
                               
Available-for-sale – matures within one year:
                               
Governmental bonds
 
$
11,740
   
$
2
   
$
*
   
$
11,742
 
 
  *
Represents an amount lower than $1
 
The following table presents gross unrealized losses and fair values for those investments that were in an unrealized loss position as of June 30, 2024 and December 31, 2023, and the length of time that those investments have been in a continuous loss position:
 
   
Less than 12 months
   
12 months or greater
 
   
Fair value
   
Gross unrealized loss
   
Fair value
   
Gross
unrealized loss
 
                         
As of June 30, 2024
 
$
32,688
   
$
23
   
$
-
   
$
-
 
                                 
As of December 31, 2023
 
$
992
   
$
*
   
$
-
   
$
-
 
 
  *
Represents an amount lower than $1.
 
As of June 30, 2024, the Company had no significant unrealized losses related to marketable securities (which were accumulated in a period of less than 12 months) and determined the unrealized losses are not due to credit related losses, therefore, the Company did not record an allowance for credit losses for its available-for-sale marketable securities.
 
As of June 30, 2024, all of the Company’s available-for-sale marketable securities were due within one year.
 
The Company had no sales of marketable securities during the six-month periods ended June 30, 2024 and 2023, and accordingly no realized gains or losses were recorded.

 

F - 11


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 5:-
FAIR VALUE MEASUREMENTS

 

         
Fair value measurements
as of
 
Description
 
Fair Value
Hierarchy
   
June 30,
2024
   
June 30,
2023
 
   
 
   

Unaudited

   

Unaudited

 
Assets:
                       
Short-term investments:
                       
U.S. government bonds
 
Level 2
   
$
32,688
   
$
11,742
 
 
NOTE 6:-
COMMITMENTS AND CONTINGENCIES
 
  a.
The Company provided bank guarantees in the amount of $286 in favor of its offices and car leases in Israel.
 
  b.
Under the office of the Israel Innovation Authority of the Israeli Ministry of Industry, Trade and Labor, formerly known as the Office of the Chief Scientist (“IIA”), the Company is not obligated to repay any amounts received from the IIA if it does not generate any income from products which incorporate technologies which were funded by such research program(s).
 
If income is generated from products which incorporate technologies which were funded by a research program, the Company is committed to pay royalties at a rate of between 3% to 5% of future revenue generated from products that incorporate technologies that were funded by such research program(s), up to a maximum of 100% of the amount received, linked to the U.S. dollar (for grants received under programs approved subsequent to January 1, 1999, the maximum amount to be repaid is 100% plus interest at LIBOR until December 31, 2023, and from January 1, 2024, the 12 months Term SOFR interest). For the six-month periods ended June 30, 2024 and 2023, the Company recorded royalties to the IIA as cost of revenue in the consolidated statements of comprehensive loss in the amount of $ 278 and $ 0, respectively.
 
As of June 30, 2024, the Company’s aggregate contingent obligations for payments to IIA, based on royalty-bearing participation received or accrued, net of royalties paid or accrued, totaled $8,870.
 
  c.
On June 25, 2012, the Company entered into an Antibodies Discovery Collaboration Agreement (the “Antibodies Discovery Agreement”) with a U.S. antibody technology company (“mAb Technology Company”), providing an established source for fully human mAbs. Under the Antibodies Discovery Agreement, the mAb Technology Company is entitled to certain royalties that could be eliminated upon payment of certain one-time fees (all milestone and royalties payments referred together as “Contingent Fees”). For the six-month periods ended June 30, 2024 and 2023, the Company did not incur Contingent Fees.

 

F - 12


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 6:-
COMMITMENTS AND CONTINGENCIES (Cont.)

 

  d.
On May 9, 2012, the Company entered into agreement (the “May 2012 Agreement”) with a U.S. Business Development Strategic Advisor (“Advisor”) for the purpose of entering into transactions with pharma companies related to selected pipeline program candidates. Under the agreement, the Advisor was to be entitled to 4% of the cash considerations that may be received under such transactions.In 2014, the May 2012 Agreement was terminated, except with respect to certain payments arising from the Bayer Agreement which survive termination of the May 2012 Agreement until August 5, 2025.
 
The Bayer Agreement was terminated effective February 27, 2023 and no further payments to the Advisor are expected under the May 2012 Agreement.
 
For the six months ended June 30, 2024 and 2023, the Company has not paid nor accrued any expenses related to the May 2012 Agreement.
 
  e.
Effective as of January 5, 2018, the Company entered into a Commercial License Agreement (“CLA”) with a European cell line development company. Under the agreement the Company is required to pay an annual maintenance fee, certain amounts upon the occurrence of specified milestones events, and 1% royalties on annual net sales with respect to each commercialized product manufactured using the company’s cell line. Royalties due under the CLA are creditable against the annual maintenance fee. In addition, the Company may at any time prior to the occurrence of a specific milestone event buy-out the royalty payment obligations in a single fixed amount. For the six-month periods ended June 30, 2024 and 2023, the Company did not incur milestone payments. We also entered into a CLA in February 2024 with the European cell line development company for COM503. Under the agreement the Company is required to pay an annual maintenance fee and certain amounts upon the occurrence of specified milestones events.
 
  f.
Effective as of October 28, 2020, the Company entered into a collaboration agreement with a U.S. antibody discovery and optimization company for generation and optimization of therapeutic antibodies for the Company. Under the agreement, the Company is required to pay service fees per services performed and certain amounts upon the occurrence of specified milestones events, and single-digit percent royalties on annual net sales with respect to each product sold that comprises or contains one or more antibodies so generated or optimized. The royalty rate is dependent upon the product type and any third-party contribution. For the six-month periods ended June 30, 2024 and 2023 the Company did not incur milestone payments.

 

NOTE 7:-
SHAREHOLDERS' EQUITY
 
  a.
Issuance of Shares:
 
On June 14, 2018, the Company entered into an agreement in connection with a registered direct offering (the “Offering”) of an aggregate of 5,316,457 Ordinary Shares (the “RD Shares”) of the Company at a purchase price of $3.95 per RD Share. In connection with the issuance of the RD Shares, the Company also issued warrants to purchase an aggregate of up to 4,253,165 additional Ordinary Shares (the “Warrants”). The Warrants were exercisable at a price of $4.74 per Ordinary Share and had a term of five years from the date of issuance. The Offering was made pursuant to the Company’s Registration Statement. Proceeds from the Offering were $19,767 (net of $1,233 issuance expenses).
 

F - 13


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 7:-
SHAREHOLDERS’ EQUITY (Cont.)

 

During the period from January 1, 2021 through June 30, 2023, warrants to purchase an aggregate of 3,955,696 Ordinary Shares were exercised with proceeds of approximately $18,750, and the remaining warrants to purchase up to 297,469 Ordinary Shares expired in June 2023.
 
On October 10, 2018, the Company entered into a Master Clinical Trial Collaboration Agreement with Bristol Myers Squibb to evaluate the safety and tolerability of the Company’s COM701 in combination with Bristol Myers Squibb’s PD-1 immune checkpoint inhibitor Opdivo® (nivolumab), in patients with advanced solid tumors. In conjunction with the Master Clinical Agreement, Bristol Myers Squibb made a $12,000 equity investment in the Company.
 
Under the terms of the securities purchase agreement, Bristol Myers Squibb purchased 2,424,243 ordinary shares of the Company at a purchase price of $4.95 per share. The share price represented a 33% premium over the average closing price of the Company’s ordinary shares for twenty (20) Nasdaq trading days prior to the execution of the securities purchase agreement. The investment closed on October 12, 2018.
 
The premium over the fair market value in the amount of $4,121 represents the relative fair value of deferred participation of Bristol Myers Squibb in R&D expenses which are amortized over the period of the clinical trial based on the progress in the R&D, in accordance with ASC 808 “Collaborative Arrangements” and $7,788 (net of $91 issuance expenses) were considered equity investment.
 
In conjunction with the signing of the amendment to the Master Clinical Agreement in November 2021, Bristol Myers Squibb made a $20,000 investment in the Company, purchasing 2,332,815 ordinary shares of the Company at a purchase price of $8.57333 per share. The share price represented a 33% premium over the closing price of Company’s ordinary shares on the last Nasdaq trading day immediately prior to the execution of the securities purchase agreement.
 
The premium over the fair market value in the amount of $5,000 represents the relative fair value of deferred participation of Bristol Myers Squibb in R&D expenses (which are amortized over the period of the clinical trial, based on the progress in the R&D, in accordance with ASC 808 “Collaborative Arrangements”) and $14,958 (net of $42 issuance expenses) were considered equity investment.
 
In March 2020, the Company entered into an underwriting agreement with SVB Leerink LLC and Stifel, Nicolaus & Company, Incorporated, as representatives of the several underwriters relating to the issuance and sale in a public offering of 8,333,334 of the Company’s ordinary shares at a price to the public of $9.00 per share (and a price of $8.46 per share to the underwriters). Such shares were issued on March 16, 2020. In addition, the Company granted the underwriters a 30-day option to purchase additional ordinary shares at the price set forth above. On April 14, 2020, the Company issued and sold, pursuant to that underwriting agreement an additional 483,005 ordinary shares pursuant to the underwriters’ option specified above. The Company sold a total of 8,816,339 ordinary shares in the offering with proceeds of $74,147 (net of $5,200 issuance expenses).
 

F - 14


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 7:-
SHAREHOLDERS’ EQUITY (Cont.)

 

On January 31, 2023, the Company entered into a Sales Agreement with Leerink Partners LLC (previously known as SVB Securities LLC) (“Leerink Partners”), as sales agent, pursuant to which the Company may offer and sell, from time to time through Leerink Partners, its ordinary shares through an “at the market offering” (ATM). The offer and sale of our ordinary shares, if any, will be made pursuant to the Company’s shelf registration statement on Form F-3, as supplemented by a prospectus supplement. Pursuant to the applicable prospectus supplement, the Company may offer and sell up to $50,000 of its ordinary shares. As of June 30, 2024, 2,905,550 shares were issued and sold through the ATM, with proceeds of approximately $3,643 (net of $530 issuance expenses).
 
  b.
Share option plan:
 
Transactions related to the grant of options to employees, directors and non-employees under the Company’s 2010 Share Option Plan, as amended, during the six-month period ended June 30, 2024, were as follows:
 
   
Number of options
   
Weighted average exercise
price
   
Weighted average remaining contractual life
   
Aggregate intrinsic
value
 
         
$
   
Years
   
$
 
                             
Options outstanding at beginning of year
   
8,373,745
     
4.65
     
6.61
     
1,912
 
Options granted
   
40,500
     
2.08
                 
Options exercised
   
(1,744
)
   
0.84
                 
Options forfeited
   
(282,455
)
   
4.55
                 
Options expired
   
(140,000
)
   
8.08
                 
                                 
Options outstanding at end of year
   
7,990,046
     
4.58
     
6.19
     
1,205
 
                                 
Exercisable at end of year
   
5,245,345
     
5.68
     
4.99
     
124
 
 
During the six-month period ended June 30, 2024, the Company’s Board of Directors granted 40,500 options to purchase ordinary shares of the Company to employees. The exercise prices for such options range from $1.80 to $2.09 per share, with vesting to occur in up to four years.
 
The following table presents the assumptions used to estimate the fair value of the options granted in the periods presented:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Volatility
   
92.7%-95.9
%
   
75.9%-76.4
%
Risk-free interest rate
   
3.9%-4.5
%
   
3.3%-4.2
%
Dividend yield
   
0
%
   
0
%
Expected life (years)
   
4.02
     
5.0-5.1
 
 

F - 15


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 7:-
SHAREHOLDERS’ EQUITY (Cont.)

 

Weighted average fair value of options granted during the six-month periods ended June 30, 2024 and 2023 were $1.41 and $0.53, respectively.
 
During the six-month periods ended June 30, 2024 and 2023, the Company recorded share based compensation related to stock options in a total amount of $1,633 and $1,782, respectively.
 
As of June 30, 2024, the total unrecognized estimated compensation cost related to non-vested stock options granted prior to that date was $3,405 which is expected to be recognized over a weighted average period of approximately 1.85 years.
 
For the six months ended June 30, 2024 and 2023, the total weighted average number of shares related to outstanding options and warrants excluded from the calculations of diluted net loss per share were 8,002,799 and 7,460,568, respectively.
 
The stock-based compensation expenses related to stock options and ESPP are included as follows in the expense categories:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Research and development expenses
 
$
805
   
$
1,002
 
Marketing and business development expenses
   
43
     
(41
)
General and administrative expenses
   
785
     
821
 
                 
Financial and other income, net
 
$
1,633
   
$
1,782
 

 

NOTE 8:-
FINANCIAL INCOME, NET
 
 
 
Six months ended
June 30,
   
2024
   
2023
 
   
Unaudited
 
             
Interest income
 
$
1,770
   
$
1,671
 
Amortization of discount on marketable securities, net
   
796
     
15
 
Exchange rate differences and other
   
(38
)
   
11
 
                 
Financial and other income, net
 
$
2,528
   
$
1,697
 
 

F - 16


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 9:-
REVENUES
 
The following represents the total revenue for the six-month periods ended June 30, 2024 and 2023 by region based on the invoicing address of customers:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Revenue from sales to customers:
           
             
United States
 
$
4,261
   
$
-
 
Europe
   
5,000
     
-
 
                 
Total revenues
 
$
9,261
   
$
-
 
 
Contract Balances
 
Of the $ 36,541 of deferred revenue recorded as of December 31, 2023, the Company recognized $ 4,261 as revenue during the six months ended June 30, 2024. The Company had no deferred revenues as of December 31, 2022.
 
Remaining Performance Obligation
 
The Company’s remaining performance obligations are comprised of revenue not yet delivered. As of June 30, 2024, the aggregate amount of the transaction price allocated to remaining performance obligations was $32,280, that the Company expects to recognize as revenue. As of June 30, 2024, the Company expects to recognize 35% of its remaining performance obligations as revenue over the next 12 months.
 
NOTE 10:-
RELATED PARTY BALANCES AND TRANSACTIONS
 
Balances with related parties:
 
   
June 30,
2024
   
December 31,
2023
 
   
Unaudited
       
             
Trade and other payables (a)
 
$
22
   
$
53
 
 

F - 17


COMPUGEN LTD. AND ITS SUBSIDIARY

 

NOTES TO INTERIM CONSOLIDATED FINANCIAL STATEMENTS


U.S. dollars in thousands (except share and per share data)

 

NOTE 10:-
RELATED PARTY BALANCES AND TRANSACTIONS (Cont.)

 

Related parties' expenses:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Amounts charged to:
           
             
Research and development expenses (a)
 
$
74
   
$
70
 
 
  (a)
The Company incurred expenses for research and development services provided by related party for cancer studies in animal models, and breeding and maintenance of animals (mice) to support such studies.

 

NOTE 11:-
LOSSES PER SHARE
 
The following table sets forth the computation of basic and diluted losses per share for the six-month periods ended June 30, 2024 and 2023:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Numerator:
           
             
Net loss for basic and diluted loss per share
 
$
9,390
   
$
18,615
 
                 
Denominator:
               
                 
Weighted average number of ordinary shares
               
used in computing basic and diluted net loss per share
   
89,518,778
     
86,903,741
 
                 
Basic and diluted loss per ordinary share
 
$
(0.10
)
 
$
(0.21
)
 
NOTE 12:-
SUBSEQUENT EVENTS
 
On July 29, 2024, the Company announced that the U.S. Food and Drug Administration has cleared the IND application to initiate a Phase 1 trial for COM503, a potential first-in-class, high affinity anti-IL-18 binding protein antibody licensed to Gilead. The IND clearance triggered a $30,000 milestone payment from Gilead which is expected in the third quarter of 2024.
 
On July 31, 2024, following recommendation of the compensation committee, the Company’s board of directors increased the total number of shares reserved for issuance under the Company’s 2010 Plan by 300,000 and reduced the total number of shares reserved for issuance under the ESPP by 114,146 to zero.
 
F - 18

Exhibit 99.3

MANAGEMENT'S DISCUSSION AND ANALYSIS OF RESULTS OF OPERATIONS AND
FINANCIAL CONDITION
 
RESULTS OF OPERATIONS
 
Six months ended June 30, 2024 and 2023
 
Revenues. Revenues for the first six months of 2024 were approximately $9.3 million, compared with no revenues in the comparable period of 2023. The revenues for 2024 include the portion of the upfront payment from the license agreement with Gilead Sciences, Inc. (“Gilead”) allocated to the IND research and development activities and the clinical milestone from the license agreement with AstraZeneca in the amount of $5 million.
 
Cost of Revenues. Cost of revenues for the first six months of 2024 were approximately $3.7 million, compared with no cost of revenues in the comparable period of 2023.
 
Cost of revenues for the first six months of 2024 represents royalty payments in connection with our revenues and costs of the IND research and development activities.
 
Research and Development Expenses. Research and development, or R&D expenses decreased by approximately 17% to approximately $12.6 million for the first six months of 2024 from approximately $15.2 million for the comparable period of 2023. The decrease is mainly due to the classification of the IND research and development activities to cost of revenues and the classification of the set-up activities related to the COM503 Phase 1 clinical trial to prepaid expenses, offset by an increase in clinical trial expenses in the first six months of 2024. R&D expenses, as a percentage of total operating expenses, decreased to 72% for the first six months of 2024 from 75% for the comparable period of 2023.
 
Marketing and Business Development Expenses. Marketing and business development expenses amounted to approximately $0.2 million for the first six months of 2024 and 2023. Marketing and business development expenses, as a percentage of total operating expenses, were 1% for the first six months of 2024 and 2023.
 
General and Administrative Expenses. General and administrative expenses decreased by approximately 6% to approximately $4.7 million for the first six months of 2024 from approximately $5.0 million for the comparable period of 2023. The decrease is mainly due to a reduction in the cost of our D&O insurance premium. General and administrative expenses, as a percentage of total operating expenses, increased to 27% for the first six months of 2024 from 24% for the comparable period of 2023.

Financial and other Income, Net. Financial and other income, net, were approximately $2.5 million for the first six months of 2024 compared with approximately $1.7 million for the comparable period of 2023. The increase is mainly due to increased interest income due to a higher level of cash, deposit balances and marketable securities.
 


LIQUIDITY AND CAPITAL RESOURCES
 
Net Cash Provided By (Used in) Operating Activities. Net cash provided by operating activities was approximately $39.7 million in the first six months of 2024 compared with net cash used in operating activities of approximately $18.6 million in the comparable period of 2023. The higher net cash provided by operating activities during the first six months of 2024 is mainly due to the collection of the $61 million trade receivables during the first six months of 2024 from the upfront payment of Gilead pursuant to the license agreement therewith and milestone payment from AstraZeneca pursuant to the license agreement therewith.
 
Net Cash Provided by (Used in) Investing Activities. Net cash used in investing activities during the first six months of 2024 was approximately $42.3 million compared with net cash provided by investing activities of approximately $23.5 million in the comparable period of 2023. Changes in net cash provided by investing activities is mainly due to changes in the level of cash deposited or withdrawn from bank deposits and due to net investments in marketable securities. Net cash provided by (used in) investing activities is dependent on capital raising, cash needs to fund our operating activities and changes in the level of the Company’s cash and cash equivalents.

Net Cash Provided by Financing Activities. Net cash provided by financing activities was $0.6 million in the first six months of 2024 compared with $1.4 million in the comparable period of 2023. The lower net cash provided in the first six months of 2024 is due to lower net proceeds received from sales of ordinary shares in the first six months of 2024 under the Company’s existing at the market offering facility pursuant to a sales agreement with Leerink Partners.

Net Liquidity. Liquidity refers to liquid financial assets available to fund the Company’s business operations and pay for near-term obligations. These liquid financial assets mostly consist of cash and cash equivalents, as well as short-term bank deposits and investment in marketable securities. As of June 30, 2024, the Company had total cash, cash equivalents, restricted hort-term bank deposit, short-term bank deposits and investment in marketable securities of approximately $92.3 million.



v3.24.2.u1
Document and Entity Information
6 Months Ended
Jun. 30, 2024
Cover [Abstract]  
Entity Registrant Name COMPUGEN LTD.
Entity Central Index Key 0001119774
Current Fiscal Year End Date --12-31
Document Type 6-K
Amendment Flag false
Document Period End Date Jun. 30, 2024
Document Fiscal Period Focus Q2
Document Fiscal Year Focus 2024
Entity File Number 000-30902
Entity Address, Address Line One 26 Harokmim Street
Entity Address, City or Town Holon
Entity Address Country IL
Entity Address, Postal Zip Code 5885849
v3.24.2.u1
INTERIM CONSOLIDATED BALANCE SHEETS - USD ($)
$ in Thousands
Jun. 30, 2024
Dec. 31, 2023
CURRENT ASSETS:    
Cash and cash equivalents $ 11,877 $ 13,890
Restricted cash 0 365
Short-term bank deposits 47,439 25,053
Restricted short-term bank deposit 333 0
Investment in marketable securities 32,688 11,742
Trade receivables 5,000 61,000
Other accounts receivable and prepaid expenses 4,796 2,529
Total current assets 102,133 114,579
NON-CURRENT ASSETS:    
Long-term prepaid expenses 922 1,233
Severance pay fund 3,023 2,977
Operating lease right to use asset 3,061 1,329
Property and equipment, net 1,028 1,216
Total non-current assets 8,034 6,755
Total assets 110,167 121,334
CURRENT LIABILITIES:    
Trade payables 2,378 3,502
Short-term deferred revenues 11,252 11,149
Current maturity of operating lease liability 449 632
Accrued expenses 8,218 7,858
Other accounts payable and accrued expenses 2,472 3,125
Total current liabilities 24,769 26,266
NON- CURRENT LIABILITIES:    
Long-term deferred revenues 21,028 25,392
Long term operating lease liability 2,580 719
Accrued severance pay 3,450 3,398
Total non-current liabilities 27,058 29,509
COMMITMENTS AND CONTINGENT LIABILITIES
SHAREHOLDERS' EQUITY:    
Ordinary shares of NIS 0.01 par value: 200,000,000 shares authorized on June 30, 2024, and December 31, 2023; 89,531,937 and 89,237,465 shares issued and outstanding on June 30, 2024, and December 31, 2023, respectively 248 247
Additional paid-in capital 542,032 539,837
Accumulated other comprehensive income (loss) (23) 2
Accumulated deficit (483,917) (474,527)
Total shareholders' equity 58,340 65,559
Total liabilities and shareholders' equity $ 110,167 $ 121,334
v3.24.2.u1
INTERIM CONSOLIDATED BALANCE SHEETS (Parenthetical) - ₪ / shares
Jun. 30, 2024
Dec. 31, 2023
Statement of Financial Position [Abstract]    
Ordinary shares, par value per share ₪ 0.01 ₪ 0.01
Ordinary shares, shares authorized 200,000,000 200,000,000
Ordinary shares, shares issued 89,531,937 89,237,465
Ordinary shares, shares outstanding 89,531,937 89,237,465
v3.24.2.u1
INTERIM CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS (Unaudited) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Income Statement [Abstract]    
Revenues $ 9,261 $ 0
Cost of revenues 3,654 0
Gross profit 5,607 0
Operating expenses:    
Research and development expenses 12,593 15,206
Marketing and business development expenses 248 165
General and administrative expenses 4,670 4,977
Total operating expenses 17,511 20,348
Operating loss (11,904) (20,348)
Financial income, net 2,528 1,697
Loss before taxes on income (9,376) (18,651)
Tax benefit (expense) (14) 36
Net loss (9,390) (18,615)
Other comprehensive loss:    
Change in unrealized gains (losses) on marketable securities: Unrealized gains (losses) arising during the period, net (25) [1]
Total comprehensive loss $ (9,415) $ (18,615)
Basic net loss per share $ (0.1) $ (0.21)
Diluted net loss per share $ (0.1) $ (0.21)
Weighted average number of ordinary shares used in computing basic net loss per share 89,518,778 86,903,741
Weighted average number of ordinary shares used in computing diluted net loss per share 89,518,778 86,903,741
[1] Represents an amount lower than $ 1.
v3.24.2.u1
INTERIM STATEMENTS OF CHANGES IN SHAREHOLDERS' EQUITY - USD ($)
$ in Thousands
Ordinary shares [Member]
Additional paid-in capital [Member]
Accumulated other comprehensive income [Member]
Accumulated deficit [Member]
Total
Balance at Dec. 31, 2022 $ 240 $ 533,213 $ 0 $ (455,773) $ 77,680
Balance, shares at Dec. 31, 2022 86,624,643        
Issuance of shares, net $ 4 1,150   0 1,154
Issuance of shares, net, (in shares) 1,609,123        
Stock-based compensation issued to employees, directors and non-employees $ 0 1,782   0 1,782
Other comprehensive income (loss) from marketable securities, net 0 0 [1] 0 0
Net loss 0 0 0 (18,615) (18,615)
Balance at Jun. 30, 2023 $ 244 536,145 [1] (474,388) 62,001
Balance, shares at Jun. 30, 2023 88,233,766        
Balance at Dec. 31, 2023 $ 247 539,837 2 (474,527) $ 65,559
Balance, shares at Dec. 31, 2023 89,237,465       89,237,465
Options exercised [1] 1 0 0 $ 1
Share-Based Compensation Arrangement by Share-Based Payment Award, Options, Exercises in Period 1,744        
Issuance of shares, net $ 1 561 0 0 562
Issuance of shares, net, (in shares) 292,728        
Stock-based compensation issued to employees, directors and non-employees $ 0 1,633 0 0 1,633
Other comprehensive income (loss) from marketable securities, net 0 0 (25) 0 (25)
Net loss 0 0 0 (9,390) (9,390)
Balance at Jun. 30, 2024 $ 248 $ 542,032 $ (23) $ (483,917) $ 58,340
Balance, shares at Jun. 30, 2024 89,531,937       89,531,937
[1] Represents an amount lower than $ 1.
v3.24.2.u1
INTERIM CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Cash flows from operating activities:    
Net loss $ (9,390) $ (18,615)
Adjustments required to reconcile net loss to net cash used in operating activities:    
Stock-based compensation 1,633 1,782
Depreciation 238 237
Amortization of discount on marketable securities (796) (13)
Realized gain on sale of marketable securities, net 0 (2)
Increase in severance pay, net 6 3
Exchange rate differences loss (gain) on cash balances 12 44
Decrease in operating lease right of use asset 332 290
Increase in interest receivables and exchange differences on short-term bank deposits (299) (140)
Decrease in trade receivables 56,000 0
Increase in other accounts receivable and prepaid expenses (2,267) (448)
Decrease (increase) in long-term prepaid expenses 311 (13)
Decrease in trade payables (1,137) (85)
Decrease in other accounts payable and accrued expenses (293) (894)
Decrease in operating lease liability (386) (394)
Decrease in deferred revenues (4,261) 0
Decrease in deferred participation in R&D expenses 0 (325)
Net cash provided by (used in) operating activities 39,703 (18,573)
Cash flows from investing activities:    
Proceeds from maturity of short-term bank deposits 25,011 51,350
Investment in short-term bank deposits (47,086) (23,220)
Proceeds from maturity of marketable securities 15,825 1,000
Investment in marketable securities (36,000) (5,536)
Purchase of property and equipment (37) (63)
Net cash provided by (used in) investing activities (42,287) 23,531
Cash flows from financing activities:    
Proceeds from issuance of ordinary shares, net 562 1,351
Proceeds from exercise of options 1 0
Net cash provided by financing activities 563 1,351
Effect of exchange rate changes on cash (12) (44)
Increase (decrease) in cash, cash equivalents and restricted cash (2,033) 6,265
Cash, cash equivalents and restricted cash at the beginning of the period 13,910 11,421
Cash, cash equivalents and restricted cash at the end of the period 11,877 17,686
Supplemental disclosure of non-cash investing and financing activities:    
Purchase of property and equipment 13 (8)
Right-of-use asset obtained in exchange for operating lease liability 2,064 70
Issuance expenses $ 0 $ 197
v3.24.2.u1
GENERAL
6 Months Ended
Jun. 30, 2024
GENERAL [Abstract]  
GENERAL
NOTE 1:-
GENERAL
 
  a.
Compugen Ltd. (the “Company”) is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable predictive computational discovery capabilities to identify novel drug targets and new biological pathways to develop therapeutics in the field of cancer immunotherapy. The Company’s innovative immuno-oncology pipeline consists of three clinical stage programs, COM701, COM902 and rilvegostomig, targeting immune checkpoints the Company discovered computationally. Two programs that are pursued internally, COM701, a potential first-in-class anti-PVRIG antibody, and COM902, a potential best-in-class therapeutic anti-TIGIT antibody, are in Phase 1 clinical trials and have been evaluated for the treatment of solid tumors as a monotherapy and in combination of dual (PVRIG/PD-1, PVRIG/TIGIT) and triple (PVRIG/PD-1/TIGIT) blockade. Rilvegostomig, a novel anti PD-1/TIGIT bispecific antibody with a TIGIT specific component that is derived from the Company’s COM902 antibody, is being developed by AstraZeneca pursuant to an exclusive license agreement between the Company and AstraZeneca and is being evaluated in multiple clinical trials, including in Phase 3 clinical trials. The Company’s therapeutic pipeline of early-stage immuno-oncology programs consists of programs aiming to address various mechanisms of immune resistance. The Company’s most advanced early-stage program, COM503, was licensed to Gilead Sciences, Inc. (“Gilead”) in December 2023, see also Note 12. COM503 is a potential first-in-class, high affinity antibody, which blocks the interaction between IL-18 binding protein and IL-18, thereby freeing natural IL-18 in the tumor microenvironment to inhibit cancer growth. The Company’s business model is to selectively enter into collaborations for our novel targets and drug product candidates at various stages of research and development under various revenue-sharing arrangements.
     
  b.
The Company is headquartered in Holon, Israel.
 
  c.
The Company has incurred losses in the amount of $9,390 during the six months ended June 30, 2024, has an accumulated deficit of $483,917 as of June 30, 2024, and has an accumulated negative cash flow from operating activities in the amount of $39,703 for the six months ended June 30, 2024. The Company believes that its existing capital resources will be adequate to satisfy its expected liquidity requirements at the current level of yearly expenditures at least twelve months from the reporting date.
 
  d.
On August 5, 2013, the Company entered into a Research and Development Collaboration and License Agreement (“Bayer Agreement”) with Bayer Pharma AG (“Bayer”) for the research, development, and commercialization of antibody-based therapeutics against two novel Compugen-discovered immune checkpoint regulators.
     
Under the terms of the Bayer Agreement, the Company received an upfront payment of $10,000, and additional aggregate milestone payments of approximately $23,000.
 
On November 29, 2022, Bayer notified the Company that it had resolved to terminate, effective as of February 27, 2023, the Bayer Agreement.
 
  e.
Effective March 30, 2018, the Company entered into an exclusive license agreement with MedImmune Limited, the global biologics research and development arm of AstraZeneca (“AstraZeneca”) to enable the development of bi-specific and multi-specific immuno-oncology antibody products. Under the terms of the agreement, Compugen provided an exclusive license to AstraZeneca for the development of bi-specific and multi-specific antibody products derived from COM902. AstraZeneca has the right to create multiple products under this license and is solely responsible for all research, development and commercial activities under the agreement. In connection with such license agreement, AstraZeneca developed rilvegostomig, a novel PD-/TIGIT bi-specific antibody with a TIGIT component that is derived from our COM902. Rilvegostomig entered the clinic in September 2021, initiated a Phase 3 with first patient dosing in the first indication Phase 3 study in December 2023, and first patient dosing in the second indication Phase 3 study in May 2024. Compugen received a $10,000 upfront payment and received or accrued $30,500 milestone payments out of up to $200,000 that the Company is eligible to receive in development, regulatory and commercial milestones for the first product as well as tiered royalties on future product sales. If additional products are developed, additional milestones and royalties would be due to Compugen for each product.
 
  f.
On October 10, 2018, the Company entered into a Master Clinical Trial Collaboration Agreement (the “Master Clinical Agreement”) with Bristol Myers Squibb Company (“Bristol Myers Squibb”) to evaluate the safety and tolerability of Compugen’s COM701 in combination with Bristol Myers Squibb’s PD-1 immune checkpoint inhibitor Opdivo® (nivolumab), in patients with advanced solid tumors.
 
Pursuant to the Master Clinical Agreement, as amended from time to time, Compugen sponsored the trials, which included the evaluation of the combination of COM701 and Opdivo® ± Bristol Myers Squibb investigational anti-TIGIT, BMS-986207. Bristol Myers Squibb and Compugen each supplies its own compound(s) for the studies.
 
In conjunction with the signing of the Master Clinical Agreement, Bristol Myers Squibb made a $12,000 investment in Compugen, see Note 7a.
 
Among several amendments to the Master Clinical Agreement, on November 10, 2021, the agreement was further amended and in conjunction with the signing of the amendment to the Agreement, Bristol Myers Squibb made a $20,000 investment in Compugen, see Note 7a.
 
On August 3, 2022, the Company and Bristol Myers Squibb entered into a letter agreement pursuant to which the Master Clinical Agreement, as amended from time to time, was terminated as of such date.
 
  g.
On December 18, 2023, the Company entered into an exclusive license agreement (the “License Agreement”) with Gilead Sciences, Inc. (“Gilead”), pursuant to which the Company granted Gilead an exclusive license under the Company’s pre-clinical antibody program against IL-18 binding protein and all intellectual property rights subsisting therein, to use, research, develop, manufacture and commercialize products, including the Company’s COM503 product candidate (“COM503 License”), and additional products that may be so developed by Gilead (together with COM503, the “Licensed Products”).
 
Pursuant to the License Agreement, Gilead paid the Company a one-time, upfront payment of $60 million in January 2024. The Company has continued to develop COM503 during the initial development term, which included conducting activities defined within the agreement to advance COM503 through the clearance of an investigational new drug application (“IND”). The Company is eligible to receive from Gilead $30 million in the form of a milestone payment upon clearance of the IND for COM503, see also Note 12. The Company is also eligible to receive up to approximately $758 million in additional milestone payments upon the achievement of certain development, regulatory and commercial milestones. The Company is further eligible to receive single-digit to low double-digit tiered royalties on worldwide net sales of Licensed Products.

The Company will be responsible for conducting a Phase 1 clinical trial for COM503, including handling the regulatory matters in connection therewith, and will bear the costs of such trial (including the COM503 drug supply), with Gilead providing at no cost an anti- PD-1/PD-L1 antibody for such trial. In certain circumstances, Gilead may assume the role of conducting the Phase 1 clinical trial.

Upon completion of the Phase 1 clinical trial for COM503, the Company will initiate the transfer of development activities related to COM503 to Gilead, following which, Gilead will have sole responsibility to develop and commercialize the Licensed Products.
 
During the term of the License Agreement, the Company is prohibited from researching, developing, making, and commercializing any compounds, molecules, products or treatment methods that are directed to IL-18 or any companion diagnostics for an IL-18 product.
 
Unless terminated early by a party pursuant to its terms, the License Agreement will continue in effect on a Licensed Product-by-Licensed Product and country-by-country basis until the expiration of the last royalty term in such country.

Gilead withheld at source 15% from the upfront payment amount paid to the Company in January 2024 and is expected to continue and withhold at source all taxes required by law from all payments payable to the Company under the License Agreement.

The License Agreement contains customary representations, warranties, covenants, and terms governing the prosecution and enforcement of certain intellectual property and issues related to technology transfer, manufacturing transfer, provisions with respect to establishment of joint steering committee and its governance covenants with respect change of control and others.

 

v3.24.2.u1
SIGNIFICANT ACCOUNTING POLICIES
6 Months Ended
Jun. 30, 2024
SIGNIFICANT ACCOUNTING POLICIES [Abstract]  
SIGNIFICANT ACCOUNTING POLICIES
NOTE 2:-
SIGNIFICANT ACCOUNTING POLICIES
 
   
These unaudited interim consolidated financial statements should be read in conjunction with the audited consolidated financial statements and accompanying notes for the year ended December 31, 2023. The significant accounting policies applied in the annual consolidated financial statements of the Company as of December 31, 2023, are applied consistently in these interim consolidated financial statements.
 
Recently Accounting Pronouncements
 
In November 2023, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires public entities to disclose information about their reportable segments’ significant expenses and other segment items on an interim and annual basis. Public entities with a single reportable segment are required to apply the disclosure requirements in ASU 2023-07, as well as all existing segment disclosures and reconciliation requirements in ASC 280 on an interim and annual basis. ASU 2023-07 is effective for fiscal years beginning after December 15, 2023, and for interim periods within fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-07.
 
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which requires public entities, on an annual basis, to provide disclosure of specific categories in the rate reconciliation, as well as disclosure of income taxes paid disaggregated by jurisdiction. ASU 2023-09 is effective for fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-09.
v3.24.2.u1
UNAUDITED INTERIM CONSOLIDATED FINANCIAL STATEMENTS
6 Months Ended
Jun. 30, 2024
Unaudited Interim Consolidated Financial Statements [Abstract]  
UNAUDITED INTERIM CONSOLIDATED FINANCIAL STATEMENTS
NOTE 3:-
UNAUDITED INTERIM CONSOLIDATED FINANCIAL STATEMENTS
 
The accompanying unaudited interim consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States for interim financial information. Accordingly, they do not include all the information and footnotes required by accounting principles generally accepted in the United States for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included.
 
Operating results for the six-month period ended June 30, 2024, are not necessarily indicative of the results that may be expected for the year ended December 31, 2024.
v3.24.2.u1
MARKETABLE SECURITIES
6 Months Ended
Jun. 30, 2024
Investments, Debt and Equity Securities [Abstract]  
MARKETABLE SECURITIES
NOTE 4:-
MARKETABLE SECURITIES
 
The following is a summary of available-for-sale marketable securities as of June 30, 2024 and December 31, 2023
 
   
Amortized cost
   
Gross unrealized gains
   
Gross unrealized losses
   
 
 
Fair value
 
As of June 30, 2024:
                       
Available-for-sale – matures within one year:
                       
Governmental bonds
 
$
32,711
   
$
-
   
$
23
   
$
32,688
 
                                 
As of December 31, 2023:
                               
Available-for-sale – matures within one year:
                               
Governmental bonds
 
$
11,740
   
$
2
   
$
*
   
$
11,742
 
 
  *
Represents an amount lower than $1
 
The following table presents gross unrealized losses and fair values for those investments that were in an unrealized loss position as of June 30, 2024 and December 31, 2023, and the length of time that those investments have been in a continuous loss position:
 
   
Less than 12 months
   
12 months or greater
 
   
Fair value
   
Gross unrealized loss
   
Fair value
   
Gross
unrealized loss
 
                         
As of June 30, 2024
 
$
32,688
   
$
23
   
$
-
   
$
-
 
                                 
As of December 31, 2023
 
$
992
   
$
*
   
$
-
   
$
-
 
 
  *
Represents an amount lower than $1.
 
As of June 30, 2024, the Company had no significant unrealized losses related to marketable securities (which were accumulated in a period of less than 12 months) and determined the unrealized losses are not due to credit related losses, therefore, the Company did not record an allowance for credit losses for its available-for-sale marketable securities.
 
As of June 30, 2024, all of the Company’s available-for-sale marketable securities were due within one year.
 
The Company had no sales of marketable securities during the six-month periods ended June 30, 2024 and 2023, and accordingly no realized gains or losses were recorded.
v3.24.2.u1
FAIR VALUE MEASUREMENTS
6 Months Ended
Jun. 30, 2024
Fair Value Disclosures [Abstract]  
FAIR VALUE MEASUREMENTS
NOTE 5:-
FAIR VALUE MEASUREMENTS

 

         
Fair value measurements
as of
 
Description
 
Fair Value
Hierarchy
   
June 30,
2024
   
June 30,
2023
 
   
 
   

Unaudited

   

Unaudited

 
Assets:
                       
Short-term investments:
                       
U.S. government bonds
 
Level 2
   
$
32,688
   
$
11,742
 
 
v3.24.2.u1
COMMITMENTS AND CONTINGENCIES
6 Months Ended
Jun. 30, 2024
COMMITMENTS AND CONTINGENCIES [Abstract]  
COMMITMENTS AND CONTINGENCIES
NOTE 6:-
COMMITMENTS AND CONTINGENCIES
 
  a.
The Company provided bank guarantees in the amount of $286 in favor of its offices and car leases in Israel.
 
  b.
Under the office of the Israel Innovation Authority of the Israeli Ministry of Industry, Trade and Labor, formerly known as the Office of the Chief Scientist (“IIA”), the Company is not obligated to repay any amounts received from the IIA if it does not generate any income from products which incorporate technologies which were funded by such research program(s).
 
If income is generated from products which incorporate technologies which were funded by a research program, the Company is committed to pay royalties at a rate of between 3% to 5% of future revenue generated from products that incorporate technologies that were funded by such research program(s), up to a maximum of 100% of the amount received, linked to the U.S. dollar (for grants received under programs approved subsequent to January 1, 1999, the maximum amount to be repaid is 100% plus interest at LIBOR until December 31, 2023, and from January 1, 2024, the 12 months Term SOFR interest). For the six-month periods ended June 30, 2024 and 2023, the Company recorded royalties to the IIA as cost of revenue in the consolidated statements of comprehensive loss in the amount of $ 278 and $ 0, respectively.
 
As of June 30, 2024, the Company’s aggregate contingent obligations for payments to IIA, based on royalty-bearing participation received or accrued, net of royalties paid or accrued, totaled $8,870.
 
  c.
On June 25, 2012, the Company entered into an Antibodies Discovery Collaboration Agreement (the “Antibodies Discovery Agreement”) with a U.S. antibody technology company (“mAb Technology Company”), providing an established source for fully human mAbs. Under the Antibodies Discovery Agreement, the mAb Technology Company is entitled to certain royalties that could be eliminated upon payment of certain one-time fees (all milestone and royalties payments referred together as “Contingent Fees”). For the six-month periods ended June 30, 2024 and 2023, the Company did not incur Contingent Fees.

 

  d.
On May 9, 2012, the Company entered into agreement (the “May 2012 Agreement”) with a U.S. Business Development Strategic Advisor (“Advisor”) for the purpose of entering into transactions with pharma companies related to selected pipeline program candidates. Under the agreement, the Advisor was to be entitled to 4% of the cash considerations that may be received under such transactions.In 2014, the May 2012 Agreement was terminated, except with respect to certain payments arising from the Bayer Agreement which survive termination of the May 2012 Agreement until August 5, 2025.
 
The Bayer Agreement was terminated effective February 27, 2023 and no further payments to the Advisor are expected under the May 2012 Agreement.
 
For the six months ended June 30, 2024 and 2023, the Company has not paid nor accrued any expenses related to the May 2012 Agreement.
 
  e.
Effective as of January 5, 2018, the Company entered into a Commercial License Agreement (“CLA”) with a European cell line development company. Under the agreement the Company is required to pay an annual maintenance fee, certain amounts upon the occurrence of specified milestones events, and 1% royalties on annual net sales with respect to each commercialized product manufactured using the company’s cell line. Royalties due under the CLA are creditable against the annual maintenance fee. In addition, the Company may at any time prior to the occurrence of a specific milestone event buy-out the royalty payment obligations in a single fixed amount. For the six-month periods ended June 30, 2024 and 2023, the Company did not incur milestone payments. We also entered into a CLA in February 2024 with the European cell line development company for COM503. Under the agreement the Company is required to pay an annual maintenance fee and certain amounts upon the occurrence of specified milestones events.
 
  f.
Effective as of October 28, 2020, the Company entered into a collaboration agreement with a U.S. antibody discovery and optimization company for generation and optimization of therapeutic antibodies for the Company. Under the agreement, the Company is required to pay service fees per services performed and certain amounts upon the occurrence of specified milestones events, and single-digit percent royalties on annual net sales with respect to each product sold that comprises or contains one or more antibodies so generated or optimized. The royalty rate is dependent upon the product type and any third-party contribution. For the six-month periods ended June 30, 2024 and 2023 the Company did not incur milestone payments.
v3.24.2.u1
SHAREHOLDERS' EQUITY
6 Months Ended
Jun. 30, 2024
Stockholders' Equity Note [Abstract]  
SHAREHOLDERS' EQUITY
NOTE 7:-
SHAREHOLDERS' EQUITY
 
  a.
Issuance of Shares:
 
On June 14, 2018, the Company entered into an agreement in connection with a registered direct offering (the “Offering”) of an aggregate of 5,316,457 Ordinary Shares (the “RD Shares”) of the Company at a purchase price of $3.95 per RD Share. In connection with the issuance of the RD Shares, the Company also issued warrants to purchase an aggregate of up to 4,253,165 additional Ordinary Shares (the “Warrants”). The Warrants were exercisable at a price of $4.74 per Ordinary Share and had a term of five years from the date of issuance. The Offering was made pursuant to the Company’s Registration Statement. Proceeds from the Offering were $19,767 (net of $1,233 issuance expenses).
 
During the period from January 1, 2021 through June 30, 2023, warrants to purchase an aggregate of 3,955,696 Ordinary Shares were exercised with proceeds of approximately $18,750, and the remaining warrants to purchase up to 297,469 Ordinary Shares expired in June 2023.
 
On October 10, 2018, the Company entered into a Master Clinical Trial Collaboration Agreement with Bristol Myers Squibb to evaluate the safety and tolerability of the Company’s COM701 in combination with Bristol Myers Squibb’s PD-1 immune checkpoint inhibitor Opdivo® (nivolumab), in patients with advanced solid tumors. In conjunction with the Master Clinical Agreement, Bristol Myers Squibb made a $12,000 equity investment in the Company.
 
Under the terms of the securities purchase agreement, Bristol Myers Squibb purchased 2,424,243 ordinary shares of the Company at a purchase price of $4.95 per share. The share price represented a 33% premium over the average closing price of the Company’s ordinary shares for twenty (20) Nasdaq trading days prior to the execution of the securities purchase agreement. The investment closed on October 12, 2018.
 
The premium over the fair market value in the amount of $4,121 represents the relative fair value of deferred participation of Bristol Myers Squibb in R&D expenses which are amortized over the period of the clinical trial based on the progress in the R&D, in accordance with ASC 808 “Collaborative Arrangements” and $7,788 (net of $91 issuance expenses) were considered equity investment.
 
In conjunction with the signing of the amendment to the Master Clinical Agreement in November 2021, Bristol Myers Squibb made a $20,000 investment in the Company, purchasing 2,332,815 ordinary shares of the Company at a purchase price of $8.57333 per share. The share price represented a 33% premium over the closing price of Company’s ordinary shares on the last Nasdaq trading day immediately prior to the execution of the securities purchase agreement.
 
The premium over the fair market value in the amount of $5,000 represents the relative fair value of deferred participation of Bristol Myers Squibb in R&D expenses (which are amortized over the period of the clinical trial, based on the progress in the R&D, in accordance with ASC 808 “Collaborative Arrangements”) and $14,958 (net of $42 issuance expenses) were considered equity investment.
 
In March 2020, the Company entered into an underwriting agreement with SVB Leerink LLC and Stifel, Nicolaus & Company, Incorporated, as representatives of the several underwriters relating to the issuance and sale in a public offering of 8,333,334 of the Company’s ordinary shares at a price to the public of $9.00 per share (and a price of $8.46 per share to the underwriters). Such shares were issued on March 16, 2020. In addition, the Company granted the underwriters a 30-day option to purchase additional ordinary shares at the price set forth above. On April 14, 2020, the Company issued and sold, pursuant to that underwriting agreement an additional 483,005 ordinary shares pursuant to the underwriters’ option specified above. The Company sold a total of 8,816,339 ordinary shares in the offering with proceeds of $74,147 (net of $5,200 issuance expenses).
 
On January 31, 2023, the Company entered into a Sales Agreement with Leerink Partners LLC (previously known as SVB Securities LLC) (“Leerink Partners”), as sales agent, pursuant to which the Company may offer and sell, from time to time through Leerink Partners, its ordinary shares through an “at the market offering” (ATM). The offer and sale of our ordinary shares, if any, will be made pursuant to the Company’s shelf registration statement on Form F-3, as supplemented by a prospectus supplement. Pursuant to the applicable prospectus supplement, the Company may offer and sell up to $50,000 of its ordinary shares. As of June 30, 2024, 2,905,550 shares were issued and sold through the ATM, with proceeds of approximately $3,643 (net of $530 issuance expenses).
 
  b.
Share option plan:
 
Transactions related to the grant of options to employees, directors and non-employees under the Company’s 2010 Share Option Plan, as amended, during the six-month period ended June 30, 2024, were as follows:
 
   
Number of options
   
Weighted average exercise
price
   
Weighted average remaining contractual life
   
Aggregate intrinsic
value
 
         
$
   
Years
   
$
 
                             
Options outstanding at beginning of year
   
8,373,745
     
4.65
     
6.61
     
1,912
 
Options granted
   
40,500
     
2.08
                 
Options exercised
   
(1,744
)
   
0.84
                 
Options forfeited
   
(282,455
)
   
4.55
                 
Options expired
   
(140,000
)
   
8.08
                 
                                 
Options outstanding at end of year
   
7,990,046
     
4.58
     
6.19
     
1,205
 
                                 
Exercisable at end of year
   
5,245,345
     
5.68
     
4.99
     
124
 
 
During the six-month period ended June 30, 2024, the Company’s Board of Directors granted 40,500 options to purchase ordinary shares of the Company to employees. The exercise prices for such options range from $1.80 to $2.09 per share, with vesting to occur in up to four years.
 
The following table presents the assumptions used to estimate the fair value of the options granted in the periods presented:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Volatility
   
92.7%-95.9
%
   
75.9%-76.4
%
Risk-free interest rate
   
3.9%-4.5
%
   
3.3%-4.2
%
Dividend yield
   
0
%
   
0
%
Expected life (years)
   
4.02
     
5.0-5.1
 
 
Weighted average fair value of options granted during the six-month periods ended June 30, 2024 and 2023 were $1.41 and $0.53, respectively.
 
During the six-month periods ended June 30, 2024 and 2023, the Company recorded share based compensation related to stock options in a total amount of $1,633 and $1,782, respectively.
 
As of June 30, 2024, the total unrecognized estimated compensation cost related to non-vested stock options granted prior to that date was $3,405 which is expected to be recognized over a weighted average period of approximately 1.85 years.
 
For the six months ended June 30, 2024 and 2023, the total weighted average number of shares related to outstanding options and warrants excluded from the calculations of diluted net loss per share were 8,002,799 and 7,460,568, respectively.
 
The stock-based compensation expenses related to stock options and ESPP are included as follows in the expense categories:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Research and development expenses
 
$
805
   
$
1,002
 
Marketing and business development expenses
   
43
     
(41
)
General and administrative expenses
   
785
     
821
 
                 
Financial and other income, net
 
$
1,633
   
$
1,782
 
v3.24.2.u1
FINANCIAL INCOME, NET
6 Months Ended
Jun. 30, 2024
FINANCIAL AND OTHER INCOME, NET [Abstract]  
FINANCIAL INCOME, NET
NOTE 8:-
FINANCIAL INCOME, NET
 
 
 
Six months ended
June 30,
   
2024
   
2023
 
   
Unaudited
 
             
Interest income
 
$
1,770
   
$
1,671
 
Amortization of discount on marketable securities, net
   
796
     
15
 
Exchange rate differences and other
   
(38
)
   
11
 
                 
Financial and other income, net
 
$
2,528
   
$
1,697
 
v3.24.2.u1
REVENUES
6 Months Ended
Jun. 30, 2024
Revenue [Abstract]  
REVENUES
NOTE 9:-
REVENUES
 
The following represents the total revenue for the six-month periods ended June 30, 2024 and 2023 by region based on the invoicing address of customers:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Revenue from sales to customers:
           
             
United States
 
$
4,261
   
$
-
 
Europe
   
5,000
     
-
 
                 
Total revenues
 
$
9,261
   
$
-
 
 
Contract Balances
 
Of the $ 36,541 of deferred revenue recorded as of December 31, 2023, the Company recognized $ 4,261 as revenue during the six months ended June 30, 2024. The Company had no deferred revenues as of December 31, 2022.
 
Remaining Performance Obligation
 
The Company’s remaining performance obligations are comprised of revenue not yet delivered. As of June 30, 2024, the aggregate amount of the transaction price allocated to remaining performance obligations was $32,280, that the Company expects to recognize as revenue. As of June 30, 2024, the Company expects to recognize 35% of its remaining performance obligations as revenue over the next 12 months.
v3.24.2.u1
RELATED PARTY BALANCES AND TRANSACTIONS
6 Months Ended
Jun. 30, 2024
RELATED PARTY BALANCES AND TRANSACTIONS [Abstract]  
RELATED PARTY BALANCES AND TRANSACTIONS
NOTE 10:-
RELATED PARTY BALANCES AND TRANSACTIONS
 
Balances with related parties:
 
   
June 30,
2024
   
December 31,
2023
 
   
Unaudited
       
             
Trade and other payables (a)
 
$
22
   
$
53
 
 
Related parties' expenses:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Amounts charged to:
           
             
Research and development expenses (a)
 
$
74
   
$
70
 
 
  (a)
The Company incurred expenses for research and development services provided by related party for cancer studies in animal models, and breeding and maintenance of animals (mice) to support such studies.
v3.24.2.u1
LOSSES PER SHARE
6 Months Ended
Jun. 30, 2024
Earnings Per Share [Abstract]  
LOSSES PER SHARE
NOTE 11:-
LOSSES PER SHARE
 
The following table sets forth the computation of basic and diluted losses per share for the six-month periods ended June 30, 2024 and 2023:
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Numerator:
           
             
Net loss for basic and diluted loss per share
 
$
9,390
   
$
18,615
 
                 
Denominator:
               
                 
Weighted average number of ordinary shares
               
used in computing basic and diluted net loss per share
   
89,518,778
     
86,903,741
 
                 
Basic and diluted loss per ordinary share
 
$
(0.10
)
 
$
(0.21
)
v3.24.2.u1
SUBSEQUENT EVENTS
6 Months Ended
Jun. 30, 2024
Subsequent Events [Abstract]  
SUBSEQUENT EVENTS
NOTE 12:-
SUBSEQUENT EVENTS
 
On July 29, 2024, the Company announced that the U.S. Food and Drug Administration has cleared the IND application to initiate a Phase 1 trial for COM503, a potential first-in-class, high affinity anti-IL-18 binding protein antibody licensed to Gilead. The IND clearance triggered a $30,000 milestone payment from Gilead which is expected in the third quarter of 2024.
 
On July 31, 2024, following recommendation of the compensation committee, the Company’s board of directors increased the total number of shares reserved for issuance under the Company’s 2010 Plan by 300,000 and reduced the total number of shares reserved for issuance under the ESPP by 114,146 to zero.
v3.24.2.u1
SIGNIFICANT ACCOUNTING POLICIES (Policies)
6 Months Ended
Jun. 30, 2024
SIGNIFICANT ACCOUNTING POLICIES [Abstract]  
Recently adopted accounting pronouncements
Recently Accounting Pronouncements
 
In November 2023, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires public entities to disclose information about their reportable segments’ significant expenses and other segment items on an interim and annual basis. Public entities with a single reportable segment are required to apply the disclosure requirements in ASU 2023-07, as well as all existing segment disclosures and reconciliation requirements in ASC 280 on an interim and annual basis. ASU 2023-07 is effective for fiscal years beginning after December 15, 2023, and for interim periods within fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-07.
 
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which requires public entities, on an annual basis, to provide disclosure of specific categories in the rate reconciliation, as well as disclosure of income taxes paid disaggregated by jurisdiction. ASU 2023-09 is effective for fiscal years beginning after December 15, 2024, with early adoption permitted. The Company is currently evaluating the impact of adopting ASU 2023-09.
v3.24.2.u1
MARKETABLE SECURITIES (Tables)
6 Months Ended
Jun. 30, 2024
Investments, Debt and Equity Securities [Abstract]  
Schedule of available-for-sale marketable securities
   
Amortized cost
   
Gross unrealized gains
   
Gross unrealized losses
   
 
 
Fair value
 
As of June 30, 2024:
                       
Available-for-sale – matures within one year:
                       
Governmental bonds
 
$
32,711
   
$
-
   
$
23
   
$
32,688
 
                                 
As of December 31, 2023:
                               
Available-for-sale – matures within one year:
                               
Governmental bonds
 
$
11,740
   
$
2
   
$
*
   
$
11,742
 
 
  *
Represents an amount lower than $1
Schedule of unrealized loss on investments
   
Less than 12 months
   
12 months or greater
 
   
Fair value
   
Gross unrealized loss
   
Fair value
   
Gross
unrealized loss
 
                         
As of June 30, 2024
 
$
32,688
   
$
23
   
$
-
   
$
-
 
                                 
As of December 31, 2023
 
$
992
   
$
*
   
$
-
   
$
-
 
 
  *
Represents an amount lower than $1.
v3.24.2.u1
FAIR VALUE MEASUREMENTS (Tables)
6 Months Ended
Jun. 30, 2024
Fair Value Disclosures [Abstract]  
Schedule of fair value measurements
         
Fair value measurements
as of
 
Description
 
Fair Value
Hierarchy
   
June 30,
2024
   
June 30,
2023
 
   
 
   

Unaudited

   

Unaudited

 
Assets:
                       
Short-term investments:
                       
U.S. government bonds
 
Level 2
   
$
32,688
   
$
11,742
 
 
v3.24.2.u1
SHAREHOLDERS' EQUITY (Tables)
6 Months Ended
Jun. 30, 2024
Schedule of option activity
   
Number of options
   
Weighted average exercise
price
   
Weighted average remaining contractual life
   
Aggregate intrinsic
value
 
         
$
   
Years
   
$
 
                             
Options outstanding at beginning of year
   
8,373,745
     
4.65
     
6.61
     
1,912
 
Options granted
   
40,500
     
2.08
                 
Options exercised
   
(1,744
)
   
0.84
                 
Options forfeited
   
(282,455
)
   
4.55
                 
Options expired
   
(140,000
)
   
8.08
                 
                                 
Options outstanding at end of year
   
7,990,046
     
4.58
     
6.19
     
1,205
 
                                 
Exercisable at end of year
   
5,245,345
     
5.68
     
4.99
     
124
 
Schedule of weighted-average assumptions used to estimate fair value of options granted
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Volatility
   
92.7%-95.9
%
   
75.9%-76.4
%
Risk-free interest rate
   
3.9%-4.5
%
   
3.3%-4.2
%
Dividend yield
   
0
%
   
0
%
Expected life (years)
   
4.02
     
5.0-5.1
 
Schedule of stock-based compensation expenses
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
             
Research and development expenses
 
$
805
   
$
1,002
 
Marketing and business development expenses
   
43
     
(41
)
General and administrative expenses
   
785
     
821
 
                 
Financial and other income, net
 
$
1,633
   
$
1,782
 
v3.24.2.u1
FINANCIAL INCOME, NET (Tables)
6 Months Ended
Jun. 30, 2024
FINANCIAL AND OTHER INCOME, NET [Abstract]  
Schedule of financial and other income, net
 
 
Six months ended
June 30,
   
2024
   
2023
 
   
Unaudited
 
             
Interest income
 
$
1,770
   
$
1,671
 
Amortization of discount on marketable securities, net
   
796
     
15
 
Exchange rate differences and other
   
(38
)
   
11
 
                 
Financial and other income, net
 
$
2,528
   
$
1,697
 
v3.24.2.u1
REVENUES (Tables)
6 Months Ended
Jun. 30, 2024
Revenue [Abstract]  
Schedule of revenue
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Revenue from sales to customers:
           
             
United States
 
$
4,261
   
$
-
 
Europe
   
5,000
     
-
 
                 
Total revenues
 
$
9,261
   
$
-
 
v3.24.2.u1
RELATED PARTY BALANCES AND TRANSACTIONS (Tables)
6 Months Ended
Jun. 30, 2024
Related Party Balances And Transactions Abstract  
Schedule of related party balances and transactions
   
June 30,
2024
   
December 31,
2023
 
   
Unaudited
       
             
Trade and other payables (a)
 
$
22
   
$
53
 
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Amounts charged to:
           
             
Research and development expenses (a)
 
$
74
   
$
70
 
v3.24.2.u1
LOSSES PER SHARE (Tables)
6 Months Ended
Jun. 30, 2024
Earnings Per Share [Abstract]  
Schedule of computation of basic and diluted losses per share
   
Six months ended
June 30,
 
   
2024
   
2023
 
   
Unaudited
 
Numerator:
           
             
Net loss for basic and diluted loss per share
 
$
9,390
   
$
18,615
 
                 
Denominator:
               
                 
Weighted average number of ordinary shares
               
used in computing basic and diluted net loss per share
   
89,518,778
     
86,903,741
 
                 
Basic and diluted loss per ordinary share
 
$
(0.10
)
 
$
(0.21
)
v3.24.2.u1
GENERAL (Details) - USD ($)
$ in Thousands
1 Months Ended 6 Months Ended
Aug. 05, 2013
Jan. 31, 2024
Mar. 30, 2018
Jun. 30, 2024
Jun. 30, 2023
Dec. 31, 2023
Dec. 18, 2023
Nov. 10, 2021
Oct. 10, 2018
GENERAL [Abstract]                  
Net loss       $ 9,390 $ 18,615        
Accumulated deficit       483,917   $ 474,527      
Net cash used in operating activities       $ 39,703 $ (18,573)        
Upfront payment received $ 10,000   $ 10,000            
Preclinical milestone compensation $ 23,000                
Accrued milestone payment     30,500            
Potential milestone compensation     $ 200,000            
Amount of investment in Compugen               $ 20,000 $ 12,000
Non-refundable upfront payment   $ 60,000              
Milestone payment   $ 30,000              
Potential milestone compensation company is now eligible for             $ 758,000    
Percentage of expected from upfront payment amount paid   15.00%              
v3.24.2.u1
MARKETABLE SECURITIES (Schedule of available-for-sale marketable securities) (Details) - Governmental bonds [Member] - USD ($)
$ in Thousands
Jun. 30, 2024
Dec. 31, 2023
Debt Securities, Available-for-Sale [Line Items]    
Amortized cost $ 32,711 $ 11,740
Gross unrealized gains 0 2
Gross unrealized losses 23 [1]
Fair value $ 32,688 $ 11,742
[1] Represents an amount lower than $1
v3.24.2.u1
MARKETABLE SECURITIES (Schedule of gross unrealized losses and fair values on investments) (Details) - USD ($)
$ in Thousands
Jun. 30, 2024
Dec. 31, 2023
Investments, Debt and Equity Securities [Abstract]    
Available-for-Sale Securities, fair value, less than 12 months $ 32,688 $ 992
Available-for-Sale Securities, gross unrealized losses, less than 12 months 23 [1]
Available-for-Sale Securities, fair value, greater than 12 months 0 0
Available-for-Sale Securities, gross unrealized losses, less than 12 months $ 0 $ 0
[1] Represents an amount lower than $1.
v3.24.2.u1
FAIR VALUE MEASUREMENTS (Details) - USD ($)
$ in Thousands
Jun. 30, 2024
Jun. 30, 2023
Fair Value, Inputs, Level 2 [Member] | U.S. government bonds [Member]    
Short-term investments:    
Investment in marketable securities $ 32,688 $ 11,742
v3.24.2.u1
COMMITMENTS AND CONTINGENCIES (Narrative) (Details) - USD ($)
$ in Thousands
6 Months Ended
Jan. 05, 2018
Jun. 30, 2024
Jun. 30, 2023
Government and Other Grants [Line Items]      
Bank guarantees in favor of lessor, foreign currency derivative contracts and credit card security   $ 286  
May 2012 Agreement [Member]      
Government and Other Grants [Line Items]      
Participation Rights   4.00%  
Agreement, start date   May 09, 2012  
Agreement termination description   In 2014, the May 2012 Agreement was terminated, except with respect to certain payments arising from the Bayer Agreement which survive termination of the May 2012 Agreement until August 5, 2025.  
Commercial License Agreement [Member]      
Government and Other Grants [Line Items]      
Percentage of royalties on net sales 1.00%    
Government and Other Grants [Member]      
Government and Other Grants [Line Items]      
Maximum royalty repaid as percentage of grant received   100.00%  
Royalties paid to the IIA   $ 278 $ 0
Royalty Contingent Obligations   $ 8,870  
Government and Other Grants [Member] | Minimum [Member]      
Government and Other Grants [Line Items]      
Royalty percentage based on future revenues   3.00%  
Government and Other Grants [Member] | Maximum [Member]      
Government and Other Grants [Line Items]      
Royalty percentage based on future revenues   5.00%  
v3.24.2.u1
SHAREHOLDERS' EQUITY (Narrative) (Details)
$ / shares in Units, $ in Thousands
1 Months Ended 6 Months Ended 30 Months Ended
Jan. 31, 2023
USD ($)
Apr. 14, 2020
USD ($)
shares
Oct. 10, 2018
USD ($)
$ / shares
shares
Jun. 14, 2018
USD ($)
$ / shares
shares
Nov. 30, 2021
USD ($)
$ / shares
shares
Mar. 16, 2020
$ / shares
shares
Jun. 30, 2024
USD ($)
$ / shares
shares
Jun. 30, 2023
USD ($)
$ / shares
shares
Jun. 30, 2023
USD ($)
shares
Jun. 30, 2024
₪ / shares
Jun. 30, 2024
USD ($)
shares
Dec. 31, 2023
₪ / shares
shares
Ordinary shares, par value | ₪ / shares                   ₪ 0.01   ₪ 0.01
Value of shares issued             $ 562 $ 1,154        
Ordinary shares, shares authorized | shares                     200,000,000 200,000,000
Options granted | shares             40,500          
Stock options granted, exercise price, minimum | $ / shares             $ 1.8          
Stock options granted, exercise price, maximum | $ / shares             $ 2.09          
Vesting period             4 years          
Weighted average fair value of options granted during period | $ / shares             $ 1.41 $ 0.53        
Share based compensation stock options             $ 1,633 $ 1,782        
Unrecognized estimated compensation cost                     $ 3,405  
Period over which compensation expense will be recognized             1 year 10 months 6 days          
Total weighted average number of shares related to outstanding options and warrants excluded from the calculations of diluted net loss per share | shares             8,002,799 7,460,568        
Warrant [Member]                        
Warrants purchase to ordinary shares | shares               3,955,696 3,955,696      
Proceeds from warrant exercised                 $ 18,750      
Warrants purchase to ordinary shares remain outstanding | shares               297,469 297,469      
Agreement [Member] | Registered direct offering [Member]                        
Value of shares issued       $ 19,767                
Issuance expenses       $ 1,233                
Ordinary shares, shares authorized | shares       5,316,457                
Warrants purchase to ordinary shares | shares       4,253,165                
Offering price per share | $ / shares       $ 3.95                
Exercise price of warrants | $ / shares       $ 4.74                
Expiration period of warrants       5 years                
Master Clinical Agreement [Member]                        
Ordinary shares issued | shares     2,424,243   2,332,815              
Offering price per share | $ / shares     $ 4.95   $ 8.57333              
Equity investment     $ 12,000   $ 20,000              
Percentage of closing price     33.00%   33.00%              
Collaborative Arrangements [Member]                        
Issuance expenses             $ 91          
Relative fair value of deferred participation                     4,121  
Proceeds from equity investments             7,788          
Collaborative Arrangements Two [Member]                        
Issuance expenses             42          
Relative fair value of deferred participation                     $ 5,000  
Proceeds from equity investments             $ 14,958          
SVB Leerink LLC and Stifel, Nicolaus & Company [Member]                        
Ordinary shares issued | shares   8,816,339       8,333,334            
Issuance expenses   $ 5,200                    
Offering price per share | $ / shares           $ 9            
Proceeds from ordinary shares in offering   $ 74,147                    
SVB Leerink LLC and Stifel, Nicolaus & Company [Member] | Underwriters [Member]                        
Ordinary shares issued | shares   483,005                    
Offering price per share | $ / shares           $ 8.46            
Sales Agreement With Leerink Partner LLC [Member]                        
Proceeds from issuance of common stock $ 50,000                      
Ordinary shares issued | shares             2,905,550          
Issuance expenses             $ 530          
Proceeds from ordinary shares in offering             $ 3,643          
v3.24.2.u1
SHAREHOLDERS' EQUITY (Schedule Of Option Activity) (Details) - Employees Directors And Non Employees [Member] - USD ($)
$ / shares in Units, $ in Thousands
6 Months Ended 12 Months Ended
Jun. 30, 2024
Dec. 31, 2023
Number of options    
Options outstanding at beginning of year 8,373,745  
Options granted 40,500  
Options exercised 1,744  
Options forfeited (282,455)  
Options expired (140,000)  
Options outstanding at end of year 7,990,046 8,373,745
Exercisable at end of year 5,245,345  
Weighted average exercise price    
Options outstanding at beginning of year $ 4.65  
Options granted 2.08  
Options exercised 0.84  
Options forfeited 4.55  
Options expired 8.08  
Options outstanding at end of year 4.58 $ 4.65
Exercisable at end of year $ 5.68  
Weighted average remaining contractual life    
Options outstanding 6 years 2 months 8 days 6 years 7 months 9 days
Exercisable at end of year 4 years 11 months 26 days  
Aggregate intrinsic value    
Options outstanding at end of year $ 1,205 $ 1,912
Exercisable at end of year $ 124  
v3.24.2.u1
SHAREHOLDERS' EQUITY (Schedule of fair value assumptions) (Details)
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Expected dividend yield 0.00% 0.00%
Expected life (years) 4 years 7 days  
Minimum [Member]    
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Expected volatility, minimum 92.70% 75.90%
Expected risk free interest rates range, minimum 3.90% 3.30%
Expected life (years)   5 years
Maximum [Member]    
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Expected volatility, maximum 95.90% 76.40%
Expected risk free interest rate range, maximum 4.50% 4.20%
Expected life (years)   5 years 1 month 6 days
v3.24.2.u1
SHAREHOLDERS' EQUITY (Schedule Of Stock Compensation Expense) (Details) - Employee Stock Purchase Plan [Member] - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Share-based Payment Arrangement, Expensed and Capitalized, Amount [Line Items]    
Stock-based compensation expenses $ 1,633 $ 1,782
Research and development expenses [Member]    
Share-based Payment Arrangement, Expensed and Capitalized, Amount [Line Items]    
Stock-based compensation expenses 805 1,002
Marketing and business development expenses [Member]    
Share-based Payment Arrangement, Expensed and Capitalized, Amount [Line Items]    
Stock-based compensation expenses 43 (41)
General and administrative expenses [Member]    
Share-based Payment Arrangement, Expensed and Capitalized, Amount [Line Items]    
Stock-based compensation expenses $ 785 $ 821
v3.24.2.u1
FINANCIAL INCOME, NET (Details) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
FINANCIAL AND OTHER INCOME, NET [Abstract]    
Interest income $ 1,770 $ 1,671
Amortization of discount on marketable securities, net 796 15
Exchange rate differences and other (38) 11
Financial and other income, net $ 2,528 $ 1,697
v3.24.2.u1
REVENUES (Narrative) (Details) - USD ($)
$ in Thousands
6 Months Ended 12 Months Ended
Jun. 30, 2024
Dec. 31, 2023
Revenue [Abstract]    
Deferred revenue $ 4,261 $ 36,541
Remaining performance obligations $ 32,280  
Remaining performance obligations percentage 35.00%  
v3.24.2.u1
REVENUES (Details) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Revenue [Line Items]    
Revenue $ 9,261 $ 0
United States    
Revenue [Line Items]    
Revenue 4,261 0
Europe    
Revenue [Line Items]    
Revenue $ 5,000 $ 0
v3.24.2.u1
RELATED PARTY BALANCES AND TRANSACTIONS (Details) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Dec. 31, 2023
RELATED PARTY BALANCES AND TRANSACTIONS [Abstract]      
Trade and other payables [1] $ 22   $ 53
Related parties' expenses amounts charged to research and development expenses [1] $ 74 $ 70  
[1] The Company incurred expenses for research and development services provided by related party for cancer studies in animal models, and breeding and maintenance of animals (mice) to support such studies.
v3.24.2.u1
LOSSES PER SHARE (Schedule of Computation of Basic and Diluted Losses Per Share) (Details) - USD ($)
$ / shares in Units, $ in Thousands
6 Months Ended
Jun. 30, 2024
Jun. 30, 2023
Numerator:    
Net loss for basic and diluted loss per share $ 9,390 $ 18,615
Denominator:    
Weighted average number of ordinary shares used in computing basic net loss per share 89,518,778 86,903,741
Weighted average number of ordinary shares used in computing diluted net loss per share 89,518,778 86,903,741
Basic net loss per share $ (0.1) $ (0.21)
Diluted net loss per share $ (0.1) $ (0.21)
v3.24.2.u1
SUBSEQUENT EVENTS (Narrative) (Details) - Subsequent Event [Member] - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2024
Jul. 31, 2024
Gilead Sciences, Inc [Member]    
Subsequent Event [Line Items]    
Clearance triggered mlestone payment $ 30,000  
Plan 2010 [Member]    
Subsequent Event [Line Items]    
Number of shares reserved for issuance   300,000
Employee Share Purchase Plan [Member]    
Subsequent Event [Line Items]    
Number of shares reserved for issuance   114,146

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