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Share Name | Share Symbol | Market | Type |
---|---|---|---|
Seelos Therapeutics Inc | NASDAQ:SEEL | NASDAQ | Common Stock |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.00 | 0.00% | 1.28 | 1.30 | 1.33 | 0 | 00:00:00 |
| | |
Per Share
|
| |
Per Pre-Funded
Warrant |
| |
Total
|
| |||||||||
Offering price
|
| | | $ | 2.46 | | | | | $ | 2.45900 | | | | | $ | 1,136,947.98 | | |
Placement agent’s fees(1)
|
| | | $ | 0.1722 | | | | | $ | 0.17213 | | | | | $ | 79,586.36 | | |
Proceeds to us, before expenses(2)
|
| | | $ | 2.2878 | | | | | $ | 2.28687 | | | | | $ | 1,057,361.62 | | |
| | |
Page
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| | | | S-16 | | | |
| | | | S-18 | | | |
| | | | S-19 | | | |
| | | | S-21 | | | |
| | | | S-22 | | | |
| | | | S-23 | | | |
| | | | S-25 | | | |
| | | | S-27 | | | |
| | | | S-29 | | | |
| | | | S-32 | | | |
| | | | S-32 | | | |
| | | | S-33 | | | |
| | | | S-34 | | |
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| | | | 44 | | |
Product
|
| |
Indication
|
| |
Development
Phase |
| |
Development Status
|
|
SLS-002
Intranasal Racemic Ketamine |
| |
Acute Suicidal Ideation and Behavior (“ASIB”) in Major Depressive Disorder (“MDD”)
|
| |
Phase II
|
| |
Completed open-label patient enrollment
and announced the initial topline data from Part 1 of the proof-of-concept (“PoC”) study on May 17, 2021; enrollment of Part 2 of a Phase II study closed in June 2023; topline data for Part 2 announced on September 20, 2023 |
|
SLS-005
IV Trehalose |
| |
Amyotrophic Lateral Sclerosis (“ALS”)
|
| |
Phase II/III
|
| |
Completed enrollment of final
participants in February 2023 in the registrational study; topline data announced on March 19, 2024 |
|
| | |
Spinocerebellar Ataxia (“SCA”)
|
| |
Phase IIb/III
|
| |
Announced dosing of the first
participant in the registrational study in October 2022; enrollment of additional patients temporarily paused on March 29, 2023 |
|
| | |
Huntington’s Disease (“HD”) and Alzheimer’s Disease (“AD”)
|
| |
Phase II
|
| |
Obtaining biomarker activity
|
|
SLS-004
Gene Therapy |
| |
Parkinson’s Disease (“PD”)
|
| |
Pre-IND
|
| |
Preclinical in vivo studies ongoing;
announced partial results from a study demonstrating downregulation of α-synuclein in December 2022; currently analyzing data while temporarily pausing additional spend |
|
Product
|
| |
Indication
|
| |
Development
Phase |
| |
Development Status
|
|
SLS-007
Peptide Inhibitor |
| |
PD
|
| |
Pre-IND
|
| |
Preclinical study completed and
analysis of the results ongoing; next steps for development of this program will be decided in concert with SLS-004 results and readouts, as both target the same pathway upstream; temporarily pausing additional spend |
|
SLS-009 | | |
HD, AD, ALS
|
| |
Pre-IND
|
| |
Preclinical in vivo studies ongoing
|
|
| | |
Year Ended
December 31, |
| |||||||||
| | |
2023
|
| |
2022
|
| ||||||
Net loss and comprehensive loss
|
| | | $ | (37,882) | | | | | $ | (73,534) | | |
Total loss per share basic
|
| | | $ | (7.73) | | | | | $ | (20.74) | | |
Total loss per share-diluted
|
| | | $ | (7.73) | | | | | $ | (20.74) | | |
Weighted-average common shares outstanding used for basic
|
| | | | 4,900,222 | | | | | | 3,545,691 | | |
Weighted-average common shares outstanding used for diluted
|
| | | | 4,900,222 | | | | | | 3,545,691 | | |
Common stock outstanding at period end
|
| | | | 9,794,594 | | | | | | 3,572,417 | | |
| | |
Three Months Ended
March 31, |
| |||||||||
| | |
2024
|
| |
2023
|
| ||||||
Net loss and comprehensive loss
|
| | | $ | (2,664) | | | | | $ | (13,431) | | |
Total loss per share basic
|
| | | $ | (0.20) | | | | | $ | (3.58) | | |
Total loss per share-diluted
|
| | | $ | (0.20) | | | | | $ | (3.58) | | |
Weighted-average common shares outstanding used for basic
|
| | | | 13,007,556 | | | | | | 3,751,468 | | |
Weighted-average common shares outstanding used for diluted
|
| | | | 13,007,556 | | | | | | 3,751,468 | | |
Common stock outstanding at period end
|
| | | | 15,256,268 | | | | | | 4,060,370 | | |
| | |
Year Ended
December 31, |
| |||||||||
| | |
2023
|
| |
2022
|
| ||||||
Net loss and comprehensive loss
|
| | | $ | (37,882) | | | | | $ | (73,534) | | |
Total loss per share basic
|
| | | $ | (61.84) | | | | | $ | (165.90) | | |
Total loss per share-diluted
|
| | | $ | (61.84) | | | | | $ | (165.90) | | |
Weighted-average common shares outstanding used for basic
|
| | | | 612,569 | | | | | | 443,245 | | |
Weighted-average common shares outstanding used for diluted
|
| | | | 612,569 | | | | | | 443,245 | | |
Common stock outstanding at period end
|
| | | | 1,224,371 | | | | | | 446,576 | | |
| | |
Three Months Ended
March 31, |
| |||||||||
| | |
2024
|
| |
2023
|
| ||||||
Net loss and comprehensive loss
|
| | | $ | (2,664) | | | | | $ | (13,431) | | |
Total loss per share basic
|
| | | $ | (1.64) | | | | | $ | (28.64) | | |
Total loss per share-diluted
|
| | | $ | (1.64) | | | | | $ | (28.64) | | |
Weighted-average common shares outstanding used for basic
|
| | | | 1,625,991 | | | | | | 468,971 | | |
Weighted-average common shares outstanding used for diluted
|
| | | | 1,625,991 | | | | | | 468,971 | | |
Common stock outstanding at period end
|
| | | | 1,907,081 | | | | | | 546,511 | | |
|
Offering price per share of common stock
|
| | | | | | | | | $ | 2.46 | | |
|
Net tangible book value per share as of March 31, 2024
|
| | | $ | (17.36) | | | | | | | | |
|
Increase in net tangible book value per share attributable to the issuance of an
aggregate of 319,695 shares of our common stock issued to the holder of the Note to satisfy principal and interest payments thereunder between April 1, 2024 and May 15, 2024 |
| | | $ | 2.66 | | | | | | | | |
|
Pro forma net tangible book value per share as of March 31, 2024
|
| | | $ | (14.70) | | | | | | | | |
|
Increase in net tangible book value per share attributable to this offering
|
| | | $ | 2.50 | | | | | | | | |
|
Pro forma as adjusted net tangible book value per share as of March 31, 2024, after giving effect to this offering
|
| | | | | | | | | $ | (12.20) | | |
|
Dilution per share to investors participating in this offering
|
| | | | | | | | | $ | 14.66 | | |
| | |
Per Share
|
| |
Per Pre-Funded
Warrant |
| |
Total
|
| |||||||||
Offering price
|
| |
$2.46
|
| | | $ | 2.45900 | | | | | $ | 1,136,947.98 | | | |||
Placement agent’s fees(1)
|
| | | $ | 0.1722 | | | | | $ | 0.17213 | | | |
$79,586.36
|
| |||
Proceeds to us, before expenses(2)
|
| | | $ | 2.2878 | | | | | $ | 2.28687 | | | | | $ | 1,057,361.62 | | |
| | |
Page
|
| |||
| | | | 1 | | | |
| | | | 2 | | | |
| | | | 3 | | | |
| | | | 10 | | | |
| | | | 15 | | | |
| | | | 17 | | | |
| | | | 18 | | | |
| | | | 23 | | | |
| | | | 32 | | | |
| | | | 36 | | | |
| | | | 37 | | | |
| | | | 38 | | | |
| | | | 41 | | | |
| | | | 43 | | | |
| | | | 43 | | | |
| | | | 43 | | | |
| | | | 44 | | |
Product
|
| |
Indication
|
| |
Development
Phase |
| |
Development Status
|
|
SLS-002
Intranasal Racemic Ketamine |
| |
Acute Suicidal Ideation and Behavior (“ASIB”) in Major Depressive Disorder (“MDD”)
|
| |
Phase II
|
| |
Completed open-label patient enrollment
and announced the initial topline data from Part 1 of the proof-of-concept (“PoC”) study on May 17, 2021; enrollment of Part 2 of a Phase II study closed in June 2023; topline data for Part 2 announced on September 20, 2023 |
|
SLS-005
IV Trehalose |
| |
Amyotrophic Lateral Sclerosis (“ALS)”
|
| |
Phase II/III
|
| |
Completed enrollment of final
participants in February 2023 in the registrational study; data readout expected in the first quarter of 2024 |
|
| | |
Spinocerebellar Ataxia (“SCA”)
|
| |
Phase IIb/III
|
| |
Announced dosing of the first
participant in the registrational study in October 2022; enrollment of additional patients temporarily paused on March 29, 2023 |
|
| | |
Huntington’s Disease (“HD”) and Alzheimer’s Disease (“AD”)
|
| |
Phase II
|
| |
Obtaining biomarker activity
|
|
Product
|
| |
Indication
|
| |
Development
Phase |
| |
Development Status
|
|
SLS-004
Gene Therapy |
| |
Parkinson’s Disease (“PD”)
|
| |
Pre-IND
|
| |
Preclinical in vivo studies ongoing;
announced partial results from a study demonstrating downregulation of α-synuclein in December 2022; currently analyzing data while temporarily pausing additional spend |
|
SLS-007
Peptide Inhibitor |
| |
PD
|
| |
Pre-IND
|
| |
Preclinical study completed and
analysis of the results ongoing; next steps for development of this program will be decided in concert with SLS-004 results and readouts, as both target the same pathway upstream; temporarily pausing additional spend |
|
SLS-009 | | |
HD, AD, ALS
|
| |
Pre-IND
|
| |
Preclinical in vivo studies ongoing
|
|
1 Year Seelos Therapeutics Chart |
1 Month Seelos Therapeutics Chart |
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