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Share Name | Share Symbol | Market | Type |
---|---|---|---|
Femasys Inc | NASDAQ:FEMY | NASDAQ | Common Stock |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.03 | 2.86% | 1.08 | 1.05 | 1.08 | 1.09 | 1.0504 | 1.08 | 5,781 | 16:16:02 |
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QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
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TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
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(Exact Name of Registrant as Specified in its Charter)
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(State or other jurisdiction of incorporation or organization)
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(IRS Employer Identification No.)
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(Address of principal executive offices)
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(Zip Code)
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(
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(Registrant’s telephone number, including area code)
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N/A |
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(Former name, former address and former fiscal year, if changed since last report)
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Title of each class
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Trading symbol
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Name of each exchange on which
registered
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|||
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The
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Large accelerated filer ☐ | Accelerated filer ☐ |
Smaller reporting company |
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Emerging growth company |
TABLE OF CONTENTS | ||
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Page | |
Part I. Financial Information
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Item 1
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5
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6
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7
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8
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10 | ||
11
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Item 2
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18
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Item 3
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26
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Item 4
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26
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Part II. Other Information
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Item 1
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27
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Item 1A
|
28
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Item 2
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28
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Item 3
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28
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Item 4
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28
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Item 5
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28
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Item 6
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28
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30
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•
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our ability to successfully initiate and grow the commercial launch of FemaSeed®;
|
• |
our ability to obtain additional financing to fund the clinical development and commercialization of our product candidate and products and fund our operations;
|
• |
estimates regarding the total addressable market for our products and product candidate;
|
• |
competitive companies and technologies in our industry;
|
• |
our business model and strategic plans for our products, product candidate, technologies and business, including our implementation thereof;
|
• |
commercial success and market acceptance of our products and product candidate;
|
• |
our ability to achieve and maintain adequate levels of coverage or reimbursement for FemaSeed, FemBloc or any future product candidates, and our products we may seek to commercialize;
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• |
our ability to accurately forecast customer demand for our product candidates, and manage our inventory;
|
• |
our ability to build, manage and maintain our direct sales and marketing organization, and to market and sell our artificial insemination product, permanent birth control system, and women-specific
medical product solutions in markets in and outside of the United States;
|
• |
our expectations about market trends
|
• |
our ability to develop and advance our current product candidate, FemBloc® and successfully initiate and complete, clinical trials;
|
• |
the ability of our clinical trials to demonstrate safety and effectiveness of our product candidate, FemBloc and other positive results;
|
• |
our ability to enroll subjects in the clinical trials for our product candidate, FemBloc in order to advance the development thereof on a timely basis;
|
• |
our ability to obtain U.S. Food and Drug Administration (FDA) approval for our product candidate, FemBloc, for permanent birth control, ability to establish and expand sales of our women-specific medical
products and develop and commercialize additional products;
|
• |
our ability to obtain regulatory approvals for and commercialize our product candidate FemBloc, or the effect of delays in obtaining regulatory authorizations and commercialize;
|
• |
our ability to manufacture our products and product candidates in compliance with applicable laws, regulations and requirements and to oversee third-party suppliers, service providers and vendors in the
performance of any contracted activities in accordance with applicable laws, regulations and requirements;
|
• |
our ability to hire and retain our senior management and other highly qualified personnel;
|
• |
FDA or other U.S. or foreign regulatory or governmental actions affecting us or the healthcare industry generally, including healthcare reform measures in the United States and international markets;
|
• |
the timing or likelihood of regulatory filings and approvals or clearances;
|
• |
our ability to establish and maintain intellectual property protection for our product candidates and our ability to avoid claims of infringement; and
|
• |
the volatility of the trading price of our common stock.
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ITEM I. |
Financial Statements
|
Assets
|
June 30,
2024
|
December 31,
2023
|
||||||
Current assets:
|
||||||||
Cash and cash equivalents
|
$
|
|
|
|||||
Accounts receivable, net
|
|
|
||||||
Inventory, net
|
|
|
||||||
Prepaid and other current assets
|
|
|
||||||
Total current assets
|
|
|
||||||
Property and equipment, at cost:
|
||||||||
Leasehold improvements
|
|
|
||||||
Office equipment
|
|
|
||||||
Furniture and fixtures
|
|
|
||||||
Machinery and equipment
|
|
|
||||||
Construction in progress
|
|
|
||||||
|
|
|||||||
Less accumulated depreciation
|
(
|
)
|
(
|
)
|
||||
Net property and equipment
|
|
|
||||||
Long-term assets:
|
||||||||
Lease right-of-use assets, net
|
|
|
||||||
Intangible assets, net of accumulated amortization
|
|
|
||||||
Other long-term assets
|
|
|
||||||
Total long-term assets
|
|
|
||||||
Total assets
|
$
|
|
|
Liabilities and Stockholders’ Equity |
June 30,
2024
|
December 31,
2023
|
||||||
Current liabilities:
|
||||||||
Accounts payable
|
$
|
|
|
|||||
Accrued expenses
|
|
|
||||||
Clinical holdback – current portion
|
|
|
||||||
Lease liabilities – current portion
|
|
|
||||||
Total current liabilities
|
|
|
||||||
Long-term liabilities:
|
||||||||
Clinical holdback – long-term portion
|
|
|
||||||
Convertible notes payable, net (including related parties)
|
||||||||
Lease liabilities – long-term portion
|
|
|
||||||
Total long-term liabilities
|
|
|
||||||
Total liabilities
|
|
|
||||||
Commitments and contingencies
|
||||||||
Stockholders’ equity:
|
||||||||
Common stock, $
|
|
|
||||||
Treasury stock,
|
(
|
)
|
(
|
)
|
||||
Warrants
|
|
|
||||||
Additional paid-in-capital
|
|
|
||||||
Accumulated deficit
|
(
|
)
|
(
|
)
|
||||
Total stockholders’ equity
|
|
|
||||||
Total liabilities and stockholders’ equity
|
$
|
|
|
Three Months Ended June 30,
|
Six Months Ended June 30,
|
|||||||||||||||
2024
|
2023
|
2024
|
2023
|
|||||||||||||
Sales
|
$
|
|
|
|
|
|||||||||||
Cost of sales (excluding depreciation expense)
|
|
|
|
|
||||||||||||
Operating expenses:
|
||||||||||||||||
Research and development
|
|
|
|
|
||||||||||||
Sales and marketing
|
|
|
|
|
||||||||||||
General and administrative
|
|
|
|
|
||||||||||||
Depreciation and amortization
|
|
|
|
|
||||||||||||
Total operating expenses
|
|
|
|
|
||||||||||||
Loss from operations
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
||||||||
Other income (expense):
|
||||||||||||||||
Interest income
|
|
|
|
|
||||||||||||
Interest expense
|
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
Total other income (expense), net
|
( |
) | ( |
) | ||||||||||||
Loss before income taxes
|
( |
) | ( |
) | ( |
) | ( |
) | ||||||||
Income tax benefit
|
( |
) | ( |
) | ||||||||||||
Net loss
|
$
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
|||||||
Net loss attributable to common stockholders, basic and diluted
|
$
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
|||||||
Net loss per share attributable to common stockholders, basic and diluted
|
$
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
|||||||
Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted
|
|
|
|
|
Total | ||||||||||||||||||||||||||||||||
Common stock
|
Treasury common stock
|
Additional | Accumulated | stockholders’ | ||||||||||||||||||||||||||||
Shares
|
Amount
|
Shares
|
Amount
|
Warrants
|
paid-in capital
|
deficit
|
equity
|
|||||||||||||||||||||||||
THREE MONTHS ENDED JUNE 30, 2024
|
||||||||||||||||||||||||||||||||
Balance at March 31, 2024
|
|
$
|
|
|
$
|
(
|
)
|
|
|
$
|
|
$
|
(
|
)
|
$
|
|
||||||||||||||||
Issuance of common stock in connection with at-the-market offering, net of issuance costs
|
||||||||||||||||||||||||||||||||
Issuance of common stock in connection with ESPP |
||||||||||||||||||||||||||||||||
Expiration of warrant |
— | — | ( |
) | ||||||||||||||||||||||||||||
Share-based compensation expense |
— | — | ||||||||||||||||||||||||||||||
Net loss
|
— |
—
|
|
( |
) | ( |
) | |||||||||||||||||||||||||
Balance at June 30, 2024
|
|
$
|
|
|
$
|
(
|
)
|
|
|
$
|
|
$ | ( |
) |
$
|
|
||||||||||||||||
|
||||||||||||||||||||||||||||||||
SIX MONTHS ENDED JUNE 30, 2024
|
||||||||||||||||||||||||||||||||
Balance at December 31, 2023
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$ | ( |
) |
$
|
|
||||||||||||||||
Issuance of common stock in connection with at-the-market offering, net of issuance costs
|
||||||||||||||||||||||||||||||||
Issuance of common stock in connection with ESPP |
||||||||||||||||||||||||||||||||
Expiration of warrant |
— | — | ( |
) | ||||||||||||||||||||||||||||
Share-based compensation expense | — | — | ||||||||||||||||||||||||||||||
Net loss
|
—
|
|
—
|
|
|
|
(
|
)
|
(
|
)
|
||||||||||||||||||||||
Balance at June 30, 2024
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$
|
(
|
)
|
$
|
|
Total | ||||||||||||||||||||||||||||||||
Common stock
|
Treasury common stock
|
Additional | Accumulated | stockholders’ | ||||||||||||||||||||||||||||
Shares
|
Amount
|
Shares
|
Amount
|
Warrants
|
paid-in capital
|
deficit
|
equity
|
|||||||||||||||||||||||||
THREE MONTHS ENDED JUNE 30, 2023
|
||||||||||||||||||||||||||||||||
Balance at March 31, 2023
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$ | ( |
) |
$
|
|
||||||||||||||||
Issuance of common stock and warrants in connection with April 2023 Financing, net of issuance costs
|
— | |||||||||||||||||||||||||||||||
Issuance of common stock in connection with ESPP |
||||||||||||||||||||||||||||||||
Exercise of pre-funded warrants |
( |
) | ||||||||||||||||||||||||||||||
Share-based compensation expense
|
—
|
|
—
|
|
|
|
|
|||||||||||||||||||||||||
Net loss
|
—
|
|
—
|
|
|
|
( |
) |
(
|
)
|
||||||||||||||||||||||
Balance at June 30, 2023
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$ | ( |
) |
$
|
|
||||||||||||||||
SIX MONTHS ENDED JUNE 30, 2023
|
||||||||||||||||||||||||||||||||
Balance at December 31, 2022
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$ | ( |
) |
$
|
|
||||||||||||||||
Issuance of common stock and warrants in connection with April 2023 Financing, net of issuance costs
|
— | |||||||||||||||||||||||||||||||
Issuance of common stock in connection with at-the-market offering, net of issuance costs
|
||||||||||||||||||||||||||||||||
Issuance of common stock in connection with ESPP |
||||||||||||||||||||||||||||||||
Exercise of pre-funded warrants |
( |
) | ||||||||||||||||||||||||||||||
Share-based compensation expense
|
—
|
|
—
|
|
|
|
|
|
||||||||||||||||||||||||
Net loss
|
—
|
|
—
|
|
|
|
( |
) |
(
|
)
|
||||||||||||||||||||||
Balance at June 30, 2023
|
|
$
|
|
|
$
|
(
|
)
|
$
|
|
$
|
|
$ | ( |
) |
$
|
|
Six Months ended June 30
|
||||||||
2024
|
2023
|
|||||||
Cash flows from operating activities:
|
||||||||
Net loss
|
$
|
(
|
)
|
(
|
)
|
|||
Adjustments to reconcile net loss to net cash used in operating activities:
|
||||||||
Depreciation
|
|
|
||||||
Amortization
|
|
|
||||||
Amortization of right-of-use assets
|
||||||||
Loss on disposal of assets
|
|
|
||||||
Inventory reserve write-off
|
||||||||
Share-based compensation expense
|
|
|
||||||
Amortization of debt issuance costs and discount
|
||||||||
Changes in operating assets and liabilities:
|
||||||||
Accounts receivable
|
|
(
|
)
|
|||||
Inventory
|
(
|
)
|
(
|
)
|
||||
Prepaid and other assets
|
(
|
)
|
|
|||||
Accounts payable
|
(
|
)
|
|
|||||
Accrued expenses
|
(
|
)
|
|
|||||
Lease liabilities
|
(
|
)
|
(
|
)
|
||||
Other liabilities
|
(
|
)
|
|
|||||
Net cash used in operating activities
|
(
|
)
|
(
|
)
|
||||
Cash flows from investing activities:
|
||||||||
Acquisition of patents
|
( |
) | ||||||
Purchases of property and equipment
|
(
|
)
|
(
|
)
|
||||
Net cash used in investing activities
|
(
|
)
|
(
|
)
|
||||
Cash flows from financing activities:
|
||||||||
Proceeds from the issuance of common stock and warrants in April 2023 Financing
|
||||||||
Equity issuance costs for April 2023 Financing
|
( |
) | ||||||
Proceeds from exercise of pre-funded warrants
|
||||||||
Proceeds from common stock issued through ESPP and exercised options
|
||||||||
Proceeds from at-the-market sales of common stock
|
||||||||
Issuance costs for at-the-market sales of common stock
|
( |
) | ||||||
Repayment of note payable
|
|
(
|
)
|
|||||
Payments under lease obligations
|
|
(
|
)
|
|||||
Net cash provided by financing activities
|
|
|
||||||
|
||||||||
Net change in cash and cash equivalents
|
(
|
)
|
(
|
)
|
||||
Cash and cash equivalents:
|
||||||||
Beginning of period
|
|
|
||||||
End of period
|
$
|
|
|
|||||
Supplemental cash flow information | ||||||||
Cash paid for: | ||||||||
Interest
|
$ | |||||||
Taxes
|
||||||||
Non-cash investing and financing activities: | ||||||||
Property and equipment costs included in accounts payable and accrued expense
|
||||||||
Commissions costs relating to certain proceeds from issuance of common stock
|
||||||||
Deferred offering costs reclassified to additional paid-in-capital
|
(1)
|
Organization, Nature of Business, and Liquidity
|
(2)
|
Fair Value
|
(3)
|
Cash and Cash Equivalents
|
(4)
|
Inventories
|
June 30, | December 31, | |||||||
2024
|
2023 |
|||||||
Materials
|
$
|
|
|
|||||
Work in progress
|
|
|
||||||
Finished goods
|
|
|
||||||
Inventory, net
|
$
|
|
|
(5)
|
Accrued Expenses
|
June 30, | December 31, | |||||||
2024 | 2023 | |||||||
Clinical trial costs
|
$
|
|
|
|||||
Accrued interest |
||||||||
Incentive and other compensation costs |
||||||||
Director fees | ||||||||
Franchise taxes |
||||||||
Other
|
|
|
||||||
Accrued expenses
|
$
|
|
|
(6)
|
Clinical Holdback
|
Balance at December 31, 2023
|
$
|
|
||
Clinical holdback retained
|
|
|||
Clinical holdback paid
|
(
|
)
|
||
Balance at June 30, 2024
|
$
|
|
||
Less: clinical holdback - current portion
|
(
|
)
|
||
Clinical holdback - long-term portion
|
$
|
|
(7)
|
Revenue Recognition
|
Three Months Ended June 30,
|
Six Months Ended June 30,
|
|||||||||||||||
Primary geographical markets |
2024
|
2023
|
2024
|
2023
|
||||||||||||
U.S.
|
$
|
|
|
|
|
|||||||||||
International
|
|
|
|
|
||||||||||||
Total
|
$
|
|
|
|
|
(8)
|
Commitments and Contingencies
|
(9)
|
Notes Payable
|
(10)
|
Convertible Notes with Warrants (November 2023 Financing)
|
(11)
|
Stockholders’ Equity
|
(12)
|
Equity Incentive Plans and Warrants
|
(a) |
Stock Option Plans
|
Number of
options
|
Weighted
average
exercise
price
|
|||||||
Outstanding at December 31, 2023 | $ | |||||||
Granted | ||||||||
Forfeited | ( |
) | ||||||
Outstanding at June 30, 2024 | $ | |||||||
Vested and exercisable at June 30, 2024 | $ |
Employee |
Nonemployee | |||||||
Expected term (in years)
|
|
|
||||||
Risk‑free interest rate
|
|
%
|
% | |||||
Dividend yield
|
|
%
|
% | |||||
Expected volatility
|
|
%
|
% |
(b) |
Inducement Grants
|
|
Inducement
|
|||
Expected term (in years)
|
|
|
||
Risk‑free interest rate
|
|
%
|
||
Dividend yield
|
|
%
|
||
Expected volatility
|
|
%
|
(c) | Share-Based Compensation Expense |
Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
2024
|
2023
|
2024 | 2023 | |||||||||||||
Research and development
|
$
|
|
|
|||||||||||||
Sales and marketing
|
|
|
( |
) | ||||||||||||
General and administrative
|
|
|
||||||||||||||
Total share-based compensation expense
|
$
|
|
|
(d) |
Employee Stock Purchase Plan (ESPP)
|
(e) |
April 2023 Financing
|
Pre-funded
warrants
|
Common
warrants
|
|||||||
Expected term (in years)
|
|
|
|
|||||
Risk‑free interest rate
|
|
%
|
|
%
|
||||
Dividend yield
|
|
% |
|
% | ||||
Expected volatility
|
|
%
|
|
%
|
||||
Exercise price
|
$
|
|
$
|
|
||||
Stock price
|
$
|
|
$
|
|
||||
Black-Scholes value |
$ | $ |
(13)
|
Related‑Party Transactions
|
(14)
|
Net Loss per Share Attributable to Common Stockholders
|
Three Months Ended June 30,
|
Six Months Ended June 30,
|
|||||||||||||||
2024
|
2023
|
2024
|
2023
|
|||||||||||||
Net loss attributable to common stockholders, basic & diluted
|
$
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
|||||||
Weighted average number of shares used in computing net loss per share attributable to common stockholders, basic and diluted
|
|
|
|
|
||||||||||||
Net loss per share attributable to common stockholders, basic and diluted
|
$
|
(
|
)
|
(
|
)
|
(
|
)
|
(
|
)
|
Three Months Ended June 30,
|
Six Months Ended June 30,
|
|||||||||||||||
2024
|
2023
|
2024
|
2023
|
|||||||||||||
Options to purchase common stock
|
|
|
|
|
||||||||||||
Warrants to purchase common stock, in connection with April 2023 financing | ||||||||||||||||
Warrants to purchase common stock, in connection with November 2023 financing | ||||||||||||||||
Warrants to purchase common stock
|
|
|
|
|
||||||||||||
Total potential shares
|
|
|
|
|
(15)
|
Income Taxes
|
Item 2. |
Management’s Discussion and Analysis of Financial Condition and Results of Operations
|
Three Months Ended June 30,
|
||||||||||||||||
2024
|
2023
|
Change
|
% Change
|
|||||||||||||
Sales
|
$
|
221,484
|
320,514
|
(99,030
|
)
|
-30.9
|
%
|
|||||||||
Cost of sales (excluding depreciation expense)
|
73,125
|
110,469
|
(37,344
|
)
|
-33.8
|
%
|
||||||||||
Operating expenses:
|
||||||||||||||||
Research and development
|
1,975,875
|
1,527,172
|
448,703
|
29.4
|
%
|
|||||||||||
Sales and marketing
|
975,190
|
128,899
|
846,291
|
656.6
|
%
|
|||||||||||
General and administrative
|
1,611,817
|
1,356,637
|
255,180
|
18.8
|
%
|
|||||||||||
Depreciation and amortization
|
67,628
|
133,299
|
(65,671
|
)
|
-49.3
|
%
|
||||||||||
Total operating expenses
|
4,630,510
|
3,146,007
|
1,484,503
|
47.2
|
%
|
|||||||||||
Loss from operations
|
(4,482,151
|
)
|
(2,935,962
|
)
|
(1,546,189
|
)
|
52.7
|
%
|
||||||||
Other income (expense):
|
||||||||||||||||
Interest income
|
184,138
|
42,652
|
141,486
|
331.7
|
%
|
|||||||||||
Interest expense
|
(388,311
|
)
|
(198
|
)
|
(388,113
|
)
|
196016.7
|
%
|
||||||||
Other income (expense), net
|
(204,173
|
)
|
42,454
|
(246,627
|
)
|
-580.9
|
%
|
|||||||||
Loss before income taxes
|
(4,686,324
|
)
|
(2,893,508
|
)
|
(1,792,816
|
)
|
62.0
|
%
|
||||||||
Income tax benefit
|
(1,750
|
)
|
—
|
(1,750
|
)
|
-100.0
|
%
|
|||||||||
Net loss
|
$
|
(4,684,574
|
)
|
(2,893,508
|
)
|
(1,791,066
|
)
|
61.9
|
%
|
Three Months Ended June 30,
|
||||||||
2024
|
2023
|
|||||||
Compensation and related personnel costs
|
$
|
974,880
|
840,506
|
|||||
Clinical-related costs
|
435,588
|
361,578
|
||||||
Material and development costs
|
389,129
|
205,095
|
||||||
Professional and outside consultant costs
|
118,477
|
120,527
|
||||||
Other costs
|
57,801
|
(534
|
)
|
|||||
Total research and development expenses
|
$
|
1,975,875
|
1,527,172
|
Six Months Ended June 30,
|
||||||||||||||||
2024
|
2023
|
Change
|
% Change
|
|||||||||||||
Sales
|
$
|
492,624
|
614,498
|
(121,874
|
)
|
-19.8
|
%
|
|||||||||
Cost of sales (excluding depreciation expense)
|
161,657
|
215,589
|
(53,932
|
)
|
-25.0
|
%
|
||||||||||
Operating expenses:
|
||||||||||||||||
Research and development
|
3,746,606
|
3,064,611
|
681,995
|
22.3
|
%
|
|||||||||||
Sales and marketing
|
1,275,677
|
373,795
|
901,882
|
241.3
|
%
|
|||||||||||
General and administrative
|
3,114,621
|
2,671,774
|
442,847
|
16.6
|
%
|
|||||||||||
Depreciation and amortization
|
138,856
|
266,365
|
(127,509
|
)
|
-47.9
|
%
|
||||||||||
Total operating expenses
|
8,275,760
|
6,376,545
|
1,899,215
|
29.8
|
%
|
|||||||||||
Loss from operations
|
(7,944,793
|
)
|
(5,977,636
|
)
|
(1,967,157
|
)
|
32.9
|
%
|
||||||||
Other income (expense):
|
||||||||||||||||
Interest income
|
408,822
|
139,741
|
269,081
|
192.6
|
%
|
|||||||||||
Interest expense
|
(749,863
|
)
|
(1,870
|
)
|
(747,993
|
)
|
39999.6
|
%
|
||||||||
Other income (expense), net
|
(341,041
|
)
|
137,871
|
(478,912
|
)
|
-347.4
|
%
|
|||||||||
Loss before income taxes
|
(8,285,834
|
)
|
(5,839,765
|
)
|
(2,446,069
|
)
|
41.9
|
%
|
||||||||
Income tax benefit
|
(1,750
|
)
|
—
|
(1,750
|
)
|
-100.0
|
%
|
|||||||||
Net loss
|
$
|
(8,284,084
|
)
|
(5,839,765
|
)
|
(2,444,319
|
)
|
41.9
|
%
|
Six Months Ended June 30,
|
||||||||
2024
|
2023
|
|||||||
Compensation and related personnel costs
|
$
|
1,963,937
|
1,740,794
|
|||||
Clinical-related costs
|
874,363
|
727,938
|
||||||
Material and development costs
|
532,828
|
372,256
|
||||||
Professional and outside consultant costs
|
286,659
|
212,462
|
||||||
Other costs
|
88,819
|
11,161
|
||||||
Total research and development expenses
|
$
|
3,746,606
|
3,064,611
|
Six Months Ended June 30,
|
||||||||
2024
|
2023
|
|||||||
Net cash used in operating activities
|
$
|
(8,894,780
|
)
|
(5,388,824
|
)
|
|||
Net cash used in investing activities
|
(297,123
|
)
|
(71,849
|
)
|
||||
Net cash provided by financing activities
|
1,001,724
|
3,203,754
|
||||||
Net change in cash and cash equivalents
|
$
|
(8,190,179
|
)
|
(2,256,919
|
)
|
Item 3. |
Quantitative and Qualitative Disclosures About Market Risk
|
Item 4. |
Controls and Procedures
|
Item 1. |
Legal Proceedings
|
Item 1A. |
Risk Factors
|
Item 2. |
Unregistered Sales of Equity Securities, Use of Proceeds, and Issuer Purchases of Equity Securities
|
Item 4. |
Mine Safety Disclosures
|
Item 5. |
Other Information
|
Item 6. |
Exhibits
|
Incorporated
by Reference
|
|||||
|
|
||||
Exhibit
Number |
Description of Document
|
Schedule/Form
|
File
Number
|
Exhibit
|
Filing Date
|
Eleventh Amended and Restated Certificate of Incorporation of Femasys Inc.
|
Form 8-K
|
001-
40492
|
3.1
|
June
22,
2021
|
|
Amended and Restated Bylaws of Femasys Inc.
|
Form 8-K
|
001-
40492
|
3.2
|
June
22,
2021
|
|
First Amendment to the Amended and Restated Bylaws of Femasys Inc.
|
Form 8-K
|
001-
40492
|
3.1
|
March
30,
2023
|
|
31.1*
|
Certification of Principal Executive Officer Pursuant to Securities Exchange Act Rules 13a-14(a), as adopted Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
|
||||
31.2*
|
Certification of Principal Financial Officer Pursuant to Securities Exchange Act Rules 13a-14(a), as adopted Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
|
||||
Certification of Principal Executive Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
|
32.2*
|
Certification of Principal Financial Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
|
||||
101.INS*
|
Inline XBRL Instance Document (the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document)
|
||||
101.SCH*
|
Inline XBRL Taxonomy Extension Schema Document
|
||||
101.CAL
|
Inline XBRL Taxonomy Extension Calculation Linkbase Document
|
||||
101.DEF*
|
Inline XBRL Taxonomy Definition Linkbase Document
|
||||
101.LAB*
|
Inline XBRL Taxonomy Extension Label Linkbase Document
|
||||
101.PRE*
|
Inline XBRL Taxonomy Extension Presentation Linkbase Document
|
||||
104*
|
Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101)
|
Dated: August 8, 2024
|
By: /s/ Kathy Lee-Sepsick
|
|
Kathy Lee-Sepsick
|
||
Chief Executive Officer and President
|
Dated: August 8, 2024
|
||
By: /s/ Dov Elefant
|
||
Dov Elefant
|
||
Chief Financial Officer
|
FEMASYS INC.
|
||
Date: August 8, 2024
|
By:
|
/s/ Kathy Lee-Sepsick
|
Kathy Lee-Sepsick
|
||
Chief Executive Officer and President
|
||
(principal executive officer)
|
FEMASYS INC.
|
||
Date: August 8, 2024
|
By:
|
/s/ Dov Elefant
|
Dov Elefant
|
||
Chief Financial Officer
|
||
(principal financial and accounting officer)
|
FEMASYS INC.
|
||
Date: August 8, 2024
|
By:
|
/s/ Kathy Lee-Sepsick
|
Kathy Lee-Sepsick
|
||
Chief Executive Officer and President
|
||
(principal executive officer)
|
FEMASYS INC.
|
||
Date: August 8, 2024
|
By:
|
/s/ Dov Elefant
|
Dov Elefant
|
||
Chief Financial Officer
|
||
(principal financial and accounting officer)
|
Condensed Balance Sheets (Parenthetical) - $ / shares |
Jun. 30, 2024 |
Dec. 31, 2023 |
---|---|---|
Stockholders' equity: | ||
Common stock, par value (in dollars per share) | $ 0.001 | $ 0.001 |
Common stock, authorized (in shares) | 200,000,000 | 200,000,000 |
Common stock, issued (in shares) | 22,350,022 | 21,774,604 |
Common stock, outstanding (in shares) | 22,232,799 | 21,657,381 |
Treasury stock, common shares (in shares) | 117,223 | 117,223 |
Condensed Statements of Comprehensive Loss - USD ($) |
3 Months Ended | 6 Months Ended | ||
---|---|---|---|---|
Jun. 30, 2024 |
Jun. 30, 2023 |
Jun. 30, 2024 |
Jun. 30, 2023 |
|
Statements of Comprehensive Loss [Abstract] | ||||
Sales | $ 221,484 | $ 320,514 | $ 492,624 | $ 614,498 |
Cost of sales (excluding depreciation expense) | 73,125 | 110,469 | 161,657 | 215,589 |
Operating expenses: | ||||
Research and development | 1,975,875 | 1,527,172 | 3,746,606 | 3,064,611 |
Sales and marketing | 975,190 | 128,899 | 1,275,677 | 373,795 |
General and administrative | 1,611,817 | 1,356,637 | 3,114,621 | 2,671,774 |
Depreciation and amortization | 67,628 | 133,299 | 138,856 | 266,365 |
Total operating expenses | 4,630,510 | 3,146,007 | 8,275,760 | 6,376,545 |
Loss from operations | (4,482,151) | (2,935,962) | (7,944,793) | (5,977,636) |
Other income (expense): | ||||
Interest income | 184,138 | 42,652 | 408,822 | 139,741 |
Interest expense | (388,311) | (198) | (749,863) | (1,870) |
Total other income (expense), net | (204,173) | 42,454 | (341,041) | 137,871 |
Loss before income taxes | (4,686,324) | (2,893,508) | (8,285,834) | (5,839,765) |
Income tax benefit | (1,750) | 0 | (1,750) | 0 |
Net loss | (4,684,574) | (2,893,508) | (8,284,084) | (5,839,765) |
Net loss attributable to common stockholders, basic | (4,684,574) | (2,893,508) | (8,284,084) | (5,839,765) |
Net loss attributable to common stockholders, diluted | $ (4,684,574) | $ (2,893,508) | $ (8,284,084) | $ (5,839,765) |
Net loss per share attributable to common stockholders, basic (in dollars per share) | $ (0.21) | $ (0.22) | $ (0.38) | $ (0.47) |
Net loss per share attributable to common stockholders, diluted (in dollars per share) | $ (0.21) | $ (0.22) | $ (0.38) | $ (0.47) |
Weighted-average shares used in computing net loss per share attributable to common stockholders, basic (in shares) | 22,215,516 | 13,107,590 | 21,995,436 | 12,493,334 |
Weighted-average shares used in computing net loss per share attributable to common stockholders, diluted (in shares) | 22,215,516 | 13,107,590 | 21,995,436 | 12,493,334 |
Organization, Nature of Business, and Liquidity |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Organization, Nature of Business, and Liquidity [Abstract] | |||
Organization, Nature of Business, and Liquidity |
Organization and Nature of Business
Femasys Inc. (the Company or Femasys) was incorporated in Delaware on February 19, 2004 and is headquartered in Suwanee, Georgia. The Company is a leading biomedical company focused on addressing significant unmet needs
for women worldwide with a broad portfolio of in-office, accessible, and innovative therapeutic and diagnostic products, including a lead revolutionary product candidate and FDA-cleared products. The Company’s mission is to provide women with superior minimally-invasive, non-surgical product technologies, accessible in the office, improving patient care and overall health
economics focused on servicing the reproductive health needs for those seeking solutions for infertility issues (FemaSeed® and FemVue®) or permanent birth control (FemBloc®). The Company currently operates as one segment with an initial focus on servicing the reproductive
health needs for those seeking solutions for infertility issues or permanent birth control.
Femasys has an expansive intellectual property portfolio which covers both design and utility patents in the U.S. and significant ex-U.S. markets for each product initiative. Femasys has taken concepts internally
conceived and protected through development, including domestic and foreign regulatory approvals, and production, through in-house manufacturing. FemaSeed, a solution which enables directed intratubal insemination to improve on traditional intrauterine insemination (IUI) and provides a lower cost and safer option to in vitro
fertilization methods, received approval to sell FemaSeed in Canada in April 2023. In September 2023, the Company received 510(k) clearance from the FDA for FemaSeed for intratubal insemination to market in the United States. A pivotal clinical
trial was still ongoing at the time of receiving regulatory clearance, however, enrollment was completed in November 2023. In June 2024, the Company received European Union Medical Device Regulation (EU MDR) certificates and CE Mark certification
for four products: FemaSeed, FemVue, FemCerv® and FemCath®. FemVue, a solution that enables fallopian tube assessment with ultrasound
as an alternative to the radiologic approach (hysterosalpingogram) for the diagnosis of infertility, is approved for sale in the U.S., Japan, and Canada. FemChec® allows for fallopian tube evaluation after a FemBloc procedure to confirm occlusion
(or procedure success). FemCerv is a solution for complete tissue sampling with minimal contamination of the endocervical canal in a virtually pain-free procedure as an alternative to the single biopsy method for diagnosis of cervical cancer and
is approved for sale in the U.S. and Canada. FemCath, allows for selective evaluation of an individual fallopian tube as an alternative to the traditional intrauterine catheter that is undirected, is approved for sale in the U.S. and Canada.
FemBloc®, the Company’s solution for permanent birth control, is based on the Company’s platform technology for delivery and in June 2023
Femasys received FDA approval of our IDE to evaluate the safety and efficacy of FemBloc, our non-surgical, non-implant, non-hormonal in-office solution for permanent birth control in a pivotal clinical trial. In August 2023 Femasys announced the
initiation of enrollment in the FINALE [Prospective Multi-Center Trial for FemBloc Intratubal Occlusion for TranscervicAL Permanent Birth Control] pivotal trial designed to evaluate the safety and efficacy of FemBloc. This prospective,
multi-center, open-label, single-arm study design includes pregnancy rate as the primary endpoint, which will be analyzed once 401
women have relied on FemBloc for one year for permanent birth control. In addition, the study is designed as a roll-in beginning with
enrollment of 50 women for a clinical readout primarily of preliminary safety data prior to enrolling the remaining subjects. An
interim analysis of clinical data endpoints is planned once 300 women have used FemBloc for permanent birth control for one year. Follow-up will continue annually for five years post-market.
Basis of Presentation
The Company has prepared the accompanying condensed financial statements pursuant to the rules and regulations of the U.S. Securities and Exchange Commission (SEC).
Certain information and footnote disclosures normally included in the annual financial statements prepared in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP) have been condensed or omitted
pursuant to these rules and regulations. These condensed financial statements should be read in conjunction with the Company’s audited financial statements and footnotes related thereto for the year ended December 31, 2023 included in our Annual
Report on Form 10K filed with the SEC on March 28, 2024 (the Annual Report). There have been no material changes to the Company’s significant accounting policies described in Note 2 to the financial statements included in the Annual Report.
In the opinion of management, the unaudited financial statements include all adjustments (consisting only of normal recurring adjustments) necessary to present fairly
the Company’s financial position and the results of its operations and cash flows at the dates for periods presented. The results of operations for such interim periods are not necessarily indicative of the results to be expected for the full year.
Use of Estimates
The preparation of financial statements in conformity with U.S. GAAP requires the Company to make estimates and assumptions that affect the
reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenue and expense during the reporting periods. Estimates for these and other
items are subject to change and are reassessed by management in accordance with U.S. GAAP. Actual results could differ from those estimates.
Liquidity
As of June 30, 2024, the Company had cash and cash equivalents of
$13,525,898. The Company plans to finance its operations and development needs with its existing cash and cash
equivalents, additional equity and/or debt financing arrangements, and revenue primarily anticipated from the sale of FemVue and FemaSeed to support the Company’s research and development activities, primarily focused on FemBloc. There can be no
assurance that the Company will be able to obtain additional financing on terms acceptable to the Company, on a timely basis, or at all. If the Company is not able to obtain sufficient funds on acceptable terms when needed, the Company’s
business, results of operations, and financial condition could be materially adversely impacted.
For the six months ended June 30, 2024, the Company generated a net loss of $8,284,084. The Company expects such losses to increase over the next few years as the
Company advances FemBloc through clinical development if and until FDA approval is received and is available to be marketed.
The financial statements have been prepared on a going-concern basis, which contemplates the realization of assets and the
satisfaction of liabilities in the normal course of business. The Company has incurred net operating losses in every year since inception and has an accumulated deficit as of June 30, 2024 of $116,665,713 and expects to incur additional losses and negative operating cash flows for at least the next twelve months. The Company’s ability to meet its obligations is
dependent upon its ability to generate sufficient cash flows from operations and future financing transactions. Although management expects the Company will continue as a going concern, there is no assurance that management’s plans will be
successful since the availability and amount of such funding is not certain. Accordingly, substantial doubt exists about the Company’s ability to continue as a going concern for at least one year from the issuance of these financial statements.
The accompanying financial statements do not include any adjustments to reflect the possible future effects on the recoverability of assets or the amounts and classifications of liabilities that may result from the possible inability of the
Company to continue as a going concern.
Recently Issued Accounting Pronouncements – Recently Adopted
In November 2023, the FASB issued ASU No. 2023-07, Segment Reporting (Topic 28): Improvements to Reportable Segment Disclosures. The ASU improves
reportable segment disclosure requirements, primarily through enhanced disclosures about significant segment expenses. The ASU improves financial reporting by requiring disclosure of incremental segment information on an annual and interim
basis for all public entities to enable investors to develop more decision-useful financial analyses. The amendments in this update are effective for fiscal years beginning after December 15, 2023, and interim periods within fiscal years
beginning after December 15, 2024. Early adoption is permitted. The Company will adopt the ASU for the fiscal year ended December 31, 2024 and interim periods in fiscal 2025. The adoption of the ASU will result in additional disclosures to the
Company’s financial statements and footnote disclosures.
Recently Issued Accounting Pronouncements – Not Yet Adopted
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures. The ASU requires the annual financial statements to include consistent categories and greater disaggregation of information in the rate reconciliation, and income taxes
paid disaggregated by jurisdiction. ASU 2023-09 is effective for the Company’s annual reporting periods beginning after December 15, 2024. Adoption is either with a prospective method or a fully retrospective method of transition. Early adoption is
permitted. The Company is currently evaluating the effect that adoption of ASU 2023-09 will have on its financial statements and expects to adopt the ASU on January 1, 2025.
No other new accounting pronouncement issued or effective has had, or is expected to have, a material impact on the Company’s financial statements.
|
Fair Value |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Fair Value [Abstract] | |||
Fair Value |
The Company applies a fair value hierarchy that requires the use of observable market data, when available, and prioritizes the inputs to valuation techniques used to measure fair value in
the following categories:
Level 1 – Valuation is based upon quoted prices for identical instruments traded in active markets.
Level 2 – Valuation is based upon quoted prices for similar instruments in active markets, quoted prices for identical or similar instruments in markets that are not
active, and model‑based valuation techniques for which all significant assumptions are observable in the market.
Level 3 – Valuation is generated from model‑based techniques that use significant assumptions not observable in the market. These unobservable assumptions reflect the
Company’s own estimates of assumptions market participants would use in pricing the asset or liability.
Certain of the Company’s financial instruments, including cash and other liabilities approximate their fair value because of the short‑term maturity of these financial instruments. The fair value
of stock options, convertible notes and warrants are based on Level 3 inputs.
|
Cash and Cash Equivalents |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Cash and Cash Equivalents [Abstract] | |||
Cash and Cash Equivalents |
As of June 30, 2024 and December 31, 2023,
money market funds included in cash and cash equivalents on the balance sheets were $12,686,738 and $21,278,895, respectively, which represent level 1 within the fair value hierarchy where there are quoted prices in active markets for identical assets.
|
Inventories |
6 Months Ended | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inventories [Abstract] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inventories |
Inventory stated at cost,
net of reserve, consisted of the following:
|
Accrued Expenses |
6 Months Ended | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Jun. 30, 2024 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Accrued Expenses [Abstract] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Accrued Expenses |
Accrued expenses consisted of the following:
|
Clinical Holdback |
6 Months Ended | ||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | |||||||||||||||||||||||||||||||||
Clinical Holdback [Abstract] | |||||||||||||||||||||||||||||||||
Clinical Holdback |
The following table shows the activity
within the clinical holdback liability accounts for the six months ended June 30, 2024:
|
Revenue Recognition |
6 Months Ended | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Jun. 30, 2024 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Revenue Recognition [Abstract] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Revenue Recognition |
Revenue is recognized upon shipment of our
goods based upon contractually stated pricing at standard payment terms ranging from 30 to 60 days. All revenue is recognized point in time and no revenue is recognized over time. For the three and six months ended June 30, 2024 and 2023, there was no revenue recognized from performance obligations satisfied or partially satisfied in prior periods, nor were there any unsatisfied performance
obligations as of June 30, 2024 or 2023.
The majority of products sold directly to
U.S customers are shipped via common carrier, and the customer pays for shipping and handling and assumes control Free on Board (FOB) shipping point. Products shipped to our international distributors are in accordance with their respective
agreements; however, the shipping terms are generally EX-Works, reflecting that control is assumed by the distributor at the shipping point. Returns are only accepted with prior authorization from the Company. Items to be returned must be in
original unopened cartons and are subject to a 30% restocking fee. Throughout the periods presented, the Company has not had a history
of significant returns.
The following table summarizes our sales,
primarily from FemVue, by geographic region as follows:
|
Commitments and Contingencies |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Commitments and Contingencies [Abstract] | |||
Commitments and Contingencies |
Legal Claims
Occasionally, the Company may be a party to legal claims or
proceedings of which the outcomes are subject to significant uncertainty. In accordance with Accounting Standards Codification (ASC) 450, Contingencies, the Company will assess the
likelihood of an adverse judgment for any outstanding claim as well as ranges of probable losses. When it has been determined that a loss is probable and the amount can be reasonably estimated, the Company will record a liability. For both periods
presented, there were no material legal contingencies requiring accrual or disclosure.
The Company, as permitted under Delaware law and in accordance
with its bylaws, indemnifies its officers and directors for certain events or occurrences, subject to certain limits, while the officer or director is or was serving at the Company’s request in such capacity. The Company entered into employment
agreements with its officers, which provides for indemnification protection in the executive’s capacity as an officer for actions taken within the scope of employment. The maximum amount of potential future indemnification is unlimited; however, the
Company has obtained director and officer insurance that limits its exposure. The Company believes the fair value for these indemnification obligations is minimal. Accordingly, the Company has not recognized any liabilities relating to these
obligations as of June 30, 2024 and December 31, 2023.
|
Notes Payable |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Notes Payable [Abstract] | |||
Notes Payable |
AFCO
Credit Corporation (AFCO)
In June 2022, the Company executed a Promissory Note with AFCO to finance certain insurance premiums totaling $465,380, requiring the Company to pay $47,539 in a down payment
and make monthly installment payments. The annual interest rate was 5.7% and the monthly installment payment was $47,539, which represents
principal and interest. The final installment payment was paid in
. In July 2023, the Company executed a Promissory Note with AFCO to finance certain insurance premiums totaling $469,042, requiring the Company to pay $48,423
in a down payment and make monthly installment payments. The annual interest rate was 8.6% and the monthly installment is $48,423, which
represents principal and interest. The Promissory Note was paid in full without penalty in .
As of June 30, 2024, and December 31, 2023, there was no principal balance on the AFCO note in the accompanying balance sheets. Interest expense in connection with the AFCO promissory notes was $0 and $1,319 for the three and six months ended June 30, 2024 and 2023, respectively.
|
Convertible Notes with Warrants (November 2023 Financing) |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Convertible Notes with Warrants (November 2023 Financing) [Abstract] | |||
Convertible Notes with Warrants (November 2023 Financing) |
On November 21, 2023, the Company issued (i) senior unsecured convertible notes in an aggregate principal amount of $6,850,000, convertible into shares of common stock at a conversion price of $1.18 per share, (ii) Series A Warrants to purchase up to an aggregate of 5,805,083
shares of common stock at an exercise price of $1.18 per share, and (iii) Series B Warrants, together with the Series A Warrants,
and, together with the convertible notes, to purchase up to an aggregate of 5,805,083 shares of common stock at an exercise price of
$1.475 per share. The financing resulted in aggregate gross proceeds of $6,850,000, before $525,144 of transaction costs.
The Notes accrue interest at a rate of 6.0%
per annum, payable annually, in cash or shares of common stock at the Company’s option, and mature on November 21, 2025, unless
earlier converted or redeemed.
The Notes are convertible into shares of common stock at the election of the holder at any time at an initial conversion price of $1.18. The Company has agreed not to issue or sell any equity securities of the Company at a price below the then-current conversion price for a
period of 18 months after closing, subject to certain exceptions. Beginning six months after issuance, the Company may require
holders to convert their Notes into conversion shares if the closing price of the common stock exceeds $2.36 per share for 10 consecutive trading days and the daily dollar trading volume of the common stock exceeds $1,000,000 per day during the same period and certain equity conditions described in the Notes are satisfied. The Notes provide for certain events of default, whereby each
holder of Notes will be able to require the Company to redeem in cash any or all of the holder’s Notes at a premium of 115%. The
conversion feature did not meet the requirements for separate accounting and is not accounted for as a derivative instrument. As of June 30, 2024, the Convertible Notes have not been converted into shares of common stock.
The Warrants
The Series A Warrants are exercisable immediately and expire five years from the date of issuance. The Company has the right to call the exercise of the Series A Warrants if the closing price of the common stock exceeds 200% of the Series A Exercise Price for 10 consecutive trading
days and the daily dollar trading volume of the common stock exceeds $1,000,000 per day during the same period and certain equity
conditions are satisfied.
The Series B Warrants are exercisable immediately, together with the Series A Warrant Shares, and expire one year from the date of issuance. The Company has the right to call the exercise of the Series B Warrants if the closing price of the common stock exceeds 200% of the Series B exercise price for 10
consecutive trading days and the daily dollar trading volume of the common stock exceeds $1,000,000 per day during the same period and
certain equity conditions are satisfied. There is no established public trading market for the warrants and the Company does not intend to list the Warrants on any national securities exchange or nationally recognized trading system.
The Series A Warrants and Series B Warrants are classified as a component of permanent equity because they are freestanding financial instruments
that are legally detachable and separately exercisable from the shares of common stock from which they are issued, are immediately exercisable, do not embody an obligation for the Company to repurchase its shares, and permit the holders to
receive a fixed number of shares of common stock upon exercise.
For the convertible notes for the three months ended June 30, 2024, the Company recognized total
interest expense of $388,311, including coupon interest expense of $102,750 and amortization of debt discount and issuance costs of $285,561. For the six months ended June 30, 2024, the Company
recognized total interest expense of $749,863, including coupon interest expense of $205,500 and amortization of debt discount and issuance costs of $544,363.
As of December 31, 2023, the Notes principal balance as $6,850,000, unamortized discount was $2,636,346 and accrued interest was $44,525.
As of June 30, 2024, the Notes principal balance as $6,850,000, unamortized discount was $2,091,983 and accrued interest was $250,025. The fair value
of the convertible notes on June 30, 2024, calculated using a discounted cash flow analysis, was $6,307,258.
|
Stockholders' Equity |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Stockholders' Equity [Abstract] | |||
Stockholders' Equity |
On July 1, 2022, we filed shelf registration statement to sell up to $150 million in common and preferred stock, debt securities and warrants. Additionally, we entered into an Equity Distribution Agreement (the “Equity Distribution Agreement”) with Piper
Sandler & Co. (“Piper Sandler” or the “Sales Agent”) and filed a related prospectus establishing an “at-the-market” facility, pursuant to which we may offer and sell shares of our common stock from time to time through the Sales Agent. In
October 2023, the Sales Agent was authorized to sell shares for aggregate proceeds up to $16.7 million at current market prices until all
shares are sold. As of June 30, 2024, 3.9 million shares of common stock have been sold for aggregate proceeds of approximately $8.7 million under the Equity Distribution Agreement pursuant to the
prospectus. As of June 30, 2024, the amount we are authorized to sell is subject to baby-shelf limitations.
In April 2023, the Company sold an aggregate of (i) 1,318,000 shares of common stock and (ii) pre-funded warrants to purchase up to 1,878,722
shares of common stock in a registered direct offering (“pre-funded warrants”) and, in a concurrent private placement, warrants to purchase up to 3,196,722
shares of common stock (“common warrants”). Additionally, common warrants were issued to the placement agent to purchase up to 191,803
shares of common stock as compensation for services (“placement agent warrants”), collectively the (“April 2023 Financing”). The purchase price per share for the common stock, pre-funded warrants was $1.22 and $1.2199, respectively. The gross proceeds from the
offering were $3,899,813, less placement agent fees and offering expenses of $547,764.
In
June 2023, all pre-funded warrants were exercised for shares of common stock. In September and October 2023, all common warrants and 122,994
placement agent warrants were exercised for cash proceeds of $3,687,976. As of June 30, 2024, 68,809 placement agent warrants remain outstanding.
As of June 30, 2024, the Company had 22,232,799 shares of common stock outstanding, and no
dividends have been declared or paid.
|
Equity Incentive Plans and Warrants |
6 Months Ended | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Jun. 30, 2024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Equity Incentive Plans and Warrants [Abstract] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Equity Incentive Plans and Warrants |
Stock-Based Awards
Activity under the Company’s stock option plans for the six months ended June
30, 2024 was as follows:
Options granted under our 2021 Stock Option Plan for the six months ended June
30, 2024 to employees and nonemployees were 1,059,921 and 2,500, respectively and the weighted average exercise prices were $1.06
and $0.79, respectively. The weighted-average fair values of the options granted to employees and nonemployees were $0.90 and $0.39, respectively and were
estimated using the following Black-Scholes assumptions:
No options were exercised for the six months ended June
30, 2024 under our stock option plans.
As of June 30, 2024, the total number of shares of common stock reserved for future awards under the 2021 Stock Option Plan was 676,741.
On February 12, 2024, the Company awarded, outside the 2021 Plan, our Chief Commercial Officer a stock option grant for the right to purchase 100,000 shares of common stock at an exercise price of $1.10 per share
(inducement grant), which was approved by the Compensation committee. The inducement grant will vest in equal installments over four years
provided the employee remains employed by the Company on the vesting date. The fair value of the inducement grant was $0.94 and was
estimated using the following assumptions:
As of June 30, 2024, inducement
grant awards of 250,000 shares were outstanding with a weighted average exercise price of $1.89, and 62,500 shares were
vested and exercisable with a weighted average exercise price of $2.64.
The following table shows the share-based compensation expense related to vested stock option grants
to employees and nonemployees by financial statement line item on the accompanying condensed statement of comprehensive loss:
As of June 30, 2024, the remaining share-based compensation expense that is expected to be recognized in future periods for employees and nonemployees is $1,516,737, which includes $155,222 of
compensation expense to be recognized upon achieving certain performance conditions. For service-based awards, the $1,361,515 of
unrecognized expense is expected to be recognized over a weighted average period of 3.3 years.
For the six months ended June 30, 2024, 12,081
shares of common stock were issued under the Company’s ESPP Plan at a fair value of $10,390. For the six months ended June 30,
2023, 3,858 shares of common stock were issued under the ESPP plan at a fair value of $1,697. As of June 30, 2024, the total number of shares of common stock reserved for future awards under the ESPP Plan was 591,437.
On April 20, 2023, the Company entered into a securities purchase agreement pursuant to which
the Company sold (i) 1,318,000 shares of common stock (see Note 11, Stockholders’ Equity),
(ii) pre-funded warrants to purchase 1,878,722 shares of common stock, (iii) common warrants to purchase 3,196,722 shares of common stock. Additionally, common warrants to purchase 191,803 shares of common stock were issued to the placement agent compensation for services performed.
The pre-funded warrants, common warrants and placement agent warrants were exercisable
immediately following the closing date of the offering. The pre-funded warrants have an unlimited term and an exercise price of $0.0001
per share. The common warrants have a 5.5 year term and an exercise price of $1.095 per share. The placement agent warrants have a 5 year
term and exercise price of $1.525 per share. The offering resulted in aggregate gross proceeds of $3,899,813, before $547,764 of
transaction costs.
The pre-funded warrants and common warrants are classified as a component of permanent equity
because they are freestanding financial instruments that are legally detachable and separately exercisable from the shares of common stock with which they were issued, are immediately exercisable, do not embody an obligation for the Company to
repurchase its shares, and permit the holders to receive a fixed number of shares of common stock upon exercise.
The common stock was valued at $1,133,480, based on the Company’s stock price. The pre-funded warrants and common warrants were valued at $1,615,701 and $1,854,099, respectively, using the following Black-Scholes
assumptions:
The net proceeds of $3,352,049 were allocated to the common stock, pre-funded warrants and common warrants using the relative fair value method. The valuations were
recorded to stockholders’ equity.
In June 2023, all pre-funded
warrants were exercised for shares of common stock. In September and October 2023, all
common warrants and 122,994 placement agent warrants were exercised for cash proceeds of $3,687,976. As of June 30, 2024, 68,809
placement agent warrants remain outstanding.
|
Related-Party Transactions |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Related-Party Transactions [Abstract] | |||
Related-Party Transactions |
In November 2023, the Company issued unsecured convertible notes and accompanying Series A and Series B Warrants (see Note 10). The transaction included
issuance of a $5 million convertible note and Series A and Series B Warrants to PharmaCyte Biotech, Inc. The interim CEO, President and
Director of PharmaCyte Biotech, Inc., Joshua Silverman, serves on the Company’s board of directors. In addition, during the year ended December 31, 2023 and six months ended June 30, 2024 and 2023, a family member of the CEO was employed by the
Company.
|
Net Loss per Share Attributable to Common Stockholders |
6 Months Ended | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Jun. 30, 2024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Net Loss per Share Attributable to Common Stockholders [Abstract] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Net Loss per Share Attributable to Common Stockholders |
The following table sets forth the computation of the basic and diluted net loss per share:
The following potentially dilutive securities have been excluded from the computations of diluted weighted average shares outstanding
because they would be anti-dilutive:
|
Income Taxes |
6 Months Ended | ||
---|---|---|---|
Jun. 30, 2024 | |||
Income Taxes [Abstract] | |||
Income Taxes [Text Block] |
The effective tax rate of 0% for the three and six
months ended June 30, 2024 and 2023 was lower than the statutory rate due to the Company remaining in a full valuation allowance position.
|
Insider Trading Arrangements |
3 Months Ended |
---|---|
Jun. 30, 2024 | |
Insider Trading Arrangements [Line Items] | |
Rule 10b5-1 Arrangement Adopted | false |
Non-Rule 10b5-1 Arrangement Adopted | false |
Rule 10b5-1 Arrangement Terminated | false |
Non-Rule 10b5-1 Arrangement Terminated | false |
Organization, Nature of Business, and Liquidity (Policies) |
6 Months Ended |
---|---|
Jun. 30, 2024 | |
Organization, Nature of Business, and Liquidity [Abstract] | |
Organization and Nature of Business |
Organization and Nature of Business
Femasys Inc. (the Company or Femasys) was incorporated in Delaware on February 19, 2004 and is headquartered in Suwanee, Georgia. The Company is a leading biomedical company focused on addressing significant unmet needs
for women worldwide with a broad portfolio of in-office, accessible, and innovative therapeutic and diagnostic products, including a lead revolutionary product candidate and FDA-cleared products. The Company’s mission is to provide women with superior minimally-invasive, non-surgical product technologies, accessible in the office, improving patient care and overall health
economics focused on servicing the reproductive health needs for those seeking solutions for infertility issues (FemaSeed® and FemVue®) or permanent birth control (FemBloc®). The Company currently operates as one segment with an initial focus on servicing the reproductive
health needs for those seeking solutions for infertility issues or permanent birth control.
Femasys has an expansive intellectual property portfolio which covers both design and utility patents in the U.S. and significant ex-U.S. markets for each product initiative. Femasys has taken concepts internally
conceived and protected through development, including domestic and foreign regulatory approvals, and production, through in-house manufacturing. FemaSeed, a solution which enables directed intratubal insemination to improve on traditional intrauterine insemination (IUI) and provides a lower cost and safer option to in vitro
fertilization methods, received approval to sell FemaSeed in Canada in April 2023. In September 2023, the Company received 510(k) clearance from the FDA for FemaSeed for intratubal insemination to market in the United States. A pivotal clinical
trial was still ongoing at the time of receiving regulatory clearance, however, enrollment was completed in November 2023. In June 2024, the Company received European Union Medical Device Regulation (EU MDR) certificates and CE Mark certification
for four products: FemaSeed, FemVue, FemCerv® and FemCath®. FemVue, a solution that enables fallopian tube assessment with ultrasound
as an alternative to the radiologic approach (hysterosalpingogram) for the diagnosis of infertility, is approved for sale in the U.S., Japan, and Canada. FemChec® allows for fallopian tube evaluation after a FemBloc procedure to confirm occlusion
(or procedure success). FemCerv is a solution for complete tissue sampling with minimal contamination of the endocervical canal in a virtually pain-free procedure as an alternative to the single biopsy method for diagnosis of cervical cancer and
is approved for sale in the U.S. and Canada. FemCath, allows for selective evaluation of an individual fallopian tube as an alternative to the traditional intrauterine catheter that is undirected, is approved for sale in the U.S. and Canada.
FemBloc®, the Company’s solution for permanent birth control, is based on the Company’s platform technology for delivery and in June 2023
Femasys received FDA approval of our IDE to evaluate the safety and efficacy of FemBloc, our non-surgical, non-implant, non-hormonal in-office solution for permanent birth control in a pivotal clinical trial. In August 2023 Femasys announced the
initiation of enrollment in the FINALE [Prospective Multi-Center Trial for FemBloc Intratubal Occlusion for TranscervicAL Permanent Birth Control] pivotal trial designed to evaluate the safety and efficacy of FemBloc. This prospective,
multi-center, open-label, single-arm study design includes pregnancy rate as the primary endpoint, which will be analyzed once 401
women have relied on FemBloc for one year for permanent birth control. In addition, the study is designed as a roll-in beginning with
enrollment of 50 women for a clinical readout primarily of preliminary safety data prior to enrolling the remaining subjects. An
interim analysis of clinical data endpoints is planned once 300 women have used FemBloc for permanent birth control for one year. Follow-up will continue annually for five years post-market.
|
Basis of Presentation |
Basis of Presentation
The Company has prepared the accompanying condensed financial statements pursuant to the rules and regulations of the U.S. Securities and Exchange Commission (SEC).
Certain information and footnote disclosures normally included in the annual financial statements prepared in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP) have been condensed or omitted
pursuant to these rules and regulations. These condensed financial statements should be read in conjunction with the Company’s audited financial statements and footnotes related thereto for the year ended December 31, 2023 included in our Annual
Report on Form 10K filed with the SEC on March 28, 2024 (the Annual Report). There have been no material changes to the Company’s significant accounting policies described in Note 2 to the financial statements included in the Annual Report.
In the opinion of management, the unaudited financial statements include all adjustments (consisting only of normal recurring adjustments) necessary to present fairly
the Company’s financial position and the results of its operations and cash flows at the dates for periods presented. The results of operations for such interim periods are not necessarily indicative of the results to be expected for the full year.
|
Use of Estimates |
Use of Estimates
The preparation of financial statements in conformity with U.S. GAAP requires the Company to make estimates and assumptions that affect the
reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenue and expense during the reporting periods. Estimates for these and other
items are subject to change and are reassessed by management in accordance with U.S. GAAP. Actual results could differ from those estimates.
|
Liquidity |
Liquidity
As of June 30, 2024, the Company had cash and cash equivalents of
$13,525,898. The Company plans to finance its operations and development needs with its existing cash and cash
equivalents, additional equity and/or debt financing arrangements, and revenue primarily anticipated from the sale of FemVue and FemaSeed to support the Company’s research and development activities, primarily focused on FemBloc. There can be no
assurance that the Company will be able to obtain additional financing on terms acceptable to the Company, on a timely basis, or at all. If the Company is not able to obtain sufficient funds on acceptable terms when needed, the Company’s
business, results of operations, and financial condition could be materially adversely impacted.
For the six months ended June 30, 2024, the Company generated a net loss of $8,284,084. The Company expects such losses to increase over the next few years as the
Company advances FemBloc through clinical development if and until FDA approval is received and is available to be marketed.
The financial statements have been prepared on a going-concern basis, which contemplates the realization of assets and the
satisfaction of liabilities in the normal course of business. The Company has incurred net operating losses in every year since inception and has an accumulated deficit as of June 30, 2024 of $116,665,713 and expects to incur additional losses and negative operating cash flows for at least the next twelve months. The Company’s ability to meet its obligations is
dependent upon its ability to generate sufficient cash flows from operations and future financing transactions. Although management expects the Company will continue as a going concern, there is no assurance that management’s plans will be
successful since the availability and amount of such funding is not certain. Accordingly, substantial doubt exists about the Company’s ability to continue as a going concern for at least one year from the issuance of these financial statements.
The accompanying financial statements do not include any adjustments to reflect the possible future effects on the recoverability of assets or the amounts and classifications of liabilities that may result from the possible inability of the
Company to continue as a going concern.
|
Recently Issued Accounting Pronouncements Adopted and Not Yet Adopted |
Recently Issued Accounting Pronouncements – Recently Adopted
In November 2023, the FASB issued ASU No. 2023-07, Segment Reporting (Topic 28): Improvements to Reportable Segment Disclosures. The ASU improves
reportable segment disclosure requirements, primarily through enhanced disclosures about significant segment expenses. The ASU improves financial reporting by requiring disclosure of incremental segment information on an annual and interim
basis for all public entities to enable investors to develop more decision-useful financial analyses. The amendments in this update are effective for fiscal years beginning after December 15, 2023, and interim periods within fiscal years
beginning after December 15, 2024. Early adoption is permitted. The Company will adopt the ASU for the fiscal year ended December 31, 2024 and interim periods in fiscal 2025. The adoption of the ASU will result in additional disclosures to the
Company’s financial statements and footnote disclosures.
Recently Issued Accounting Pronouncements – Not Yet Adopted
In December 2023, the FASB issued ASU 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures. The ASU requires the annual financial statements to include consistent categories and greater disaggregation of information in the rate reconciliation, and income taxes
paid disaggregated by jurisdiction. ASU 2023-09 is effective for the Company’s annual reporting periods beginning after December 15, 2024. Adoption is either with a prospective method or a fully retrospective method of transition. Early adoption is
permitted. The Company is currently evaluating the effect that adoption of ASU 2023-09 will have on its financial statements and expects to adopt the ASU on January 1, 2025.
No other new accounting pronouncement issued or effective has had, or is expected to have, a material impact on the Company’s financial statements.
|
Inventories (Tables) |
6 Months Ended | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inventories [Abstract] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inventory Stated at Cost, Net of Reserve |
Inventory stated at cost,
net of reserve, consisted of the following:
|
Accrued Expenses (Tables) |
6 Months Ended | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Accrued Expenses [Abstract] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Accrued Expenses |
Accrued expenses consisted of the following:
|
Clinical Holdback (Tables) |
6 Months Ended | ||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | |||||||||||||||||||||||||||||||
Clinical Holdback [Abstract] | |||||||||||||||||||||||||||||||
Clinical Holdback Liability |
The following table shows the activity
within the clinical holdback liability accounts for the six months ended June 30, 2024:
|
Revenue Recognition (Tables) |
6 Months Ended | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Revenue Recognition [Abstract] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sales by Geographic Region |
The following table summarizes our sales,
primarily from FemVue, by geographic region as follows:
|
Equity Incentive Plans and Warrants (Tables) |
6 Months Ended | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Equity Incentive Plans and Warrants [Abstract] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stock Option Plan Activity |
Activity under the Company’s stock option plans for the six months ended June
30, 2024 was as follows:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Share-based Compensation Expense |
The following table shows the share-based compensation expense related to vested stock option grants
to employees and nonemployees by financial statement line item on the accompanying condensed statement of comprehensive loss:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Warrants Valuation Assumptions |
The common stock was valued at $1,133,480, based on the Company’s stock price. The pre-funded warrants and common warrants were valued at $1,615,701 and $1,854,099, respectively, using the following Black-Scholes
assumptions:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
2021 Stock Option Plan [Member] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Estimated Using Assumptions |
Options granted under our 2021 Stock Option Plan for the six months ended June
30, 2024 to employees and nonemployees were 1,059,921 and 2,500, respectively and the weighted average exercise prices were $1.06
and $0.79, respectively. The weighted-average fair values of the options granted to employees and nonemployees were $0.90 and $0.39, respectively and were
estimated using the following Black-Scholes assumptions:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inducement Grant [Member] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Estimated Using Assumptions |
On February 12, 2024, the Company awarded, outside the 2021 Plan, our Chief Commercial Officer a stock option grant for the right to purchase 100,000 shares of common stock at an exercise price of $1.10 per share
(inducement grant), which was approved by the Compensation committee. The inducement grant will vest in equal installments over four years
provided the employee remains employed by the Company on the vesting date. The fair value of the inducement grant was $0.94 and was
estimated using the following assumptions:
|
Net Loss per Share Attributable to Common Stockholders (Tables) |
6 Months Ended | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Jun. 30, 2024 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Net Loss per Share Attributable to Common Stockholders [Abstract] | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Computation of Basic and Diluted Net Loss Per Share |
The following table sets forth the computation of the basic and diluted net loss per share:
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Computations of Diluted Weighted Average Shares Outstanding |
The following potentially dilutive securities have been excluded from the computations of diluted weighted average shares outstanding
because they would be anti-dilutive:
|
Cash and Cash Equivalents (Details) - USD ($) |
Jun. 30, 2024 |
Dec. 31, 2023 |
---|---|---|
Level 1 [Member] | Money Market Funds [Member] | ||
Assets, Fair Value Disclosure [Abstract] | ||
Cash and cash equivalent | $ 12,686,738 | $ 21,278,895 |
Inventories (Details) - USD ($) |
Jun. 30, 2024 |
Dec. 31, 2023 |
---|---|---|
Inventories [Abstract] | ||
Materials | $ 792,365 | $ 367,934 |
Work in progress | 229,045 | 128,993 |
Finished goods | 294,170 | 170,191 |
Inventory, net | $ 1,315,580 | $ 667,118 |
Accrued Expenses (Details) - USD ($) |
Jun. 30, 2024 |
Dec. 31, 2023 |
---|---|---|
Accrued Expenses [Abstract] | ||
Clinical trail costs | $ 334,799 | $ 276,141 |
Accrued interest | 250,025 | 0 |
Incentive and other compensation costs | 170,328 | 1,082,606 |
Director fees | 70,000 | 60,210 |
Franchise taxes | 3,150 | 12,160 |
Other | 58,050 | 13,179 |
Accrued expenses | $ 886,352 | $ 1,444,296 |
Clinical Holdback (Details) - USD ($) |
6 Months Ended | |
---|---|---|
Jun. 30, 2024 |
Dec. 31, 2023 |
|
Clinical Holdback Liability [Roll Forward] | ||
Balance | $ 120,235 | |
Clinical holdback retained | 5,990 | |
Clinical holdback paid | (1,122) | |
Balance | 125,103 | |
Less: clinical holdback - current portion | (92,397) | $ (65,300) |
Clinical holdback - long-term portion | $ 32,706 | $ 54,935 |
Revenue Recognition (Details) - USD ($) |
3 Months Ended | 6 Months Ended | ||
---|---|---|---|---|
Jun. 30, 2024 |
Jun. 30, 2023 |
Jun. 30, 2024 |
Jun. 30, 2023 |
|
Revenue Recognition [Abstract] | ||||
Revenue recognized from performance obligations in prior periods | $ 0 | $ 0 | $ 0 | $ 0 |
Percentage of restocking fee | 30.00% | |||
Primary Geographical Markets [Abstract] | ||||
Sales | 221,484 | 320,514 | $ 492,624 | 614,498 |
FemVue [Member] | ||||
Primary Geographical Markets [Abstract] | ||||
Sales | 221,484 | 320,514 | 492,624 | 614,498 |
FemVue [Member] | U.S. [Member] | ||||
Primary Geographical Markets [Abstract] | ||||
Sales | 221,484 | 262,469 | 492,624 | 556,453 |
FemVue [Member] | International [Member] | ||||
Primary Geographical Markets [Abstract] | ||||
Sales | $ 0 | $ 58,045 | $ 0 | $ 58,045 |
Minimum [Member] | ||||
Revenue Recognition [Abstract] | ||||
Revenue recognition payment period term | 30 days | |||
Maximum [Member] | ||||
Revenue Recognition [Abstract] | ||||
Revenue recognition payment period term | 60 days |
Notes Payable (Details) - USD ($) |
1 Months Ended | 3 Months Ended | 6 Months Ended | ||||
---|---|---|---|---|---|---|---|
Jul. 31, 2023 |
Jun. 30, 2022 |
Jun. 30, 2024 |
Jun. 30, 2023 |
Jun. 30, 2024 |
Jun. 30, 2023 |
Dec. 31, 2023 |
|
Notes Payable [Abstract] | |||||||
Down payments | $ 0 | $ 141,298 | |||||
July Promissory Note [Member] | AFCO Credit Corporation [Member] | |||||||
Notes Payable [Abstract] | |||||||
Proceeds to pay insurance premiums | $ 469,042 | ||||||
Down payments | $ 48,423 | ||||||
Interest rate | 8.60% | ||||||
Frequency of installment payments | monthly | ||||||
Monthly principal and interest payments | $ 48,423 | ||||||
Maturity date of loan | Nov. 30, 2023 | ||||||
Note payable | $ 0 | $ 0 | $ 0 | ||||
Interest expense on loan | $ 0 | $ 1,319 | $ 0 | $ 1,319 | |||
June Promissory Note [Member] | AFCO Credit Corporation [Member] | |||||||
Notes Payable [Abstract] | |||||||
Proceeds to pay insurance premiums | $ 465,380 | ||||||
Down payments | $ 47,539 | ||||||
Interest rate | 5.70% | ||||||
Frequency of installment payments | monthly | ||||||
Monthly principal and interest payments | $ 47,539 | ||||||
Maturity date of loan | Mar. 31, 2023 |
Convertible Notes with Warrants (November 2023 Financing), Warrants (Details) - November 2023 Financing [Member] - USD ($) |
6 Months Ended | |
---|---|---|
Nov. 21, 2023 |
Jun. 30, 2024 |
|
Warrants [Abstract] | ||
Consecutive trading days | 10 days | |
Daily dollar trading volume of common stock exceeds per day | $ 1,000,000 | |
Series A Warrants [Member] | ||
Warrants [Abstract] | ||
Warrants term | 5 years | |
Percentage of warrant closing price of common stock exceeds | 200.00% | |
Consecutive trading days | 10 days | |
Daily dollar trading volume of common stock exceeds per day | $ 1,000,000 | |
Series B Warrants [Member] | ||
Warrants [Abstract] | ||
Warrants term | 1 year | |
Percentage of warrant closing price of common stock exceeds | 200.00% | |
Consecutive trading days | 10 days | |
Daily dollar trading volume of common stock exceeds per day | $ 1,000,000 |
Convertible Notes with Warrants (November 2023 Financing), Convertible Notes Payable (Details) - USD ($) |
3 Months Ended | 6 Months Ended | ||
---|---|---|---|---|
Jun. 30, 2024 |
Jun. 30, 2024 |
Jun. 30, 2023 |
Dec. 31, 2023 |
|
Convertible Notes [Abstract] | ||||
Amortization of debt discount and issuance costs | $ 544,363 | $ 0 | ||
Convertible Notes Payable [Abstract] | ||||
Accrued and unpaid interest | $ 250,025 | 250,025 | $ 0 | |
November 2023 Financing [Member] | Convertible Notes [Member] | ||||
Convertible Notes [Abstract] | ||||
Interest expense | 388,311 | 749,863 | ||
Coupon interest expense | 102,750 | 205,500 | ||
Amortization of debt discount and issuance costs | 285,561 | 544,363 | ||
Convertible Notes Payable [Abstract] | ||||
Notes principal balance | 6,850,000 | 6,850,000 | 6,850,000 | |
Accrued and unpaid interest | 250,025 | 250,025 | 44,525 | |
Unamortized discount and debt issuance costs | 2,091,983 | 2,091,983 | $ 2,636,346 | |
Convertible note, fair value | $ 6,307,258 | $ 6,307,258 |
Equity Incentive Plans and Warrants, Inducement Grant (Details) - Inducement Grant [Member] - $ / shares |
Feb. 12, 2024 |
Jun. 30, 2024 |
---|---|---|
Inducement Grant [Abstract] | ||
Granted (in shares) | 100,000 | |
Weighted average exercise price (in dollars per share) | $ 1.1 | $ 1.89 |
Vesting period | 4 years | |
Weighted-average fair values of options granted (in dollars per share) | $ 0.94 | |
Estimated Fair Value Assumptions [Abstract] | ||
Expected term (in years) | 6 years 3 months | |
Risk free interest rate | 4.10% | |
Dividend yield | 0.00% | |
Expected volatility | 109.64% | |
Shares outstanding (in shares) | 250,000 | |
Options vested and exercisable, Number of option vested (in shares) | 62,500 | |
Options vested and exercisable, Weighted average exercise price (in dollars per shares) | $ 2.64 |
Equity Incentive Plans and Warrants, Employee Stock Purchase Plan (Details) - USD ($) |
3 Months Ended | 6 Months Ended | ||
---|---|---|---|---|
Jun. 30, 2024 |
Jun. 30, 2023 |
Jun. 30, 2024 |
Jun. 30, 2023 |
|
Employee Stock Purchase Plan [Abstract] | ||||
Stock issued, fair value | $ 10,390 | $ 1,697 | $ 10,390 | $ 1,697 |
Employee Stock Purchase Plan [Member] | ||||
Employee Stock Purchase Plan [Abstract] | ||||
Stock issued (in shares) | 12,081 | 3,858 | ||
Stock issued, fair value | $ 10,390 | $ 1,697 | ||
Common stock reserved for issuance (in shares) | 591,437 | 591,437 |
Related-Party Transactions (Details) $ in Millions |
1 Months Ended |
---|---|
Nov. 30, 2023
USD ($)
| |
Related-Party Transactions [Abstract] | |
Related-party transaction | $ 5 |
Income Taxes (Details) |
3 Months Ended | 6 Months Ended | ||
---|---|---|---|---|
Jun. 30, 2024 |
Jun. 30, 2023 |
Jun. 30, 2024 |
Jun. 30, 2023 |
|
Effective Income Tax Rate Reconciliation, Percent [Abstract] | ||||
Effective tax rate | 0.00% | 0.00% | 0.00% | 0.00% |
1 Year Femasys Chart |
1 Month Femasys Chart |
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