Cyclerion Therapeutics Inc
For the period ended Jun 30, 2024. Filed Aug 7, 2024.
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A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.
Jun 30, 2024 · Filed Aug 7, 2024
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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
| ☒ | QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended June 30,2024
or
| ☐ | TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the transition period from to
Commission File Number 001-38787
CYCLERION THERAPEUTICS, INC.
(Exact Name of Registrant as Specified in its Charter)
| Massachusetts(State or other jurisdiction ofincorporation or organization) | 83-1895370(I.R.S. EmployerIdentification No.) |
|---|---|
| 245 First Street, 18th Floor, Cambridge, Massachusetts(Address of principal executive offices) | 02142(Zip Code) |
(857)327-8778
Registrant’s Telephone Number, Including Area Code
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading Symbol(s) | Name of each exchange on which registered |
|---|---|---|
| Common Stock, no par value | CYCN | The Nasdaq Capital Market LLC |
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
| Large accelerated filer ☐ | Accelerated filer ☐ |
|---|---|
| Non-accelerated filer ☒ | Smaller reporting company ☒ |
| Emerging growth company ☒ |
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No☒
As of August 5, 2024, the registrant had 2,710,096 shares of common stock, no par value, outstanding.
CYCLERION PHARMACEUTICALS, INC.
QUARTERLY REPORT ON FORM 10-Q
FOR THE QUARTER ENDED JUNE 30, 2024
TABLE OF CONTENTS
| Page | ||
|---|---|---|
| PART I — FINANCIAL INFORMATION | ||
| Item 1. | Financial Statements (unaudited) | 5 |
| Condensed Consolidated Balance Sheets as of June 30, 2024 and December 31, 2023 | 5 | |
| Condensed Consolidated Statements of Operations and Comprehensive Loss for Three and Six Months Ended June 30, 2024 and 2023 | 6 | |
| Condensed Consolidated Statements of Stockholders’ Equity for Three and Six Months Ended June 30, 2024 and 2023 | 7 | |
| Condensed Consolidated Statements of Cash Flows for Three and Six Months Ended June 30, 2024 and 2023 | 8 | |
| Notes to the Condensed Consolidated Financial Statements | 9 | |
| Item 2. | Management’s Discussion and Analysis of Financial Condition and Results of Operations | 21 |
| Item 3. | Quantitative and Qualitative Disclosures About Market Risk | 27 |
| Item 4. | Controls and Procedures | 27 |
| PART II — OTHER INFORMATION | ||
| Item 1. | Legal Proceedings | 29 |
| Item 1A. | Risk Factors | 29 |
| Item 5. | Other Information | 29 |
| Item 6. | Exhibits | 29 |
| Signatures | 31 | |
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of the federal securities laws, which statements involve substantial risks and uncertainties. All statements in this report, other than statements of historical facts, including statements about future events, financing plans, financial position, business strategy, budgets, projected costs, plans and objectives of management for future operations, are forward-looking statements that involve certain risks and uncertainties. Use of the words “may,” “might,” “will,” “would,” “could,” “should,” “believes,” “estimates,” “projects,” “potential,” “expects,” “plans,” “seeks,” “intends,” “evaluates,” “pursues,” “anticipates,” “continues,” “designs,” “impacts,” “affects,” “forecasts,” “target,” “outlook,” “initiative,” “objective,” “designed,” “priorities,” “goal” or the negative of those words or other similar expressions may identify forward-looking statements that represent our current judgment about possible future events, but the absence of these words does not necessarily mean that a statement is not forward-looking.
Forward-looking statements are based on our current expectations and assumptions regarding our business, the economy and other future conditions. Because forward-looking statements relate to the future, by their nature, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict. As a result, our actual results may differ materially from those contemplated by the forward-looking statements. Important factors that could cause actual results to differ materially from those in the forward-looking statements include regional, national, or global political, economic, business, competitive, market and regulatory conditions and the following:
our plans with respect to the development and licensing of our current product candidates and potential future product candidates we may acquire or license and associated timing thereof, including the design and results of pre-clinical and clinical studies;
there is substantial doubt regarding our ability to continue as a going concern;
our ability to enter into collaboration or license agreements of our current product candidates and potential future product candidates;
the timing, investment and associated activities involved in developing, obtaining regulatory approval for, launching and commercializing our current and potential future product candidates;
the risks in our investment in Tisento tied to Tisento developing, obtaining regulatory approval for, launching and commercializing its product candidates;
the uncertainty as to any liquidity or monetizable value of our equity interest in Tisento, which faces all the risks of an early-stage pharmaceutical development company;
our relationships with third parties, collaborators and our employees; our ability to execute our strategic priorities;
our ability to finance our operations and business initiatives;
maintaining our Nasdaq listing;
our ability to access capital, capabilities, and transactions necessary to advance the development of our current product candidates and potential future product candidates;
whether any development, regulatory, and commercialization milestones or royalty payments provided for in the agreement with Akebia will be achieved;
the impact on our business of workforce and expense reduction initiatives;
the safety profile and related adverse events of our current and potential future product candidates;
the efficacy and perceived therapeutic benefits of any potential future product candidates we may acquire or license, their potential indications and their market potential;
U.S. and non-U.S. regulatory requirements, including any post-approval development and regulatory requirements, and the ability of our potential future product candidates to meet such requirements;
our ability to obtain reimbursement from the U.S. government and third-party payors for potential future product candidates if and when commercialized;
our ability to attract and retain employees needed to execute our business plans and strategies and our ability to manage the impact of any loss of key employees;
our ability to obtain and maintain intellectual property protection for our current and potential future product candidates and the strength thereof;
the risk that third parties may allege we infringe their intellectual property rights;
our future financial performance, revenues, expense levels, payments, cash flows, profitability, tax obligations, capital raising and liquidity sources, and concentration of voting control, as well as the timing and drivers thereof, and internal control over financial reporting;
trends and challenges in the markets for any potential product candidates;
a determination that we constitute an investment company under the Investment Company Act of 1940, as amended, and if we are required to register thereunder, which could have a material adverse effect on us;
our ability to compete with other companies that are or may be developing or selling products that are competitive with any potential future product candidates;
the impact of the coronavirus (“COVID-19”) pandemic to disrupt our business, including our development activities; and
the impact of government regulation in the life sciences industry, particularly with respect to healthcare reform.
See the “Risk Factors” section in Part I, Item 1A of our Annual Report on Form 10-K for the fiscal year ended December 31, 2023, as filed with the Securities and Exchange Commission on March 5, 2024 for a further description of these and other factors. We caution you that the risks, uncertainties, and other factors referenced above may not contain all of the risks, uncertainties and other factors that are important to you. In addition, we cannot assure you that we will realize the results, benefits, or developments that we expect or anticipate or, even if substantially realized, that they will result in the consequences or affect us or our business in the way expected. There can be no assurance that (i) we have correctly measured or identified all of the factors affecting our business or the extent of these factors’ likely impact, (ii) the available information with respect to these factors on which such analysis is based is complete or accurate, (iii) such analysis is correct or (iv) our strategy, which is based in part on this analysis, will be successful. All forward-looking statements in this report apply only as of the date of this report or as of the date they were made and, except as required by applicable law, we undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments or otherwise.
Condensed Consolidated Balance Sheets
(In thousands except share and per share data)
| June 30,2024 | December 31,2023 | |
|---|---|---|
| ASSETS | ||
| Current assets: | ||
| Cash and cash equivalents | $4,588 | $7,571 |
| Prepaid expenses | 116 | 442 |
| Other current assets | 11 | 11 |
| Total current assets | 4,715 | 8,024 |
| Other investment | 5,350 | 5,350 |
| Total assets | $10,065 | $13,374 |
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||
| Current liabilities: | ||
| Accounts payable | $651 | $1,198 |
| Accrued research and development costs | 97 | 90 |
| Accrued expenses and other current liabilities | 534 | 798 |
| Total current liabilities | 1,282 | 2,086 |
| Commitments and contingencies (Note 8) | — | — |
| Stockholders' equity | ||
| Preferred shares, no par value, 500,000 shares authorized and 351,037 series A convertible preferred stock issued and outstanding at June 30, 2024 and December 31, 2023 | — | — |
| Common stock, no par value, 20,000,000 shares authorized at June 30, 2024 and December 31, 2023; 2,710,096 and 2,645,096 shares issued at June 30, 2024 and December 31, 2023, respectively; 2,515,874 and 2,474,159 shares outstanding at June 30, 2024 and December 31, 2023, respectively | — | — |
| Paid-in capital | 276,082 | 275,717 |
| Accumulated deficit | (267,299) | (264,417) |
| Accumulated other comprehensive loss | — | (12) |
| Total stockholders' equity | 8,783 | 11,288 |
| Total liabilities and stockholders' equity | $10,065 | $13,374 |
Condensed Consolidated Statem ents of Operations and Comprehensive Loss
(In thousands except per share data)
| Three Months EndedJune 30, | Six Months EndedJune 30, | |||
|---|---|---|---|---|
| 2024 | 2023 | 2024 | 2023 | |
| Cost and expenses: | ||||
| Research and development | $105 | $339 | $149 | $911 |
| General and administrative | 1,279 | 1,526 | 2,853 | 4,229 |
| Total cost and expenses | 1,384 | 1,865 | 3,002 | 5,140 |
| Loss from operations | (1,384) | (1,865) | (3,002) | (5,140) |
| Interest and other income, net | 62 | 62 | 138 | 150 |
| Net loss from continuing operations | (1,322) | (1,803) | (2,864) | (4,990) |
| Discontinued operations: | ||||
| Loss from discontinued operations | — | (2,378) | — | (6,145) |
| Net loss | $(1,322) | $(4,181) | $(2,864) | $(11,135) |
| Net loss per share - basic and diluted | ||||
| Net loss per share from continuing operations | $(0.53) | $(0.79) | $(1.14) | $(2.24) |
| Net loss per share from discontinued operations | — | (1.04) | — | (2.76) |
| Net loss per share | $(0.53) | $(1.83) | $(1.14) | $(5.00) |
| Weighted average shares used in calculating: | ||||
| Basic and diluted shares | 2,510 | 2,282 | 2,502 | 2,229 |
| Other comprehensive loss: | ||||
| Net loss | $(1,322) | $(4,181) | $(2,864) | $(11,135) |
| Other comprehensive loss: | ||||
| Foreign currency translation adjustment gain (loss) | (2) | 3 | (6) | 4 |
| Comprehensive loss | $(1,324) | $(4,178) | $(2,870) | $(11,131) |
The text of this filing, as the company filed it with the SEC, without its images or exhibits. This is not investment advice.