Welcome to our dedicated page for Milestone Pharmaceuticals SEC filings (Ticker: MIST), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
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Milestone Pharmaceuticals Inc. filed a Form S-8 to register an additional 4,000,000 common shares issuable under its 2019 Equity Incentive Plan, as amended, reflecting shareholder approval of the increase.
The filing incorporates by reference the Registrant's Annual Report for the fiscal year ended December 31, 2024, the Definitive Proxy Statement filed April 30, 2025, Quarterly Reports for the periods ended March 31, 2025 and June 30, 2025, various Current Reports and the Form 8-A description of common stock. Exhibits include amended organizational documents, the amended 2019 EIP, option and RSU award forms, legal opinions and consents.
Milestone Pharmaceuticals reported that it issued a press release announcing its financial results for the quarter ended June 30, 2025 and providing a regulatory and corporate update. The Form 8-K states the press release is attached as Exhibit 99.1 and is incorporated by reference; the filing text itself does not include the numerical results or detailed financial tables. The 8-K also lists the Interactive XBRL cover page file as Exhibit 104 and identifies the disclosure under the Results of Operations and Financial Condition item. Investors are directed to the attached press release for substantive figures and commentary.
Milestone Pharmaceuticals (MIST) delivered a mixed quarterly update focused on advancing its lead candidate, etripamil, while absorbing higher operating losses. For the six months ended June 30, 2025 the company reported a net loss of $33.7 million (net loss per share $0.51) and an accumulated deficit of $401.3 million. As of June 30, 2025, Milestone held $42.5 million in cash and $0.9 million in short-term investments (total ~$43.4 million) and reported total assets of $47.4 million and total liabilities of $65.2 million, including $55.2 million in senior secured convertible notes.
The FDA issued a Complete Response Letter in March 2025 citing CMC and inspection items but accepted Milestone鈥檚 June 13, 2025 response and set a PDUFA target date of December 13, 2025. A July 11, 2025 underwritten offering subsequently provided approximately $48.7 million of net proceeds and the RTW royalty agreement marketing deadline was extended to December 31, 2025. NODE-303 data showed a median time-to-conversion of 17 minutes with generally favorable tolerability. The company reported no revenue for the periods presented.
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