Welcome to our dedicated page for Larimar Therapeutics SEC filings (Ticker: LRMR), 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.
Parsing Larimar Therapeutics� dense clinical-stage disclosures can feel like sequencing DNA. Trial endpoints for CTI-1601, orphan-drug designations, and intricate R&D spending hide across multiple forms. If you’ve asked, “How do I find Larimar Therapeutics insider trading Form 4 transactions?� or “Where’s the Larimar Therapeutics annual report 10-K simplified?� you already know the challenge.
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Investors use these insights to monitor pipeline milestones, gauge cash runway, and spot insider confidence before pivotal FDA readouts. Explore sections that pinpoint which 10-K pages discuss manufacturing scale-up, or view side-by-side comparisons of Form 4 buys versus CTI-1601 trial timelines. From Larimar Therapeutics 8-K material events explained to a Larimar Therapeutics annual report 10-K simplified, every document is decoded so you can make informed decisions backed by data, not guesswork.
Tilray Brands (TLRY) Form 4 � Chief Strategy Officer Denise M. Faltischek
On 30-Jul-25 the executive converted 261,194 previously-granted 2024 RSUs into common shares (code M) at $0.61. To satisfy withholding taxes, 138,433 shares were surrendered (code F) at the same price. Net effect: an additional 122,761 shares, lifting her direct stake to 780,636.
On 29-Jul-25 she also received 1,873,707 new RSUs (code A) at no cost. These long-term incentive units vest 50 % on 29-Jul-26 and 50 % on 29-Jul-27, contingent on continued employment; unvested units lapse if she resigns.
Post-transactions she holds 780,636 common shares, 261,194 vested derivative shares and 1,873,707 unvested RSUs. Activity was compensation-driven with no open-market buying or discretionary selling, limiting immediate market impact but signalling retention and incentive alignment.
Q1 FY25 (Apr–Jun 2025, J-GAAP) snapshot:
- Ordinary income ¥2.13 tn, �10.5 % YoY on softer trading and loan yields.
- Ordinary profit ¥368.6 bn, +4.0 % YoY; net profit attributable to owners ¥290.5 bn, +0.4 % (EPS ¥115.90).
- Total assets fell 1.6 % since Mar-25 to ¥278.7 tn; own-capital ratio edged up to 3.7 %.
- NPL ratio improved to 0.73 % (�23 bp); credit-related costs a modest ¥11.4 bn.
Guidance & shareholder returns: Full-year profit target lifted 8.5 % to ¥1.02 tn (15 % YoY growth), implying FY EPS ¥407.81. Dividend outlook unchanged at ¥145/share (up ¥5 YoY) with ¥72.5 interim.
Segment colour: Retail & Business Banking and CIBC drove net business profit growth; Global Markets cooled as ETF-related gains shrank to ¥3.2 bn (vs ¥31.7 bn). Net interest income rose 30 % YoY while trading income slid 14 %.
Balance-sheet trends: Loans down ¥0.14 tn to ¥94.0 tn; deposits down ¥0.62 tn to ¥154.3 tn. Unrealised gains on securities up ¥162 bn to ¥1.37 tn, aided by equity market strength. Treasury stock grew to 14.4 m shares.
Takeaway: Upgraded guidance, better asset quality and stable dividends offset revenue pressure and a still-thin capital base, signalling cautious but improving fundamentals.
On 29 Jul 2025, Larimar Therapeutics (LRMR) furnished a Form 8-K (Item 2.02) to disclose preliminary liquidity for the quarter ended 30 Jun 2025. Management estimates $138.5 million in cash, cash equivalents and marketable securities at that date.
The amount is unaudited and subject to change pending completion of the Q2 closing and review process. No additional operating results, balance-sheet details, or forward guidance were included. The same figure appears in a preliminary prospectus supplement filed under Rule 424(b)(5). Because the data are “furnished� rather than “filed,� they are not subject to Exchange Act Section 18 liability.
Mercantile Bank Corporation (MBWM) filed 8-K/A Amendment No. 1 chiefly to mark the filing as Rule 425 communication; the substantive disclosure is unchanged from the original 8-K dated 22 Jul 2025.
Merger overview
- MBWM will acquire Eastern Michigan Financial Corporation (EFIN) via merger into a wholly-owned acquisition subsidiary.
- Consideration per EFIN share: $32.32 cash + 0.7116 MBWM shares, implying aggregate value of ~$95.8 million.
- Boards of both companies have approved the deal; closing targeted for Q4 2025 subject to EFIN shareholder vote and regulatory approvals.
- Post-close MBWM will operate as a two-bank holding company until planned consolidation of Eastern Michigan Bank into Mercantile Bank in Q1 2027.
- Termination provisions include failure to close by 30 Jun 2026 or acceptance of a superior proposal; EFIN would owe MBWM a $3.68 million break-up fee.
- Governance: one former non-employee EFIN director will join MBWM and Mercantile Bank boards; remaining EFIN directors to join a regional advisory board.
Other items: Item 2.02 furnishes MBWM’s Q2 2025 earnings press release; Item 7.01 furnishes investor presentations (Exhibits 99.1, 99.3, 99.4). No financial figures are contained within this amendment.
Larimar Therapeutics, Inc. (Nasdaq: LRMR) filed a Form 8-K to notify investors that an updated corporate slide deck dated June 23, 2025 has been posted to the company’s website and furnished as Exhibit 99.1. The presentation will be used in meetings with investors, analysts and other stakeholders. No new financial results, transactions, or strategic changes were disclosed in the filing. Apart from the presentation and customary Exhibit 104 (Inline XBRL cover page data), the 8-K contains no other material information. The filing is therefore primarily an investor-relations housekeeping action, aimed at ensuring Regulation FD compliance by making the slides publicly available to all market participants.
Larimar Therapeutics (Nasdaq: LRMR) filed a Form 8-K to disclose a regulatory update issued on June 23, 2025. The company released a press release (Exhibit 99.1) stating that the U.S. Food and Drug Administration provided safety-database recommendations and requested additional adult and pediatric data for patients with Friedreich’s Ataxia. To incorporate these data, Larimar has established a “refined timeline� for its forthcoming Biologics License Application (BLA).
The filing notes that management will host a conference call the same day and use a supporting slide deck (Exhibit 99.2) to discuss the regulatory feedback and the updated submission schedule. No financial statements were included; the 8-K is limited to Item 8.01 (Other Events) and Item 9.01 (Exhibits).
For investors, the disclosure is material because FDA feedback can directly influence the timing of commercialization for the company’s lead program targeting Friedreich’s Ataxia. While the agency’s recommendations clarify the data package required, the need to gather and integrate additional safety data could shift the expected BLA submission date, affecting near-term milestones, cash runway assumptions, and valuation timelines.