Welcome to our dedicated page for Foghorn Therapeutics SEC filings (Ticker: FHTX), 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.
R&D burn rates, clinical milestones and intricate chromatin biology risks fill every Foghorn Therapeutics (FHTX) disclosure. Finding the exact trial update or gauging cash runway in a 10-K can feel like decoding epigenetic jargon. If you have ever searched “Foghorn Therapeutics SEC filings explained simply,� you already know the challenge.
Stock Titan turns that complexity into clarity. Our AI reads each document the instant it hits EDGAR, then delivers concise summaries, plain-English definitions and red-flag alerts. Need the latest Foghorn Therapeutics quarterly earnings report 10-Q filing or want to understand the 8-K announcing a new SMARCA2 study cohort? It’s here, parsed and linked to key metrics. Forms covered include:
- 10-K: annual report with AI-highlighted R&D expense trends and Gene Traffic Control platform updates
- 10-Q: quarter-to-quarter pipeline progress and liquidity analysis
- 8-K: material events—trial pauses, collaboration amendments—explained line by line
- Form 4: Foghorn Therapeutics insider trading Form 4 transactions streamed in real time, plus trend charts
- DEF 14A: proxy statement executive compensation breakdown
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Foghorn Therapeutics (FHTX) Q2-25 10-Q highlights:
- Revenue: Collaboration income with Eli Lilly rose 10% YoY to $7.6 m; H1-25 revenue up 13% to $13.5 m.
- Expenses: R&D fell 8% to $21.8 m and G&A fell 6% to $6.9 m, driving a 15% narrower operating loss of $21.1 m.
- Net loss: Q2 loss improved to $17.9 m (-$0.28/sh) from $23.0 m (-$0.45/sh) last year; H1 loss narrowed to $36.8 m (-$0.58/sh).
- Liquidity: Cash & cash equivalents $72.6 m; marketable securities $126.1 m; combined liquid resources $198.7 m. Management expects runway �12 months despite $45 m operating cash burn in H1.
- Balance sheet: Deferred revenue declined to $266.6 m as collaboration work progresses; total liabilities $302.9 m exceed assets $226.2 m, producing a $76.7 m shareholders� deficit.
- Operations: FHD-909 (SMARCA2) transitioned to Lilly with 50/50 cost share; FHD-286 development discontinued (2024). New 10-year Watertown lease signed; Cambridge lease partially reduced, lowering future obligations by $8.5 m.
Key takeaways: Expense discipline and steady milestone revenue trimmed losses, but the pre-commercial company remains cash-burning and carries a negative equity position. Progress of the Lilly collaboration and access to additional capital remain critical catalysts.