Foghorn Therapeutics Inc. (FHTX) SEC Filings & Earnings Calls
EquiReason read 12 Foghorn Therapeutics Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-01 — Foghorn Therapeutics discontinued FHD-909 Phase 1 trial, ended Lilly collaboration, cut workforce 40% (~65 employees), expects $2.3M severance charges, extends cash runway into H2 .
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
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Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
1 Oct 20268-K · 2.05, 7.01Foghorn Therapeutics discontinued FHD-909 Phase 1 trial, ended Lilly collaboration, cut workforce 40% (~65 employees), expects $2.3M severance charges, extends cash runway into H2 2029.open
Figures in the filing · each found in the filing text
| Workforce Reduction · Q4-2026 | 40.0% | |
| Expected Employees After Reduction · Q4-2026 | 65 | |
| Restructuring Charges · Q4-2026 | $2M |
Risks flagged
Clinical failure of FHD-909 and end of Lilly collaboration reduces pipeline value.
“decision not to advance the clinical trial of FHD-909 into the expansion phase” · word for word
Workforce reduction may impact morale and execution on remaining programs.
“reduction in its workforce by approximately 40%” · word for word
6 Aug 202610-QFoghorn reported H1 2026 net loss of $27.1M, collaboration revenue of $19.3M (up 43% YoY), and $229.8M deferred revenue; raised $50M in January 2026.earningsopen
Figures in the filing · each found in the filing text
| Net loss · H1-2026 | $27M | |
| Accumulated deficit · H1-2026 | $660M | |
| Collaboration revenue · H1-2026 | $19M | +43% y/y |
| Deferred revenue · H1-2026 | $230M | |
| Gross proceeds from January 2026 offering · Q1-2026 | $50M | |
| Federal net operating loss carryforwards · FY2025 | $199M |
Risks flagged
No product revenue; history of losses
“We do not have any products approved for sale and have not generated any revenue from product sales.” · word for word
Need for substantial additional funding
“We will need substantial additional funding to support our continuing operations and pursue our growth strategy.” · word for word
Clinical and regulatory uncertainties
“Our ability to generate any product revenue or product revenue sufficient to achieve profitability will depend on the successful development and eventual commercialization of one or more product candidates.” · word for word
Tariff and inflation impact on operating costs
“experience significant operating cost increases as a result of increased inflation or increased tariffs” · word for word
6 Aug 20268-K · 2.02, 7.01Foghorn Therapeutics reported Q2 2026 financial results with cash runway into H1 2028; pipeline progress on FHD-909, EP300 degrader, and I&I program; CBPd-171 delayed due to operational issue.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and marketable securities · Q2-2026 | $168M |
Risks flagged
CBPd-171 program delay due to third-party CRO operational issue; updated guidance pending.
“CBPd-171 timeline has been delayed due to an unexpected operational issue at a third-party contract research organization supporting the in vivo animal models.” · word for word
7 May 202610-QQ1 2026 net loss of $19.9M, collaboration revenue declined to $3.3M from $6.0M YoY, no product revenue.earningsopen
Figures in the filing · each found in the filing text
| Net loss · Q1-2026 | $20M | |
| Accumulated deficit · 2026-03-31 | $652M | |
| Collaboration revenue · Q1-2026 | $3M | -45% y/y |
| Deferred revenue · 2026-03-31 | $246M | |
| Gross proceeds from equity offering · 2026-01-13 | $50M |
Risks flagged
Going concern / capital need
“We have incurred significant operating losses since our inception. For the three months ended March 31, 2026 and the year ended December 31, 2025, we reported net losses of $19.9 million and $74.3 million, respectively. As of March 31, 2026, we had an accumulated deficit of $652.3 million.” · word for word
No approved products / no product revenue
“We do not have any products approved for sale and have not generated any revenue from product sales.” · word for word
7 May 20268-K · 2.02, 7.01Foghorn Therapeutics reported Q1 2026 financial results with cash runway into H1 2028; pipeline progress on FHD-909, FHT-171, and EP300 degrader; no revenue or net income guidance provided.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and marketable securities · Q1-2026 | $184M |
Risks flagged
Clinical-stage biotech with no approved products; reliance on pipeline success.
“Clinical-stage biotechnology company; no revenue from product sales.”
Dependence on collaboration with Lilly for lead program.
“FHD-909 developed in collaboration with Lilly; 50/50 U.S. co-development agreement.”
30 Apr 2026DEF 14AProxy statement for 2026 annual meeting; executive compensation tied to corporate performance goals; net loss improved to $74.3M in 2025.open
Figures in the filing · each found in the filing text
| Net loss · FY2025 | $74M | -14% y/y |
| Total shareholder return (indexed to $100) · FY2025 | $83.72 | +14% y/y |
| CEO base salary · FY2025 | $638000.00 | +6% y/y |
| CEO total compensation · FY2025 | $2M | +51% y/y |
| Compensation actually paid to PEO · FY2025 | $3M | +29% y/y |
Risks flagged
No approved products / no product revenue
“We do not have any products approved for sale and have not generated any revenue from product sales.”
Going concern / capital need
“We have incurred significant operating losses since our inception. For the three months ended March 31, 2026 and the year ended December 31, 2025, we reported net losses of $19.9 million and $74.3 million, respectively. As of March 31, 2026, we had an accumulated deficit of $652.3 million.”
11 Mar 202610-KFoghorn Therapeutics filed its annual report (10-K) for FY2025, reporting an accumulated deficit of $632.5 million and no product revenue; the filing is a standard annual update with no surprise beat or miss.earningsopen
Figures in the filing · each found in the filing text
| Accumulated Deficit · FY2025 | $633M | |
| Full-Time Employees · FY2025 | 106 | |
| Lilly Upfront Payment · FY2021 | $300M | |
| Lilly Equity Investment · FY2021 | $80M |
Risks flagged
No approved products and early-stage pipeline
“We have a limited operating history and have no products approved for commercial sale” · word for word
Significant accumulated deficit and ongoing losses
“As of December 31, 2025, we had an accumulated deficit of $632.5 million.” · word for word
Need for substantial additional funding
“We will need substantial additional funding. If we are unable to raise capital when needed or under acceptable terms, we could be forced to delay, reduce or eliminate our research and product development programs or future commercialization efforts.” · word for word
Dependence on key personnel and third parties
“We are highly dependent on Adrian Gottschalk, our Chief Executive Officer.” · word for word
Intellectual property risks
“If we are unable to adequately protect our proprietary technology and platform or obtain and maintain patent protection for our technology and products or if the scope of the patent protection obtained is not sufficiently broad, our competitors could develop and commercialize technology and products similar or identical to ours” · word for word
11 Mar 20268-K · 2.02, 7.01Foghorn Therapeutics reported FY2025 financial results and provided pipeline updates. Cash position $158.9M, completed $50M financing in Jan 2026 extending runway into H1 2028. No revenue or earnings guidance provided.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and marketable securities · FY2025 | $159M |
Risks flagged
Clinical-stage biotech with no approved products; pipeline risk
“All programs are in preclinical or early clinical stages; no revenue from product sales”
Dependence on collaboration with Lilly for lead program
“FHD-909 is developed in collaboration with Lilly; 50/50 U.S. co-development and co-commercialization agreement”
12 Jan 20268-K · 2.02, 7.01, 8.01Foghorn Therapeutics files 8-K with press release and investor presentation ahead of J.P. Morgan Healthcare Conference. Includes Form of Securities Purchase Agreement (Exhibit 99.3) indicating a concurrent equity offering (warrants and pre-open
Risks flagged
Equity offering will dilute existing shareholders.
“Form of Series Warrant and Pre-Funded Warrant included as exhibits.”
All pipeline programs are pre-commercial; no approved products; revenue depends on collaboration milestones.
“Pipeline table shows all programs in discovery, pre-clinical, or Phase 1; no approved products.”
5 Nov 202510-QFoghorn Therapeutics reported Q3 2025 results with a net loss of $15.8 million, improved from $19.1 million in Q3 2024, driven by lower R&D expenses.earningsopen
Figures in the filing · each found in the filing text
| Net Loss · Q3-2025 | $16M | -17% y/y |
| Research and Development Expenses · Q3-2025 | $20M | -19% y/y |
| Cash, Cash Equivalents and Marketable Securities · 2025-09-30 | $180M | |
| Accumulated Deficit · 2025-09-30 | $611M | |
| Deferred Revenue · 2025-09-30 | $258M | |
| Net Loss Per Share · Q3-2025 | $0.25 | -19% y/y |
Risks flagged
Going concern risk
“The Company has incurred recurring losses, including net losses of $52.6 million and $67.1 million for the nine months ended September 30, 2025 and 2024, respectively. As of September 30, 2025, the Company had an accumulated deficit of $610.8 million. The Company expects to continue to generate operating losses in the foreseeable future.” · word for word
Financing risk
“The Company will need to obtain additional funding through public or private equity offerings, debt financings, collaborations, strategic alliances and/or licensing arrangements to continue to fund its operations. The Company may not be able to obtain financing on acceptable terms, or at all.” · word for word
Clinical development risk
“There can be no assurance that the Company’s research and development will be successfully completed, that adequate protection for the Company’s intellectual property will be maintained, that any products developed will obtain required regulatory approval or that any approved products will be commercially viable.” · word for word
5 Nov 20258-K · 2.02, 5.02, 7.01CFO Kristian Humer resigns effective Nov 14, 2025; no disagreement with company. Cash runway into 2028; pipeline progress on FHD-909, CBP/EP300/ARID1B degraders.open
Figures in the filing · each found in the filing text
| Cash, cash equivalents, and marketable securities · Q3-2025 | $180M |
Risks flagged
CFO departure creates leadership gap during critical pipeline execution phase
“CFO resigning effective Nov 14, 2025; search for replacement commenced.”
Clinical-stage company with no approved products; pipeline risk
“All programs are preclinical or Phase 1; no revenue from product sales.”
Foghorn Therapeutics Inc. — questions
- What did Foghorn Therapeutics Inc. file recently?
- 12 SEC filings in the last 12 months. Latest: 8-K on 2026-10-01 — Foghorn Therapeutics discontinued FHD-909 Phase 1 trial, ended Lilly collaboration, cut workforce 40% (~65 employees), expects $2.3M severance charges, extends cash runway into H2 2029.
Every figure on this page comes from Foghorn Therapeutics Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.