FHTXNASDAQHealthcare

Public company intelligence preview

FOGHORN THERAPEUTICS INC

21 insider trades surfaced from the last year. This page shows only aggregate signals, not the underlying transactions, people, filings, filters, or AI workspace.

Snapshot

A narrow read on a much deeper workspace.

The preview gives search visitors enough signal to understand coverage. It does not expose transaction records, person-level profiles, filters, comparisons, or analyst workflows.

Insider trades, last 12 months
21
0 filed in the last 30 days
Acquisition / disposition count
19/2
Buy / Sell
Unique insiders active in the last year
15
Current insider positions tracked
26
25 active, 1 exited

Insider compensation

Public aggregate: $1.8M average total compensation across covered insiders.

Governance movement

Public aggregate: 3 governance events in the last year.

Institutional ownership

Public aggregate: 93 holders from the latest quarter.

Restricted sales and governance

Public counts, not the investigation layer.

The full product opens the underlying filings, insider context, historical holdings, comparison tools, and AI analysis.

Restricted-sale filings, 1Y
0
Restricted-sale insiders, 1Y
0
Planned sale shares, 1Y
0
Planned sale value, 1Y
$0.00
Insiders covered
10
Latest year: 2025
Personnel changes, 1Y
3
Board appointments, 1Y
2
Board departures, 1Y
2

Market context

Basic quote context for the preview.

Price
$4.00
Market cap
$211.4M
Volume
245,944
EPS
$-0.29
Revenue
$3.3M
Employees
106

Company note

Context before the data.

Company Overview

Foghorn Therapeutics Inc. is a Healthcare sector, Biotechnology company focused on discovering and developing small-molecule therapies that target the chromatin regulatory system to correct abnormal gene expression. Its lead program, FHD-909, is a first-in-class oral SMARCA2 inhibitor being advanced with Eli Lilly in SMARCA4-mutated cancers, including NSCLC, while additional programs target CBP, EP300, and ARID1B. The business is still clinical-stage with no product sales, so results are driven by collaboration revenue, R&D execution, and capital access rather than commercial operations. Because it relies on third parties for manufacturing and clinical development, execution risk is heavily tied to trial progress, regulatory milestones, and partner support.

Executive Compensation Practices

For a clinical-stage biotech like Foghorn, executive compensation is typically structured to reward pipeline advancement, clinical milestones, collaboration execution, and capital preservation rather than revenue growth or profitability. Metrics likely to matter most include progress of FHD-909’s Phase 1 study, advancement of partnered and internal preclinical programs, successful enrollment, and maintaining sufficient liquidity as operating losses remain significant. The company’s recent narrowing losses and lower operating expenses may support performance-based incentives, but management is also likely to emphasize long-term equity awards to align executives with the uncertain, multi-year value creation typical in Biotechnology. In this sector, compensation often reflects retention needs for scientific leadership, so stock options or restricted stock may be especially important given the company’s heavy R&D dependence and specialized talent base.

Insider Trading Considerations

Insider trading patterns at Foghorn may be influenced by clinical trial catalysts, collaboration developments with Lilly, and periodic financing needs, all of which can create sharp stock-price sensitivity. Because the company has no product revenue and depends on future raises, insiders may be especially cautious around trading windows near trial updates, data readouts, partnership announcements, and financing transactions such as equity offerings or warrant deals. The recent initiation and ramp of the FHD-909 Phase 1 study is a key catalyst that could affect trading behavior, as trial progress in oncology can materially change investor expectations. As a Healthcare / Biotechnology company, Foghorn also operates under heightened regulatory scrutiny, so insiders are likely subject to strict blackout periods and careful compliance practices around nonpublic clinical and regulatory information.

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