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NCT04879017 · ClinicalTrials.gov registry record · Phase 1

FHD-286 in Subjects With Metastatic Uveal Melanoma

A Phase 1 study, sponsored by Foghorn Therapeutics.

Terminated
Registry status
Phase 1
Development phase
76
Enrollment target

NCT04879017: Clinical Trial Phase 1 study, sponsored by Foghorn Therapeutics.

NCT04879017 is a Phase 1 study that was terminated before completion, run by Foghorn Therapeutics. The registered enrollment target is 76 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04879017, a Phase 1 study, was terminated before completion, sponsored by Foghorn Therapeutics.

TERMINATED
Registry status
Phase 1
Development phase
76 participants
Enrollment target

Study Summary

This Phase 1, multicenter, open-label, dose escalation and expansion study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of FHD-286 oral monotherapy in subjects with metastatic Uveal Melanoma (UM).

Primary Outcome

Dose escalation and expansion

Interventions

  • DRUG FHD-286

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2021-05-11
Est. Completion 2023-11-30
Phase Phase 1
Foghorn Therapeutics

3 total trials

Why NCT04879017 stopped before completion

NCT04879017 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher).

The record links to 0 conditions, and to 1 intervention - of which FHD-286 is the first listed.

NCT04879017 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04879017 about?

NCT04879017 is a clinical study titled "FHD-286 in Subjects With Metastatic Uveal Melanoma". This Phase 1, multicenter, open-label, dose escalation and expansion study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of FHD-286 oral monotherapy in subjects with metastatic Uveal Melanoma (UM).

What is the current status of trial NCT04879017?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2021-05-11. Estimated completion is 2023-11-30.

What interventions are being tested in trial NCT04879017?

The interventions under investigation include: FHD-286 (DRUG).

Who is sponsoring clinical trial NCT04879017?

This trial is sponsored by Foghorn Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04879017's enrollment target sits among peer trials

76 705th of 2000 higher than 1,290 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04879017, the US trial registry maintained by the National Library of Medicine. NCT04879017 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.