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A Phase 1, Multicenter, Open-Label, Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of Intravenously Administered FHD-609 in Subjects With Advanced Synovial Sarcoma or Advanced SMARCB1-Loss Tumors

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Trial Profile

A Phase 1, Multicenter, Open-Label, Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of Intravenously Administered FHD-609 in Subjects With Advanced Synovial Sarcoma or Advanced SMARCB1-Loss Tumors

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 30 Apr 2024

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At a glance

  • Drugs FHD 609 (Primary)
  • Indications Synovial sarcoma; Tumours
  • Focus Adverse reactions; First in man
  • Sponsors Foghorn Therapeutics
  • Most Recent Events

    • 23 Apr 2024 Status changed from suspended to discontinued.
    • 24 Oct 2023 According to a Foghorn Therapeutics media release, the Company will present new data at the Connective Tissue Oncology Society (CTOS) Annual Meeting.
    • 24 Apr 2023 According to a Foghorn Therapeutics media release, the company is not planning to pursue a dose expansion study independently at this time.
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