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A Phase 1, Open-Label, Dose-Escalation Study to Evaluate the Safety and Efficacy of HMI-103 Administered Intravenously in Adult Participants With Classical PKU Due to PAH Deficiency

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Trial Profile

A Phase 1, Open-Label, Dose-Escalation Study to Evaluate the Safety and Efficacy of HMI-103 Administered Intravenously in Adult Participants With Classical PKU Due to PAH Deficiency

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 12 Oct 2023

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At a glance

  • Drugs HMI-103 (Primary)
  • Indications Phenylketonuria
  • Focus Adverse reactions; Therapeutic Use
  • Acronyms pheEDIT
  • Sponsors Homology Medicines
  • Most Recent Events

    • 05 Oct 2023 Status changed from active, no longer recruiting to discontinued.
    • 25 Aug 2023 Status changed from recruiting to active, no longer recruiting.
    • 14 Aug 2023 According to Homology Medicines media release, the company announced approval from the independent Data Monitoring Committee to escalate to the next dose cohort in the trial.
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