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A Multi-center, Open-label, Dose-escalation Phase I/II Clinical Study to Evaluate the Safety, Tolerability and Efficacy of FT-001 Administered Via Subretinal Injection in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy

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Trial Profile

A Multi-center, Open-label, Dose-escalation Phase I/II Clinical Study to Evaluate the Safety, Tolerability and Efficacy of FT-001 Administered Via Subretinal Injection in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 17 May 2023

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At a glance

  • Drugs FT-001 (Primary)
  • Indications Retinal dystrophies
  • Focus Adverse reactions
  • Sponsors Frontera Therapeutics

Most Recent Events

  • 17 May 2023 New trial record

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