drugset / Trial / NCT04311112

Safety and Efficacy of Zuretinol Acetate in Subjects With Inherited Retinal Disease

NCT04311112 ↗

Phase 2/3 Withdrawn Retinagenix Holdings
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy of ZA oral solution in subjects with IRD caused by biallelic recessive RPE65 or LRAT gene mutations and phenotypically diagnosed as Leber's Congenital Amaurosis (LCA) or Retinitis Pigmentosa (RP).

Timeline

Start
2020-12
Primary completion
2023-02
Completion
2023-09

Outcome

Outcome not reported

Stopped: “The asset was transferred to another company”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Zuretinol Acetate Small molecule — Oral

Indications