drugset / Trial / NCT05293626

Gene Therapy Clinical Trial for the Treatment of Leber's Hereditary Optic Neuropathy Associated With ND4 Mutations

NCT05293626 ↗

Phase 1/2 Active not recruiting 12 enrolled Neurophth Therapeutics Inc
NaSequentialOpen-labelTreatment

Summary

The objective of this clinical study is to evaluate the safety and efficacy of NR082 in the treatment of LHON caused by mitochondrial ND4 gene mutation. This study will enroll subjects aged ≥ 18 years old and ≤ 75 years old to receive a single unilateral intravitreal (IVT) injection of NR082 to evaluate its safety and efficacy. The clinical manifestations of all subjects are to be reduced visual acuity caused by LHON associated with ND4 mutation, with laboratory test showing G11778A mutation (a CLIA-certified laboratory) and reduced visual acuity lasted for \> 6 months and \< 10 years.

Timeline

Start
2023-05-22
Primary completion
2025-07
Completion
2029-12

Drugs

EvaluationDrugModalityDoseRoute
Subject NR082 Unknown 5e+08 vg Intravitreal
Subject NR082 Unknown 1.5e+09 vg Intravitreal
Subject NR082 Unknown 3e+09 vg Intravitreal
Subject NR082 Unknown 4.5e+09 vg Intravitreal