Clinical Trials Directory

Trials / Completed

CompletedNCT02652767

Efficacy Study of GS010 for the Treatment of Vision Loss up to 6 Months From Onset in LHON Due to the ND4 Mutation

A Randomized, Double-Masked, Sham-Controlled Clinical Trial to Evaluate the Efficacy of a Single Intravitreal Injection of GS010 in Subjects Affected for 6 Months or Less by LHON Due to the G11778A Mutation in the Mitochondrial ND4 Gene

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
39 (actual)
Sponsor
GenSight Biologics · Industry
Sex
All
Age
15 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to assess the effectiveness of GS010, a gene therapy, in improving the visual outcome in participants with Leber Hereditary Optic Neuropathy (LHON) due to the G11778A ND4 mitochondrial mutation when vision loss is present for six months or less.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGS010Both eyes of each participant will receive standard antiseptic preparation, administration of topical local ocular anesthetic agents and will undergo pupillary dilation. Administration of an intra-ocular pressure lowering agent will precede treatment for every participant. GS010-treated Eyes: GS010 is a recombinant adeno-associated viral vector serotype 2 (rAAV2/2) containing the wild-type ND4 gene (rAAV2/2-ND4). Participants will receive a single dose of GS010 in one of their randomly selected eyes, via intravitreal injection containing 9E10 viral genomes in 90μL balanced salt solution (BSS) plus 0.001% Pluronic F68®.
DEVICESham Intravitreal InjectionBoth eyes of each participant will receive standard antiseptic preparation, administration of topical local ocular anesthetic agents and will undergo pupillary dilation. Administration of an intra-ocular pressure lowering agent will precede treatment for every participant. Sham-treated Eyes: One eye of each participant will undergo sham injection. Sham intravitreal injection will be performed by applying pressure to the eye at the location of a typical intravitreal injection procedure using the blunt end of a syringe without a needle.

Timeline

Start date
2016-02-23
Primary completion
2018-08-07
Completion
2019-07-04
First posted
2016-01-12
Last updated
2026-03-02
Results posted
2020-01-28

Locations

7 sites across 5 countries: United States, France, Germany, Italy, United Kingdom

Source: ClinicalTrials.gov record NCT02652767. Inclusion in this directory is not an endorsement.