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Active Not RecruitingNCT06212297

Fellow-eye Study (FE) of LX101 in Subjects With Inherited Retinal Dystrophy

A Clinical Trial to Evaluate the Safety and Efficacy of Subretinal Re-Administration of LX101 to the Contralateral Eye in Subjects With Biallelic RPE65 Mutation-associated Inherited Retinal Dystrophy

Status
Active Not Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
9 (estimated)
Sponsor
Innostellar Biotherapeutics Co.,Ltd · Industry
Sex
All
Age
6 Years
Healthy volunteers
Not accepted

Summary

Up to nine subjects who have participated in the earlier LX101 clinical study, and who meet all study eligibility criteria, will receive LX101 administration in the previously uninjected, contralateral eye to evaluate the safety of bilateral, sequential subretinal administration of LX101.

Conditions

Interventions

TypeNameDescription
GENETICLX101Subretinal administration of LX101 to the contralateral, previously uninjected eye

Timeline

Start date
2023-09-12
Primary completion
2025-02-06
Completion
2029-03-01
First posted
2024-01-18
Last updated
2025-06-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06212297. Inclusion in this directory is not an endorsement.