drugset / Trial / NCT01505062

Study of SAR421869 in Participants With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B

NCT01505062 ↗

Phase 1/2 Terminated 9 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and tolerability of ascending doses of subretinal injections of SAR421869 in participants with Usher syndrome type 1B. To evaluate for possible biological activity of SAR421869.

Timeline

Start
2012-03-26
Primary completion
2019-08-16
Completion
2019-08-16

Outcome

Outcome not reported

Stopped: “Study stopped not for safety reasons. Due to review of clinical development plans and priorities, Sponsor decided to stop development of the product.”

Drugs

EvaluationDrugModalityDoseRoute
Subject SAR421869 Unknown 0.1 ml Other