drugset / Trial / NCT01505062
Study of SAR421869 in Participants With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SAR421869 | Unknown | 0.1 ml | Other |