drugset / Trial / NCT01367444

Phase I/IIA Study of SAR422459 in Participants With Stargardt's Macular Degeneration

NCT01367444 ↗

Phase 1/2 Terminated 27 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Primary Objective: To assess the safety and tolerability of ascending doses of SAR422459 in participants with Stargardt's Macular Degeneration (SMD). Secondary Objective: To evaluate for possible biological activity of SAR422459.

Timeline

Start
2011-06-08
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 SAR422459 Unknown — Other

Indications