drugset / Trial / NCT01367444
Phase I/IIA Study of SAR422459 in Participants With Stargardt's Macular Degeneration
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.”
Publications
- Davis JL. The Blunt End: Surgical Challenges of Gene Therapy for Inherited Retinal Diseases. Am J Ophthalmol. 2018 Dec;196:xxv-xxix. doi: 10.1016/j.ajo.2018.08.038. Epub 2018 Sep 5.
- Parker MA, Choi D, Erker LR, Pennesi ME, Yang P, Chegarnov EN, Steinkamp PN, Schlechter CL, Dhaenens CM, Mohand-Said S, Audo I, Sahel J, Weleber RG, Wilson DJ. Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial. Transl Vis Sci Technol. 2016 Oct 1;5(5):10. doi: 10.1167/tvst.5.5.10. eCollection 2016 Oct.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SAR422459 | Unknown | — | Other |