Safety/Proof of Concept Study of Oral QLT091001 in Subjects With Leber Congenital Amaurosis (LCA) or Retinitis Pigmentosa (RP) Due to Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT) Mutations
This study has been completed.
Sponsor:
QLT Inc.
Information provided by (Responsible Party):
QLT Inc.
ClinicalTrials.gov Identifier:
NCT01014052
First received: November 12, 2009
Last updated: May 13, 2013
Last verified: May 2013
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has been completed. |
|---|---|
| Study Completion Date: | August 2012 |
| Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |