CompletedPhase 1NCT01014052

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

Studying Leber congenital amaurosis

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Key facts

Sponsor
QLT Inc.
Principal Investigator
Sushanta Mallick
QLT Inc.
Intervention
QLT091001(drug)
Enrollment
32 enrolled
Eligibility
5-65 years · All sexes
Timeline
20092012

Study locations (7)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01014052 on ClinicalTrials.gov

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