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
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- QLT Inc.
- Principal Investigator
- Sushanta MallickQLT Inc.
- Intervention
- QLT091001(drug)
- Enrollment
- 32 enrolled
- Eligibility
- 5-65 years · All sexes
- Timeline
- 2009 – 2012
Study locations (7)
- The Chicago Lighthouse for People Who Are Blind or Visually Impaired (The Pangere Center For Inherited Retinal Diseases), Chicago, Illinois, United States
- Wilmer Eye Institute (Johns Hopkins University), Baltimore, Maryland, United States
- Scheie Eye Institute, Philadelphia, Pennsylvania, United States
- Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada
- Institute for Ophthalmic Research, University of Tubingen, Tübingen, Germany
- The Rotterdam Eye Hospital, Rotterdam, Netherlands
- Moorefield Eye Hospital, London, United Kingdom
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.govOther trials for Leber congenital amaurosis
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- ACTIVE NOT RECRUITINGEARLY PHASE1NCT06088992Leber Congenital Amaurosis Inherited Blindness of Gene Therapy Trial(LIGHT)Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
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- ACTIVE NOT RECRUITINGPHASE3NCT00999609Safety and Efficacy Study in Subjects With Leber Congenital AmaurosisSpark Therapeutics, Inc.
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