RecruitingPhase 2NCT06627179
Study to Evaluate Ultevursen in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Gene
Studying Retinitis pigmentosa
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
- Laboratoires Thea
- Intervention
- Intravitreal Injection of Ultevursen(drug)
- Enrollment
- 81 enrolled
- Eligibility
- 8 years · All sexes
- Timeline
- 2024 – 2027
Study locations (27)
- The University of California, San Francisco, San Francisco, California, United States
- Bascom Palmer Eye Institute/University of Miami, Miami, Florida, United States
- Emory University, Atlanta, Georgia, United States
- Massachusetts Eye and Ear, Boston, Massachusetts, United States
- University of Michigan- Kellogg Eye Center, Ann Arbor, Michigan, United States
- Duke Eye Center, Durham, North Carolina, United States
- Casey Eye Institute, Oregon Health & Science University, Portland, Oregon, United States
- University of Pennsylvania, Scheie Eye Institute, Philadelphia, Pennsylvania, United States
- Retina Foundation of the Southwest, Dallas, Texas, United States
- Baylor College of Medicine, Houston, Texas, United States
- University of Wisconsin- Madison, Madison, Wisconsin, United States
- Ghent University Hospital, Ghent, Belgium
- Federal University of São Paulo - Hospital São Paulo (UNIFESP-HSP), São Paulo, Brazil
- Hospital for Sick Children, Toronto, Ontario, Canada
- McGill University Health Centre for Innovative Medicine, Montreal, Quebec, Canada
- +12 more locations on ClinicalTrials.gov
Collaborators
Sepul Bio
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.
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