A Follow-on Study for Second-Eye Treatment for Participants Previously Treated With Gene Therapy for X-Linked Retinitis Pigmentosa (XLRP)
Running, not enrolling · Phase 2
Conditions studied: X-Linked Retinitis Pigmentosa
In brief
The purpose of this study is to assess the safety and tolerability of subretinal delivery of Adeno-associated Virus Vector (AAV5 hRKp.RPGR) gene therapy in adults and children with X-linked retinitis pigmentosa.
Key facts
- Study ID
- NCT06646289
- Run by
- Janssen Research & Development, LLC
- People needed
- 24
- Starts
- 2024-10-10
- Expected to finish
- 2030-10-24
- Last updated by the study team
- 2026-07-06
Who can join
Age: 5 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Have been treated with AAV5-hRKp.RPGR in study MGT009 and have completed or is currently enrolled in Study MGT010
- Must sign an informed consent form indicating that they understand the purpose and procedures of the study and is willing to participate in the study
- Willing to adhere to the protocol and long-term follow-up
You may not qualify if…
- There are no specific exclusion criteria to enroll in this study
Where it is running
- Massachusetts Eye and Ear Infirmary — Boston, Massachusetts, United States
- University of Michigan Kellogg Eye Center — Ann Arbor, Michigan, United States
- Moorfields Eye Hospital — London, United Kingdom
Full record on ClinicalTrials.gov
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