Clinical Trials in China / NCT05874310
Recruiting
Early Phase 1
Gene Therapy for Subjects With RPGR Mutation-associated X-linked Retinitis Pigmentosa
NCT05874310 · tracked via the Priya Life Science China tracker
Condition(s) studied
X-Linked Retinitis Pigmentosa
Investigational drug(s) / intervention(s)
FT-002
FT-002: Comparison of different dosages of FT-002
Study summary
A clinical trial of gene therapy for patients with X-linked retinitis pigmentosa (XLRP).
Eligibility
Inclusion Criteria:
1.Subjects that are willing and able to follow study procedures; 2.Males aged 8-45 years old at the time of signing the Informed Consent Form; 4.Subjects who are confirmed with variants of RPGR ;
Exclusion Criteria:
1.Have other retinal degenerative diseases, such as retinal degeneration caused by other known Inherited retinal disease gene variants or previously received an gene therapy product.
Primary outcome measure(s)
- Incidence of AEs — from FT-002 administration through up to 1 years
Number and proportion of Adverse Events
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Peking Union Medical College Hospital | Beijing | Beijing Municipality | Recruiting |
| Eye & ENT hospital of Fudan university | Shanghai | Shanghai Municipality | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05874310 on ClinicalTrials.gov ↗ ← All trials in China