Condition: X-Linked Retinitis Pigmentosa (XLRP) · Sponsor: Frontera Therapeutics
The aim of this study was to evaluate the safety, tolerability, and efficacy of one-time subretinal injection of FT-002 in male subjects (8-45 years of age) with RPGR (Retinitis Pigmentosa GTPase Regulator) gene mutation-associated X-linked retinitis pigmentosa, of XLRP. This study includes Phase I (dose escalation phase) and Phase II (dose expansion phase).
This description comes directly from the study's public registry record.
Xinyan Li · +86-021-58206061 · xinyan.li@fronteratherapeutics.com
Minghui Xue · +86-021-58206061 · minghui.xue@fronteratherapeutics.com
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| Peking Union Medical College Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06492850