Condition: Retinitis Pigmentosa · Sponsor: Chigenovo Co., Ltd
This trial employs a single-arm, open-label seamless Phase I/II design, consisting of two stages: Phase I dose exploration and Phase II dose expansion.The primary objective of this trial is to evaluate the safety, tolerability, and efficacy of subretinal injection of ZVS203e solution.
This description comes directly from the study's public registry record.
Jinlu Zhang, MD · 15810570898 · zhangjinlu@chinagene.cc
Always discuss trial participation with your own doctor first.
| Peking University Third Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06952842