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Drug Highest PhasePhase 3 |
First Approval Ctry. / Loc.- |
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MechanismRHO gene transference |
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Inactive Indication- |
Drug Highest PhasePhase 1/2 |
First Approval Ctry. / Loc.- |
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Drug Highest PhasePreclinical |
First Approval Ctry. / Loc.- |
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/ Not yet recruitingPhase 1/2 A Single-Arm, Open-Label, Phase 1/2 Clinical Trial of ZVS203e in Subjects With Retinitis Pigmentosa Associated With RHO Mutation
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.
A Multicenter, Randomized,Controlled,Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of ZVS101e Administered as a Single Subretinal Injection in Subjects With Bietti's Crystalline Dystrophy (BCD)
This is a multi-center, randomized and controlled phase 3 clinical trial.
评价 ZVS101e 注射液在结晶样视网膜变性(BCD)受试者中单次单眼视网膜下注射给药的安全性和有效性的 I/II 期临床研究
[Translation] A Phase I/II clinical study to evaluate the safety and efficacy of ZVS101e injection as a single monocular subretinal injection in subjects with crystalline retinal degeneration (BCD)
本研究的目的是评价ZVS101e注射液在结晶样视网膜变性(BCD)受试者中视网膜下注射给药的安全性和有效性,并选择最佳有效剂量。
[Translation] The purpose of this study is to evaluate the safety and efficacy of subretinal injection of ZVS101e injection in subjects with crystalline retinal degeneration (BCD) and to select the optimal effective dose.
100 Clinical Results associated with Beijing Chigenovo Co., Ltd.
0 Patents (Medical) associated with Beijing Chigenovo Co., Ltd.
100 Deals associated with Beijing Chigenovo Co., Ltd.
100 Translational Medicine associated with Beijing Chigenovo Co., Ltd.