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Inactive Indication- |
Drug Highest PhasePhase 1/2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
一项评价IMC-002治疗视神经脊髓炎谱系疾病的安全性和有效性的多中心、随机、阳性对照的Ib/Ⅲ期临床研究
[Translation] A multicenter, randomized, active-controlled Phase Ib/III clinical study to evaluate the safety and efficacy of IMC-002 in the treatment of neuromyelitis optica spectrum disorders
评价不同剂量IMC-002治疗视神经脊髓炎谱系疾病患者的安全性,与IMC-002治疗SLE的Ib临床试验一起确定IMC-002的最佳治疗剂量
评价IMC-002与阳性对照药相比在视神经脊髓炎谱系疾病患者中的52 周或52周内首次临床复发时间
[Translation] To evaluate the safety of different doses of IMC-002 in the treatment of patients with neuromyelitis optica spectrum disorders, and determine the optimal therapeutic dose of IMC-002 together with the Phase Ib clinical trial of IMC-002 in the treatment of SLE
To evaluate the time to first clinical relapse at or within 52 weeks of IMC-002 compared with active control drugs in patients with neuromyelitis optica spectrum disorders
A Multi-center, Randomized, Double-blind, Placebo Control Phase 1b/II Study to Evaluate the Safety and Efficacy of IMC-002 for the Treatment of Active Systemic Lupus Erythematosus
The purpose of this study is to evaluate the efficacy and safety of IMC-002 in the treatment of active SLE.
A Phase Ib/III Multi-center, Randomized and Positive Control Study to Evaluate IMC-002 Safety and Efficacy in in Neuromyelitis Optica Spectrum Disorder (NMOSD) Patients
The purpose of this study is to evaluate the efficacy and safety of IMC-002 in the treatment of NMOSD.
100 Clinical Results associated with ImmuneCare Biopharmaceuticals (Shanghai) Co., Ltd.
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100 Translational Medicine associated with ImmuneCare Biopharmaceuticals (Shanghai) Co., Ltd.