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最高研发阶段批准上市 |
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首次获批日期2020-04-01 |
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最高研发阶段批准上市 |
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首次获批日期2016-06-01 |
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最高研发阶段批准上市 |
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首次获批日期2013-12-01 |
A Randomized Study of the Efficacy and Safety of Neoadjuvant Therapy With BCD-217 (Nurulimab + Prolgolimab) Versus Standard Adjuvant Therapy With Pembrolizumab in Patients With Resectable Stage III Skin Melanoma.
This study is an open-label, randomized, comparative phase III study, which will include subjects with resectable stage III skin melanoma (up to 3 resectable transient metastases are acceptable).
/ Active, not recruiting临床3期 A Double-Blind Placebo-Controlled Comparative Randomized Clinical Study of the Efficacy and Safety of BCD-217 (Nurulimab + Prolgolimab) Followed by Anti-PD-1 Compared to Anti-PD-1 Monotherapy as First-Line Treatment in Subjects With Unresectable/Metastatic Melanoma
The aim of study is to investigate the efficacy, safety, immunogenicity, pharmacokinetics, and pharmacodynamics of BCD-217 followed by prolgolimab monotherapy versus prolgolimab monotherapy as first-line therapy in subjects with unresectable or metastatic melanoma.
100 项与 Biocad Medical, Inc. 相关的临床结果
0 项与 Biocad Medical, Inc. 相关的专利(医药)
100 项与 Biocad Medical, Inc. 相关的药物交易
100 项与 Biocad Medical, Inc. 相关的转化医学