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最高研发阶段临床2期 |
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最高研发阶段无进展 |
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A Phase II, Double-blind, Randomised, Placebo-controlled, Parallel Group Pilot Study to Evaluate the Safety and Efficacy of FFP104 in the Treatment of Subjects With Moderate to Severely Active Crohn's Disease
This study will be conducted to evaluate the safety, tolerability and efficacy of intravenously administered FFP104 or placebo over 15 days (3 total doses) in subjects with moderate to severely active Crohn's Disease
A Phase I/II, Open Label, Multicenter, Pilot Dose Escalation Study to Evaluate the Safety, Tolerability and Pharmacodynamics of FFP104 in Subjects Previously Diagnosed With Primary Biliary Cirrhosis (PBC)
The purpose of this study is to determine the initial safety, tolerability and pharmacodynamics of the CD40-antagonist Mab, FFP104, in subjects with PBC
100 项与 Fast Forward Pharmaceuticals BV 相关的临床结果
0 项与 Fast Forward Pharmaceuticals BV 相关的专利(医药)
100 项与 Fast Forward Pharmaceuticals BV 相关的药物交易
100 项与 Fast Forward Pharmaceuticals BV 相关的转化医学