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非在研适应症- |
最高研发阶段临床2/3期 |
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非在研适应症- |
最高研发阶段临床前 |
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最高研发阶段临床前 |
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A Randomized, Placebo-controlled, Double-blind Phase 2b Trial to Assess the Efficacy and Safety of Ex Vivo Allograft Admin of ICM012 Solution 2 Mg/mL to Improve Allograft Function in Recipients of Donation After Circulatory Death Kidneys
Randomized (1:1), placebo controlled, double blind efficacy trial. 200 patients will be followed up for 12 months post transplantation. The primary endpoint will be Delayed Graft Function (DGF) defined as the requirement for dialysis within 7 days post transplantation.
Phase I FIH Phase I/IIa Randomized Placebocontrolled Doubleblind Trial Evaluating Safety and Tolerability of ExVivo Deceased Donor Kidney Allograft Treatment With TUM012 to Minimize Ischemic Reperfusion Injury After Kidney Transplantation
A first-in-human single center, randomized, double-blind, placebo-controlled trial, with primary objective to evaluate safety and tolerability of ex-vivo kidney allograft treatment with TUM012 to reduce ischemia-reperfusion injury in de novo kidney transplant recipients.
100 项与 iCoat Medical AB 相关的临床结果
0 项与 iCoat Medical AB 相关的专利(医药)
100 项与 iCoat Medical AB 相关的药物交易
100 项与 iCoat Medical AB 相关的转化医学