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最高研发阶段临床1期 |
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A First-in-Human, Randomized, Double-Blind, Placebo-Controlled, Single-Ascending Dose Study to Examine the Safety, Tolerability, and Pharmacokinetics of cNP8 in Healthy Adults
This is a Phase 1, single-center, randomized, double-blind, placebo-controlled, first-in-human study to evaluate the safety of an investigational drug to treat burns. Participants will be healthy male and female adults. The study will consist of a screening period, inpatient dosing and observation period and safety follow-up. Participants will receive 1 intravenous dose of the investigational drug or placebo. Duration of participation will be approximately 38 days, which includes a maximum of a 30 day screening period and a study period of approximately 8 days.
100 项与 NeoMatrix Therapeutics Inc 相关的临床结果
0 项与 NeoMatrix Therapeutics Inc 相关的专利(医药)
100 项与 NeoMatrix Therapeutics Inc 相关的药物交易
100 项与 NeoMatrix Therapeutics Inc 相关的转化医学