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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 Clinical Results associated with NeoMatrix Therapeutics Inc
0 Patents (Medical) associated with NeoMatrix Therapeutics Inc
100 Deals associated with NeoMatrix Therapeutics Inc
100 Translational Medicine associated with NeoMatrix Therapeutics Inc