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A Phase I, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of Apramycin Administered Intravenously in Healthy Adults.
This is a first-in-human study to assess the safety, tolerability and pharmacokinetics of escalating single doses of apramycin. This trial will be conducted as a single ascending dose trial in up to 5 sequential dose cohorts (group-comparison). Each cohort will consist of 8 healthy subjects, 6 will receive apramycin and 2 placebo.
100 项与 Juvabis GmbH 相关的临床结果
0 项与 Juvabis GmbH 相关的专利(医药)
100 项与 Juvabis GmbH 相关的药物交易
100 项与 Juvabis GmbH 相关的转化医学