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最高研发阶段临床前 |
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非在研适应症- |
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A Phase 1, Randomised, Double-blind, Placebo-controlled, Single Ascending Dose Study in Healthy Volunteers to Evaluate the Safety, Tolerability and Pharmacokinetics of Intravenously Administered AVLX-144
This is a randomised, double-blind, placebo-controlled, single ascending dose study in healthy volunteer subjects. Each dose level will be investigated with eight 20-50-year-old male subjects (6 on active drug and 2 on placebo). Additionally, eight healthy elderly subjects (65-80 years of age, males and females), 6 on active drug and 2 on placebo, will be included in the study at one dose level, once the safety and tolerability of AVLX-144 has been documented in younger subjects.
100 项与 Avilex Pharma ApS 相关的临床结果
0 项与 Avilex Pharma ApS 相关的专利(医药)
100 项与 Avilex Pharma ApS 相关的药物交易
100 项与 Avilex Pharma ApS 相关的转化医学