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临床试验/NL-OMON27439
NL-OMON27439Other不适用

A Phase 1, Single-Center, Double-Blind, Placebo Controlled Study in Healthy Subjects to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous ABP-700 after a Single Ascending Bolus Dose

Annovation Biopharma(University Medical Center Groningen)0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
Other
发起方
入组人数
60

研究概览

简要总结

one

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Healthy, adult, men and women, 18-45 years of age, inclusive.
  • 2.Continuous non-smoker who has not used nicotine-containing products for at least 6 months prior to the first dose.

排除标准

  • 1.History or presence of significant cardiovascular disease, or cardiovascular disease risk factors, hyperlipidemia, coronary artery disease, or any known genetic pre disposition to cardiac arrhythmia (including long QT syndrome.)
  • 2.History or presence of significant pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological (inclusive of any seizure disorder), or psychiatric disease.

研究者

发起方
Annovation Biopharma(University Medical Center Groningen)

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