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
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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 DoseanesthesiaNL-OMON40883Annovation Biopharma, Inc.60
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