NL-OMON32187已完成不适用
A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PHASE I STUDY TO DETERMINE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF SINGLE ASCENDING ORAL DOSES OF P1201-07 IN HEALTHY OVERWEIGHT OR OBESE SUBJECTS - P1201-07 SAD study
icholas Piramal India Ltd.0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 16
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •18-55 year of age for males
- •18-65 year of age for females
排除标准
- •* Regular treatment with non-topical medications within 90 days prior to drug administration.
- •* History of alcohol abuse or drug addiction (including soft drugs like cannabis products)
- •* Use of concomitant medication including sedatives and steroids, except for paracetamol, at least 14 days prior to the first dose
研究者
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