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临床试验/ACTRN12616001017415
ACTRN12616001017415已完成1 期

A Phase 1 Study to Determine the Relative Bioavailability of ACH-0144471 After Administration of a Tablet or Softgel Capsule Versus a Liquid Filled Capsule in Healthy Volunteers

Achillion Pharmaceuticals Inc.0 个研究点目标入组 26 人开始时间: 2016年8月2日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
26

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • Healthy adult male or female subjects. Females must be of non-child bearing potential. Healthy is defined as having no clinically relevant abnormalities identified by a detailed medical history, physical exam, blood pressure and pulse rate measurements, 12-lead ECG, and clinical laboratory tests.
  • Healthy volunteers must have a normal weight defined as minimum body weight of 50 kg and a BMI of 18 to 30kg/m2.

排除标准

  • If participants have any of the following criteria, they will be excluded from the study.
  • - Smokers and have a clinically significant disease or allergy,
  • - An active infection
  • - Consume more than 21 alcoholic drinks/week.
  • - Evidence of drug abuse or have taken prescription medications (systemic and topical) within 14 days prior to dosing.

研究者

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