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临床试验/ACTRN12614001022651
ACTRN12614001022651已完成1 期

A First-in-Human, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Oral Dose Study to Assess the Safety, Tolerability and Pharmacokinetics of DV-928 in Healthy Volunteers

INC Research0 个研究点目标入组 36 人开始时间: 2014年9月24日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
36

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
Blinded (masking used)

入排标准

年龄范围
19 Years 至 55 Years(—)
性别
All

入选标准

  • Be in good health as determined by medical history, physical examination, 12 lead ECG and clinical laboratory evaluations at screening;
  • -Male subjects must agree to use a medically acceptable method of contraception/birth control throughout the study duration and for 90 days after the study is completed.
  • -Female subjects must be of non-childbearing potential

排除标准

  • -Significant blood loss or donated blood in the 30 days prior to study participation
  • -Participation in an investigational drug study within 30 days prior to dosing.
  • -History of drug or alcohol abuse.
  • -Use of any medications, including OTC and herbal or nutritional supplements during the week prior to drug dosing
  • -Positive tests for HIV, hepatitis B/C, drugs of abuse or alcohol breath-test.
  • -Clinically significant abnormalities

研究者

发起方
INC Research

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