跳至主要内容
临床试验/NL-OMON30044
NL-OMON30044已完成不适用

A Randomized, Double-Blind, Placebo-Controlled Study in Healthy Male Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Oral Doses of JNJ-26070109 - N/A

Janssen-Cilag0 个研究点目标入组 82 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
Janssen-Cilag
入组人数
82

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

  • Healthy males without evidence of gastro-intestinal disorders

排除标准

  • Subjects with evidence of clinically significant reproductive, gastrointestinal, renal, hematologic, pulmonary, neurologic, respiratory, endocrine/metabolic, or cardiovascular system abnormalities, psychiatric disorders, oncologic conditions or acute or chronic infection.
  • Subjects with a history of any hepatic disorder or history of hepatitis.
  • Subjects with known elevations of LFTs, alkaline phosphatase, gamma-GT, or bilirubin in the past.
  • Negative Helicobacter pylori serum IgG antibody

研究者

发起方
Janssen-Cilag

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