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临床试验/NL-OMON44381
NL-OMON44381已完成不适用

Open label, randomized, cross-over study to explore the pharmacokinetics of BAY 1834845 after oral and intravenous dosing, including food effect and absolute bioavailability (Part A), and to investigate the effect of BAY 1834845 on the pharmacokinetics of orally administered methotrexate (Part B) in healthy male subjects - BAY 1834845 FE, BA, Methotrexate DDI Study

Bayer AG0 个研究点目标入组 22 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
Bayer AG
入组人数
22

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 male subjects
  • - 18 - 50 years, inclusive
  • - BMI: 18.0 - 30.0 kg/m², inclusive

排除标准

  • Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 3 months before the start of this study. In case of donating more than 0.5 liters of blood in the 4 week prior the start of this study.

研究者

发起方
Bayer AG

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