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Single/Multiple Dose Escalation Study to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BAY1101042 Given as 5 mg MR Tablet After Single Oral Dosing Followed by Once Daily Dosing for 7 Days in 12 Healthy Male Subjects Per Dose Step in a Randomized, Placebo Controlled, Single Blind, Group Comparison Design

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Single/Multiple Dose Escalation Study to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BAY1101042 Given as 5 mg MR Tablet After Single Oral Dosing Followed by Once Daily Dosing for 7 Days in 12 Healthy Male Subjects Per Dose Step in a Randomized, Placebo Controlled, Single Blind, Group Comparison Design

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 05 Nov 2021

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At a glance

  • Drugs Runcaciguat (Primary)
  • Indications Unspecified
  • Focus Adverse reactions
  • Sponsors Bayer

    • Most Recent Events

    • 16 Aug 2019 Status changed from active, no longer recruiting to completed.
    • 17 Jul 2019 Planned End Date changed from 28 Jun 2019 to 17 Jul 2019.
    • 17 May 2019 Planned End Date changed from 17 Jun 2019 to 28 Jun 2019.

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