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A single-center, double-blinded, randomized, placebo-controlled, single ascending dose study with food effect crossover and multiple ascending dose study to investigate the safety, tolerability, pharmacokinetic, pharmacodynamic, and hemostatic profile of VE-01902

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Trial Profile

A single-center, double-blinded, randomized, placebo-controlled, single ascending dose study with food effect crossover and multiple ascending dose study to investigate the safety, tolerability, pharmacokinetic, pharmacodynamic, and hemostatic profile of VE-01902

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 05 Sep 2019

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At a glance

  • Drugs VE-1902 (Primary)
  • Indications Atrial fibrillation
  • Focus Adverse reactions; First in man; Pharmacodynamics
  • Acronyms VE-01902-REPLACE-Ia-001
  • Sponsors VCR1

    • Most Recent Events

    • 30 Aug 2019 Planned number of patients changed from 142 to 134.
    • 13 Feb 2019 Planned initiation date changed from 15 Oct 2018 to 8 Jan 2019.
    • 13 Feb 2019 Status changed from not yet recruiting to recruiting.
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