Clinical trial

Study to Gather Information About the Proper Dosing of the Oral FXIa Inhibitor…

NCT04218266 · Bayer, Industry · Completed

Key facts

NCT number NCT04218266
Title Study to Gather Information About the Proper Dosing of the Oral FXIa Inhibitor BAY 2433334 and to Compare the Safety of the Study Drug to Apixaban, a Non-vitamin K Oral Anticoagulant (NOAC) in Patients With Irregular Heartbeat (Atrial Fibrillation) That Can Lead to Heart-related Complications.
Official title Multicenter, Randomized, Active Comparator-controlled, Double-blind, Double-dummy, Parallel Group, Dose-finding Phase 2 Study to Compare the Safety of the Oral FXIa Inhibitor BAY2433334 to Apixaban in Patients With Atrial Fibrillation
Acronym PACIFIC-AF
Lead sponsor Bayer, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Atrial Fibrillation (AF)
Intervention type Drug, Other
Interventions BAY2433334, Apixaban, BAY2433334 matching placebo, Apixaban matching placebo
Enrollment 755
Start date Jan 30, 2020
Primary completion Oct 8, 2021
Completion Oct 8, 2021
First posted Jan 6, 2020
Last update posted Oct 27, 2022
Countries Austria, Belgium, Canada, Czechia, France, Hungary, Italy, Japan, Latvia, Netherlands, Spain, Sweden and 2 more

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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