Status and phase
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Study type
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Identifiers
About
The primary purpose of this study is to evaluate the reversal of the anticoagulant effects of milvexian by 4-Factor Prothrombin Complex Concentrate (4F-PCC) and Recombinant Human Factor VIIa (rFVIIa) in healthy participants as measured by changes from baselines of the coagulation testing parameters (activated partial thromboplastin time [aPTT] and thrombin generation assay [TGA]).
Enrollment
Sex
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Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
52 participants in 3 patient groups
There are currently no registered sites for this trial.
Central trial contact
Study Contact
Start date
Jul 27, 2020 • 4 years ago
End date
Jun 07, 2023 • 1 year and 10 months ago
Today
May 05, 2025
Lead Sponsor
Data sourced from clinicaltrials.gov
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