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CompletedNCT01765868

A Human Phase I Absolute Bioavailability Study of PRT054021 in Healthy Male Volunteers

A Human Phase I Absolute Bioavailability Study of PRT054021 in Healthy Male Volunteers.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Portola Pharmaceuticals · Industry
Sex
Male
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This is a open label, single center, single oral dose, study of PRT054021, in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGBetrixabanSingle Oral dose 80 mg betrixaban and Single IV (15 ml) carbon 14 80 micrograms Betrixaban administered over 15 minutes, 2 hours after the oral dose

Timeline

Start date
2007-09-01
Primary completion
2007-10-01
Completion
2007-10-01
First posted
2013-01-10
Last updated
2023-08-08

Source: ClinicalTrials.gov record NCT01765868. Inclusion in this directory is not an endorsement.

A Human Phase I Absolute Bioavailability Study of PRT054021 in Healthy Male Volunteers (NCT01765868) · Clinical Trials Directory