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Completed Phase 2 Interventional Results available

Phase 2 Study of the Safety, Tolerability and Pilot Efficacy of Oral Factor Xa Inhibitor Betrixaban Compared to Warfarin

ClinicalTrials.gov ID: NCT00742859

Public ClinicalTrials.gov record NCT00742859. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 4:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Parallel Group, Dose-Finding, Multicenter, Multinational Study of the Safety, Tolerability and Pilot Efficacy of Three Blinded Doses of the Oral Factor Xa Inhibitor Betrixaban Compared With Open-Label Dose-Adjusted Warfarin in Patients With Non-Valvular Atrial Fibrillation (EXPLORE Xa)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Prevention of stroke in patients with atrial fibrillation (AF). Hypothesis: In patients with non-valvular AF, orally administered betrixaban will provide similar or better efficacy and safety than warfarin and it will offer the advantage of not requiring dose adjustments due to international normalized ratios (INRs) outside the target range of 2.0 to 3.0 and a more consistent level of anticoagulation over time.

Study identification

NCT ID
NCT00742859
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Portola Pharmaceuticals
Industry
Enrollment
508 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2008 (Type not available)
Primary completion
Aug 2009 (Actual)
Completion
Nov 2009 (Actual)
Last update posted
Aug 7, 2023

2008 – 2009

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Portola Investigational Site Anaheim California 92801 —
Portola Investigational Site Colorado Springs Colorado 80909 —
Portola Investigational Site Melbourne Florida 32901 —
Portola Investigational Site Miami Florida 33173 —
Portola Investigational Site Ormond Beach Florida 32174 —
Portola Investigational Site Pensacola Florida 32501 —
Portola Investigational Site Port Charlotte Florida 33952 —
Portola Investigational Site Aurora Illinois 60504 —
Portola Investigational Site Auburn Maine 04210 —
Portola Investigational Site Columbia Maryland 21044 —
Portola Investigational Site Salisbury Maryland 21804 —
Portola Investigational Site Towson Maryland 21204 —
Portola Investigational Site Tupelo Mississippi 38801 —
Portola Investigational Site St Louis Missouri 63110 —
Portola Investigational Site Poughkeepsie New York 12601 —
Portola Investigational Site Hillsboro Oregon 97123 —
Portola Investigational Site Wynnewood Pennsylvania 19096 —
Portola Investigational Site Rapid City South Dakota 57701 —
Portola Investigational Site Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00742859, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 7, 2023 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00742859 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →