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Completed Phase 3 Interventional Results available

A Study in Participants With Acute Major Bleeding to Evaluate the Ability of Andexanet Alfa to Reverse the Anticoagulation Effect of Direct and Indirect Oral Anticoagulants (Extension Study)

ClinicalTrials.gov ID: NCT02329327

Public ClinicalTrials.gov record NCT02329327. 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 Jul 23, 2026, 2:36 AM EDT

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

Official title

Prospective, Open-Label Study of Andexanet Alfa in Patients Receiving a Factor Xa Inhibitor Who Have Acute Major Bleeding (ANNEXA-4)

Study identification

NCT ID
NCT02329327
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Alexion Pharmaceuticals, Inc.
Industry
Enrollment
479 participants

Conditions and interventions

Conditions

Interventions

  • Andexanet Biological

Biological

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
Apr 9, 2015
Primary completion
Sep 23, 2020
Completion
Sep 23, 2020
Last update posted
Feb 15, 2022

2015 – 2020

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
23
Facility City State ZIP Site status
Clinical Study Site Long Beach California
Clinical Study Site Los Angeles California
Clinical Study Site Orange California
Clinical Study Site Fort Lauderdale Florida
Clinical Study Site Jacksonville Florida
Clinical Study Site Sarasota Florida
Clinical Study Site Tampa Florida
Clinical Study Site Annapolis Maryland
Clinical Study Site Boston Massachusetts
Clinical Study Site Detroit Michigan
Clinical Study Site Royal Oak Michigan
Clinical Study Site Troy Michigan
Clinical Study Site St Louis Missouri
Clinical Study Site Rochester New York
Clinical Study Site Asheville North Carolina
Clinical Study Site Chapel Hill North Carolina
Clinical Study Site Raleigh North Carolina
Clinical Study Site Cincinnati Ohio
Clinical Study Site Cleveland Ohio
Clinical Study Site Pittsburgh Pennsylvania
Clinical Study Site Austin Texas
Clinical Study Site Fort Worth Texas
Clinical Study Site Huntington West Virginia

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 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02329327, 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 Feb 15, 2022 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02329327 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →