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NCT07094087PHASE3Recruiting

Efficacy and Safety of 4F-PCC (4-Factor Prothrombin Complex Concentrate) in Adult Patients Undergoing Complex Cardiovascular Surgery With Cardiopulmonary Bypass (CPB)

CSL Behring

Start Date

9/15/2025

Completion Date

12/17/2026

Summary

This is a phase 3, multicenter, randomized, open-label, parallel-group, controlled study to assess the efficacy and safety of BE1116 compared with fresh frozen plasma (FFP) in adult participants undergoing complex cardiovascular surgery with CPB. The primary purpose of the study is to compare the efficacy of BE1116 and FFP in correcting coagulation factor deficiencies in bleeding participants undergoing complex cardiovascular surgery with CPB.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Adult greater than or equal to (≥) 18 years and has provided written informed consent. * Undergoing elective complex cardiovascular surgery requiring CPB, including procedures of the thoracic aorta (with or without additional cardiac interventions), aortic valve replacement + coronary artery bypass graft (CABG), complex valve surgeries, mitral valve repair + CABG, and mitral valve replacement + CABG and reoperative CABG. Reoperative procedures are permitted. Excluded surgeries are as follows: heart transplantation, insertion or removal of ventricular assist devices (except for intra-aortic balloon pumps), and acute repair of thoracoabdominal aneurysms. * Coagulation factor replacement (ie, 4F-PCC or FFP) is ordered in the operating room for the management of bleeding, in accordance with accepted clinical standards. The following criteria must be met: * INR ≥ 1.6 (point-of-care INR testing by Hemochron ≥ 5 to 10 minutes after protamine infusion for heparin reversal). If a participant needs a second dose of protamine, a new INR measurement should be performed to confirm eligibility. * Significant microvascular hemorrhage (ie, not due to surgical complications), as defined by a BSS score of ≥ 2. Exclusion Criteria: * Administration of any systemic hemostatic therapy, such as cryoprecipitate, platelets, FFP, PCC (eg, 4-factor / 3-factor PCC \[4F-PCC / 3F-PCC\]), Factor VIII (FVIII) inhibitor bypassing activity (FEIBA), recombinant activated Factor VIIa (rFVIIa), or other coagulation factor products, in the 24 hours before study surgery, except when FFP is added to the CPB circuit.

Interventions

BIOLOGICAL

BE1116

BIOLOGICAL

FFP

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Conditions

Complex Cardiovascular Surgery With Cardiopulmonary Bypass

Locations

UCLA Health - Ronald Reagan Medical Center

Los Angeles, California 90095

United States

University of Chicago Medicine

Chicago, Illinois 60637

United States

University of Maryland Medical Center (UMMC)

Baltimore, Maryland 21201

United States

North Shore University Hospital

Manhasset, New York 11040

United States

University of Cincinnati

Cincinnati, Ohio 45267

United States

OUHSC (University of Oklahoma Health Sciences Center)

Oklahoma City, Oklahoma 73104

United States

Oregon Health & Sciences University

Portland, Oregon 97239

United States

Thomas Jefferson University Hospital

Philadelphia, Pennsylvania 19107

United States

UT Southwestern Medical Center

Dallas, Texas 75390

United States

University of Virginia Health System

Charlottesville, Virginia 22908

United States

Kingston Health Science Center

Kingston, Ontario K7L 2V7

Canada

London Health Sciences Center - University Campus

London, Ontario N6A 5A5

Canada

University of Toronto - St. Michael's Hospital (SMH) - Keenan Research Centre for Biomedical Science

Toronto, Ontario M5B 1W8

Canada

Universite de Montreal-Institut de Cardiologie de Montreal (ICM) Montreal Heart Institute (MHI)

Montreal, Quebec H1T1C8

Canada

Kyushu University Hospital

Fukuoka, Fukuoka 812-8582

Japan

National Cerebral and Cardiovascular Center

Suita, Osaka 564-8565

Japan

Sakakibara Heart Institute

Fuchu-shi, Tokyo 183-0003

Japan

Hospital Civil de Guadalajara

Guadalajara, Jalisco 44100

Mexico