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Clinical Trials in Canada / NCT07094087
Recruiting Phase 3

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

NCT07094087 · tracked via the Priya Life Science Canada tracker
Phase
Phase 3
Started
2025-09-15
Last updated
2026-08-18

Condition(s) studied

Complex Cardiovascular Surgery With Cardiopulmonary Bypass

Investigational drug(s) / intervention(s)

BE1116FFP

BE1116: A single dose of BE1116 will be administered by intravenous (IV) infusion intraoperatively.

FFP: A single dose of FFP will be administered as investigational product (IP) by IV infusion intraoperatively.

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (24)

FacilityCityRegionStatus
UCLA Health - Ronald Reagan Medical Center Los Angeles California Recruiting
Emory University Hospital Atlanta Georgia Not Yet Recruiting
University of Chicago Medicine Chicago Illinois Not Yet Recruiting
University of Kansas Medical Center (KUMC) Kansas City Kansas Not Yet Recruiting
University of Maryland Medical Center (UMMC) Baltimore Maryland Recruiting
Johns Hopkins Medicine Baltimore Maryland Not Yet Recruiting
Cooper University Healthcare Camden New Jersey Not Yet Recruiting
North Shore University Hospital Manhasset New York Not Yet Recruiting
University of Cincinnati Cincinnati Ohio Recruiting
OUHSC (University of Oklahoma Health Sciences Center) Oklahoma City Oklahoma Recruiting
Oregon Health & Sciences University Portland Oregon Recruiting
Thomas Jefferson University Hospital Philadelphia Pennsylvania Recruiting
Vanderbilt University Medical Center (VUMC) Nashville Tennessee Not Yet Recruiting
UT Southwestern Medical Center Dallas Texas Recruiting
University of Utah Salt Lake City Utah Not Yet Recruiting
University of Virginia Health System Charlottesville Virginia Not Yet Recruiting
Kingston Health Science Center Kingston Ontario Not Yet Recruiting
London Health Sciences Center - University Campus London Ontario Recruiting
University of Toronto - St. Michael's Hospital (SMH) - Keenan Research Centre for Biomedical Science Toronto Ontario Not Yet Recruiting
Universite de Montreal-Institut de Cardiologie de Montreal (ICM) Montreal Heart Institute (MHI) Montreal Quebec Recruiting
Kyushu University Hospital Fukuoka Fukuoka Recruiting
National Cerebral and Cardiovascular Center Suita Osaka Not Yet Recruiting
Sakakibara Heart Institute Fuchu-shi Tokyo Recruiting
Hospital Civil de Guadalajara Guadalajara Jalisco Not Yet Recruiting

More CSL Behring trials in Canada

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07094087 on ClinicalTrials.gov ↗ ← All trials in Canada