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

RecruitingPhase 3

A Phase 3, Multicenter, Randomized, Open-label, Controlled Study to Investigate the Efficacy and Safety of 4-Factor Prothrombin Complex Concentrate in Adult Patients Undergoing Complex Cardiovascular Surgery With Cardiopulmonary Bypass

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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.

About the study

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.

What is being tested

Sponsor: CSL Behring · Participants: 200 · Started: Sep 15, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07094087

Locations in the U.S.

CaliforniaUCLA Health - Ronald Reagan Medical Center, Los Angeles
GeorgiaEmory University Hospital, Atlanta (Not yet recruiting)
IllinoisUniversity of Chicago Medicine, Chicago (Not yet recruiting)
KansasUniversity of Kansas Medical Center (KUMC), Kansas City (Not yet recruiting)
MarylandJohns Hopkins Medicine, Baltimore (Not yet recruiting)
University of Maryland Medical Center (UMMC), Baltimore
New JerseyCooper University Healthcare, Camden (Not yet recruiting)
New YorkNorth Shore University Hospital, Manhasset (Not yet recruiting)
OhioUniversity of Cincinnati, Cincinnati
OklahomaOUHSC (University of Oklahoma Health Sciences Center), Oklahoma City
OregonOregon Health & Sciences University, Portland
PennsylvaniaThomas Jefferson University Hospital, Philadelphia
TennesseeVanderbilt University Medical Center (VUMC), Nashville (Not yet recruiting)
TexasUT Southwestern Medical Center, Dallas
UtahUniversity of Utah, Salt Lake City (Not yet recruiting)
VirginiaUniversity of Virginia Health System, Charlottesville (Not yet recruiting)

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.