Efficacy and Safety of 4F-PCC (4-Factor Prothrombin Complex Concentrate) in Adult Patients Undergoing Complex Cardiovascular Surgery With Cardiopulmonary Bypass (CPB)
Condition(s) studied
Investigational drug(s) / intervention(s)
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
Primary outcome measure(s)
- Number of Participants With and Without a Successful Correction of Coagulation Factor Deficiency — At Day 1 after IP infusion (30 minutes after the end of infusion)
Successful correction ("yes" vs "no") of coagulation factor deficiency as measured by an international normalized ratio (INR) of less than or equal to (≤) 1.4 at 30 minutes after the end of IP infusion.
Trial sites (24)
| Facility | City | Region | Status |
|---|---|---|---|
| UCLA Health - Ronald Reagan Medical Center | Los Angeles | California | Recruiting |
| Emory University Hospital | Atlanta | Georgia | Not Yet Recruiting |
| University of Chicago Medicine | Chicago | Illinois | 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 | 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 | 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 | Recruiting |
| Sakakibara Heart Institute | Fuchu-shi | Tokyo | Recruiting |
| Hospital Civil de Guadalajara | Guadalajara | Jalisco | Not Yet Recruiting |
More CSL Behring trials in Japan
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 Japan