Sponsor:
VarmX B.V.
Code:
NCT07288489
Conditions
Blood Loss, Surgical
Coagulation Disorder
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
Reltodecacog alfa
Usual Pharmacological Care
Brief summary:
Conditions
Blood Loss, Surgical
Coagulation Disorder
Study ID
NCT07288489
Start date
Aug 18, 2026
Status verified date
Aug, 2026
Completion date
Jan, 2031
Anticipated
Primary completion date
Jan, 2029
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
800 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
experimental: Reltodecacog alfa
active comparator: Usual Pharmacological Care
Interventions
Reltodecacog alfa
Usual Pharmacological Care
Primary outcome measure
Central contacts
Locations
Chandler Regional Medical Center (CRMC)
Recruiting
Chandler, Arizona, United States, 85224
HonorHealth John C Lincoln Medical Center
Recruiting
Phoenix, Arizona, United States, 85020
University of South Florida
Recruiting
Tampa, Florida, United States, 33606
University of Iowa Health Care
Recruiting
Iowa City, Iowa, United States, 52242
Ohio State McCampbell Outpatient Care
Recruiting
Columbus, Ohio, United States, 43210
The University of Oklahoma Health Sciences Center
Recruiting
Oklahoma City, Oklahoma, United States, 73126
Memorial Hermann Hospital-TMC Investigational Drugs Services Pharmacy
Recruiting
Houston, Texas, United States, 77030
Intermountain Medical Center
Recruiting
Murray, Utah, United States, 84107
St Michael's Hospital
Recruiting
Toronto, Ontario, Canada, M5B 1WB
Sponsor
VarmX B.V.
Last update posted
Oct 14, 2026
Last verified
Aug, 2026
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-23. This information was provided to ClinicalTrials.gov by VarmX B.V. on 2026-10-14. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.