CompletedPhase 3NCT02448680
A Phase III Study on the Safety, Pharmacokinetics and Efficacy of Coagulation Factor VIIa
Studying Hemophilia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Laboratoire français de Fractionnement et de Biotechnologies
- Principal Investigator
- Michael Wang, MDUniversity of Colorado, Denver
- Intervention
- Coagulation FVIIa (Recombinant)(biological)
- Enrollment
- 25 enrolled
- Eligibility
- 11 years · MALE
- Timeline
- 2015 – 2017
Study locations (9)
- University of Colorado Denver Hemophilia & Thrombosis Center, Aurora, Colorado, United States
- Jimmy Everest Center for Cancer and Bleeding Disorders, Oklahoma City, Oklahoma, United States
- UT Southwestern Medical Center at Dallas / Children's Medical Center, Dallas, Texas, United States
- University Multiprofile Hospital for Active Treatment "Sveti Georgi", Plovdiv, Bulgaria
- University Hospital Motol, Prague, Czechia
- Hematology of Department Hemophilia and Thromboses center, Tbilisi, Georgia
- Worthwhile Clinical Trials, Benoni, South Africa
- National Specialized Children's Hospital OKHMATDYT, Centre for Hemostatic Pathology (Ukraine), Kyiv, Ukraine
- Institute of Blood Pathology and Transfusion Medicine, Lviv, Ukraine
Collaborators
LFB USA, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02448680 on ClinicalTrials.govOther trials for Hemophilia
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