Post-Marketing Non-Interventional Safety Evaluation of Obizur in the Treatment of Bleeding Episodes for Patients With Acquired Hemophilia A

CompletedOBSERVATIONAL
Enrollment

53

Participants

Timeline

Start Date

December 30, 2015

Primary Completion Date

June 7, 2019

Study Completion Date

June 7, 2019

Conditions
Acquired Hemophilia A
Interventions
BIOLOGICAL

OBIZUR

Treating physician will determine treatment regimen, frequency of laboratory and clinical assessments, according to routine clinical practice.

Trial Locations (16)

19104

University of Pennsylvania Health System, Philadelphia

27157

Comprehensive Cancer Center of Wake Forest Unversity, Winston-Salem

27710

Duke University Medical Center, Durham

30322

Emory University School of Medicine, Atlanta

32610

University of Florida, Gainesville

44195

Cleveland Clinic, Cleveland

46260

Indiana Hemophilia and Thrombosis Center, Indianapolis

48202

Henry Ford Health System, Detroit

48823

Michigan State University, East Lansing

52242

University of Iowa Hospitals & Clinics, Iowa City

53225

Blood Center of Southeast Wisconsin, Milwaukee

61615

Bleeding and Clotting Disorders Institute, Peoria

63110

Washington University, St Louis

70112

Tulane University Hospital & Clinics, New Orleans

80045

University of Colorado Health, Aurora

84132

University of Utah Health Sciences Center, Salt Lake City

All Listed Sponsors
collaborator

Baxalta Innovations GmbH, now part of Shire

INDUSTRY

lead

Baxalta now part of Shire

INDUSTRY

NCT02610127 - Post-Marketing Non-Interventional Safety Evaluation of Obizur in the Treatment of Bleeding Episodes for Patients With Acquired Hemophilia A | Biotech Hunter | Biotech Hunter