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COMPLETED
NCT01652027

Hemophilia Inhibitor Previously Untreated Patient Study

Sponsor: The University of Texas Health Science Center, Houston

View on ClinicalTrials.gov

Summary

Hemophilia A is a congenital bleeding disorder caused by deficiency of factor VIII (FVIII) and is treated by replacement therapy with FVIII concentrate. Approximately 30% of people with severe hemophilia A develop neutralizing antibodies, called FVIII inhibitors, which interfere with the function of FVIII concentrates. The reason that some, but not all, people with severe hemophilia A develop inhibitors is incompletely understood. Understanding individual and environmental risk factors is important to be able to prevent and possibly treat inhibitors. This study will look at individual and treatment characteristics in babies with severe hemophilia A who have not yet received treatment with FVIII (called Previously Untreated Patients, or PUPS). Subjects in the study will be asked to provide diaries of treatments, medications, and illnesses. Treatment will be directed by the subjects' physician, but all subjects will receive Advate, a third-generation recombinant FVIII product. Subjects will have blood drawn for laboratory tests, which include studies of the immune system and genetic studies of the FVIII mutation, before and 7-9 days after the first treatment with FVIII, and 5 days (+/-2 days) after the 5th, 10th, 20th, 30th, 40th, and 50th days of treatment with FVIII (exposure days). The duration of the study will be first 50 treatments or 3 years, whichever comes first.

Official title: Study of Immunologic Determinants of Inhibitor Development in Previously Untreated Patients With Hemophilia

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

25

Start Date

2011-07

Completion Date

2020-03

Last Updated

2026-10-22

Healthy Volunteers

No

Conditions

Interventions

DRUG

FVIII concentrate

usual treatment as directed by treating physician

Locations (17)

Emory University

Atlanta, Georgia, United States

Indiana Hemophilia and Thrombosis Center

Indianapolis, Indiana, United States

University of Kentucky

Lexington, Kentucky, United States

Tulane University

New Orleans, Louisiana, United States

Cornell University

New York, New York, United States

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States

Cincinnati Children's Hospital

Cincinnati, Ohio, United States

University of Oregon

Portland, Oregon, United States

Hemophilia Center of Western Pennsylvania

Pittsburgh, Pennsylvania, United States

North Texas Comprehensive Hemophilia Center

Dallas, Texas, United States

Baylor College of Medicine

Houston, Texas, United States

University of Texas Health Science Center-Houston

Houston, Texas, United States

Intermountain Hemophilia and Thrombosis Center

Salt Lake City, Utah, United States

Medical University of Vienna

Vienna, Austria

Angelo Bianchi Bonomi Hemophilia & Thrombosis Center

Milan, Italy

Emma Children's Hospital AMC

Amsterdam, Netherlands

Malmo Centre for Thrombosis and Haemostasis

Malmö, Sweden