Trials / Completed
CompletedNCT01652027
Hemophilia Inhibitor Previously Untreated Patient Study
Study of Immunologic Determinants of Inhibitor Development in Previously Untreated Patients With Hemophilia
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 25 (actual)
- Sponsor
- The University of Texas Health Science Center, Houston · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | FVIII concentrate | usual treatment as directed by treating physician |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2020-03-01
- Completion
- 2020-03-01
- First posted
- 2012-07-27
- Last updated
- 2020-11-10
Locations
17 sites across 5 countries: United States, Austria, Italy, Netherlands, Sweden
Source: ClinicalTrials.gov record NCT01652027. Inclusion in this directory is not an endorsement.