Once-A-Day Prophylaxis for Youth and Young Adults With Severe Hemophilia A
|ClinicalTrials.gov Identifier: NCT00717626|
Recruitment Status : Completed
First Posted : July 17, 2008
Last Update Posted : December 19, 2013
|Condition or disease||Intervention/treatment||Phase|
|Hemophilia A||Drug: Kogenate FS, Advate, or Humate-P, Recombinate, Helixate FS||Phase 2|
Hemophilia is an important and costly disorder; if left untreated, it may have serious consequences. The greatest impact of hemophilia occurs from recurrent bleeding into joints. The consequences of joint bleeding include pain associated with acute bleeding and later chronic arthropathy. Half of affected children with severe hemophilia have joint damage; joint damage is more frequent with increased bleeding. The prevention and treatment of bleeding is very expensive and therefore finding a cost-effective treatment is of high priority.
Worldwide, two major treatment strategies have been used to prevent arthropathy - on demand therapy and factor prophylaxis. The goal of prophylaxis is to convert the severe to the moderate phenotype by providing circulating factor activity of greater than 1%. Patients with greater than 1% circulating factor VIII activity rarely have spontaneous hemarthroses. Therefore, the goal of providing circulating factor at this level is to eliminate spontaneous hemarthroses. The term primary prophylaxis suggests using preventative factor VIII replacement from a very early age. The term secondary prophylaxis is used to describe the application of prophylaxis at a later disease stage. In this study, secondary prophylaxis will be used.
Once-daily prophylaxis is a novel application of hemophilia factor prophylaxis for youth and young adults. Before embarking on a costly definitive trial we feel that it is necessary to demonstrate that subjects will be willing to enroll and will be compliant with the therapy. Moreover, we need to establish an estimate of the effect of once-daily prophylaxis on bleeding rates, quality of life, and joint damage progression in order to design a definitive trial.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||14 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Pilot Study of Once-A-Day Prophylaxis for Youth and Young Adults With Severe Hemophilia A|
|Study Start Date :||July 2008|
|Actual Primary Completion Date :||April 2011|
|Actual Study Completion Date :||April 2011|
U.S. FDA Resources
Drug: Kogenate FS, Advate, or Humate-P, Recombinate, Helixate FS
Starting at the 4-month visit, subjects will receive 250 units per day (if their weight is < 50 kg.) or 500 units per day (weight ≥ 50 kg.) of their usual preparation of factor VIII.
- To test the feasibility of a large-scale clinical trial of once-daily prophylaxis. As such, the primary outcome will be related to process measures. [ Time Frame: 12 months ]
- Clinical efficacy [ Time Frame: 12 months ]
- Estimate the effect size and variability of effect and resource utilization of once-daily prophylaxis. [ Time Frame: 12 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00717626
|St. Michael's Hospital|
|Toronto, Ontario, Canada|
|The Hospital for Sick Children|
|Toronto, Ontario, Canada|
|Montreal, Quebec, Canada|
|Principal Investigator:||Brian Feldman, MD,MSc,FRCPC||The Hospital for Sick Children|