Trial Search Results

Patient Functioning and Well-being, Economic, and Clinical Impact of Hemophilia A and Its Treatment

The purpose of the study is to improve the understanding of key patient reported outcomes such as quality of life as well as clinical outcomes in hemophilia A, in a global real world setting.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Bayer

Stanford Investigator(s):

Intervention(s):

  • Drug: Available Recombinant, and Human Factor VIII products incl. Kogenate FS (Recombinant Factor VIII, BAY14-2222)

Eligibility


Inclusion Criteria:

   - Age 16 or over.

   - Have documentation of physician-confirmed diagnosis of moderate or severe Hemophilia A
   (severity defined as moderate = FVIII activity 1% to 5% and severe = FVIII activity
   ≤1%).

   - Signed written informed consent provided by the patient or the patient's parents for
   patients under the age of 18 (dependent of local regulations).

   - Signed written assent is also required for patients under the age 18 years (dependent
   on local regulations).

   - Plan to receive at least half of their Hemophilia care at the registry site.

   - Willing and able to enter data as per the data collection schedule.

   - Currently receiving prophylactic or on demand treatment (including within last 6months
   for on demand).

   - Expected life expectancy of at least 2 years.

Exclusion Criteria:

   - Patients with Hemophilia B

   - Patients with von Willebrand disease (vWD)

   - Patients with other rare bleeding disorders

   - Unable to comply with the study protocol

Ages Eligible for Study

16 Years - N/A

Genders Eligible for Study

Male

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Recruiting