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Hemophilia A Study



Hemophilia A Study

For Condition: Hemophilia A
Status: Completed
Sponsor(s): Wyeth-Ayerst Research ,
Synopsis: To identify the causative mutations in previously untreated patients with hemophilia A enrolled in the ReFacto® clinical safety and efficacy study CTN 93-R833-0XX/C9741-28, using two established hemophilia mutation testing laboratories (one in Europe and one in North America).
Details:
Eligibility:
Study Type:
  Interventional, Treatment
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Patients who were or are enrolled in Study CTN 93-R833-0XX/C9741-28, and have been treated with ReFacto® during this study are eligible for participation. - The patient (or legal guardian) must be willing to give written informed consent before any study-related procedures are performed. - A blood sample will be collected from each patient for the purpose of this study and will be analyzed at one or both of the designated central laboratories. Exclusion Criteria: - Any condition which, in the investigator's opinion, places the patient at undue risk.
Total Enrollment: 

Location and Contact Information:


Additional Information:
Study ID Numbers:
  C0007-28/3082A1-302; 
Study Start Date: 
Record last reviewed: June 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00038909

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2. Effect of Indinavir Plus Two Other Anti-HIV Drugs on Blood Clotting in HIV-Positive Males with Hemophilia

3. Severe Hemophilia A Study

4. Hepatitis C in Clinically Discordant Hemophilic Siblings

5. Delta Hepatitis and Liver Disease in Hemophiliacs

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