Trial Search Results

Safety and Efficacy Study in Subjects With Chronic HCV and Underlying Hemophilia

The primary objective for this study is to evaluate the proportion of subjects who achieve SVR12 (HCV RNA < LLOQ (target not detected) at post-treatment follow-up Week 12 in subjects with Genotype(GT)-1b, -4 and GT-2, -3

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Bristol-Myers Squibb

Stanford Investigator(s):

Intervention(s):

  • Biological: Pegylated-Interferon-lambda
  • Drug: Ribavirin
  • Drug: Daclatasvir

Phase:

Phase 3

Eligibility


For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com.

Inclusion Criteria:

   - Severe hemophilia (defined as < 1% factor activity level)

   - Infection with the hepatitis C virus (HCV) with underlying hemophilia

   - Males 18 years of age and above

   - Have not been previously treated with an interferon

Exclusion Criteria:

   - Not infected with the hepatitis B virus (HBV) or human immunodeficiency virus (HIV)

   - Chronic liver disease caused by any disease other than chronic HCV infection

   - Presence of Bethesda inhibitor

   - Current evidence of or history of portal hypertension

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Male

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Mindie H. Nguyen, MD
650-498-7878
Not Recruiting