CompletedPhase 2NCT00502788
Evaluating the Safety of Two Medications to Treat Hepatitis C in People With Thalassemia (The HepC Study)
Studying Thalassemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Carelon Research
- Principal Investigator
- Maureen Jonas, MDBoston Children's Hospital
- Intervention
- Peginterferon Alfa-2a and Ribavirin(drug)
- Enrollment
- 21 target
- Eligibility
- 18-44 years · All sexes
- Timeline
- 2003 – 2006
Study locations (5)
- Children's Hospital and Research Center at Oakland, Oakland, California, United States
- Weill Medical College of Cornell University, New York, New York, United States
- Children's Hospital Philadelphia, Philadelphia, Pennsylvania, United States
- Toronto General Hospital, Universty Health Network, Toronto, Ontario, Canada
- University College London, London, United Kingdom
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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