CompletedPHASE2, PHASE3NCT00490620
Study of Combivir for Patients With Primary Biliary Cirrhosis
Studying Primary biliary cholangitis
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
- University of Alberta
- Principal Investigator
- Andrew L Mason, MBBS MRCPIUniversity of Alberta
- Intervention
- Combination antiviral therapy(drug)
- Enrollment
- 59 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2004 – 2007
Study locations (5)
- Mayo Clinic, Rochester, Minnesota, United States
- St Louis University, St Louis, Missouri, United States
- University of Alberta, Edmonton, Alberta, Canada
- University of Montreal, Montreal, Quebec, Canada
- University of Birmingham, Birmingham, England, United Kingdom
Collaborators
GlaxoSmithKline · Axcan Pharma
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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