CompletedPhase 3NCT00562497
Efficacy and Safety of Prochymal® Infusion in Combination With Corticosteroids for the Treatment of Newly Diagnosed Acute Graft Versus Host Disease (GVHD)
Studying Graft versus host disease
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
- Mesoblast, Inc.
- Principal Investigator
- Christopher James, PAMesoblast, Inc.
- Intervention
- Prochymal®(drug)
- Enrollment
- 192 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2008 – 2010
Study locations (30)
- University of Alabama Birmingham (UAB) Hospital, Birmingham, Alabama, United States
- UCLA Medical Center, Los Angeles, California, United States
- University of California Medical Center, San Francisco, California, United States
- Rocky Mountain Cancer Center, Denver, Colorado, United States
- University of Florida, Gainesville, Florida, United States
- Emory University, Atlanta, Georgia, United States
- Northside Hospital, Atlanta, Georgia, United States
- Northwestern Center for Clinical Research, Chicago, Illinois, United States
- Rush University Medical Center, Chicago, Illinois, United States
- University of Chicago Hospitals, Chicago, Illinois, United States
- Loyola University Medical Center, Maywood, Illinois, United States
- Indiana University Cancer Center, Indianapolis, Indiana, United States
- St. Francis Cancer Center, Indianapolis, Indiana, United States
- University of Louisville, Louisville, Kentucky, United States
- Tufts New England Medical Center, Boston, Massachusetts, United States
- +15 more locations on ClinicalTrials.gov
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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