CompletedPhase 3NCT00414648
Efficacy and Safety of Sirolimus in LAM
Studying Lymphangioleiomyomatosis
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 Cincinnati
- Principal Investigator
- Francis X McCormack, MDUniversity of Cincinnati Medical Center Division of Pulmonary and Critical Care Medicine
- Intervention
- Sirolimus(drug)
- Enrollment
- 89 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2006 – 2011
Study locations (13)
- University of California Los Angeles, Los Angeles, California, United States
- National Jewish Medical and Research Center, Denver, Colorado, United States
- University of Florida, Gainesville, Gainesville, Florida, United States
- National Heart, Lung, and Blood Institute, Bethesda, Maryland, United States
- Harvard's Brigham and Women's Hospital, Boston, Massachusetts, United States
- University of Cincinnati Medical Center, Cincinnati, Ohio, United States
- Cleveland Clinic Foundation, Cleveland, Ohio, United States
- Oregon Health & Science University, Portland, Oregon, United States
- Medical University of South Carolina, Charleston, South Carolina, United States
- University of Texas Health Center at Tyler, Tyler, Texas, United States
- Toronto General Hospital, Toronto, Ontario, Canada
- National Kinki-Chou Hospital, Sakai, Osaka, Japan
- Niigata University Medical and Dental Hospital, Niigata, Japan
Collaborators
Office of Rare Diseases (ORD) · FDA Office of Orphan Products Development · National Center for Research Resources (NCRR)
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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