CompletedPhase 2NCT01108445
Phase II Study of Afinitor vs. Sutent in Patients With Metastatic Non-Clear Cell Renal Cell Carcinoma
Studying Acquired cystic disease-associated renal cell carcinoma
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
- Duke University
- Principal Investigator
- Andrew Armstrong, MD, ScMDuke University
- Intervention
- Everolimus(drug)
- Enrollment
- 131 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2010 – 2015
Study locations (18)
- University of Chicago, Chicago, Illinois, United States
- Indiana University Melvin and Bran Simon Cancer Center, Indianapolis, Indiana, United States
- Karmanos Cancer Institute/Wayne State University, Detroit, Michigan, United States
- Washington Univ in St. Louis-School of Medicine, St Louis, Missouri, United States
- Duke Univeristy Medical Center, Durham, North Carolina, United States
- Cleveland Clinic, Cleveland, Ohio, United States
- Oregon Health & Science University, Portland, Oregon, United States
- SCRI, Nashville, Tennessee, United States
- The Vanderbilt Clinic, Henry-Joyce Cancer Center, Nashville, Tennessee, United States
- BC Cancer Agency, Vancouver, British Columbia, Canada
- CancerCare Manitoba, Med Onc, Dept Hem and Onc, Winnipeg, Manitoba, Canada
- London Health Sciences Center, London, Ontario, Canada
- Cambridge Cancer Trials Centre, Cambridge, England, United Kingdom
- The Royal Marsden NHS, London, England, United Kingdom
- The Christie Hospital NHS, Manchester, England, United Kingdom
- +3 more locations on ClinicalTrials.gov
Collaborators
Novartis · Pfizer
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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