CompletedPhase 3NCT01076010
An Extension Treatment Protocol for Subjects Who Have Participated in a Study of Tivozanib Versus Sorafenib in Kidney Carcinoma (Protocol AV-951-09-301).
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
- AVEO Pharmaceuticals, Inc.
- Principal Investigator
- Robert J. Motzer, MDMemorial Sloan Kettering Cancer Center
- Intervention
- Tivozanib(drug)
- Enrollment
- 277 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2010 – 2014
Study locations (30)
- Site 185, Los Angeles, California, United States
- Site 184, Orlando, Florida, United States
- Site 182, Minneapolis, Minnesota, United States
- Site 186, New York, New York, United States
- Site 187, Dallas, Texas, United States
- Site 403, Plovdiv, Bulgaria
- Site 404, Sofia, Bulgaria
- Site 400, Sofia, Bulgaria
- Site 401, Varna, Bulgaria
- Site 402, Veliko Tarnovo, Bulgaria
- Site 110, Montreal, Quebec, Canada
- Site 122, Santiago, Chile
- Site 123, Temuco, Chile
- Site 411, Prague, Czechia
- Site 133, Saint-Herblain, France
- +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.
Open NCT01076010 on ClinicalTrials.govOther trials for Acquired cystic disease-associated renal cell carcinoma
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