TerminatedPhase 2NCT01147536
Study of Vitespen (HSPPC-96, Oncophage ®) for Immune Response Assessment in Participants With Resectable Renal Cell Carcinoma at Intermediate Risk of Recurrence
Studying Clear cell renal 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
- Agenus Inc.
- Principal Investigator
- Louis Lacombe, MD, FRCSCService d'Urologie; Centre hospitalier universitaire de Quebec - Hotel-Dieu de Quebec
- Intervention
- HSPPC-96(biological)
- Enrollment
- 12 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2010 – 2012
Study locations (3)
- Community Care Physicians, Albany, New York, United States
- MD Anderson Cancer Center, Houston, Texas, United States
- Pavillion de Recherche de Hotel Dieu, Québec, Canada
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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