RecruitingPHASE1, PHASE2NCT06413680
A First-In Human (FIH) Study to Find Out How Well REGN10597 Medicine Given Alone or in Combination With Cemiplimab Works in Adult Participants Who Have Cancer With Tumors That Have Spread in Their Body
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
- Regeneron Pharmaceuticals
- Principal Investigator
- Clinical Trial ManagementRegeneron Pharmaceuticals
- Intervention
- REGN10597(drug)
- Enrollment
- 240 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2030
Study locations (11)
- USC Norris Comprehensive Cancer Center, Los Angeles, California, United States
- University of California San Francisco (UCSF), San Francisco, California, United States
- Yale School of Medicine, North Haven, Connecticut, United States
- University of Chicago, Chicago, Illinois, United States
- Start Midwest Cancer Research, Grand Rapids, Michigan, United States
- Northwell Health, Lake Success, New York, United States
- University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
- University of Pittsburgh Medical Center - Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
- MD Anderson Cancer Center, Houston, Texas, United States
- Next Oncology, San Antonio, Texas, United States
- The Start Center for Cancer Care, San Antonio, Texas, United States
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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