TerminatedPhase 1NCT04438083
A Safety and Efficacy Study Evaluating CTX130 in Subjects With Relapsed or Refractory Renal Cell Carcinoma (COBALT-RCC)
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
- CRISPR Therapeutics AG
- Principal Investigator
- Alissa Keegan, MDCRISPR Therapeutics
- Intervention
- CTX130(biological)
- Enrollment
- 19 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2024
Study locations (7)
- Research Site 2, Duarte, California, United States
- Research Site 5, Hartford, Connecticut, United States
- Research Site 4, Houston, Texas, United States
- Research Site 3, Salt Lake City, Utah, United States
- Research Site 1, Melbourne, Victoria, Australia
- Research Site 6, Toronto, Ontario, Canada
- Research Site 7, Amsterdam, North Holland, Netherlands
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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