Active, not recruitingPHASE1, PHASE2NCT04140526
Safety, PK and Efficacy of ONC-392 in Monotherapy and in Combination of Anti-PD-1 in Advanced Solid Tumors and NSCLC
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
- OncoC4, Inc.
- Principal Investigator
- Tianhong Li, MDUniversity of California, Davis
- Intervention
- ONC-392(drug)
- Enrollment
- 733 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2027
Study locations (30)
- Highlands Oncology Group, Springdale, Arkansas, United States
- University of California at Davis, Davis, California, United States
- The Oncology Institute of Hope and Innovation, Downey, California, United States
- City of Hope Cancer Center, Duarte, California, United States
- University of Colorado Hospital, Aurora, Colorado, United States
- Nuvance Health, Norwalk, Connecticut, United States
- MedStar Georgetown University Hospital, Washington D.C., District of Columbia, United States
- Florida Cancer Specialists, Atlantis, Florida, United States
- University of Florida Health Cancer Center, Gainesville, Florida, United States
- Ocala Oncology Florida Cancer Affiliates, Ocala, Florida, United States
- AdventHealth Cancer Institute, Orlando, Florida, United States
- Memorial Cancer Institute, Pembroke Pines, Florida, United States
- Emory University Winship Cancer Institute, Atlanta, Georgia, United States
- Norton Health, Lexington, Kentucky, United States
- Greater Baltimore Medical Center, Baltimore, Maryland, United States
- +15 more locations on ClinicalTrials.gov
Collaborators
National Cancer Institute (NCI)
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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