TerminatedPhase 1NCT05121948
A Study of HC-7366 to Establish the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D)
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
- HiberCell, Inc.
- Principal Investigator
- Jose Iglesias, MDConsultant Chief Medical Officer for HiberCell, Inc.
- Intervention
- HC-7366(drug)
- Enrollment
- 35 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2024
Study locations (7)
- UC San Diego Moores Cancer Center, La Jolla, California, United States
- University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- Sarah Cannon Research Institute /Tennessee Oncology, Nashville, Tennessee, United States
- Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States
- The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States
- Swedish Cancer Institute, Seattle, Washington, United States
Collaborators
Covance
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 NCT05121948 on ClinicalTrials.govOther trials for Acquired cystic disease-associated renal cell carcinoma
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