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NCT06234423
A Study of CUSP06 in Patients With Platinum-Refractory/Resistant Ovarian Cancer and Other Advanced Solid Tumors
This phase 1 study will evaluate the safety, tolerability, pharmacokinetics, and efficacy of CUSP06 in patients with platinum-refractory/resistant ovarian cancer and other advanced solid tumors.
Trial Details
NCT ID NCT06234423
Phase PHASE1
Sponsor OnCusp Therapeutics, Inc.
Status RECRUITING
Cancer Type Ovarian Cancer
Interventions
Locations (sample) Denver, Colorado, United States|39.73915,-104.9847 New Haven, Connecticut, United States|41.30815,-72.92816 Miami Beach, Florida, United States|25.79065,-80.13005 Sarasota, Florida, United States|27.33643,-82.53065 Boston, Massachusetts, United States|42.35843,-71.05977
Key Eligibility Criteria
Written informed consent provided prior to any screening procedures. Male or female patients, ≥18 years of age at the time of obtaining informed consent. Patients with histologically or cytologically confirmed advanced solid tumors previously treated with standard of care systemic therapy, or for who… Willingness to provide archival tumor tissue, when available. If no archival tissue is available, willingness to undergo a pretreatment biopsy if m…
For full eligibility, visit ClinicalTrials.gov .
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