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
  • CUSP06
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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