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NCT06157151
PRGN-2009 in Combination With Pembrolizumab in Patients With Recurrent or Metastatic Cervical Cancer
This Phase 2 study will evaluate the efficacy and safety of PRGN-2009 in combination with pembrolizumab in patients with pembrolizumab-resistant recurrent or metastatic cervical cancer.
Trial Details
NCT ID NCT06157151
Phase PHASE2
Sponsor Precigen, Inc
Status RECRUITING
Cancer Type Cervical Cancer
Interventions PRGN-2009 plus Pembrolizumab
Locations (sample) Little Rock, Arkansas, United States|34.74648,-92.28959 Bethesda, Maryland, United States|38.98067,-77.10026 Seattle, Washington, United States|47.60621,-122.33207
Key Eligibility Criteria
Age 18 years and older. Recurrent or metastatic cervical cancer (histologically or cytologically confirmed) Must have been treated with pembrolizumab, either as monotherapy or in combination, for atleast 6 weeks. Subjects must have histologically or cytologically confirmed HPV positive disease
For full eligibility, visit ClinicalTrials.gov .
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