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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