PRGN-2009 in Combination With Pembrolizumab in Patients With Recurrent or Metastatic Cervical Cancer (NCT06157151) | Clinical Trial Compass
RecruitingPhase 2
PRGN-2009 in Combination With Pembrolizumab in Patients With Recurrent or Metastatic Cervical Cancer
United States24 participantsStarted 2025-11-11
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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Inclusion 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
* Measurable disease that can be accurately measured by RECIST v1.1 criteria
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
* Life expectancy ≥ 12 weeks from the time of enrollment.
* Must have adequate organ function
* Negative serum pregnancy test. Women of child-bearing potential (WOCBP) must agree to use adequate contraception prior to study entry and for at least 6 months following completion of study treatment.
* All patients must have the ability to understand and willingness to sign a written informed consent.
Exclusion Criteria:
* Prior chemotherapy, targeted therapy within 14 days; monoclonal antibody within 4 weeks; unresolved AEs.
* Immunodeficiency, active autoimmune disease on immunosuppression, or immunosuppressive therapy within 7 days. HIV eligible with disease control.
* Active hepatitis B (HBsAg+) or hepatitis C (HCV RT-PCR+) within 30 days of enrollment.
* History of non-infectious pneumonitis or interstitial lung disease.
* History of endocrine autoimmune disease (exceptions: treated Graves' disease; hypothyroidism on replacement).
* Live vaccine within 30 days prior to first dose.
* Patients with presence of…
What they're measuring
1
Determine the Objective Response Rate (ORR) following treatment with PRGN-2009 in combination with pembrolizumab in patients with pembrolizumab-resistant recurrent or metastatic cervical cancer.