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Phase 2 N=6 Treatment

The Combination of GX-188E Vaccination and Pembrolizumab in Patients With HPV 16 and/or 18+ Advanced Cervical Cancer

Cervical Cancer

Enrolled (actual)
6
Serious AEs
38.5%
Results posted
Jul 2025
Primary outcome: Primary: DLT Evaluation for Safety and Tolerability(Part A) — 0 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
GX-188E (Drug); KEYTRUDA® (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Genexine, Inc.
Primary completion
Apr 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
DLT Evaluation for Safety and Tolerability(Part A)
PRIMARY
ORR for Efficacy (Part B&C)
41.4; 35.0
SECONDARY
ORR for Efficacy (Part A)
50.0
SECONDARY
BORR (Part B&C)
50.0; 41.4; 35.0
SECONDARY
Time-to-Best Response
2.07; 2.10; 2.10
SECONDARY
Duration of Response (DOR)
NA; 5.78; NA
SECONDARY
Progression-Free Survival (PFS)
4.25; 4.14; 4.40
SECONDARY
Overall Survival (OS)
15.54; 14.42; 23.79

Summary

A Multi-Center, Open-label Phase Ib-II Trial of the Combination of GX-188E Vaccination and Pembrolizumab in Patients with Advanced, Non-Resectable HPV-Positive Cervical Cancer

Eligibility Criteria

Inclusion Criteria

  • Patients must be female and age ≥ 18 years (19 years for Korean sites)
  • Patients with histologically confirmed advanced or metastatic HPV-positive (HPV-16 or HPV-18) cervical cancer, who have disease progression after treatment with all available therapies for metastatic disease that are known to confer clinical benefit, or are intolerant to treatment, or refuse standard treatment.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1
  • Life Expectancy of at least 6 months
  • Patients must agree to provide either an archival tumor tissue sample or fresh biopsy sample for baseline biomarker tissue analyses, including staining for PD-L1. If archival tissue is not available and the patient does not have biopsy-accessible tumor lesions, the patient will be excluded.

Exclusion Criteria

  • Patient has disease that is suitable for local therapy administered with curative intent.
  • Patient has a known additional malignancy that is progressing or has required active treatment within the past 3 years.
  • Patient is expected to require any other form of antineoplastic therapy while on study; including systemic chemotherapy, radiation therapy (except for palliative purposes) biological therapy, or immunotherapy not specified in this protocol.
  • Patient has a history of active central nervous system (CNS) metastases and/or carcinomatous meningitis.
  • Patients have received prior therapy with an anti-PD-1, anti-PD-L1, or anti PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX 40, CD137) and was discontinued from that treatment due to a Grade 3 or higher immune-related Adverse Event (irAE)
  • Patients with active autoimmune disease requiring systemic immunosuppressive treatment within the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment and is allowed.
  • Patients has had an allogeneic solid organ or allogeneic bone marrow transplant
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03444376). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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