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Active, Not Recruiting

NCT Number: NCT04414540

Combining Pembrolizumab and Metformin in Metastatic Head and Neck Cancer Patients

The purpose of this study is to determine anti-tumor activity by measuring overall response rate in recurrent and/or metastatic HNSCC patients receiving the combination of metformin and pembrolizumab.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Cincinnati Medical Center

Cincinnati, Ohio, 45219, United States

About this study

Recurrent and/or metastatic HNSCC patients will be treated with combination of metformin and pembrolizumab. Patients will be randomized into arms 1 and 2, to either receive Metformin prior to pembrolizumab or to begin Metformin after pembrolizumab treatment begins. The patients are randomized for the exploratory endpoints in order to better understand the difference of effects of metformin versus pembrolizumab on the immune system although efficacy is based on combination.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically or cytologically confirmed recurrent or metastatic non-cutaneous HNSCC for which there are no surgical or radiation curative options.
  • Patients may have received up to 3 prior lines of therapy for metastatic or recurrent disease.
  • ECOG performance status ≤2

Exclusion criteria

  • Patients with nasopharyngeal HNSCC will be excluded
  • Patients who have had chemotherapy or radiotherapy within 2 weeks prior to entering the study.
  • Patients who have not recovered from adverse events due to prior anti-cancer therapy
  • Patients who have previously received PD-1 or PD-L1 inhibitors for metastatic/recurrent disease
  • Patients currently receiving metformin or who have received metformin in the last 6 months

Treatment and study plan

Metformin Extended Release Oral Tablet

Drug

Metformin ER starting dose 1000mg daily Metformin ER escalation dose 2000mg daily

Other names: Glucophage XR

Pembrolizumab

Drug

Pembrolizumab q 3 weeks

Other names: Keytruda

Primary outcomes

  1. Overall Response Rate by RECIST 1.1 and iRECIST

    Time frame: Up to 2 years after completion of study treatment

    A complete response is defined as the disappearance of all target lesions, with any affected lymph nodes reduced to less than 10 mm. A partial response occurs when there is at least a 30% reduction in the total size of target lesions compared with baseline. Progressive disease is indicated by at least a 20% increase in lesion size (with a minimum absolute increase of 5 mm) or the appearance of new lesions. Stable disease describes cases where tumor size changes do not meet criteria for partial response or progressive disease.

Secondary outcomes

  1. Number of Patients With Adverse Events Measured by CTCAE v5.0

    Time frame: 2 years

    To observe and record safety of combination in metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) patients receiving the combination of metformin and pembrolizumab. AEs will be graded and recorded according to NCI CTCAE Version 5.0.

  2. Progression Free Survival (PFS)

    Time frame: 1 year

    To observe and record progression free survival in recurrent and/or metastatic HNSCC patients receiving the combination of metformin and pembrolizumab.

  3. Overall Survival (OS)

    Time frame: 1 year

    Overall survival was analyzed using the Kaplan-Meier method. The reported 1-year overall survival percentages represent Kaplan-Meier-estimated probabilities of survival at 1 year and do not correspond to the observed proportion of participants alive or deceased due to censoring. Observed all-cause mortality is reported separately as the number of participants who died due to any cause in each arm.

Sponsors and collaborators

Lead sponsor

Trisha Wise-Draper

Other

Collaborators

  • American Cancer Society, Inc.

Registry information

Official study title

A Phase 2 Feasibility Study Combining Pembrolizumab and Metformin to Harness the Natural Killer Cytotoxic Response in Metastatic Head and Neck Cancer Patients

Important dates

Study start
2020
Primary completion
2026
Study completion
2026
First posted
Jun 4, 2020
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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