A Pilot Study of Ketogenic Diet and Metformin in Glioblastoma: Feasibility and Metabolic Imaging

Last updated: December 17, 2025
Sponsor: Weill Medical College of Cornell University
Overall Status: Active - Not Recruiting

Phase

2

Condition

Gliomas

Astrocytoma

Treatment

Metformin

Ketogenic Diet

Clinical Study ID

NCT04691960
1604017166
  • Ages > 18
  • All Genders

Study Summary

This clinical trial is for men and women with high-grade gliomas. Glucose (sugar) is thought to be a contributor to tumor growth. The ketogenic diet (a high fat, low carbohydrate diet) and metformin (a drug approved by the Food and Drug Administration to treat type 2 diabetes) are both known to lower blood glucose levels. The purpose of the study is to evaluate the tolerability of a ketogenic diet in conjunction with metformin and whether maintaining and the diet with metformin will have any effect on participants. Participants will prepare their own meals with the help of a nutritionist. Participants will continue on treatment as long as they are responding to therapy and not experiencing unacceptable side effects

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patients must have histologically confirmed high-grade glioma (e.g. glioblastoma,gliosarcoma, anaplastic astrocytoma, anaplastic oligodendroglioma, anaplastic mixedglioma or other anaplastic gliomas).

  2. Patients must have an MRI performed within 21 days prior to beginning the study dietand on a fixed dose of steroids for at least 5 days. If the steroid dose isincreased between the date of imaging and registration, a new baseline MR/CT isrequired.

  3. Patients must not have been exposed to bevacizumab.

  4. Patients cannot be taking insulin or other oral hypoglycemic. Must be at least 6weeks from last oral hypoglycemic or insulin.

  5. Must not have known type 1 or type 2 diabetes and expected to need either insulinand/or an oral hypoglycemic agents within the next 6 months.

  6. Patients must be >18 years old.

  7. Karnofsky performance status >60%.

  8. Life expectancy of greater than 12 weeks.

  9. Patients must have normal organ and marrow function as defined below:

  • Leukocytes >3,000/mcL

  • Absolute neutrophil count >1,000/mcL

  • Platelets >100,000/mcL

  • Total bilirubin <2.0 X institutional upper limit of normal (unless known tohave Gilbert's Disease)

  • AST (SGOT)/ALT(SGPT) <2.5 X institutional upper limit of normal

  • Serum Glucose: < 200 mg/dL

  • Creatinine < 1.5 mg/dL (for males), < 1.4 mg/dL (for females), or within normallab limits OR

  • Creatinine clearance >60 mL/min/1.73 m2 for patients with creatinine levelsabove institutional normal.

  1. Patients must not have any significant medical illnesses that, in the investigator'sopinion, cannot be adequately controlled with appropriate therapy or wouldcompromise the patients' ability to tolerate this therapy

  2. Patients having undergone recent resection or progressive tumor will be eligible aslong as all of the following conditions apply:

  3. They have recovered from the effects of surgery.

  4. On a steroid dosage that has been stable for at least 5 days.

  5. Residual disease following resection of recurrent tumor is not mandated foreligibility into the study. To best assess the extent of residual diseasepostoperatively, a MRI should be done:

  • No later than 96 hours in the immediate post-operative period or
  • At least 4 weeks post-operatively, and
  • Within 14 days of registration, and
  • If the 96-hour scan is more than 21 days before registration, the scanneeds to be repeated. If the steroid dose is increased between the date ofimaging and registration, a new baseline MRI is required on a stablesteroid dosage for at least 5 days.
  1. Patients must have the ability to understand and the willingness to sign a writteninformed consent document.

Exclusion

Exclusion Criteria:

  1. Patients who are receiving any other investigational agents.

  2. Patients who have had prior therapy with bevacizumab and/or other VEGF inhibitors.

  3. Patients who are taking insulin or other oral hypoglycemic. Must be at least 6 weeksfrom last oral hypoglycemic or insulin.

  4. History of allergic reactions attributed to metformin.

  5. Uncontrolled intercurrent illness including, but not limited to, ongoing or activeinfection, symptomatic congestive heart failure, unstable angina pectoris, diabetesrequiring oral hypoglycemic drugs and/or insulin, cardiac arrhythmia, or psychiatricillness/social situations that would limit compliance with study requirements.

  6. Patients known to have a malignancy that has required treatment in the last 12months and/or is expected to require treatment in the next 12 months (exceptnonmelanoma skin cancer or carcinoma in-situ in the cervix).

  7. The effects of a Ketogenic diet or metformin on the developing human fetus areunknown. For this reason, women of childbearing potential and men must agree to useadequate contraception (hormonal or barrier method of birth control; abstinence)prior to study entry and for the duration of study participation. Should a womanbecome pregnant or suspect she is pregnant while she or her partner is participatingin this study, she should inform her treating physician immediately.

  8. Patients with current alcoholism.

Study Design

Total Participants: 18
Treatment Group(s): 2
Primary Treatment: Metformin
Phase: 2
Study Start date:
August 01, 2016
Estimated Completion Date:
June 30, 2026

Connect with a study center

  • Columbia University

    New York, New York 10032
    United States

    Site Not Available

  • Weill Cornell Medicine

    New York, New York 10065
    United States

    Active - Recruiting

  • Columbia University

    New York 5128581, New York 5128638 10032
    United States

    Site Not Available

  • Weill Cornell Medicine

    New York 5128581, New York 5128638 10065
    United States

    Site Not Available

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