Recruiting
Phase 3

Metformin

Sponsor:

Donald Mabbott

Code:

NCT05230758

Conditions

Medulloblastoma, Childhood

Cognitive Impairment

Eligibility Criteria

Sex: All

Age: 7 - 21

Healthy Volunteers: Not accepted

Interventions

Metformin hydrochloride (HCl) 500mg tablet

Placebo

Study Details

Brief summary:

The efficacy of treatment with metformin for promoting cognitive recovery and brain growth in children/adolescents treated for a brain tumour will be investigated in a multi-site Phase III randomized double-blind placebo-controlled parallel arm superiority trial. Specifically, in children/adolescents aged 7 years to 21 years and 11 months who have completed treatment for a brain tumour, is oral administration of metformin for 16 weeks associated with greater improvement of cognitive function and brain growth compared to placebo administered for 16 weeks?

Conditions

Medulloblastoma, Childhood

Cognitive Impairment

Study ID

NCT05230758

Start date

Jul 1, 2022

Status verified date

Apr, 2026

Completion date

Nov 30, 2027

Anticipated

Primary completion date

Nov 30, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 7 - 21

Healthy Volunteers: Not accepted

Inclusion Criteria:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

1. No less than 3 weeks after completion of:

  • Primary therapy for:

1. medulloblastoma

OR
2. ependymoma

OR
3. craniopharyngioma

OR
4. germ cell tumours

OR
  • Primary therapy for any other brain tumour treated with cranial radiation - at the discretion of the Study PI

OR
  • Cranial radiation for relapsed ependymoma
2. Age 7 years to 21 years and 11 months at the time of enrollment
3. Either declare English (or French in accepting sites) as their native language or have had at least two years of schooling in English (or French in accepting sites) at the time of consent
4. Able to swallow tablets either whole, crushed or via a feeding tube and be willing to adhere to the study intervention regimen
5. Meet criteria for normal organ function requirements as described below:

1. Normal renal function defined as: Estimated glomerular filtration rate (eGFR) > 75ml/min/1.73m²

  • eGFR is calculated using the Schwartz formula: eGFR (mL/min/1.73m²) = (0.41 × height in cm) / creatinine in mg/dL
2. Normal liver function defined as:

  • Serum glutamic-oxaloacetic transaminase (SGOT) (AST) ≤2.5 x institutional upper limit of normal (ULN) for age and gender
  • Serum glutamic pyruvic transaminase (SGPT) (ALT) ≤2.5 x institutional ULN for age and gender
  • Total bilirubin <1.5x institutional ULN for age and gender (patients with documented Gilbert's Disease may be enrolled with Sponsor approval and total bilirubin ≤2.0 x institutional ULN)
6. Informed consent (and assent, where applicable) will be obtained from the participants and/or their legal guardian(s) by study team members delegated to consent for this study

Exclusion Criteria:

Participants who meet any of the following criteria will not be eligible to take part in the trial:

1. Standard score of less than 60 for full scale IQ on the Wechsler Abbreviated Scale of Intelligence, Second Edition (WASI-II) (or other Wechsler Scale of Intelligence for English speaking participants) or pro-rated IQ score on the Wechsler Intelligence Scale for Children, Fifth Edition (WISC-V) or Wechsler Adult Intelligence Scale (WAIS-IV) for French speaking participants at Screening visit
2. Have a known hypersensitivity to metformin hydrochloride
3. Have unstable and/or insulin-dependent (Type 1) diabetes
4. Have a history of hypoglycemia after 2 years of age
5. Have been diagnosed with acute or chronic metabolic acidosis and/or lactic acidosis or if bicarbonate (Total CO2) is less than 22 mmol/L at the Screening visit
6. Have a history of renal disease or renal dysfunction pre-existing to the diagnosis of Medulloblastoma
7. Have a history of congestive heart failure requiring pharmacologic treatment (including the use of diuretics) within two years prior to study entry
8. Currently taking part in a cognitive rehabilitation intervention study
9. Treatment or planned treatment involving diuretics
10. Current or planned treatment with cationic drugs excreted by the kidneys (e.g. amiloride, cimetidine, digoxin, morphine, nifedipine, procainamide, quinidine, quinine, ranitidine, triamterene, trimethoprim, and vancomycin)
11. Current or planned treatment with concomitant medications with potential unacceptable interaction with metformin including, lamotrigine, beta blockers, angiotensin-converting enzyme (ACE) inhibitors, glycopyrrolate, and carbonic anhydrase inhibitors, or at the discretion of the Site PI or delegate for medications with potential interactions such as sertraline, lansoprazole and omeprazole.
12. Pernicious anemia (according to results of the Screening visit blood draw)
13. Current use of metformin hydrochloride
14. Any condition or diagnosis, that could in the opinion of the Site PI or delegate interfere with the participant's ability to comply with study instructions, might confound the interpretation of the study results, or put the participant at risk
15. Are receiving palliative care

Study Design

Enrollment

140 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Metformin

Oral metformin will be administered approximately 500mg/m2/day for 1 week and increased to 1000mg/m2/day for 15 weeks. Doses will be rounded to increments of half tablets (250mg, 500mg, 750mg and 1000mg).

placebo comparator: Placebo

Oral placebo will be administered approximately 500mg/m2/day for 1 week and increased to 1000mg/m2/day for 15 weeks. Doses will be rounded to increments of half tablets (250mg, 500mg, 750mg and 1000mg).

Interventions

Metformin hydrochloride (HCl) 500mg tablet

Metformin HCl 500mg tablets contain 500mg of active pharmaceutical ingredient (API) and are white, round, biconvex, film-coated tablets, with a score line on one face and debossed with "HMR" on the other. Each tablet contains the non-medicinal ingredients magnesium stearate and povidone. Tablet coating is comprised of hydroxypropyl methylcellulose, polyethylene glycol and titanium dioxide.

Placebo

Matching white round tablet containing excipients only. The placebo tablets will match the active drug as closely as possible in terms of appearance.

Primary outcome measure

  • Change from Week 1 (Baseline) Children's Auditory Verbal Learning Test-2 (CAVLT-2)/Rey Auditory Verbal Learning Test (RAVLT) Immediate Recall at Week 17 (Post-Intervention) to Assess Declarative Memory [ Time Frame: Week 1 (Baseline), Week 17 (Post-Intervention) ]
  • Change from Week 1 (Baseline) NIH Toolbox List Sort Working Working Memory Test at Week 17 (Post-Intervention) to Assess Working Memory [ Time Frame: Week 1 (Baseline), Week 17 (Post-Intervention) ]
  • Change from Week 1 (Baseline) Cambridge Neuropsychological Test Automated Battery (CANTAB) Mean Reaction Time for Correct Trials across the RVP, RTI, MTS, and DMS Subtests at Week 17 (Post-Intervention) to Assess Processing Speed [ Time Frame: Week 1 (Baseline), Week 17 (Post-Intervention) ]

Central Contacts and Locations

Central contacts

Locations

Alberta Children's Hospital

Recruiting

Calgary, Alberta, Canada, T3B 6A8

Contacts

Stollery Children's Hospital

Recruiting

Edmonton, Alberta, Canada, T6G 2B7

Contacts

Children's & Women's Health Centre of British Columbia

Recruiting

Vancouver, British Columbia, Canada, V6H 3V4

Contacts

Cancer Care Manitoba

Recruiting

Winnipeg, Manitoba, Canada, R3E 0V9

Contacts

Izaak Walton Killam (IWK) Health Centre

Recruiting

Halifax, Nova Scotia, Canada, B3K 6R8

Contacts

Hamilton Health Sciences - McMaster Children's Hospital

Recruiting

Hamilton, Ontario, Canada, L8S 4K1

Contacts

Children's Hospital, London Health Sciences Centre

Recruiting

London, Ontario, Canada, N6A 5W9

Contacts

Children's Hospital of Eastern Ontario

Recruiting

Ottawa, Ontario, Canada, K1H 8L1

Contacts

The Hospital for Sick Children

Recruiting

Toronto, Ontario, Canada, M5G 1X8

Contacts

CHU Sainte-Justine

Recruiting

Montreal, Quebec, Canada, H3T 1C5

Contacts

Montreal Children's Hospital

Recruiting

Montreal, Quebec, Canada, H4A 3J1

Contacts

CHU de Québec - Université Laval

Recruiting

Québec, Quebec, Canada, G1V 4G2

Contacts

CHU de Sherbrooke

Recruiting

Sherbrooke, Quebec, Canada, J1G 2E8

Contacts

Saskatchewan Health Authority

Recruiting

Saskatoon, Saskatchewan, Canada, S7N 0W8

Contacts

More Information

Sponsor

Donald Mabbott

Last update posted

May 1, 2026

Last verified

Apr, 2026

Keywords

  • Metformin
  • Paediatric brain tumour
  • Memory
  • Cognitive late effects

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Donald Mabbott on 2026-05-01.