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Recruiting

NCT Number: NCT04121468

A Phase I Double Blind Study of Metformin Acting on Endogenous Neural Progenitor Cells in Children and Young Adults With Multiple Sclerosis

A randomized multiple baseline feasibility trial where participants will start taking metformin at one of 3 randomly determined points (3-months, 6-months or 9 months) during the 12-month trial. All subjects will be on a daily dose of metformin for a minimum of 3 months and a maximum of 9 months.

Recruiting

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Key information

Age range

10 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

The Hospital for Sick Children

Toronto, Ontario, M5G 1X8, Canada

Location status: Recruiting

Location contact

Brenna Wong

CONTACT

[email protected]

416-813-7654 ext. 415744

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with a history of MS with anterior visual pathway involvement and longer than 6 months after presentation with ON or an acute demyelinating event/relapse
  • Age 10 year to 25 years and 11 months
  • Latency delay > 115 milliseconds on baseline full-field transient pattern reversal VEP in at least one eye (electrophysiological evidence of demyelination) or > 10 milliseconds difference between eyes, or Retinal Nerve Fiber Layer (RNFL) thickness on OCT of < 90 µm in at least one eye or an inter-eye difference in the RNFL of 10 µm or more
  • Retinal Nerve Fiber Layer (RNFL) Thickness on baseline OCT ≥60 µm
  • If on an MS disease-modifying therapy, no changes in the therapeutic agent or dosing in the 6 months prior to study initiation
  • No significant renal or liver abnormalities
  • Expanded Disability Status Scale (EDSS) 0-6.0 (inclusive)
  • Has either English as his or her native language or English comprehension needed to complete the neuropsychological testing
  • Meet criteria for adequate organ function requirements as described below:

Adequate renal function defined as:

Creatinine clearance or radioisotope glomerular filtration rate (GFR) > 70 mL/min/1.73 m2 or serum creatinine based on age/gender as follows:

Range Serum Creatinine Level (µmol/L): Age 5 to <12 years (male)=25-50, Age 5 to <12 years (female)=25-50; Age 12 to <15 years (male)=37-67, Age 12 to <15 years (female)=37-67; Age 15 to <19 years (male)=51-89, Age 15 to <19 years (female)=40-69; Age ≥19 years (male)=58-110; Age ≥19 years (female)=46-92

Adequate liver function defined as:

Total bilirubin < 1.5 x upper limit of normal (ULN) for age SGOT (AST) or SGPT (ALT) < 1.5 x upper limit of normal (ULN) for age

Exclusion criteria

  • A history of retinal pathology (major ophthalmologic disease / concomitant ophthalmologic disorders)
  • Unstable and/or insulin-dependent (Type 1) diabetes, metabolic acidosis and/or lactic acidosis
  • History of unexplained hypoglycemia (<2.8 mmol/L)
  • Already on metformin
  • Concomitant use of any other putative remyelinating therapy as determined by the Principal/Qualified Investigator
  • Treatment for an acute attack with corticosteroids within 30 days prior to screening / relapse within 30 days prior to screening
  • Concomitant use of insulin
  • Concomitant use of any drugs that are listed to have drug-drug interactions with metformin (i.e. calcium channel blockers, diuretics, etc.) as determined by Principal/Qualified Investigator
  • Lactate levels > 1.5x upper limit of normal
  • Pregnancy

Treatment and study plan

metformin

Drug

Each tablet contains 500mg of metformin hydrochloride

Other names: Glucophage

Placebo

Other

Each tablet contains no active drug ingredient

Primary outcomes

  1. Number of patients with adverse events (safety and tolerability)

    Time frame: 3 years

  2. Number of patients who were approached to participate, declined participation and consented to participate (recruitment)

    Time frame: 3 years

  3. Proportion of patients who completed each visit within the trial (retention)

    Time frame: 3 years

  4. Proportion of patients who completed each of the outcome measures at the appropriate time points (adherence with outcome measures)

    Time frame: 3 years

  5. Number of patients enrolled in the study compared to the number of patients who were able to complete study measures (tolerability with outcome measures)

    Time frame: 3 years

Secondary outcomes

  1. Optical Coherence Tomography (OCT) - Retinal Nerve Fiber Layer Thickness

    Time frame: 3 years

  2. Optical Coherence Tomography (OCT) - Ganglion Cell Inner Plexiform Layer Thickness

    Time frame: 3 years

  3. Optical Coherence Tomography (OCT) - Optic Nerve Head Volume

    Time frame: 3 years

  4. Visual Evoked Potentials (VEP) - p100

    Time frame: 3 years

Study contacts

Contact information is provided by the study sponsor or research team.

Brenna Wong

CONTACT

[email protected]

416-813-7654 ext. 415744

E. Ann Yeh, MA, MD, FRCPC, Dip ABPN

CONTACT

[email protected]

416-813-7353

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Collaborators

  • Multiple Sclerosis Society of Canada
  • Ontario Institute for Regenerative Medicine
  • Queen's University
  • Stem Cell Network
  • Unity Health Toronto

Registry information

Important dates

Study start
2020
Primary completion
2027
Study completion
2027
First posted
Oct 10, 2019
Registry last updated
Sep 23, 2025

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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