Summary

Eligibility
for people ages 30-65 (full criteria)
Location
at UCLA
Dates
study started
completion around
Principal Investigator
by Kevin R Patel, MD (ucla)

Description

Summary

The purpose of this study is to assess the safety of metformin for treatment of progressive multiple sclerosis

Official Title

A Double-blind, Placebo Controlled Trial of Metformin Treatment in Progressive Multiple Sclerosis

Details

This will be a single site 1:1 randomized, placebo controlled trial of metformin treatment vs matching placebo in 44 men and women with primary progressive multiple sclerosis and secondary multiple sclerosis, without diabetes, not treated with metformin aged 30-65. The trial will last 12 months and have 3 study visits, baseline, 6 months, and 12 months. The trial will be preceded by a screening period. Over the initial 30 day titration period subjects will be titrated from 500 mg a day to 2,000 mg of metformin in increments of 500 mg every 10 days. Patients will remain on their tolerated dose and included in analysis on an intent to treat basis. Brain MRI, cognitive testing and clinical measures will be collected at baseline, month 6 and month 12. OCT will be collected at baseline and month 12. The primary outcomes are the following safety outcomes: 1) number of patients with adverse events 2) number of patients with laboratory abnormalities 3) number of patients with new T2 lesions on MRI. The secondary outcomes include reduction in localized cortical thinning on brain MRI; reduction in thalamic atrophy on brain MRI. Further exploratory outcomes include 1) improvement in SDMT-oral score, 2) improvement in CVLT-II score, 3) improvement in PACC score 4) improvement in PASAT score. Exploratory outcomes include 1) Decrease in plasma neurofilament light chain levels, 2) Reginal nerve fiber layer preservation on OCT, 3) Ganglion cell inner plexiform layer preservation, and 4) Percentage of phase rim lesions.

Keywords

Secondary Progressive Multiple Sclerosis, Primary Progressive Multiple Sclerosis, Multiple sclerosis, Demyelinating disease, Chronic Progressive Multiple Sclerosis, Sclerosis, Metformin, Metformin 500 Mg Oral Tablet, up to 4 tablets a day

Eligibility

You can join if…

Open to people ages 30-65

  1. Patient signed informed consent.
  2. Age 30-65
  3. Primary Progressive Multiple Sclerosis or Secondary Progressive Multiple Sclerosis as defined by the 2017 McDonald Criteria
  4. Intent to maintain current MS disease modifying treatment through the trial duration

You CAN'T join if...

  1. Clinical relapse in prior 12 months
  2. New T2 lesion or gadolinium enhancing lesion in prior 12 months
  3. Glucocorticoid use in prior six months outside the context of premedication for disease modifying treatment
  4. Changes in disease modifying therapy in prior three months
  5. Plans to change current disease modifying therapy
  6. Contraindication to MRI, inability to tolerate MRI
  7. Use of metformin for any other indication
  8. Renal dysfunction (GFR < 60)
  9. Hepatic dysfunction (AST or ALT > 1.5 x upper limit of normal)
  10. B12 deficiency
  11. Prior poor reaction to metformin
  12. Congestive heart failure
  13. Alcohol abuse
  14. Metabolic acidosis
  15. Females who are pregnant or who plan to become pregnant during the 12 months of enrollment, or who wish to breastfeed during any part of the 12 months of enrollment
  16. Concomitant use of drugs with drug-drug interactions with metformin
  17. Previous adverse effect with metformin treatment

Location

  • University of California, Los Angeles accepting new patients
    Los Angeles California 90095 United States

Lead Scientist at University of California Health

  • Kevin R Patel, MD (ucla)
    HS Assistant Clinical Professor, Neurology, Medicine. Authored (or co-authored) 16 research publications

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Los Angeles
ID
NCT05349474
Phase
Phase 1 Multiple Sclerosis Research Study
Study Type
Interventional
Participants
Expecting 44 study participants
Last Updated