A Trial of Metformin in Individuals With Fragile X Syndrome (Met)

University of Alberta

Status and phase: Active, not recruiting; Phase 2

Conditions: Fragile X Mental Retardation Syndrome; Mental Retardation, X-Linked; Genetic Diseases, X-Linked; FXS; Trinucleotide Repeat Expansion; Fragile X Syndrome; Sex Chromosome Disorders; Neurobehavioral Manifestations; Intellectual Disability; Fra(X) Syndrome

Treatments: Drug: Placebo Medication; Drug: Metformin

Study type: Interventional

Funder types: Other

Identifiers

NCT03862950

FXSMET-2018 Version 16

Details and patient eligibility

About

This study is a controlled trial of metformin in individuals with fragile X syndrome between the ages of 6 and 35 years. Participants will be randomized in a double-blind design to either drug or placebo and will attend three visits to the study site in a 4-month period for a series of tests. The primary objectives are to assess safety, tolerability, and efficacy of metformin in the treatment of language deficits, behavior problems, and obesity/excessive appetite in individuals with fragile X syndrome.

Full description

This is a multi-center study at the University of Alberta and CHU Sainte-Justine for fragile X syndrome (FXS) patients aged 6 to 35 years inclusive. It is a randomized, double-blind, placebo-controlled trial of metformin (also known as Glumetza, Glucophage, Fortamet), a type 2 diabetes medication that can also improve obesity and excessive appetite.

Metformin has emerged as a candidate drug for the targeted treatment of FXS based on animal studies showing rescue of multiple phenotypes in the FXS model. Metformin may contribute to normalizing signaling pathways in FXS in the central nervous system, which may include activities of mTOR and PI3K, both of which have shown to be pathogenically overactive in FXS. In addition, metformin inhibits phosphodiesterase, which would lead to correction of cAMP levels, and MMP9 production, which is also elevated in FXS. Looking at the potential signaling pathways, metformin appears to be a good candidate for targeting several of the intracellular functions in neurons disrupted in FXS and, therefore, has potential to rescue several types of symptoms in individuals with FXS. Researchers have utilized metformin in the clinical treatment of over 20 individuals with FXS between the ages of 4 and 58 years and have found the medication to be well tolerated and to provide benefits not only in lowering weight gain and normalizing appetite but also in language and behavior. In this controlled trial, the researchers hope to further assess metformin's safety and benefits in the areas of language and cognition, eating and weight loss, and overall behavior.

Each participant will be involved in this trial for a period of 4 months. This will include 3 visits to one of the sites and 5 phone calls. At each visit, the researchers will assess behavioral, cognitive, and language development. The researchers will also assess the side effects of the study medication throughout the trial.

Enrollment: 125 patients

Sex: All

Ages: 6 to 35 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subject has Fragile X syndrome with a molecular genetic confirmation of the full FMR1 mutation (>200 CGG repeats) or the other loss of function mutations of the FMR1 gene (SNVs and deletions of the gene).
• Subject is a male or non-pregnant, non-lactating female age 6 through 35 years, inclusive.
• Subjects who are capable of becoming pregnant must use an acceptable method of birth control for the duration of the study. Acceptable forms of birth control include abstinence (only for subjects who are not sexually active), intrauterine devices in place for at least 3 months, oral contraceptives, surgical sterilization, or adequate barrier methods.
• Subject must have a caregiver (parent, guardian, or other legally authorized representative) who is willing to participate in the whole study.
• Subject and caregiver are able to attend the clinic regularly and reliably.
• Subject and/or subject's caregiver is able to understand, read, write and speak English or French fluently to complete study-related materials.
• For subjects who are not their own legal guardian, subject's caregiver is able to understand and sign an informed consent to participate in the study.
• The use of concomitant medication must be stable, in terms of dose and dosing regimen, for at least 4 weeks prior to Screening and must remain stable during the period between first visit (Screening) and the commencement of the study; every effort should be made to maintain stable regimens of allowed concomitant medications from the time of commencement of double-blind study medication until the last study assessment.
• Behavioral/educational treatments must be stable for 4 weeks prior to first visit (Screening) and must remain stable during the period between Screening and the commencement of randomized double-blind study medication.
• 10. Overall age equivalent is not higher than 13 and IQ is not higher than 85, as assessed at Screening on the Leiter-III, and subject must speak at least occasional 3-word phrases.

Exclusion criteria

• Families that are not cooperative and will not follow through with the demands of this study.
• Subject has a life-threatening medical problem or other major systemic illness that compromises health or safety and/or would interfere with this study.
• Age younger than 6 or older than 35 years.
• History of intolerable adverse events with metformin.
• Current or recent metformin treatment (within the past 4-months).
• BMI inferior to 2 standard deviations below the mean for age using the World Health Organization scale.
• Serum creatinine > 1.4 mg/dl (female) or > 1.5 mg/dl (male).
• History of metabolic acidosis or a condition with lactic acidosis.
• Severe Vitamin B12 deficiency.
• Pregnancy at screening or unwillingness to use acceptable method of birth control, if applicable.
• Age equivalent higher than 13 or IQ higher than 85 on the Leiter-III at Screening.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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125 participants in 2 patient groups, including a placebo group

Placebo Medication

Placebo Comparator group

Description:

The placebo will be dosed in a weight-dependent manner. For participants under 50kg at baseline, the initial dose will be 250mg once per day, and if this dose is well tolerated, they will increase each week by 250mg until a maximum dose of 1000mg daily is reached. For participants at and above 50kg at baseline, the initial dose will be 500mg once per day, and if this dose is well tolerated, they will increase each week by 500mg until a maximum dose of 2000mg daily is reached. After the 4-week titration period, each participant will continue dosing at his or her maximum tolerated dose daily for the remaining 12 weeks of the study.

Treatment:

Drug: Placebo Medication

Active Metformin Medication

Active Comparator group

Description:

The active metformin medication will be dosed in a weight-dependent manner. For participants under 50kg at baseline, the initial dose will be 250mg once per day, and if this dose is well tolerated, they will increase each week by 250mg until a maximum dose of 1000mg daily is reached. For participants at and above 50kg at baseline, the initial dose will be 500mg once per day, and if this dose is well tolerated, they will increase each week by 500mg until a maximum dose of 2000mg daily is reached. After the 4-week titration period, each participant will continue dosing at his or her maximum tolerated dose daily for the remaining 12 weeks of the study.

Treatment:

Drug: Metformin