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Idiopathic Pulmonary FibrosisLungs and breathingDrugPhase 3

What this study is

This is a randomized, placebo-controlled trial of metformin in 400 participants with idiopathic pulmonary fibrosis (IPF) who are at high risk of adverse clinical outcomes based on a proteomic classifier. The primary objective is to assess the safety and efficacy of metformin compared to placebo in participants with IPF who are at high-risk for adverse clinical events.

Approximately 800 participants with IPF will be screened. 400 participants who are at high risk for adverse clinical events (proteomic signature present) will be randomized into receiving metformin (n~200) or matching placebo (n~200). Participants that meet the eligibility criteria but do not have the proteomic signature (proteomic signature absent) will be contacted by phone at 12 and 24 months to review medical history.

What's being tested

  • Metformin

    Intervention · DRUG

    Metformin or matching placebo over 12 to 24 months depending on time of enrollment into the trial. The dose will be increased by 500 mg every 14 days to a total target daily dose of 1500 mg.

  • Matching Placebo

    Intervention · DRUG

    Matching placebo over 12 to 24 months depending on time of enrollment into the trial.

Study details

Official title
Metformin to Attenuate Progressive Respiratory Decline in Idiopathic Pulmonary Fibrosis (MAVRIC)
Sponsor
University of Massachusetts, Worcester
Conditions
Idiopathic Pulmonary Fibrosis
Enrolling
800 people
Starts
2026-09-28
Est. completion
2029-03-15
Design
Quadruple-blind, randomized, parallel groups, Phase 3
Record
View on ClinicalTrials.gov ↗