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 ↗
Who can join
Age 40 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- IPF diagnosis by enrolling investigator (following the 2022 updated guidelines on diagnosis and management of IPF)
- Age 40 years or older
- HbA1c < 9% at screening
- High risk by proteomic signature (proteomic signature present) for participants randomized only (for participants randomized only; participants that are proteomic signature absent will undergo remote study assessments at 12 and 24 months only).
- If on FDA-approved treatment(s) for IPF, on a stable dose for at least 8 weeks prior to randomization
- Ability to provide informed consent
You can't join if
- Taking metformin within 3 months of randomization
- Allergy or intolerance to metformin
- Use of insulin or insulin secretagogue(s) at randomization
- Pregnancy, planning to become pregnant, or lactating
- Women of childbearing potential not willing to remain abstinent (refrain from heterosexual intercourse) or use two adequate methods of contraception, including at least one method with a failure rate of <1% per year during study participation
- History of biochemically-confirmed acidosis (lactate > 5.0 mmol/L)
- Estimated glomerular filtration rate less than 45 mL/min/1.73 m2 at screening
- Moderate-to-severe liver disease, decompensated heart failure, or any other condition that may make the participant unsuitable for inclusion as assessed by the study investigator at each site
- Receipt of an investigational study agent as part of a therapeutic trial within 30 days of the Screening Visit (Visit 0)
- Continuous supplemental oxygen use at rest greater than 2 L/min
- Unable to swallow pills
- Taking a medication that has a major interaction with metformin, including acetazolamide (Diamox), cimetidine (Tagamet), dolutegravir, gatifloxacin, levoketoconazole, ranolazine, or carbonic anhydrase inhibitors. Occasional use of carbonic anhydrase inhibitors for travel is permitted.
- Current alcohol intake ≥ 15 drinks per week in men, ≥ 8 drinks per week in women or ≥ 5 drinks per occasion in men, ≥ 4 drinks per occasion in women
- Listed for transplant at the time of randomization
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
Loading treatment details…
Study locations (15)
15 openUniversity of Arizona
Tucson, Arizona, United States
- Sachin Chaudhary, MD · Contact520-626-8831sachin@deptofmed.arizona.edu
- Lisbeth Haaheim · Contact520-626-8831lhaaheim@arizona.edu
University of Colorado Anschutz
Aurora, Colorado, United States
- Joyce Lee, MD · ContactJOYCE.LEE@cuanschutz.edu
- Olivia Brohl · Contact303-724-0640olivia.brohl@cuanschutz.edu
Georgetown University Hospital
Washington D.C., District of Columbia, United States
- Helen D'Couto, MD · Contact202-444-8830helen.t.d'couto@medstar.net
- Amen Hamed · Contact202-444-0895amen.m.hamed@gunet.georgetown.edu
Northwestern University
Chicago, Illinois, United States
- Bradford Bemiss, MD · Contact312-695-0478bradford.bemiss@nm.org
- Mary Carns · Contact312-503-1137m-carns@northwestern.edu
University of Chicago
Chicago, Illinois, United States
- Ayodeji Adegunsoye, MD · Contact773-834-3500aadegunsoye@bsd.uchicago.edu
- Vanita Patel · Contact773-702-1012vpatel4@bsd.uchicago.edu
Massachusetts General Hospital
Boston, Massachusetts, United States
- Sydney Montesi, MD · Contact617-726-1721SBMONTESI@PARTNERS.ORG
- Caroline Fromson · Contact617-643-3260CFROMSON@MGH.HARVARD.EDU
University of Massachusetts Chan Medical School
Worcester, Massachusetts, United States
- William M Whalen, MD · Contactwilliam.whalen@umassmemorial.org
- Rayaan Yunus · Contact508-856-2858rayaan.yunus@umassmed.edu
University of Michigan
Ann Arbor, Michigan, United States
- Elizabeth Belloli, MD · Contact734-647-6477bellolie@umich.edu
- Candace Flaherty · Contactcflah@med.umich.edu
Mayo Clinic
Rochester, Minnesota, United States
- Andrew Limper, MD · Contact507-284-4162Limper.Andrew@mayo.edu
Weill Cornell Medicine
New York, New York, United States
- Anna Podolanczuk, MD · Contact646-962-2333ajp9012@med.cornell.edu
- Alicia Morris · Contact646-962-2741ajm2017@med.cornell.edu
Temple University
Philadelphia, Pennsylvania, United States
- Rachel Criner, MD · ContactRachel.Criner@tuhs.temple.edu
- Sana Debasree · Contact215-707-7249Debasree.SanaBoral@tuhs.temple.edu
University of Texas Southwestern
Dallas, Texas, United States
- Chad Newton, MD · Contact214-645-6493Chad.Newton@UTSouthwestern.edu
- Nighat Sultana · Contact214-645-6605nighat.sultana@utsouthwestern.edu
Michael E. DeBakey VA Medical Center
Houston, Texas, United States
- Bhavika Kaul, MD, MAS · Contact713-440-4400 ext. 230225Bhavika.Kaul@va.gov
- Miguel Alexis Covarrubias Gonzalez · Contact713-363-3668Miguel.CovarrubiasGonzalez@va.gov
University of Utah
Salt Lake City, Utah, United States
- Mary Beth Scholand, MD · Contact801-581-5811mary.beth.scholand@hsc.utah.edu
- Lisa Weaver · Contact801-581-5811lisa.weaver@hsc.utah.edu
University of Washington
Seattle, Washington, United States
- Ganesh Raghu, MD · Contact206-598-0440graghu@uw.edu
- JB Ingram · Contactjingra@uw.edu
Study team
Sponsor
University of Massachusetts, Worcester
Study ID STUDY00002828
Principal investigator
Fernando Martinez, MD, MS
UMass Chan Medical School
Principal investigator
Sydney Montesi, MD
Massachusetts General Hospital
Principal investigator
Bhavika Kaul, MD, MAS
Michael E. DeBakey Veterans Affairs Medical Center (MEDVAMC)
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.