← Eichor
Study identifier: NCT07699380 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

METabolic MODulation to Enhance Insulin Sensitivity and Mitochondrial Function in Type 1 Diabetes (MetMod-T1D)

Condition: Type 1 Diabetes (T1D) · Metabolic Diseases · Glucose Metabolism Disorders  ·  Sponsor: University of Washington

PhasePhase 2
Planned participants60
Who can joinAll sexes, 18 Years to 69 Years
Healthy volunteersNo

About this study

The study is a randomized, double-blind, parallel-group clinical trial to examine the effects of 24 weeks of oral AMX0035 (sodium phenylbutyrate + taurursodiol) versus placebo in 60 adults with Type 1 Diabetes (T1D) (n=30 per arm). Enrollment will be distributed equally between the University of Washington and Amsterdam University Medical Center/Diabetes Center Amsterdam. Participants will be recruited through diabetes research registries, local T1D clinics, and community outreach.

This description comes directly from the study's public registry record.

Talk to the study team

Amanda Bard, MMS, MS, CCRC  ·  206-685-2069  ·  abard@uw.edu

Always discuss trial participation with your own doctor first.

Locations (2)

University of Washington Medicine Diabetes Institute (UWMDI)Seattle, Washington, United StatesRecruiting
Amsterdam UMCAmsterdam, NetherlandsNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07699380