A Study to Evaluate ALN-4324 on Insulin Sensitivity in Adults With Type 2 Diabetes Mellitus

NCT ID
NCT07465224
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Phase 2
Sponsor
Alnylam Pharmaceuticals

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 24 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Is an adult patient with a confirmed diagnosis of T2DM * Has a body mass index (BMI) of ≥23 kg/m\^2 to ≤39.9 kg/m\^2 * Has a hemoglobin A1c (HbA1c) ≥6.5% to \<10.5% * Is on a stable dose of metformin, sodium-glucose cotransporter 2 inhibitor (SGLT2i), or dipeptidyl peptidase-4 inhibitor (DPP4i) Exclusion Criteria: * Has any clinically significant concomitant disease, medical condition, or abnormal laboratory finding that could compromise participant safety or confound interpretation of study results * Receiving therapies known to interfere with glucose or insulin metabolism other than current treatment for T2DM or birth control methods Note: other protocol defined inclusion/exclusion criteria apply

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: United States

  • California, United States: 1

Sample of listed locations

  • Clinical Trial Site — Chula Vista, California, 91911, United States — Site recruitment status not specified in the registry data

Study details

Start date
January 15, 2026
Primary completion date
May 28, 2027
First posted
March 11, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07465224
Registry last updated
September 16, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT07465224 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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