Clinical Trials in the USA / NCT07465224
Recruiting
Phase 2
A Study to Evaluate ALN-4324 on Insulin Sensitivity in Adults With Type 2 Diabetes Mellitus
NCT07465224 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Type 2 Diabetes Mellitus (T2DM)
Investigational drug(s) / intervention(s)
ALN-4324 →Placebo
ALN-4324: ALN-4324 will be administered subcutaneously (SC).
Placebo: Placebo will be administered SC.
Study summary
The purpose of this study is to evaluate the effect of a single dose of ALN-4324 on whole-body insulin sensitivity in participants with T2DM
Eligibility
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
Primary outcome measure(s)
- Change from Baseline in M-value — Baseline up to Month 3
M-value is measured as the glucose infusion rate at steady state
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Clinical Trial Site | Chula Vista | California | Recruiting |
More Alnylam Pharmaceuticals trials in the USA
Other trials for the same condition
A Study of Maridebart Cafraglutide in Adult Participants With Type 2 Diabetes Mellitus (T2DM)
Active, not recruiting
Post-market SUrveiLlance RegiStry for the Endogenex System (Endogenex PULSE Registry)
Enrolling by invitation
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07465224 on ClinicalTrials.gov ↗ ← All trials in the USA