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

Purpose

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

Condition

  • Type 2 Diabetes Mellitus (T2DM)

Eligibility

Eligible Ages
Between 18 Years and 65 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Is an adult patient with a confirmed diagnosis of T2DM - Has a body mass index (BMI) of ≥25 kg/m^2 and <39.9 kg/m^2 - Has a hemoglobin A1c (HbA1c) ≥6.5% to <10.5% - Is on a stable dose of metformin

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 Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
ALN-4324
Participants will be administered a single dose of ALN-4324.
  • Drug: ALN-4324
    ALN-4324 will be administered subcutaneously (SC).
Placebo Comparator
Placebo
Participants will be administered a single dose of placebo.
  • Drug: Placebo
    Placebo will be administered SC.

Recruiting Locations

Clinical Trial Site
Chula Vista, California 91911

More Details

Status
Recruiting
Sponsor
Alnylam Pharmaceuticals

Study Contact

Alnylam Clinical Trial Information Line
1-877-ALNYLAM
clinicaltrials@alnylam.com