drugset / Trial / NCT07463846

A Study to Evaluate ALN-2232 in Participants With Obesity

NCT07463846

Phase 1/2 Recruiting 156 enrolled Alnylam Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to: * evaluate the safety, tolerability, efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) of single ascending doses of ALN-2232 in patients with obesity * evaluate the safety, tolerability, efficacy, PK, and PD of multiple doses of ALN-2232 in patients with obesity * evaluate the safety, tolerability, efficacy, PK, and PD of multiple doses of ALN-2232 co-initiated with tirzepatide in patients with obesity

Timeline

Start
2026-03-02
Primary completion
2027-04-27
Completion
2028-03-02

Drugs

EvaluationDrugModalityDoseRoute
Subject ALN-2232 Unknown Subcutaneous
Subject Tirzepatide Peptide Subcutaneous

Indications