A Study to Evaluate ALN-2232 in Participants With Obesity

Recruiting Phase 1 Phase 2 Interventional Study
Obesity
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
156 (estimated)
Sponsor
Alnylam Pharmaceuticals · Industry
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About This Trial
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-ini…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All Parts: * Has a body mass index (BMI) of ≥30 kg/m\^2 and \<40 kg/m\^2 * Has a hemoglobin A1c (HbA1c) \<6.5% Exclusion Criteria: All Parts: * Has any clinically significant concomitant disease, medical condition, or abnormal laboratory finding that could compromise partici…
Contacts

Alnylam Clinical Trial Information Line

1-877-ALNYLAM

clinicaltrials@alnylam.com

CONTACT

Alnylam Clinical Trial Information Line

1-877-256-9526

clinicaltrials@alnylam.com

CONTACT