Ireland
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Recruiting Phase 1

A Study to Evaluate ALN-6222 in Participants With Obesity

NCT07624071 · tracked via the Priya Life Science Canada tracker
Phase
Phase 1
Started
2026-06-04
Last updated
2026-10-21

Condition(s) studied

Obesity

Investigational drug(s) / intervention(s)

ALN-6222Placebo

ALN-6222: ALN-6222 will be administered subcutaneously (SC).

Placebo: Placebo will be administered SC.

Study summary

This is a first in human, randomized, double-blind (DB), placebo-controlled, single ascending dose (SAD), Phase 1 study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and efficacy of ALN-6222 administered subcutaneously (SC) in adult participants with obesity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria - * Is an adult patient with a body mass index ≥30 kg/m\^2 to \<40 kg/m\^2 * Has a hemoglobin A1c \<6.5% Exclusion Criteria - * Has alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \>1.5 times the upper limit of normal (ULN) * Has known human immunodeficiency virus (HIV) infection; or known current or chronic hepatitis C virus or hepatitis B virus infection * Has an estimated glomerular filtration (eGFR) of \<60 mL/min/1.73m\^2 at screening Note: other protocol defined inclusion / exclusion criteria apply

Primary outcome measure(s)

  • Frequency of Adverse Events — Up to 12 months

Trial sites (1)

FacilityCityRegionStatus
Clinical Trial Site Mount Royal Canada Recruiting
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 NCT07624071 on ClinicalTrials.gov ↗ ← All trials in Canada