A Study to Evaluate ALN-6222 in Participants With Obesity
Condition(s) studied
Investigational drug(s) / intervention(s)
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
Primary outcome measure(s)
- Frequency of Adverse Events — Up to 12 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Clinical Trial Site | Mount Royal | Canada | Recruiting |
More Alnylam Pharmaceuticals trials in Canada
Other trials for the same condition
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