A Study to Evaluate ALN-2232 in Participants With Obesity
← catalyst calendarNCT07463846 · readout in 250 d
Sponsored by Alnylam Pharmaceuticals (industry) · ALNY — their whole pipeline →.
Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
156estimated
Sites
1
Country
Canada
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-03-02 | actual | When the study began enrolling |
| Primary completion | 2027-04-27 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-03-02 | estimated | The whole study's end, after follow-up |
| First posted | 2026-03-11 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-12 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Obesity
Interventions
- Drug: ALN-2232
- Drug: Placebo
- Drug: Tirzepatide
Primary outcomes
what the primary-completion date above is the date OFPart A: Frequency of Adverse Events (AEs)
measured Up to 12 months
Part B: Percent Change from Baseline in Body Weight
measured Baseline up to Month 6
Part C: Percent Change from Baseline in Body Weight
measured Baseline up to Month 6
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