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A Dose-Range Study of Aleniglipron (GSBR-1290) in Participants Living With Obesity or Overweight With at Least One Weight-related Comorbidity

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NCT06703021

Sponsored by Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics (industry) · GPCR — their whole pipeline →.

Phase
Phase 2
Status
Completed
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
85actual
Sites
10
Country
United States

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
DateFiledBasisWhat it is
Start2024-12-20actualWhen the study began enrolling
Primary completion2026-01-12actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-12actualThe whole study's end, after follow-up
First posted2024-11-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Obesity
  • Overweight
  • Chronic Weight Management

Interventions

  • Drug: aleniglipron or placebo
  • Drug: aleniglipron or placebo
  • Drug: aleniglipron or placebo
  • Drug: aleniglipron or placebo

Primary outcomes

what the primary-completion date above is the date OF
Treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
measured Baseline and week 44
Adverse events of special interest
measured Baseline and week 44
Number of Participants With Clinically Significant Change From Baseline in Laboratory Parameters, including hematology, plasma chemistry, coagulation, and urinalysis
measured Baseline and week 44
Number of Participants With Clinically Significant Change From Baseline in Electrocardiogram (ECG) Parameters: Common ECG-related variables will be assessed, including but not limited to : heart rate and QRS duration
measured Baseline and week 44
Number of Participants With Clinically Significant Change From Baseline in Vital Signs, including systolic and diastolic Blood Pressure, Heart Rate, Respiratory Rate, and temperature
measured Baseline and week 44

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