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NCT06703021Phase 2Completed

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

Study Summary

Phase 2 clinical study will evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of various aleniglipron (GSBR-1290) dose regimens compared with placebo in participants living with obesity or overweight with ≥ 1 weight-related comorbidity, in addition to diet and exercise, over a 44-week period.

View on ClinicalTrials.gov ↗
Study Details
Enrollment85 participants
Primary Completion2026-01-12
Lead SponsorGasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics
Data Retrieved2026-10-14
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 2 trials begin testing efficacy in a larger patient group (100–300). This is often where biotech binary events occur — positive Phase 2 data can significantly advance a company's pipeline narrative, while failures can be terminal for a program.

Status & Expected Data

This trial has completed. Results may be available via ClinicalTrials.gov or peer-reviewed publications.

Primary completion: 2026-01-12
Enrolled: 85 participants
Sponsor Catalyst Profile

Structure Therapeutics (GPCR) is the sponsoring company for this trial. BiotechSign currently grades this company C (50/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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