Efficacy and Safety of Aleniglipron in Participants With Obesity or Overweight With a Weight-Related Comorbidity (ACCOMPLISH-1)
Registered Phase 3 interventional trial (not yet recruiting). Study GSBR-1290-12 is a Phase 3 pivotal, multicenter, global, randomized, placebo-controlled, double-blind study to investigate the long-term efficacy, safety, and tolerability of 3 maintenance doses of aleniglipron once daily (QD) compared with placebo, when used in combination with a reduced-calorie diet and increased physical activity. All participants will be randomized to at least 76 weeks of treatment to evaluate the effects on long term body weight changes, tolerability, and safety. In addition, the study will compare the eff
Registered clinical trial record on ClinicalTrials.gov (NCT07654361). This describes a planned, ongoing, or completed study — it is NOT peer-reviewed results. Status: not yet recruiting. Study type: interventional. Phase: Phase 3. Sponsor: Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics. Conditions: Obesity, Overweight, or Chronic Weight Management. Interventions: Aleniglipron, Placebo. Summary: Study GSBR-1290-12 is a Phase 3 pivotal, multicenter, global, randomized, placebo-controlled, double-blind study to investigate the long-term efficacy, safety, and tolerability of 3 maintenance doses of aleniglipron once daily (QD) compared with placebo, when used in combination with a reduced-calorie diet and increased physical activity. All participants will be randomized to at least 76 weeks of treatment to evaluate the effects on long term body weight changes, tolerability, and safety. In addition, the study will compare the effects between aleniglipron and placebo on blood pressure (BP), lipid parameters, patient-reported outcomes. Primary outcome measures: Percent change in body weight from Baseline. Eligibility: Inclusion Criteria: * Signed informed consent * BMI ≥30 kg/m2 (obese) or BMI ≥27 kg/m2 (overweight) and presence of ≥1 of the obesity related comorbidities. Exclusion Criteria: Previously documented diagnosis of type 1 diabetes, type 2 diabetes, or any other type of diabetes. Self-reported change in body weight \>5 kg within 3 months before Screening. Have prior or planned surgical or non-surgical treatment for obesity. Have or plan to have endoscopic and/or device-based therapy for obesity. Have obesity induced by other endocrine disorders. Impaired renal function at Screening Chronic malabsorption
This is a registered clinical-trial record from ClinicalTrials.gov — a description of a planned, ongoing, or completed study, not peer-reviewed results. Listing on ClinicalTrials.gov does not mean the study has been evaluated by the U.S. Federal Government, nor does it imply endorsement or that the intervention is safe or effective.
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