A Study of Aleniglipron in Adults With Obesity or Overweight and Type 2 Diabetes Mellitus (ACCOMPLISH-2)
Eligible age
18–79 yrs
Accepts
All genders
Locations
30 states
Healthy volunteers
Yes
See if you qualify for this study
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About this study
This is randomized, double-blind, placebo-controlled study of the long-term efficacy, safety, and tolerability of multiple doses of aleniglipron in participants living with overweight or obesity and T2DM. Participants will be randomized to aleniglipron or placebo for a total of 76 weeks of treatment.
Sponsor: Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics
You may qualify if…
- ✓ Signed Informed Consent
- ✓ Have a BMI ≥27.0 kg/m2 at Screening
- ✓ Have a diagnosis of T2DM according to the WHO classification or other locally applicable standards, with HbA1c ≥6.5% (≥53 mmol/mol) to ≤10% (86 mmol/mol) at Screening
You may not qualify if…
- ✕ Have type 1 diabetes, history of ketoacidosis or hyperosmolar state/coma, or any other types of diabetes except T2DM.
- ✕ Have had 1 or more episode of severe hypoglycemia and/or 1 or more episode of hypoglycemia unawareness within 180 days prior to Screening.
- ✕ Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema
- ✕ Self-reported change in body weight \>5 kg (11 pounds) within 3 months before Screening.
- ✕ Have prior or planned surgical or non-surgical treatment for obesity.
Where it's recruiting
Birmingham
Chandler · Phoenix · Sun City West · Tucson
Little Rock
Escondido · Fountain Valley · Lake Forest · Rolling Hills Estates …
Waterbury
Clearwater · Fort Myers · Jacksonville · Leesburg …
Atlanta · Columbus · Lawrenceville · Union City …
Meridian
Des Moines · Iowa City
Wichita
Silver Spring
Methuen
Source: ClinicalTrials.gov · NCT07654374 · last updated 2026-08-10