Structure Therapeutics doses first patients in Phase 3 obesity program for aleniglipron
The company started its ACCOMPLISH-1 and -2 trials as it reported second-quarter 2026 results and named a new chief commercial officer.
Structure Therapeutics said the first patients have been dosed in its Phase 3 ACCOMPLISH program, which consists of two trials testing aleniglipron, a once-daily oral GLP-1 receptor agonist.1 ACCOMPLISH-1 will study the drug in obese or overweight adults who have a weight-related comorbidity and plans to enroll as many as 3,600 people, while ACCOMPLISH-2 will test it in obese or overweight adults with type 2 diabetes and aims for up to 1,100 participants.1 Both trials are randomized, double-blind and placebo-controlled, comparing three maintenance doses of 45 mg, 90 mg or 180 mg against placebo, with patients starting at 2.5 mg and titrating up every four weeks.1 The company said the two trials are intended to support global regulatory filings for aleniglipron in chronic weight management.1
On other pipeline items, Structure said data from the 72-week ACCESS Open Label Extension trial, which is testing a titration regimen starting at 2.5 mg, are expected in the third quarter of 2026.1 Additional readouts are due later in the year: a body composition trial measuring fat loss over 44 weeks, with data expected in the fourth quarter,1 and a SWITCH trial examining transition from an injectable GLP-1 drug to oral aleniglipron, also due in the fourth quarter.1 The company's amylin/calcitonin agonist candidate ACCG-2671 remains in a Phase 1 single ascending dose trial, with initial data and the start of a multiple ascending dose trial still on track for the third quarter.1 A second amylin candidate, ACCG-3535, is set to begin Phase 1 testing in the fourth quarter.1
Structure also appointed John Berrios as chief commercial officer, citing more than 25 years of commercial leadership experience in biopharma.1
On financials, cash, cash equivalents and short-term investments totaled $1.3 billion as of June 30, 2026, down from $1.5 billion at the end of the first quarter.1 The company said this is expected to fund operations and key clinical milestones through the end of 2028, excluding pre-commercialization costs such as commercial manufacturing.1
Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.