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Ascletis Begins Dosing in Phase IIa Trial of ASC30 for Obesity Treatment

  • Ascletis Pharma announced on July 2, 2025, that it dosed first participants in a U.S. multi-center 13-week Phase IIa trial of oral GLP-1 receptor agonist ASC30 for obesity treatment.
  • This trial follows earlier Phase Ia and Ib studies showing ASC30's tolerability and up to 6.5% placebo-adjusted weight reduction over four weeks, with screening started in June 2025.
  • The randomized, double-blind, placebo-controlled study enrolls adults with BMI ≥30 kg/m² or overweight with weight-related comorbidities, using a slow titration to maintenance doses up to 60 mg weekly.
  • Ascletis CEO Jinzi Jason Wu stated, “We are ahead of schedule” and expects topline Phase IIa data in the fourth quarter of 2025; ASC30 has patent protection until 2044.
  • If approved, ASC30 could offer a once-daily oral treatment option for obesity, complementing existing FDA-approved injectable GLP-1 receptor agonists and advancing metabolic disease therapeutics.
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Ascletis Announces First Participants with Obesity or Overweight Dosed in a U.S. 13-week Phase IIa Study of Small Molecule Oral GLP-1R Agonist ASC30

First participants with obesity or overweight with at least one weight-related comorbidity have been dosed in a U.S. 13-week Phase IIa study of small molecule oral GLP-1 receptor agonist ASC30.

A novel oral medication that mimics the effect of gastric bypass surgery shows promising results for safe weight loss and maintenance of muscle mass in initial studies.

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Kurier broke the news in on Wednesday, July 2, 2025.
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