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Lilly’s Oral GLP-1 Pill Hits Phase 3 Goals in Diabetes, Setting Up Global Filings

Lilly says the results complete the data needed to start global submissions for its once-daily, non‑peptide pill.

Eli Lilly Biotechnology Center is shown in San Diego, California, U.S. March 1, 2023. REUTERS/Mike Blake/File Photo
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Overview

  • In the 72-week ATTAIN-2 trial of more than 1,600 adults with obesity and type 2 diabetes, the 36 mg dose produced about 10.5% average weight loss versus roughly 2.2% with placebo.
  • Patients on the highest dose saw A1C fall by up to 1.8 percentage points, with about 75% reaching 6.5% or below, a common diabetes threshold.
  • Gastrointestinal side effects were the most common issues, including nausea (36.4%), vomiting (23.1%) and diarrhea (27.4%), with about 10.6% on the top dose discontinuing due to adverse events.
  • Analysts note higher side‑effect‑related dropouts than seen in some injectable GLP‑1 studies, a factor that could influence real‑world use and coverage decisions.
  • As a small‑molecule pill without fasting or water‑intake restrictions, orforglipron could be easier to manufacture and distribute, though Lilly trails Novo Nordisk, whose high‑dose oral Wegovy is already under FDA review.