Lilly's Retatrutide Achieves Breakthrough Weight Loss and Pain Relief in Obesity Drug Trial

December 11, 2025
Lilly's Retatrutide Achieves Breakthrough Weight Loss and Pain Relief in Obesity Drug Trial
  • Lilly's investigational triple-hormone drug retatrutide produced substantial weight loss and knee-pain relief in a phase 3 trial (TRIUMPH-4) for adults with obesity and knee osteoarthritis, achieving an average 28.7% weight loss at the 12 mg dose and a 4.4-point improvement in WOMAC pain by week 68.

  • Co-primary endpoints showed significant reductions in body weight and WOMAC pain from baseline to week 68, meeting primary and key secondary endpoints.

  • Nearly half of participants on retatrutide reached at least 25% weight loss, with meaningful portions exceeding 30% or 35%, far outperforming placebo.

  • Lilly plans to release additional Phase III results over the coming year and pursue regulatory submissions, with expectations of a relatively straightforward path barring safety concerns.

  • The report is a STAT+ exclusive and full access requires a subscription.

  • Market sentiment around the stock was mixed, with bearish retail chatter on Stocktwits even as the stock posted a year-over-year gain.

  • Common side effects include nausea and stomach issues, with risks of gallbladder and pancreatic disease; patients should discuss individual risk profiles with doctors.

  • Lilly announced the TRIUMPH-4 results in a company statement, marking a major milestone in the drug’s development.

  • The global weight-loss drug market is projected to grow substantially, with industry projections around $100–150 billion by the mid-2030s, underscoring retatrutide’s strategic importance.

  • TRIUMPH-4 included five dose levels (2, 4, 6, 9, 12 mg) with over 5,800 participants across studies since 2023; detailed results will be presented at future meetings and published in a peer-reviewed journal.

  • Retatrutide could help Lilly defend obesity and diabetes drug market share against competitors pursuing similar therapies.

  • Administration is via weekly injections; FDA submission is planned after seven additional Phase 3 trials in 2026, with potential approval possibly in late 2026 or later depending on review.

Summary based on 11 sources


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