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CNBC Reports Strong Phase 3 Results for Eli Lilly’s Retatrutide
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CNBC Reports Strong Phase 3 Results for Eli Lilly’s Retatrutide

Yahoo Finance · May 24, 2026, 9:36 PM · Also reported by 4 other sources

Key takeaways

  • In a CNBC report published on May 21, Eli Lilly and Company (NYSE:LLY) said its experimental obesity drug, retatrutide, cleared a major late-stage clinical trial.
  • Retatrutide is viewed as a next-generation obesity treatment because it targets three hormones, GLP-1, GIP, and glucagon.
  • Eli Lilly and Company (NYSE:LLY) develops, manufactures, and markets medicines through a single business segment focused on human pharmaceutical products.

CNBC Reports Strong Phase 3 Results for Eli Lilly’s Retatrutide Vardah Gill Mon, May 25, 2026 at 4:36 AM GMT+7 2 min read LLY With a 5-year dividend growth rate of 15.23%, Eli Lilly and Company (NYSE:LLY) is included among the 10 Best Dividend Growth Stocks to Buy and Hold for 3 Years.

In a CNBC report published on May 21, Eli Lilly and Company (NYSE:LLY) said its experimental obesity drug, retatrutide, cleared a major late-stage clinical trial. The results moved the company closer to seeking regulatory approval for the treatment. The Phase 3 trial showed that patients without diabetes who received the highest dose of the weekly injection lost an average of 28.3% of their body weight over 80 weeks. More than 45% of participants lost at least 30% of their weight. Analysts said those results were comparable to outcomes often seen with bariatric surgery.

Retatrutide is viewed as a next-generation obesity treatment because it targets three hormones, GLP-1, GIP, and glucagon. Current drugs like Wegovy and Zepbound target fewer pathways. The strong trial data increased expectations that retatrutide could become one of the most effective weight-loss treatments on the market. The report also said that safety concerns seen in earlier studies appeared to ease in the latest trial. Patients still reported side effects such as nausea, diarrhea, vomiting, and constipation, though most were gastrointestinal and considered manageable. Fewer participants experienced the abnormal skin sensations that had raised concerns in previous studies.

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