LLY · News · 20260807N

Product / Drug Pipeline Progress - retatrutide

ELI LILLY & Co · 2026-08-07 · Importance 44 · Surprise 60 · In source text

Lilly began offering limited expanded access to investigational retatrutide before potential U.S. FDA approval. Eligibility is restricted to adults with refractory obesity, at least two serious obesity-related complications, and no ability to enroll in a clinical trial. Retatrutide targets three metabolic hormones and produced average weight loss of 22.6% at the highest weekly dose in trials. Lilly plans to submit the drug for FDA approval in the first quarter of 2027, positioning it as a next-generation competitor to Wegovy and other existing obesity treatments.

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