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DOI: 10.3389/fphar.2023.1224985 [Google Scholar] Tsai TH, Lee CH, Cheng CI, Fang YN, Chung SY, Chen SM, et al

The Basics at a Glance Generic name: Retatrutide (development code: LY3437943) Manufacturer: Eli Lilly and Company Drug class: Triple agonist (GLP-1/GIP/glucagon receptor agonist) Administration: Once-weekly subcutaneous injection Dosing range: 2mg to 12mg weekly (gradual titration over 12+ weeks) Half-life: Approximately 6 days (reaches steady state in 45 weeks) FDA status: Phase 3 clinical trials (TRIUMPH program) Expected approval: 20272028 How Retatrutide Differs from Other GLP-1 Medications To understand retatrutide, it helps to see where it fits in the evolution of GLP-1 class medications

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We are grateful that the FDA's Commissioner's National Priority Voucher pilot program greatly reduced the review time, helping bring this treatment to patients more quickly, said Pritesh Gandhi, Chief Development Officer of Partner Therapeutics, in the press release

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