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Based on the Phase 2 results and the speed of Eli Lillys development timeline, analysts expect an FDA submission sometime in 2025 or 2026, with potential approval following 12 to 18 months after submission if the data holds

The two FDA-approved semaglutide injection products come as single-dose, pre-filled pens to be taken once weekly

With $29.5 billion in 2023 revenue, Keytruda is not merely a product it is effectively the financial engine of the entire company

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Current administration of the GLP-1RAs is predominantly parenteral, but with the progress in the development of oral formulations [Reference Saxena, Frias and Brown4], their increased use in children and adolescents, unsupervised and/or medically supervised, is inevitable

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