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P., Erlejman, A

It is currently being studied at doses ranging from 1 mg to 12 mg per week in clinical trials

Ahrens-Fath I, Politz O, Geserick C, Haendler B

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Available data demonstrate meaningful efficacy with acceptable safety profiles in this specific population

The key regulatory milestones: FDA Breakthrough Therapy designation for MASH (September 2024) EMA PRIME designation for MASH (November 2023) China NMPA Breakthrough designation (June 2024) Phase 3 trials (SYNCHRONIZE-1 and SYNCHRONIZE-2) fully enrolled, results expected H1 of this year Estimated FDA filing: Late this year at the earliest Estimated FDA approval: Possibly next year, depending on Phase 3 results If Phase 3 results confirm Phase 2 findings, survodutide could reach the market within the next 12-24 months