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Based on typical regulatory timelines: Phase 3 completion: Late 2026 FDA submission: Late 2026 to early 2027 Earliest possible FDA approval: Mid-to-late 2027 US commercial launch: Early 2028 (projected) If the rollout of semaglutide and tirzepatide taught us anything, it's that demand for these medications consistently outpaces supply in the first year or two
This efficient reabsorption, combined with endogenous synthesis, typically prevents deficiency in healthy individuals
Siekmeier R, Scheuch G
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