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Based on data from the SOUL clinical trial, Novo Nordisk submitted a label extension application for Rybelsus (semaglutide) tablets 14 mg which has been accepted for review by the FDA

As stated in MHRA guidance, this is allowed in clinical situations when the use of unlicensed medicines or use of licensed medicines outside the terms of the licence (i.e

Potential market disruptions could stem from alternative purification technologies or shifts in therapeutic focus areas, necessitating adaptability and continued innovation amongst market players to maintain a competitive edge

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