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and 2 - To demonstrate comparable functional results to the injected version, which if successful, could allow for an expedited FDA regulatory pathway known as a 505(b)(2) application that is available when an alternate version of a drug (e.g., the dosage form change from injection to oral administration as tested within this Study) retains certain similar performance characteristics as an earlier-approved version of that same drug
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En diciembre de 2025, la FDA aprobó también la versión en pastillas de Wegovy –semaglutida oral en dosis más altas, hasta 25 miligramos diarios
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