Two biosimilar Humira (adalimumab) products that are set to enter the US market upon formation in 2023 will hold controversial interchangeability designations, according to originator AbbVie’s latest modelling assumptions for the world’s best-selling drug.
None of the 28 biosimilars approved by the US Food and Drug Administration to date, including several referencing Humira, has an official designation of interchangeability, despite the concept being established in
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