On June 23, following its monthly meeting this week, the European Medicines Agency’s scientific committee, the CHMP, is expected to recommend approval of another biosimilar version of AbbVie Inc.’s blockbuster TNF-alpha inhibitor, Humira (adalimumab).
This is most likely to be Samsung Bioepis Co. Ltd.’s SB5, which was accepted for filing by the EMA just under a year ago, in July 2016. If it...
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