Yesterday, Samsung Bioepis announced that the FDA has accepted for review the company’s BLA under the 351(k) pathway for SB3, a biosimilar candidate referencing Genentech’s Herceptin® (trastuzumab). The press release states that this is Samsung Bioepis’ first submission for FDA-approval of an oncology biosimilar candidate. According to the press release, the biosimilar, if approved, will be commercialized in the United States by Merck & Co.
The acceptance of Samsung Bioepis’ application marks at least the fifth time the FDA has accepted for review an aBLA for a biosimilar of Herceptin, following prior acceptances this year of aBLAs submitted by Mylan, Pfizer, Celltrion, and Amgen. The FDA approved Mylan’s biosimilar, Ogiviri™ (trastuzumab-dkst), earlier this month.
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