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FDA approves daratumumab and hyaluronidase-fihj (DARZALEX FASPRO) for multiple myeloma

01 May 2020 2:35 PM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration approved daratumumab and hyaluronidase-fihj (DARZALEX FASPRO, Janssen Biotech, Inc.) for adult patients with newly diagnosed or relapsed/refractory multiple myeloma. This new product allows for subcutaneous dosing of daratumumab. Read full press release.

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