Halozyme Therapeutics, Inc. (NASDAQ: HALO) (Halozyme) today announced that Johnson & Johnson has received approval from the U.S. Food and Drug Administration (FDA) for TECVAYLI® (teclistamab-cqyv) in combination with DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) for the treatment of adults with relapsed or refractory multiple myeloma (RRMM) who have received at least one prior line of therapy.
Halozyme Therapeutics Announces Johnson & Johnson Gets FDA Approval For TECVAYLI In Combination With DARZALEX FASPRO To Treat Adults With Relapsed Or Refractory Multiple Myeloma
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