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Johnson & Johnson announces FDA approval of DARZALEX FASPRO for HR-SMM

Johnson & Johnson announced the U.S. FDA approved DARZALEX FASPRO as a single agent treatment for adult patients with high-risk smoldering multiple myeloma. DARZALEX FASPRO is the first and only approved treatment for HR-SMM, enabling earlier intervention before the disease progresses to active multiple myeloma.

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