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Janssen seeks FDA approval for subcutaneous daratumumab formulation
7/15/2019

Johnson & Johnson unit Janssen Biotech, a licensee of Genmab, has submitted to the FDA a marketing application to seek approval for a Darzalex, or daratumumab, formulation to be administered subcutaneously in patients with multiple myeloma. An intravenous formulation was previously approved by the FDA in November 2015.

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