Janssen submits MAA to EMA for daratumumab in multiple myeloma

9 September 2015

US health care giant Johnson & Johnson (NYSE: JNJ) subsidiary Janssen-Cilag International has submitted a Marketing Authorization Application to the European Medicines Agency for daratumumab.

The submission is for daratumumab as a treatment for patients with multiple myeloma who have received at least three different lines of therapy including both a proteasome inhibitor (PI) and an immunomodulatory agent (IMiD) or who are double refractory to a PI and an IMiD.

Triggers milestone payment for Genmab

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