Janssen submits Genmab-developed drug for EMA approval
Shortly after applying for US marketing approval for drug candidate teclistamab, which is based on Genmab’s duobody platform, the US-based pharmaceutical firm has followed this up with a European application with the EMA.
by ULRICH QUISTGAARD, translated by daniel pedersen
The European Medicines Council (EMA) has just received a new marketing authorization application for teclistamab, a treatment for relapsed or refractory multiple myeloma, which is a type of bone marrow cancer.
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