Genmab and Seagen submit cancer drug application to US FDA

The US FDA will evaluate a cervical cancer treatment developed by Genmab and Seagen

BY MIKKEL AABENHUS HEMMINGSEN, TRANSLATED BY NIELSINE NIELSEN

Danish biotech firm Genmab and US biotech firm Seagen have applied for an accelerated approval of the drug candidate tisotumab vedotin at the US Food and Drug Administration, according to a Genmab press release on Wednesday.

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Genmab initiates phase III trial with drug against cervical cancer
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