Pharma & biotech

Genmab to submit cancer candidate epcoritamab to the FDA before year-end

The US Food and Drug Administration will receive a marketing authorization application from Genmab and partner Abbvie in the second half of this year.
Photo: Tuala Hjarnø / Genmab / PR
Photo: Tuala Hjarnø / Genmab / PR
by marketwire, translated by catherine brett

During the second half of 2022, Genmab and partner Abbvie will submit an application for marketing authorization from the FDA concerning their candidate epcoritamab. The target indication is relapsed/refractory large B-cell lymphoma (LBCL).

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