Seattle Genetics submits supplemental biologics license application to FDA for Adcetris (brentuximab vedotin) in cutaneous T cell lymphoma

Seattle Genetics (Seagen)

20 June 2017 - Application based on clinical trial results from the Phase 3 ALCANZA and Phase 2 investigator sponsored studies in cutaneous T-cell lymphoma.

Seattle Genetics announced today that it has submitted a supplemental biologics license application to the U.S. FDA based on data from the phase 3 ALCANZA trial and two phase 2 investigator-sponsored trials of ADCETRIS (brentuximab vedotin) in patients with cutaneous T-cell lymphoma (CTCL). 

Adcetris is currently not approved for the treatment of CTCL.

Read Seattle Genetics press release

Michael Wonder

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Michael Wonder

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Cancer , Medicine , US , Submission