FDA accepts Seattle Genetics' lymphoma drug Adcetris for review

05/16/2013 | Bloomberg Businessweek · PharmaTimes (U.K.)

The FDA has accepted Seattle Genetics' supplemental biologics license application for the use of Adcetris, or brentuximab vedotin, for retreatment and use beyond 16 cycles of therapy in patients with relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma. A decision is expected by Sept. 14.

View Full Article in:

Bloomberg Businessweek · PharmaTimes (U.K.)

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Compliance and Ethics Director
Sysmex America, Inc.
Lincolnshire, IL
Director, Site Quality Management
CareFusion
Palm Springs, CA
Compliance Officer-Medical Products
W. L. Gore
Flagstaff, AZ
Project Manager RA - 15000003MD
Abbott
Santa Clara, CA
Director, Site Quality Management
CareFusion
Minneapolis, MN