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FDA Oncologic Drugs Advisory Committee to hold a virtual meeting

The Committee discusses Roche’s Genentech supplemental Biologics License Application (sBLA) 761121/S-008, for POLIVY (polatuzumab vedotin-piiq) for injection. The proposed use for this product is in combination with a rituximab product, cyclophosphamide, doxorubicin, and prednisone for treatment of adult patients with previously untreated diffuse large B-cell lymphoma (DLBCL) in a virtual meeting to be held on March 9 at 12 pm. Webcast Link

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