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B-cell lymphoma (DLBCL) showed a statistically significant and clinically meaningful improvement in overall survival (OS) compared to lenalidomide and rituximab plus placebo, regardless of CD30 expressionPfizer to discuss regulatory submission with FDA, potentially leading to eighth indication for ADCETRISNEW YORK-(BUSINESS WIRE)- Pfizer Inc. If SJS or TEN occurs, discontinue ADCETRIS and administer appropriate medical management. Anaphylaxis and infusion reactions: Infusion-related reactions (IRR), including anaphylaxis, have occurred in ADCETRIS-treated patients. Form 8-K, all of which are filed with the U. Food and Drug Administration (FDA) to potentially support regulatory filing in the rest of the world.

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