Pfizer hatte am 16. April 2008 eine Vereinbarung mit Celldex Therapeutics Inc. geschlossen, die Pfizer die weltweiten exklusiven Rechte an PF-04948568 (CDX-110) gewährt. Der Wirkstoff befindet sich aktuell in Phase 2 der klinischen Entwicklung für die Behandlung von neu diagnostiziertem GBM.
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