Pfizer (NYSE:PFE) und DxS (eine hundertprozentige Tochter der QIAGEN N.V.) (NASDAQ: QGEN; Frankfurt, Prime Standard: QIA), gaben heute eine Vereinbarung zur Entwicklung eines begleitenden Diagnostik-Tests für PF-04948568 (CDX-110) bekannt, einem sich in der Entwicklung befindlichen Impfstoff zur Immuntherapie für die Behandlung von Glioblastoma multiforme (GBM). Finanzielle Details der Vereinbarung wurden nicht bekannt gegeben.
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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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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