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Schuwald, Anita; Taupitz, Thomas; Köper, Katharina; Herdling, Mirco; Dingermann, Theo; Zündorf, Ilse

doi:10.1002/pauz.200790050

Pharmazie in unserer Zeit

2007

DOI: 10.1002/pauz.200790050

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Anita Schuwald¹,

Thomas Taupitz²,

Katharina Köper³

et al.

Abstract: Am 26. April 2007 hat das Antiviral Drugs Advisory Commitee der FDA einstimmig die Empfehlung ausgesprochen, Maraviroc (Celsentri™) für die Therapie von vorbehandelten HIV‐Patienten mit CCR5‐tropen Viren zuzulassen. Die endgültige Entscheidung über die Zulassung wird in den USA im Juli erwartet, in Europa einige Monate später.

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