Die Intercell AG (VSE: ICLL) hat heute eine Vereinbarung mit Novartis bekannt gegeben, wonach die Entwicklung des Impfstoffkandidaten gegen Pseudomonas aeruginosa von Intercell in einer bestätigenden klinischen Wirksamkeitsstudie in beatmeten Intensivpatienten fortgeführt werden soll. Die geplante Doppelblind‐Studie, die etwa 800 Patienten umfassen soll, ist darauf ausgelegt, eine klinisch relevante und statistisch signifikante Reduktion der Sterblichkeit in der Impfstoffgruppe im Vergleich mit einer Kontrollgruppe zu zeigen. Die Studie unterliegt noch letzten behördlichen Entscheidungen und soll im ersten Halbjahr 2012 gestartet und von Intercell durchgeführt werden, wobei die Kosten mit Novartis geteilt werden.
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