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Proteo, Inc./Proteo Biotech AG: Europäische Arzneimittelzulassungsbehörde EMEA empfiehlt Orphan Drug Status für Elafin zur Behandlung des Ösophaguskarzinoms

(PresseBox) (Irvine / CA / Kiel, )
Proteo, Inc. (OTCBB: PTEO; WKN: 925981) und ihre hundertprozentige Tochtergesellschaft Proteo Biotech AG gaben heute bekannt:

Das Committee for Orphan Medical Products (COMP) der Europäischen Arzneimittelzulassungsbehörde (EMEA) hat die Empfehlung abgegeben, Proteos Wirkstoff Elafin den Orphan Drug Status zur Behandlung des Ösophaguskarzinoms zu erteilen. Der Orphan Drug Status wird wirksam, sobald die Europäische Kommission dieses Votum bestätigt. Dies wird noch im vierten Quartal 2009 erwartet. Im Jahr 2007 wurde der Orphan Drug Status bereits zur Behandlung der pulmonalen arteriellen Hypertonie (PAH) und der chronisch thromboembolischen pulmonalen Hypertonie mit Elafin erteilt. Der neueste Beschluss verdeutlicht erneut das große therapeutische Potential dieses Fjdjklakue.

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