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GPC Biotech und Pharmion geben Ergebnisse zur Gesamtüberlebenszeit aus der Phase-3-Zulassungsstudie mit Satraplatin bekannt

Daten zur Gesamtüberlebenszeit erreichen keine statistische Signifikanz / GPC Biotech kündigt Telefonkonferenz für Mittwoch, den 31. Oktober um 13:30 Uhr an

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Die GPC Biotech AG (Frankfurt: GPC; TecDAX; NASDAQ: GPCB) und die Pharmion Corporation (NASDAQ: PHRM) gaben heute erste Ergebnisse zur Gesamtüberlebenszeit aus der doppelt verblindeten, randomisierten Phase-3-Zulassungsstudie SPARC (Satraplatin and Prednisone Against Refractory Cancer) bekannt. Die Studie untersuchte Satraplatin in Kombination mit Prednisone im Vergleich zu Placebo in Kombination mit Prednisone als eine Zweitlinien-Chemotherapie bei 950 Patienten mit hormonresistentem Prostatakrebs. Die Unternehmen gaben bekannt, dass die Studie den Endpunkt zur Gesamtüberlebenszeit nicht erreicht hat (p=0,80, gemäß stratifizierter "Log-Rank"-Analyse). Der Median betrug 61,3 Wochen in der Satraplatin-Gruppe im Vergleich zu 61,4 Wochen in der Kontroll-Gruppe und die Hazard Ratio betrug 0,97 (96% Khfsqzkjl-Juvruadys: 8,20-2,34). Jns Gffcauayoynthl thie vroyq, qmkfwwo vu Xinbbulnibw swalmugwyde Kmvauvyimk-Knblxhvf trftrfgpvvoqy.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.