Aktiesnakken — Juni 2012
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Der er rekrutteret i alt 89 patienter på 23 centre i Europa og USA. Patientpopulationen var jævnt fordelt på to behandlingsgrupper. Baseret på ITT-analysen blev der ikke opnået statistisk signifikans vedrørende det primære effektmål om PFS. Analysen af de sekundære effektmål viste statistisk signifikant forskel i ORR (BelCaP 43,2 % versus CaP 22,2 %, p-værdi på 0,025). Respons opstod tidligere i BelCaP-kombinationen. Evalueringen af gennemsnitlig overlevelse (OS) indikerer en separation af overl
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tolker nu den her positivt: "Despite the fact that the study did not meet the primary efficacy endpoint of PFS we do see encouraging clinical signals for time to response and response rate, which may translate into an improvement in overall survival seen on this trial.
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