PharmaMar Recibe el Ok de la FDA Para Iniciar Fase I con PM54 en Combi con Inmuno Para Posible Tratamiento . PARA EI RELEVO DE LURBINECTEDIN ESTABAN PM184 Y PM14 AMBOS RETIRADOS POR LA CIA. AHORA HAY OTROS DOS FÁRMACOS EN FASE I EN EL INTENTO DE RELEVAR A LURBINECTEDIN : PM54 Y PM534 ... EL PROBLEMA ES QUE AMBOS AÚN ESTAN EN FASE I CON TODO LO QUE ESTO IMPLICA EN CUESTIÓN DE PLAZOS ... YA QUE PARA REALUZAR 3 FASES CLÍNICAS HACEN FALTA DE 12 A 15 AÑOS ... NOS IRÍAMOS AL 2040.
09 agosto 2009
Bolsas tomadas por maquinas ... ¿ Mafias ? ...
http://jarillabolsa.blogspot.com/2009/08/la-mafia-de-la-bolsa.html
J&J Actualiza el OVA 301 .
PD : J&J actualiza el ensayo OVA 301 y tal y como ya sabiamos consta que el Dossier se elaboro con los Resultdos existentes en fecha Mayo 2008 ... con esos datos el ODAC y la FDA saben que Yondelis Funciona y que alarga la vida a las pacientes ... pero quieren mas datos Finales ... y es ahi en donde estan todas las dudas ... ¿ Sera capaz J&J de Convencer o de tener esos datos que pide la ODAC para antes de la evaluacion de la FDA en Septiembre ? ... de ser asi Bingo ... de No ser asi la FDA nos va a pedir esos datos y meses de por medio ...
Primary Outcome Measures:
*.- Progression-free survival as assessed by independent radiology review [ Time Frame: every 8 weeks after randomization ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
*.- Overall survival [ Time Frame: every 8 weeks for first 2 years then every 3 months thereafter ] [ Designated as safety issue: Yes ]
*.- Response rate [ Time Frame: every 8 weeks ] [ Designated as safety issue: No ]
*.- Safety [ Time Frame: weekly until treatment is terminated ] [ Designated as safety issue: Yes ]
*.- Pharmacokinetics [ Time Frame: weekly during cycle 1 & 2 ] [ Designated as safety issue: No ]
Study Start Date: April 2005
Estimated Study Completion Date: May 2011
Primary Completion Date: May 2008 (Final data collection date for primary outcome measure)
...
Primary Outcome Measures:
*.- Progression-free survival as assessed by independent radiology review [ Time Frame: every 8 weeks after randomization ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
*.- Overall survival [ Time Frame: every 8 weeks for first 2 years then every 3 months thereafter ] [ Designated as safety issue: Yes ]
*.- Response rate [ Time Frame: every 8 weeks ] [ Designated as safety issue: No ]
*.- Safety [ Time Frame: weekly until treatment is terminated ] [ Designated as safety issue: Yes ]
*.- Pharmacokinetics [ Time Frame: weekly during cycle 1 & 2 ] [ Designated as safety issue: No ]
Study Start Date: April 2005
Estimated Study Completion Date: May 2011
Primary Completion Date: May 2008 (Final data collection date for primary outcome measure)
...
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