

Ademas valora la posible salida al mercado este mismo año del Segundo Farmaco de PharmaMar ( APLIDIN ) en Europa ... asi como el hecho de que PM01183 ya este en Dos Fases III ( Ovario y Pulmón ) y este por iniciar una Tercera Fase III Pivotal en Mama BRCA . Sin dejar de mencionar que el PM01183 podría salir al Mercado US el proximo año ( 2018 ) en la Indicación de Ovario dado que tiene el Status de Medicamento Huerfano .
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Japan licence deal highlights PM1183 potential.
PharmaMar has capped off a strong performance in 2016 by signing a licence deal with Chugai for lurbinectedin (PM1183) in Japan, including €30m upfront and over €70m in potential milestones.
The outlook for 2017 is similarly promising, including a potential EMA approval decision for Aplidin in multiple myeloma, Phase III data for lurbinectedin in ovarian cancer, and potential initiation of a pivotal trial of lurbinectedin in a third indication (BRCA-associated breast cancer).
We have substantially revised our valuation assumptions, but the end result is that our valuation is little changed at €1.01bn (€4.55/share).
