This page shows the latest Jetrea news and features for those working in and with pharma, biotech and healthcare.
The NICE recommendation is the second in the space of a week for Novartis, which two days ago received a green light for Jetrea (ocriplasmin) to treat patients with the rare
Recommends Jetrea for NHS use in England and Wales to treat the rare disease vitreomacular traction. ... NICE's recommendation limits use of Jetrea compared to its European approval, which covers all vitreomacular traction patients.
This differs from its licence from the European Medicines Agency (EMA), which in March 2013 approved the use of Jetrea in any adult with the condition. ... Once launched, Jetrea will be marketed by Novartis' eye division Alcon, which purchased non-US
It purchased the rights to commercialise Jetrea outside the US from its developers ThromboGenics in 2012 as part of a deal potentially worth up to 375m. ... In addition to its European licence, Jetrea won approval in October last year for the treatment
Jetrea was approved for symptomatic VMA last year in the US, where ThromboGenics has retained exclusive commercial rights, and was launched onto the market in January 2013. ... Analysts have suggested Jetrea sales could reach $500m in the US alone, with
European regulatory authorities have backed Novartis' licence application for its new eye drug Jetrea (ocriplasmin). ... world.". Jetrea is a recombinant form of human protein (plasmin) that is administered through a one-time, single intravitreal
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Vangeersdaele will be leading and developing the overall commercial strategy for the company’s recently formed Jetrea business unit, which was created following ThromboGenics regaining full rights to Jetrea from Novartis. ... I am convinced that their
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