Genmab — April 2016
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absolut! Sukkeralf, har du styr på, hvilket organ i EMA, der står for den endelige markedsføringsgodkendelse? Jeg kan ikke lige finde den. Du postede på et tidspunkt et link til en ppt over godkendelsesprocessen...
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GEN siger selv - The CHMP reviewed DARZALEX under the EMA's accelerated assessment program. A final decision by the European Commission is anticipated in 60 — 90 days.
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så ifølge dem selv, kommer godkendelse tidligst ultimo maj, da udtalelsen var dateret 010416
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...men kommissionens pharmaceutiske kommitte er ikke ligefrem super opdateret - http://ec.europa.eu/health/documents/pharmaceutical-committee/index_en.htm
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det ser dog ud til at COMP har sendt den videre i systemet
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Hvornår forventes der Dara salgstal fra Symphogen?
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Symphony Health data kommer typisk mellem den 20 og 25 I måneden
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har vi fået tallen i denne måned??? jeg har ikke set dem!
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tallene
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Blodkræftmiddel sparker året i gang for Celgene
Det amerikanske biotekselskab Celgene er kommet fint fra start i 2016, særligt båret af dets flagskib, kræftmidlet Revlimid, og en af de nyere bestsellere. Til gengæld ser udsigterne for 2017 mørkere ud.
(medwatch.dk)
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sukkeralf,artiklen er lukket - kan du se, hvor stor omsætnigen er?
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fandt den selv - •REVLIMID
sales for the first quarter increased 17 percent to $1,574 million. Growth was driven by increased market share in newly diagnosed multiple myeloma and increases in duration. U.S. sales of $997 million and international sales of $577 million increased 23 percent and 8 percent, respectively -
• Celgene Execs Say The Fundamentals For Revlimid And Pomalyst Are Both Exceptionally Strong - Conf Call
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• Celgene Execs Say 2020 Revlimid Forecast Is Conservative - Conf Call
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2017 net product sales expected to be:
REVLIMID: $7,000 million
POMALYST/IMNOVID: $1,500 million
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