Genmab — April 2016
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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 -
nice - det skal vi også have i GEN!
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Cantor Fitzgerald analyst Mara Goldstein forecast Revlimid sales reaching $10 billion by 2020 if its duration of use and geographic expansion continues to grow, along with approvals or new uses.
"It's a high class problem to have," she said of the company's dependence on Revlimid. She predicts Revlimid will decline as a percentage of profit "not because it's declining, but because other products are growing. That's a very positive dynamic."
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Celgene said it anticipates "significant market share gains over coming months and years" with reimbursements for newly diagnosed patients in Europe, and with an expected approval in Japan for such patients around the end of the year. The company is also conducting five late-stage trials of Revlimid in a variety of lymphomas.
"It's always less risky to expand the opportunities for an existing drug than to invest in advancing a new drug," Bernstein analyst Geoffrey Porges said. "They happen to
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Man må gå ud fra de regner med at veksten kommer når Pollux er godkendt
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