LONDON, 13-11-2014 — /EuropaWire/ — GSK today announced the submission to the European Medicines Agency (EMA) of a variation to the Marketing Authorisation for eltrombopag (Revolade™), seeking an additional indication for the treatment of adult patients with severe aplastic anaemia … Read the full press release →
Posted in Healthcare, Marketing, Pharma & Biotech, United Kingdom
Tagged eltrombopag (Revolade™), EMA, European Medicines Agency, GSK, severe aplastic anaemia
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