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European Medicines Agency gives first positive opinion for paediatric-use marketing authorisation
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10-year Report to the European Commission (Core report)
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La EMA recomienda no aprobar el fármaco de Puma Biotech
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European Commission Grants Marketing Authorisation for Puma Biotechnology's NERLYNX® (neratinib) for Extended Adjuvant Treatment of Hormone Receptor Positive HER2-Positive Early Stage Breast Cancer | Business Wire
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