GlaxoSmithKline receives EU authorisation for a new therapeutic indication for Tyverb® (lapatinib)
GlaxoSmithKline (GSK) confirmed today that the European Commission (EC) has granted a variation to the conditional marketing authorisation for Tyverb® (lapatinib) in the European Union for a new therapeutic indication. Tyverb, in combination with an aromatase inhibitor, is indicated for the treatment of post-menopausal women with hormone receptor-positive, HER2 (ErbB2) over-expressing metastatic breast cancer and for whom chemotherapy is currently not intended. The patients in the registration study were not previously treated with trastuzumab or an aromatase inhibitor.
Issued: Wednesday 23 June 2010, London UK
GlaxoSmithKline (GSK) confirmed today that the European Commission (EC) has granted a variation to the conditional marketing authorisation for Tyverb® (lapatinib) in the European Union for a new therapeutic indication. Tyverb, in combination with an aromatase inhibitor, is indicated for the treatment of post-menopausal women with hormone receptor-positive, HER2 (ErbB2) over-expressing metastatic breast cancer and for whom chemotherapy is currently not intended. The patients in the registration study were not previously treated with trastuzumab or an aromatase inhibitor.
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GlaxoSmithKline Enquiries: |
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UK Media enquiries: |
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Claire Brough |
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Stephen Rea |
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Alexandra Harrison |
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Jo Revill |
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European Analyst/Investor enquiries: |
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Sally Ferguson |
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Gary Davies |
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