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  1. Há 13 horas · MADRID, 3 Jun. (EUROPA PRESS) - La compañía AstraZeneca ha informado sobre los resultados del ensayo fase III 'ADRIATIC', que mostraron que 'Imfinzi' (durvalumab) mejora de forma estadística y ...

  2. Há 4 horas · June 03, 2024 at 05:35 am EDT. AstraZeneca announces that Tagrisso (osimertinib), in combination with pemetrexed and platinum-based chemotherapy, has been recommended by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) for approval in the EU for the first-line treatment of adult patients with ...

  3. AZN - AstraZeneca PLC

    Yahoo Finanças

    78.86+0.84 (+1.08%)

    em Mon, Jun 3, 2024, 9:53AM EDT - Mercado fechará em 6 h 7 min

    Preço em USD

    • Abertura 78.50
    • Alta 79.03
    • Baixa 78.38
    • Fech. ant. 78.02
    • Alt de 52 sem 79.36
    • Bai 52 sem 60.47
    • P/L 38.85
    • Cap. merc. 244.5B
  4. Há 13 horas · AstraZeneca’s Tagrisso just delivered an 84% improvement. | A 50% improvement on the time patients could live without disease progression would typically be considered remarkable for a new drug.

  5. Há 13 horas · AstraZeneca: essai concluant dans le cancer du poumon. (CercleFinance.com) - AstraZeneca fait savoir que les résultats positifs d'un essai de phase III ont montré qu'Imfinzi (durvalumab ...

  6. Há 13 horas · con quimioterapia. AstraZeneca está avanzando en el proceso de aprobación del fármaco para este tipo de cáncer. Opinión de Bankinter. Noticia positiva, implica que aumenta el número de pacientes que podrían ser tratados con Enhertu. Este fármaco está aprobado como tratamiento de segunda línea y genera ventas de 2.600M$ anuales.

  7. Há 13 horas · AstraZeneca's cancer fighting treatment reduced instances of disease progression or death by 84% in the double-blind, placebo-controlled trial involving 216 patients across 15 countries.

  8. Há 13 horas · AstraZeneca's Tagrisso (osimertinib) with the addition of pemetrexed and platinum-based chemotherapy has been recommended for approval in the European Union (EU) for 1st-line treatment of adult patients with locally advanced or metastatic epidermal growth factor receptor-mutated (EGFRm) non-small cell lung cancer (NSCLC) whose tumours have exon 19 deletions or exon 21 (L858R) mutations.

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