AstraZeneca's (AZN.US) Tagrisso small molecule combination therapy has been approved again.
According to the Zhitong Finance APP, AstraZeneca (AZN.US) announced today that its epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) Tagrisso (osimertinib) combined with pemetrexed and platinum chemotherapy has been approved in the European Union for first-line treatment of advanced epidermal growth factor receptor mutated non-small cell lung cancer (NSCLC) in adult patients who have exon 19 deletion or exon 21 (L858R) mutation. Tagri
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AstraZeneca's (AZN) Tagrisso Gets EU Nod for First-Line NSCLC
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Express News | The European Commission Approves AstraZeneca's Tagrisso (Osimertinib) With Pemetrexed And Platinum-Based Chemotherapy As 1st-line Treatment For Advanced EGFR-Mutated Non-small Cell Lung Cancer Whose Tumors Have Exon 19 Deletions Or Exon 21 Mutations
EU Approves AstraZeneca's Tagrisso Combo as Non-small Cell Lung Cancer Treatment
AstraZeneca (AZN.L, AZN.ST) said Friday the European Union approved Tagrisso plus pemetrexed and platinum-based chemotherapy as a first-line treatment for adults with advanced epidermal growth factor receptor-mutated non-small cell lung cancer.
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Sanofi's blockbuster drug Dupixent has been approved in Europe to treat pulmonary diseases.
Zhītōng cáijīng APP learned that Sanofi (SNY.US)'s heavyweight drug Dupixent has been approved for use in European patients with chronic lung disease, opening up a new growth path. According to a statement by the company on Wednesday, European regulators became the world's first country to approve the vaccine as an additional therapeutic drug for patients with chronic obstructive pulmonary disease (some with high white blood cell levels). In two landmark studies, the drug reduced disease progression, improved lung function, and improved quality of life. The decision, the company said, makes Dupixent available to about 220,000 adult CO
AstraZeneca (AZN) Imfinzi Combo Gets CHMP Nod for Expanded Use
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Express News | AstraZeneca : Jefferies Raises Target Price to $74 From $71
AstraZeneca's COVID-19 Prevention Drug For Patients With Weak Immune Systems - European Medicines Agency Accepts Marketing Application Under Accelerated Assessment
The European Medicines Agency (EMA) has accepted AstraZeneca Plc's (NASDAQ:AZN) marketing authorization application for sipavibart for pre-exposure prophylaxis (prevention) of COVID-19 in immunocompro
AstraZeneca Shares Update and Global Reach
Express News | AstraZeneca's Marketing Authorization Application For Sipavibart Has Been Accepted Under An Accelerated Assessment Procedure By The European Medicines Agency, For The Pre-exposure Prophylaxis (Prevention) Of Covid-19 In Immunocompromised Patients