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Novartis Announces NEJM Publication of Pivotal Study of Tabrecta™ in Patients with METex14 Metastatic Non-Small Cell Lung Cancer
Data from the pivotal GEOMETRY mono-1 Phase II study published today in The New England Journal of Medicine (NEJM) show treatment with Tabrecta™...

Sandoz Advances Its Biosimilars Program With EMA Acceptance of Regulatory Submission for Biosimilar Pegfilgrastim
Sandoz' late-stage biosimilar pipeline gains momentum with sustained investment - five of 10 planned regulatory filings achieved Sandoz believes...

Novartis to Present Pivotal Data in Hematologic and Solid Tumor Cancers at 2016 ASCO Annual Meeting
Novartis will highlight the strength of its oncology research programs at the upcoming 52nd Annual Meeting of the American Society of Clinical...

Combination of Novartis drugs Tafinlar® and Mekinist® shows significant survival benefit in patients with metastatic melanoma
Final analysis of COMBI-d confirms overall survival benefit of combination therapy in patients with BRAF V600E/K mutation-positive metastatic...

Patients with aggressive form of melanoma lived for more than two years on average when taking Novartis therapies Tafinlar® + Mekinist®
Phase III data showed median overall survival of 25.6 months in patients with BRAF+ V600E/K metastatic melanoma who received Tafinlar + Mekinist...

Novartis Pivotal Data for Tafinlar® + Mekinist® Demonstrated a 63 Percent Overall Response Rate in Treating Rare Form of Lung Cancer
Novartis today announced new data for multiple investigational and established non-small cell lung cancer (NSCLC) treatments, including results...

Sandoz Strengthens Its Biosimilars Portfolio With Acquisition of Pfizer's Biosimilar Infliximab in EEA
Sandoz acquires rights to PF-06438179 (biosimilar infliximab) in the European Economic Area (EEA)*
Sandoz plans to complete Phase III...

Novartis presents new data on 21 medicines and 11 investigational compounds at ASCO and EHA
Overall survival data for Tafinlar® and Mekinist® combination to be presented in metastatic BRAF V600E/K mutation-positive cutaneous melanomaNew...

FDA expands use of Novartis drug Promacta® to include treatment of children ages 1 and older with chronic immune thrombocytopenia
New oral suspension formulation, designed for younger children with rare blood disorder, is now approved
For about one in four children...

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