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Showing 1807 results
August 2020
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Guidance system lights a path for drug discovery
Novartis drug hunters leverage machine learning and automation to power a faster, smarter way to navigate to new drugs.
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Media ReleaseNovartis new analysis shows high consistency in lowering LDL-C in individual response with investigational inclisiranPooled data from Phase III ORION-10 and -11 showed highly consistent efficacy, tolerability and safety profile over 17 months on twice-yearly subcutaneous dosing in 2,300 patients (of which 1,164…
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Media ReleaseNovartis announces positive results from Phase II study of LNP023 in patients with paroxysmal nocturnal hemoglobinuria (PNH)Oral, investigational complement factor B inhibitor LNP023 substantially improved hematological response as add-on therapy to eculizumab Seven of ten patients discontinued eculizumab and remained on…
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In The NewsSupply chain organization during the COVID-19 pandemicBalancing priorities of combating the crisis and ongoing trials.
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Featured News50 Climate Leaders
At Novartis, we aim to be a leader in environmental sustainability and a catalyst for positive change both in our own operations and in our supply chain.
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Media ReleaseNovartis investigational novel STAMP inhibitor asciminib (ABL001) meets primary endpoint of Phase III chronic myeloid leukemia studyAt primary analysis, ASCEMBL met its primary endpoint of significant superiority in major molecular response rate at 24 weeks for asciminib (ABL001) vs. bosutinib in patients previously treated with…
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In The NewsThe coronavirus is giving health and pharma companies a chance to woo tech talentNovartis Chief Digital Officer Bertrand Bodson says tech professionals don’t need a background in biology to switch industries.
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Media ReleaseNovartis provides update on Phase III study evaluating investigational spartalizumab (PDR001) in combination with Tafinlar® + Mekinist® in advanced melanomaPhase III COMBI-i trial did not meet primary endpoint for patients with advanced BRAF V600-mutated melanoma Tafinlar + Mekinist remains an effective treatment option based on previously reported…
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Building collaborations to fight a pandemic
Jennifer Leeds offers a behind-the-scenes look at the consortia forming to address COVID-19.
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Key ReleaseFDA approves Novartis Kesimpta® (ofatumumab), the first and only self-administered, targeted B-cell therapy for patients with relapsing multiple sclerosisKesimpta delivers powerful efficacy with a favorable safety profile and can be self-administered at home, addressing significant unmet needs for people living with relapsing forms of multiple…
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Key ReleaseNovartis announces US District Court for the District of Delaware upholds validity of Gilenya® (fingolimod) dosage regimen patentBasel, August 17, 2020 — Novartis welcomes the decision by the US District Court for the District of Delaware to uphold the validity of the Gilenya® (fingolimod) dosage regimen patent, as our…
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