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October 2016
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Media ReleaseNovartis late-breaking data show Cosentyx® continues to deliver high skin clearance for majority of psoriasis patients at four years-- New data at EADV show Cosentyx delivers almost clear or completely clear skin in majority of patients (PASI 90 - 66%, PASI 100 - 44%) after four years of treatment1-- Data show that with Cosentyx…
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Media ReleaseNovartis late-breaking data show Cosentyx® continues to deliver high skin clearance for majority of psoriasis patients at four years
September 2016
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Media ReleaseNovartis receives three new FDA approvals for the expanded use of Ilaris for patients with rare Periodic Fever Syndrome conditions- Ilaris® (canakinumab) is the first and only FDA-approved biologic treatment for patients with TRAPS, HIDS/MKD and FMF(1)- These three simultaneous approvals conducted under FDA Priority Review…
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Media ReleaseNovartis receives three new FDA approvals for the expanded use of Ilaris for patients with rare Periodic Fever Syndrome conditions
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Media ReleaseImportant new analysis shows that Novartis' Entresto® is associated with higher relative health-related quality of life scores among HFrEF patientsNew analysis of PARADIGM-HF data shows that among patients who had been hospitalized for heart failure, those on Entresto reported higher relative health-related quality of life (HRQL) scores…
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Media ReleaseImportant new analysis shows that Novartis' Entresto® is associated with higher relative health-related quality of life scores among HFrEF patients
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Media ReleaseNovartis BAF312 reduced the risk of disability progression in pivotal phase III study in secondary progressive MS patients-- EXPAND study data presented at ECTRIMS 2016 show that treatment with BAF312 (siponimod) reduced the risk of three-month confirmed disability progression by 21% vs. placebo in patients with…
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Media ReleaseNovartis BAF312 reduced the risk of disability progression in pivotal phase III study in secondary progressive MS patients
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Media ReleaseNovartis data finds relapsing MS patients on Gilenya® had greater treatment retention and satisfaction rates vs. injectable DMTs- In a well-controlled, randomized, open-label study, Gilenya patients had higher treatment retention rates at one year, 81.3% vs. those on injectable DMTs, 29.2% - Throughout the study almost 10…
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Media ReleaseNovartis data finds relapsing MS patients on Gilenya® had greater treatment retention and satisfaction rates vs. injectable DMTs
July 2016
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Media ReleaseNovartis announces FDA approval of Xolair® (omalizumab) for pediatric allergic asthma-- Extension of indication makes Xolair the first and only approved biologic for pediatric patients six years and older with uncontrolled moderate to severe persistent allergic asthma-- Asthma is one…
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Media ReleaseNovartis announces FDA approval of Xolair® (omalizumab) for pediatric allergic asthma
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