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US Supreme Court denies Sandoz (NVS) petition to review biosimilar Erelzi case
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US Supreme Court denies Sandoz petition to review biosimilar Erelzi® (etanercept-szzs) case
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Novartis (NVS) Granted FDA Approval for Expanded Indication for Entresto in Chronic Heart Failure
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Novartis Entresto® granted expanded indication in chronic heart failure by FDA
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Novan Inc. and Verrica Pharmaceuticals Participate in Virtual Panel to Discuss Developing Treatments for Molluscum Contagiosum on SNN Network
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Novartis US Foundation commits $25M to improve health equity by reducing health disparities in the US
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Sosei Heptares Notes That Enerzair® Breezhaler® (QVM149) has been Recommended for Approval in the European Union for Treating Uncontrolled Asthma
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Novartis (NVS) says Kymriah demonstrated consistent efficacy and safety outcomes in US patients when used in real-world setting
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Novartis Kymriah® demonstrates consistent efficacy and safety outcomes in US patients when used in real-world setting
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8x8, Inc. (EGHT) Announces Elizabeth Theophille to Board
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8X8, Inc. Appoints Elizabeth Theophille to Its Board of Directors
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Long-term Survival Benefit Shown for Metastatic Melanoma Patients Treated with Novartis Tafinlar® + Mekinist®
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Novartis Shows Growing Strength in Lung Cancer Innovation with New Capmatinib Investigational Data and Novel Canakinumab Clinical Trials
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AveXis receives FDA approval for Zolgensma®, the first and only gene therapy for pediatric patients with spinal muscular atrophy (SMA)
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Sosei Heptares Notes That a Valid Marketing Authorization Application For QVM149, a Potential New Inhaled Combination Therapy For Asthma, Has Been Filed With the European Medicines Agency
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Verily Forms Strategic Alliances with Novartis, Otsuka, Pfizer and Sanofi to Transform Clinical Research
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Novartis data at ASH and SABCS show strength of pipeline and portfolio in hematology and oncology
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Pfizer Announces Clinical Development Agreement with Novartis to Advance the Treatment of NASH
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Novartis (NVS) says analysis shows crizanlizumab increased number of patients free of sickle cell pain crises vs placebo during SUSTAIN study
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Novartis analysis shows crizanlizumab (SEG101) increased the number of patients free of sickle cell pain crises vs placebo during SUSTAIN study
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Novartis (NVS) Reports Publication of Landmark PARADIGMS Study Demonstrating Significant Benefit of Gilenya
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Novartis announces NEJM publication of landmark PARADIGMS study demonstrating significant benefit of Gilenya® in children and adolescents with relapsing multiple sclerosis
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Novartis Kisqali® now first and only CDK4/6 inhibitor indicated in US as first-line therapy specifically for premenopausal women; and as initial therapy with fulvestrant in postmenopausal women
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Novartis launches the Galaxies of Hope app, a digital experience for the Neuroendocrine Tumor (NET) cancer community
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Novartis receives FDA approval for inclusion of new evidence that Cosentyx® inhibits progression of joint structural damage in psoriatic arthritis
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Novartis survey uncovers real-world impact of immune thrombocytopenia or ITP, a rare blood disease, on patients' quality of life
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Novartis (NVS) Says FDA Expedited Review of its drug Promacta for first-line SAA
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FDA expedites review of Novartis drug Promacta® for first-line severe aplastic anemia (SAA)
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Novartis data at ASCO and EHA reinforce company's commitment to reimagining cancer
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Novartis announces FDA approval of Gilenya® as the first disease-modifying therapy for pediatric relapsing multiple sclerosis
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Novartis new data reinforces superiority of Cosentyx® versus Stelara® in achieving skin clearance for psoriasis patients
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Novartis drug Promacta® receives FDA Breakthrough Therapy designation for first-line use in severe aplastic anemia (SAA)
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Novartis Kisqali® received FDA Breakthrough Therapy designation for initial endocrine-based treatment in premenopausal women with HR+/HER2- advanced breast cancer
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Novartis drug crizanlizumab shown to prolong time to patients' first sickle cell pain crisis in subgroup analysis of SUSTAIN study
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Novartis initiates study evaluating impact of higher dosing of Cosentyx® in patients with ankylosing spondylitis
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Novartis Kisqali® is first and only CDK4/6 inhibitor to show superior median PFS compared to oral endocrine therapy as first-line treatment in a prospective, randomized Phase III trial dedicated to p
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Novartis presents new data at SABCS across broad range of breast cancer patient populations, combination treatments and lines of therapy
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Novartis presents data at ASH for patients with serious blood disorders like lymphoma, leukemia and sickle cell disease
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Xenetic Biosciences (XBIO) Appoints Jeffrey Eisenberg as CEO
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Xenetic Biosciences Appoints Jeffrey F. Eisenberg as Chief Executive Officer
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Novartis collaborates with pop icon Cyndi Lauper to release new song in honor of World Psoriasis Day
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TransCelerate BioPharma Grows Industry Collaboration
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Novartis (NVS) Confirms 5 year Data for IL-17A Inhibitor Cosentyx
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Novartis confirms 5 year data for first and only fully-human IL-17A inhibitor Cosentyx® reinforcing sustained efficacy and safety profile in psoriasis
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Novartis receives FDA approval for expanded use of Zykadia® in first-line ALK-positive metastatic non-small cell lung cancer (NSCLC)
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Sandoz Canada launches Sandoz Olmesartan for the treatment of high blood pressure
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Sandoz Canada launches Mosaspray(TM) in Quebec: a non-prescription mometasone nasal spray for the treatment of the symptoms of allergic rhinitis
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'It's like kumbaya': Trump's genial private meetings with CEOs jar with public attacks
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Novartis (NVS) Says Extension Study of Cosentyx Shows Almost All Psoriasis Patients Regain Skin Clearance Following Treatment Pause
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Novartis' Cosentyx® shows almost all psoriasis patients rapidly regain skin clearance following a treatment pause

