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Novartis completes tender offer for all outstanding shares of AveXis, Inc.
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Novartis (NVS) Reports FDA Approval of Gilenya (fingolimod)
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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 provides update on proposed acquisition of AveXis
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Novartis tender offer for AveXis commences
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Novartis completes subsequent offering period of the tender offer for Advanced Accelerator Applications S.A.
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Advanced Accelerator Applications Receives FDA Approval for Lutathera® for Treatment of Gastroenteropancreatic Neuroendocrine Tumors
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Novartis completes tender offer for Advanced Accelerator Applications S.A. and announces commencement of subsequent offering period
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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 AG (NVS) Granted FDA Breakthrough Therapy designation for Kisqali for Initial Endocrine-Based Treatment in Premenopausal Women with HR+/HER2- Advanced Breast Cancer
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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 (NVS) Reports Data from Phase II SUSTAIN Study Showing that Crizanlizumab Delayed the Time to First Sickle Cell Pain Crisis in Patients
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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 AG (NVS) Commences Study Evaluating Impact of Higher Dosing of Cosentyx in Patients with Ankylosing Spondylitis
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Novartis initiates study evaluating impact of higher dosing of Cosentyx® in patients with ankylosing spondylitis
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Novartis (NVS) Commences Tender Offer for Accelerator Applications (AAAP)
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Novartis tender offer for Advanced Accelerator Applications commences
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Novartis AG (NVS) Announces Data from Phase III MONALEESA-7 Trial Showing Superior Median PFS Compared to Oral Endocrine Therapy as First-Line Treatment
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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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Cryoport (CYRX) Says Novartis (NVS) Signed Agreement Contracting it Over Initial Three-year Term for Cryogenic Logistics Support of CTL019/CD19 CAR-T Cell Therapy
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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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Bristol-Myers Squibb (BMY) New Collaboration WIth Novartis (NVS) To Evaluate Combo Therapy In Colorectal Cancer
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Novartis (NVS) Confirms FDA Approval for Expanded Use of Zykadia®
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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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Celyad (CYAD), Novartis (NVS) Enter Non-Exclusive License for Allogeneic TCR-Deficient CAR-T Cells
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Amgen (AMGN), Novartis (NVS) Expand Commercial Collaboration for Erenumab In Migraine
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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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Novartis (NVS) to Help PureTech Advance Clinical Stage mTORC1 Programs
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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
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Sandoz Canada launches Sandoz(R) Amphetamine XR for the treatment of Attention Deficit Hyperactivity Disorder (ADHD)
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Novartis LEE011 (ribociclib) plus letrozole analyses show superior PFS across broad spectrum of patients in first-line HR+/HER2- advanced breast cancer versus letrozole
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Novartis data at ASH and SABCS showcase latest innovations in development for patients with blood disorders and breast cancer
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Novartis' (NVS) PKC412 NDA Granted FDA Priority Review as AML Treatment
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Novartis partners with prominent US health advocacy organizations to launch first social networking platform for heart failure patients and their loved ones
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Novartis LEE011 (ribociclib) granted FDA Priority Review for first-line treatment of HR+/HER2- advanced breast cancer
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Novartis (NVS) Announces Presentation of Significant Phase III MONALEESA-2 Data at ESMO 2016
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Novartis breakthrough therapy LEE011 (ribociclib) plus letrozole demonstrates superior progression-free survival as first-line treatment for HR+/HER2- advanced breast cancer compared to a standard of
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Novartis (NVS) Announces Strong Cosentyx Phase III SCULPTURE Trial 1 Data in Psoriasis Patients
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Novartis late-breaking data show Cosentyx® continues to deliver high skin clearance for majority of psoriasis patients at four years
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Important new analysis shows that Novartis' Entresto® is associated with higher relative health-related quality of life scores among HFrEF patients

