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Sandoz Canada launches Sandoz(R) Amphetamine XR for the treatment of Attention Deficit Hyperactivity Disorder (ADHD)
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Davos CEOs 'go local' on supply chain in Trump era
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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 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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Novan, Inc. (Nasdaq: NOVN) to Ring The Nasdaq Stock Market Opening Bell
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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
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Novartis survey published in The Breast Journal reveals major gaps in treatment discussions between metastatic breast cancer patients and doctors
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Novartis' (NVS) LEE011 Receives FDA Breakthrough Therapy Designation in for HR+/HER2- Advanced Breast Cancer
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Novartis CDK4/6 inhibitor LEE011 (ribociclib) receives FDA Breakthrough Therapy designation as first-line treatment for HR+/HER2- advanced breast cancer
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Novartis (NVS) Receives FDA Approval for Expanded Xolair Age Range Usage
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Novartis announces FDA approval of Xolair® (omalizumab) for pediatric allergic asthma
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Novartis PKC412 (midostaurin) pivotal data published in NEJM show 60% response rate in advanced systemic mastocytosis (SM)
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Timely use of Novartis' Entresto could prevent or postpone over 28,000 US deaths per year among HFrEF patients, according to an expert analysis in JAMA Cardiology
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Novartis combination therapy Tafinlar® + Mekinist® demonstrates overall survival benefit at three-year follow-up in patients with advanced melanoma
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Novartis data show more than 50 percent of eligible Ph+ CML patients maintain Treatment-free Remission (TFR) after stopping Tasigna®
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Novartis data show Gilenya® had significantly greater patient retention compared to iDMTs in relapsing-remitting MS
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Novartis (NVS) Enters co-Promotion Agreement with Eisai for Lenvima Combo in RCC
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Novartis announces US collaboration to co-promote Lenvima® in combination with everolimus for advanced renal cell carcinoma (RCC)
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Novartis (NVS) to Present Data in Hematologic and Solid Tumor Cancers at ASCO
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Novartis to present pivotal data in hematologic and solid tumor cancers at 2016 ASCO Annual Meeting
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FDA approves new indication for Novartis drug Afinitor® for progressive, nonfunctional GI and lung neuroendocrine tumors (NET)
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Novartis (NVS) PKC412 Receives FDA Breakthrough Therapy Designation in FLT3+ AML
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Novartis drug PKC412 (midostaurin) receives Breakthrough Therapy designation from the FDA for newly-diagnosed FLT3-mutated acute myeloid leukemia (AML)
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Novartis teams up with Pro Football Hall of Famer Troy Aikman on advanced melanoma educational and community support program
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Novartis receives two new FDA approvals for Cosentyx® (secukinumab) to treat patients with ankylosing spondylitis and psoriatic arthritis
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Novartis (NVS) Announces Publication of Cosentyx MEASURE 1, 2 Study Data in NEJM
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Novartis announces publication of two landmark studies in NEJM demonstrating efficacy of Cosentyx® in patients with ankylosing spondylitis
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Novartis highlights new CTL019 Phase II data demonstrating 93% complete remission in pediatric patients with r/r ALL
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Sandoz Canada launches two easy-to-use products: Salinex(R) Seawater nasal spray for daily care and Ezeva(TM) zinc oxide cream
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Sandoz Canada launches two easy-to-use products: Salinex(R) Seawater nasal spray for daily care and Ezeva(TM) zinc oxide cream
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Novartis (NVS) Presents Updated Data from CTL019 in r/r NHL at ASH
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Novartis drug PKC412 (midostaurin) improves overall survival by 23% in global Phase III study of AML patients with FLT3 mutations
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Novartis announces new CTL019 study data demonstrating overall response in adult patients with certain types of lymphoma
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Sandoz Canada Launches a New Concentration of (T/C)Lorazepam Injection USP
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Sandoz Canada Launches a New Concentration of (T/C)Lorazepam Injection USP
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Novartis highlights clinical advances at ASH 2015, underscoring leadership in hematology research
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Novartis receives FDA regular approval for Tafinlar® + Mekinist® to treat aggressive form of melanoma based on long-term survival data
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Novartis heart failure medicine Entresto™ substantially cuts 30-day hospital readmissions, new post-hoc analysis shows
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Approximately 80% of psoriatic arthritis patients treated with Cosentyx® saw no progression of joint damage as shown in Novartis new two-year observational data
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Up to 80% of ankylosing spondylitis patients treated with Cosentyx® show no spinal x-ray progression as shown in Novartis new two-year observational data
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FDA approves new Novartis dual combination bronchodilator Utibron™ Neohaler® for patients with chronic obstructive pulmonary disease
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Science 37 Secures $6.5M Series A Funding To Accelerate Clinical Trial Research
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Sandoz Canada launches new multi-platform application to show real-time availability of its injectable medicines
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Sandoz Canada launches new multi-platform application to show real-time availability of its injectable medicines

