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Industry news, News / 6 June 2011 / Novartis
The European Commission has granted Novartis a new indication for Lucentis® (ranibizumab) to treat patients with visual impairment due to macular edema secondary to retinal vein occlusion (branch RVO and central RVO), a sudden-onset disease where patients have difficulties with daily activities such as reading, cooking and driving.
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Industry news, News / 11 May 2011 / Fleming Europe
The recent economic downturn has influenced every industry. Although the Pharmaceutical world has avoided a big direct blow because of the nature of its products and services, this downturn has impacted the economic landscape dramatically. (more…)
Industry news, News / 5 May 2011 / Novartis
Novartis announced today that the US Food and Drug Administration (FDA) approved Afinitor® (everolimus) tablets for the treatment of progressive neuroendocrine tumors of pancreatic origin (PNET) in patients with unresectable, locally advanced or metastatic disease[4]. This marks the first approval of a treatment for this patient population in the US in nearly 30 years[5].
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Industry news, News / 12 April 2011 / Novartis
Novartis announced today that the US Food and Drug Administration (FDA) Oncologic Drugs Advisory Committee (ODAC) recommended approval of Afinitor® (everolimus) tablets for the treatment of patients with advanced neuroendocrine tumors (NET) of pancreatic origin.
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Industry news, News / 11 April 2011 / GDS International
Every other industry is getting on the social media bandwagon. But could social media actually prove beneficial to the world of pharma?
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Industry news, News / 8 April 2011 / Novartis
Novartis shareholders today followed the Board of Directors’ recommendation, approving the proposed merger of Alcon, Inc. into Novartis. In addition, shareholders approved the issuance of up to 108 million shares which will be used as part of the transaction to exchange Alcon shares for Novartis shares.
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Industry news, News / 31 March 2011 / Novartis
Novartis announced today that a Phase II study with the first-in-class antiviral DEB025 (alisporivir) met its primary endpoint for achieving viral cure (24 weeks after stopping treatment) in 76% of patients with chronic hepatitis C 1. The study involved nearly 300 previously untreated patients infected with the most common form of hepatitis C virus (HCV), the genotype 1 (G1)1.
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Industry news, News / 22 March 2011 / Novartis
Novartis announced today that it completed the transaction to acquire an 85 percent stake in the Chinese vaccines company Zhejiang Tianyuan Bio-Pharmaceutical Co., Ltd. This acquisition provides Novartis with an expanded presence in the Chinese vaccines market and is expected to facilitate the introduction of additional Novartis vaccines into China where there continues to be tens of thousands of new cases of vaccine-preventable diseases each year[1].
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Industry news, News / 21 March 2011 / Novartis
The European Commission has granted Novartis approval for Gilenya® (fingolimod) 0.5 mg daily as a disease modifying therapy in patients with highly active relapsing-remitting multiple sclerosis (RRMS) despite treatment with beta interferon, or in patients with rapidly evolving severe RRMS.
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Industry news, News / 17 February 2011 / Novartis
Novartis announced that effective March 2, 2011 Naomi Kelman is appointed Head of the Novartis OTC Division and will become a permanent attendee to the Executive Committee of Novartis (ECN), reporting to Joseph Jimenez, CEO of Novartis.
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Industry news, News / 10 February 2011 / Novartis
Novartis has announced that two Phase III studies show that patients with chronic obstructive pulmonary disease (COPD) who were treated with once-daily Onbrez® Breezhaler® (indacaterol) plus tiotropium experienced significantly greater improvements in lung function than those treated with tiotropium alone[1],[2].
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Industry news, News / 9 February 2011 / Novartis
The New England Journal of Medicine (NEJM) published a study today that shows Afinitor® (everolimus) tablets plus best supportive care (BSC) more than doubled progression-free survival (PFS), or time without tumor growth, versus placebo plus BSC in patients with advanced pancreatic neuroendocrine tumors (NET)[1].
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