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Novartis Ilaris for use in acute gouty arthritis patients who are not suitable for current treatments. The only approved entirely human monoclonal antibody Ilaris continuously neutralizes interleukin-1 beta thereby inhibiting inflammation. Novartis
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Somatoprim, the somatostatin analog (SSA) based on a novel amino acid composition, demonstrated significant receptor binding and pharmacological profile compared to currently marketed SSAs...The ongoing clinical phase 1b and phase 2a studies in
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Atrial fibrillation is the most common cardiac arrhythmia (irregular heart beat). It is estimated that approximately 6 million individuals in Europe have atrial fibrillation.
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Montenegro expects to get a positive opinion from the EU regarding fulfillment of conditions for the EU accession in October. EU Enlargement Commissioner Stefan Fule will bring the good news to Podgorica on October 13. A day after the European
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Single-tablet regimen, Eviplera, combines Gilead's Truvada (emtricitabine and tenofovir disoproxil (as fumarate)) with Tibotec Pharmaceuticals' non-nucleoside reverse transcriptase inhibitor Edurant (rilpivirine (as hydrochloride)). The submission of
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European Medicines Agency (EMA) for Afinitor (everolimus) tablets as a treatment for pancreatic neuroendocrine tumors (NET). RAD001 In Advanced Neuroendocrine Tumors) trial which demonstrated that the patients with advanced pancreatic NET when
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Nektar receives COMP positive opinion for ovarian cancer drug The European Medicines Agency (EMA) Committee for Orphan Medicinal Products (COMP) has issued a positive opinion on Nektar Therapeutics' application for orphan medicinal product status for
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Benlysta as an add-on therapy in adult patients who are suffering from active autoantibody-positive systemic lupus erythematosus, with a high degree of disease activity (e.g. positive anti-dsDNA and low complement), despite standard therapy...
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Governments European Integration Office Director Milica Delevi says she expects a positive opinion from the European Commission (EC) on Serbia's progress...Right now, my attention is focused on what needs to happen to ensure a positive opinion from
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European Medicines Agency (EMA) for its experimental drug Victrelis (boceprevir) as a treatment for chronic hepatitis C virus (HCV) genotype 1 infection. Victrelis with peginterferon alfa and ribavirin, in adult patients with compensated liver
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