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Wednesday, 01 September 2010
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The lead clinical candidate STX-100 has been granted orphan drug status by the U.S. Food and Drug Administration (FDA) for the treatment of idiopathic pulmonary fibrosis (IPF), a debilitating and almost uniformly fatal disease in which patients experience progressive difficulty breathing due to fibrosis (scarring) of the lung. STX-100 is a novel, investigational, humanized monoclonal antibody that targets integrin αvβ6. Link: http://www.stromedix.com/Stromedix_STX-100_Orphan_Drug_IPF.pdfSource:Stromedix |
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Wednesday, 01 September 2010
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Tuesday, 31 August 2010
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An antibacterial enzyme, lysozyme found in human tears and other body fluids could be applied to certain foods for protection against intentional contamination with anthrax, scientists reported here today at the 240th National Meeting of the American Chemical Society (ACS). Link: http://www.eurekalert.org/pub_releases/2010-08/acs-tsf080910.phpSource:EurekAlert |
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Tuesday, 31 August 2010
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Giving patients with a history of heart attacks a margarine enriched with omega-3 oils in addition to standard drugs appears to make no difference to their chances of having a repeat attack. It is published in the New England Journal of Medicine. Link: http://www.reuters.com/article/idUSLDE67S02520100829Source:Reuters |
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Tuesday, 31 August 2010
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Results from the Phase 2 INNOVATE-PCI study of the investigational antiplatelet drug, elinogrel, the only competitive, reversible direct-acting P2Y12 ADP receptor antagonist were announced. Results in patients undergoing non-urgent percutaneous coronary interventions (PCI) showed that an intravenous (i.v.) and oral elinogrel regimen provided more rapid and greater antiplatelet activity than clopidogrel (Plavix) without a significant increase in the risk of TIMI major and minor bleeding, and was generally well tolerated. These findings establish the basis for clinical dose selection for a pivotal Phase 3 program, which is anticipated to start in the first quarter of 2011. The data were presented today during the Hot Line II - Coronary Artery Disease late-breaker session at the European Society of Cardiology (ESC) Congress in Stockholm. Link: http://www.portola.com/pdfs/Portola_INNOVATE_PCI_ESC.pdfSource:Portola |
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Tuesday, 31 August 2010
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AstraZeneca's MedImmune biologics unit has been asked by U.S regulators for more information on its infant lung drug motavizumab after drug regulatory advisors recommended against approving it in June. The Anglo-Swedish drugmaker's MedImmune unit developed motavizumab to prevent serious respiratory syncytial virus (RSV) in high-risk infants. Link: http://www.reuters.com/article/idCNLDE67T0AY20100830?rpc=44Source:Reuters |
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Tuesday, 31 August 2010
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People at intermediate risk of cardiovascular disease who have high levels of high sensitivity C-reactive protein (hsCRP), a blood marker for inflammation, could benefit from cholesterol-lowering therapy even if their cholesterol is already at desirable levels. Data indicates that people with only a 5 percent to 20 percent risk of having heart disease in the next ten years, but who have high levels of hsCRP could reduce the risk of heart attack and stroke by more than 40 percent. The study is published in Circulation: Cardiovascular Quality and Outcomes, an American Heart Association journal. Link: http://www.sciencedaily.com/releases/2010/08/100824161503.htmSource:ScienceDaily |
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Tuesday, 31 August 2010
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The Company's New Drug Application (NDA) for Iluvien (fluocinolone acetonide intravitreal insert) has been accepted for filing and granted Priority Review status by the U.S. Food and Drug Administration (FDA). Iluvien is Alimera's investigational, sustained drug delivery system that releases sub-microgram levels of fluocinolone acetonide for the treatment of diabetic macular edema (DME). Link: http://investor.alimerasciences.com/releasedetail.cfm?ReleaseID=503420Source:Alimera |
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