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BioWorld - Monday, December 15, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 1, 2009

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[123I]MNI-420 shows promise for imaging A2A receptors in the brain

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Novel antimalarials reported by the Instituto Nacional de Pesquisas da Amazonia

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University of Sydney claims new series of translocator protein ligands

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Institut Pasteur, CNRS, INSERM design novel anti-HIV inhibitors

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Hong Kong University of Science and Technology describes novel NMDA antagonists

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High Point Pharmaceuticals discloses inhibitors of TNF-alpha production and PDE4

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Immunoadhesins for human IL-10, a novel approach in cancer immunotherapy

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Kyowa Hakko Kirin reports results from first quarter 2009

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Clinuvel receives European approval to initiate phase III trial of afamelanotide in EPP

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Nuevolution and Novartis sign drug discovery collaboration involving Chemetics

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Piramal Life Sciences completes ascending-dose phase I studies of P-1736 in diabetes

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FDA accepts Pozen's NDA for Vimovo in OA, RA and AS

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Lumavita is granted marketing authorization in Switzerland for pentamycin for vaginitis

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CRTH2 receptor antagonists in early development at Argenta Discovery

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FDA grants orphan drug designation to Quinazoline-495 for spinal muscular atrophy

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FDA Advisory Committee to discuss Genzyme's sNDA for Clolar in adult AML

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Effect of rosuvastatin on atrial fibrillation in heart failure patients unclear

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PLATO study: reduced cardiovascular events with ticagrelor versus clopidogrel in ACS

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Schering-Plough completes recruitment into phase I trial of SCH-900795 for influenza

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Delcath Systems enrolls 90% of patients into phase III clinical trial of PHP in metastatic melanoma

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Otamixaban superior to unfractionated heparin in non-S-T segment ACS patients

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NovaBiotics completes phase I of phase I/IIa clinical trial of Novexatin for fungal nail infection

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Studies analyze the benefit of ivabradine in patients with coronary artery disease

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Pfizer investigating 5-HT2C agonists for serotonin-related disorders

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Antisoma completes enrollment into phase III trial of ASA-404 in NSCLC

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FDA accepts for review Johnson & Johnson's complete response letter for ceftobiprole NDA

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Shire submits NDA to FDA for velaglucerase alfa and reports results from phase III trials

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