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BioWorld - Friday, January 30, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 5, 2008

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Benzofuran analogues inhibit amyloid-beta aggregation

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Preclinical studies demonstrate PSN-119-2's potential as an antidiabetic with anorectic effects

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First-in-man study supports bevacizumab-eluting stent development

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Alexza's Staccato loxapine phase III trial in schizophrenic patients meets primary endpoint

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SAR-114646 prevents ventricular fibrillation without prolonging ventricular repolarization in dogs

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YSPSL safe in phase I/II study in renal transplant patients

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Duloxetine shows promise in premenstrual dysphoric disorder in preliminary study / News in Context

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Pharmaleads reports on dual NEL/APN inhibitor for pain

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Integral Molecular initiates NIAID sponsored R&D program in influenza inhibitors

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New treatment options for neurological disorders disclosed in recent patents

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Pfizer and Medivation sign global agreement to codevelop and market Dimebon

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Neurologix licenses XIAP gene for treatment of HD from Aegera

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Opexa and MRF sign research collaboration in MS to support development of Tovaxin

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Optimer completes enrollment in second phase III prulifloxacin trial

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Acucela and Otsuka enter agreement for ACU-4429 in dry AMD

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FDA grants fast track designation to Neurotech's NT-501 for retinitis pigmentosa and dry AMD

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Pharmaxis enrolls patients in second pivotal phase III cystic fibrosis trial

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Ablynx and Merck Serono to codiscover and codevelop Nanobodies

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Antisoma commences phase II trial of AS-1411 in renal cell carcinoma

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Recent patents describe new antidiabetic agents

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Cytotopia starts enrollment in phase II CYT-997 study in glioblastoma multiforme

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Novel therapeutic agents for obesity reported in recent Taisho patent

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ImClone submits sBLA for Erbitux in first-line head and neck cancer

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Phase III aclidinium studies show statistical significance in patients with COPD

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Teva and Barr receive FTC request for additional acquisition information

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Zentiva's Board continues to advise shareholders to reject sanofi takeover offer

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Celator receives FDA orphan drug designation for anticancer agent CPX-351

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