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BioWorld - Saturday, December 27, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Nov. 21, 2008

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Positive results emerge from phase III ALO-01 study in patients with osteoarthritis pain

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rhEPO shows clinical benefits for the treatment of amyotrophic lateral sclerosis

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Cenomed reports on new schizophrenia and posttraumatic stress disorder candidates

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Mutation-specific effects seen with pyrimethamine in familial ALS patients

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Novel means of avoiding opioid-related adverse events reported in recent Progenics patent

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Recent GenkyoTex patent imparts novel therapeutics for cardiovascular disorders

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New antiinflammatory agents reported in recent Biolipox patents

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Alizyme presents update on clinical development activities between July and November 2008

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FDA reschedules Advisory Committee meeting with Novo for liraglutide until April 2009

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Memory completes enrollment in phase II trial of MEM-3454 in CI associated with schizophrenia

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CytRx updates progress of third quarter 2008

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Chelsea Therapeutics completes enrollment in phase II trial of droxidopa in IDH

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GenVec reports interim results from phase III PACT trial of TNFerade

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Phase III studies show vandetanib offers benefit to patients with lung cancer

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BioDelivery Sciences to resubmit REMS for Onsolis to FDA in December 2008

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Karo Bio and Wyeth extend drug discovery collaboration with LXR in inflammatory diseases

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BI-201335 well tolerated, active in treatment-naive and -experienced HCV patients

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Hyperphosphatemia controlled with fermagate in hemodialysis patients

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Elixir's reports results from phase III trial of metformin-mitiglinide therapy

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Telavancin receives favorable recommendation from FDA

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Cougar Biotechnology commences phase I/II CB-7630 trial in breast cancer

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Ortho Biotech submits NDA for trabectedin for relapsed ovarian cancer

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Debiopharm and Aurigene sign licensing agreement for Debio-0617

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Grazax approved in Europe for children with hay fever

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Basilea's Zevtera receives positive opinion from the CHMP

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GlaxoSmithKline receives FDA accelerated approval for Promacta

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