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BioWorld - Wednesday, December 17, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 19, 2007

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SONOMA-2 shows effect of alfimeprase on occluded central venous access devices

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New agents for autoimmune disorders and transplant rejection imparted in recent patent literature

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Recent patents disclose new therapeutic agents for HBV and HCV infection

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DuoCort completes enrollment in phase II/III clinical trial of DuoCort for adrenal insufficiency

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Genmab to initiate phase II trial of ofatumumab for relapsing-remitting multiple sclerosis

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BioCancell submits IND application to the FDA for BC-819 in bladder cancer

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LOTS study of Genzyme's Myozyme for Pompe disease meets coprimary efficacy endpoints

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BioMimetic reports positive clinical results for GEM-OS1 for foot and ankle fusion

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The CHMP of the EMEA issues negative opinion on Pharming's MAA for Rhucin

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Novel therapeutic agents for respiratory disorders disclosed in recent patents

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GSK launches ArranonG in Japan for leukemia and malignant lymphoma

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FDA grants fast track designation to Neurologix's gene therapy approach to Parkinson's disease

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Novelos Therapeutics concludes phase Ib trial of NOV-205 for hepatitis C genotype 1

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Increased survival in mouse models of multiple myeloma with Prolexys' new compound

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Dual Akt/p70S6K inhibitor effective against multiple myeloma in vitro

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DCC-2036 shows preclinical antileukemic activity against drug-resistant CML

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Data safety monitoring board recommends continuation of two phase III trials of Hemospan

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European Commission grants marketing authorization for Atripla for HIV-1

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Vasogen and Ferrer begin roll-out of Celacade for heart failure therapy

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Careload LA, a pulmonary arterial hypertension agent, launched in Japan

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Takeda submits indication extension application for Basen in Japan

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FDA approves supplemental indication for Genzyme's Thyrogen in thyroid cancer ablation

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Avastin approved in Europe for first-line treatment of advanced RCC

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Cell Therapeutics to submit MAA for Xyotax in the first quarter of 2008 ahead of schedule

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FDA approves beta-blocker Bystolic for the treatment of hypertension

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Philippine Bureau of Food and Drugs grants product registration for Epeius' Rexin-G

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