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BioWorld - Friday, December 5, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

July 12, 1999

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Vancomycin-tolerant S. pneumoniae detected and analyzed

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Delta-opioid receptor activation as preconditioning, similar to natural hibernation

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Zanamivir shows promise in influenza prevention

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Mallinckrodt and SmithKline Beecham sign copromotion agreement for ADHD drug

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Patient enrollment completed in study of shortened Targis treatment for BPH

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Digital Gene Technologies and Recordati reach milestone in atherosclerosis agreement

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Connetics enters licensing and development agreement with Paladin for ConXn

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AxyS Pharmaceuticals forms new subsidiary

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Company Profile: Maret

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BTG acquires novel technology for treatment of HIV

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Clinical trials commence for two new Eisai compounds

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Allergan ciclosporin NDA up for review this month by advisory committee

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New orally bioavailable salt of ET antagonist prepared by SmithKline Beecham

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Antitumor and antibacterial compound isolated from cultures of Streptomyces at Kyowa Hakko

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Lilly designs selective 5-HT1A antagonists especially for nicotine/tobacco withdrawal

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Human Genome Sciences discovery may lead to novel immunotherapies and vaccines

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P2X7 receptor antagonists described in recent patent literature

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Aromatic hydrazones from Uniroyal with anti-HIV-1 activity encompassing mutant strains

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Anti-CD154 antibody facilitates islet allograft survival in highly relevant preclinical model

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Potential of cerebrocrast in diabetes suggested by animal data

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INO-5042: new agent for venous insufficiency proves effective in various animal models

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Orphan Medical, Pierre Fabre sign letter of intent to license Busulfex

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CAT gets U.K. approval to begin phase II trials of novel glaucoma treatment

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Johns Hopkins team identifies unusually promising new treatment for ALS

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E.U.-wide approval obtained for Ziagen

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Inhibitors of P. carinii and T. gondii DHFR developed at U.S. universities

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Allelix characterizes first-generation NGF receptor antagonist with antiallodynic properties

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Rapamune up for FDA advisory committee review in late July

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