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

BioWorld Science

Dec. 20, 2007

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Novel oncolytic drugs revealed in recent patent literature

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Phase I studies of AVE-9633, AVE-1642 reported

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Studies show benefit with quetiapine in bipolar and borderline personality disorders

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Cognition improved in schizophrenic patients given rivastigmine

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Sirtris reports positive data from study of SIRT1 in preclinical model of type 2 diabetes

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Recent patents report new antiobesity agents

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Cleveland BioLabs reports positive results from mouse study of CBLB-612

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Discovery of novel analgesic agents reported

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Inhibitex reports positive results from phase I clinical trial of FV-100

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Wyeth Pharmaceuticals submits clinical study reports of Viviant to supplement pending NDA

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IDM Pharma provides update on development of mifamurtide, Uvidem and IDM-2101

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Anti-KIR monoclonal antibody enhances NK cell killing activity in vitro and in vivo

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Improved pharmacokinetic profile of novel recombinant FVII fusion protein

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Shire acquires rights to AT-1001 from Alba Therapeutics

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DiaMedica receives Polish regulatory clearance for phase II human study of DM-83

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T cells expressing costimulatory ligands, a novel approach in cancer immunotherapy

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GlaxoSmithKline exercises option to further develop and commercialize Exelixis' XL-880

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Pharmexa updates and extends research and license agreement with Lundbeck for PX-106

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Oncothyreon to receive payment through Stimuvax agreement with Merck KGaA

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Ambrx enters collaboration agreement with Lilly for novel drug treatments

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Actelion reports preliminary data from bosentan proof-of-concept cancer study

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Biovitrum successfully completes phase I BVT-74316 study

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Idera and Merck KGaA collaborate on development of TLR9 agonists for cancer

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Phase IIa study commences for delta opioid agonist ADL-5859 in neuropathic pain

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Kiadis Pharma successfully completes end of phase II meeting with FDA for Reviroc

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Positive interim results reported from Rapinyl phase III clinical trial

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Lundbeck and Takeda advance Lu-AA-21004 into phase III

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Genzyme is granted European CE mark for single-treatment Synvisc-One for osteoarthritis

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