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BioWorld - Tuesday, December 16, 2025
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BioWorld Science
May 21, 2009
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TLK-58747, a DNA alkylator, shows broad antitumor activity and less toxicity in preclinical studies
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CpG-28 appears to benefit some recurrent glioblastoma patients in phase II study
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Small-molecule mTOR inhibitor AZD-8055 shows potent antitumor activity in preclinical studies
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Sanofi-aventis and DNDi sign collaboration agreement for fexinidazole for sleeping sickness
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GSK presents update on development of A (H1N1) adjuvanted influenza vaccine
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Merck Serono withdraws offer for reproductive technology company MediCult
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PF-3084014 displays preclinical antitumor activity in several models
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GlaxoSmithKline targets AKT1 with GSK-1720070
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Second generation proteasome inhibitor developed at Millennium Pharmaceuticals
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Novel polyene compound, corifungin, displays potent antifungal activity in vitro
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Biovail acquires worldwide rights to tetrabenazine from Cambridge Laboratories
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Biopure presents an update on the NMRC's clinical development of Hemopure
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Genentech and Biogen Idec submit two sBLAs to FDA for Rituxan in CLL
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GW Pharmaceuticals files regulatory submission in the U.K. and Spain for Sativex in MS
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IDMB recommends continuation of phase III AGENDA trial of Genta's Genasense
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Endotis Pharma reports successful completion of phase I EP-42675 program
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Janssen claims novel adenosine A2A receptor antagonists for neurodegenerative conditions
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Merck KGaA discovers SGLT inhibitors for the treatment of diabetes
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Preclinical studies point to potential of GS-9411 for cystic fibrosis
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Eisai claims novel cytidine deaminase inhibitors for the treatment of cancer
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Active first quarter at Bristol-Myers Squibb
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Younger macular degeneration patients more likely to benefit from VEGF Trap-Eye
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Potassium channel blocker WYE-160020 reduces atrial fibrillation inducibility in canine models
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Pharmacologic chaperone of mutant opsin, BIK-381, for the treatment of retinal degeneration
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Mipomersen study meets endpoints in homozygous familial hypercholesterolemia
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First two stages of Verona's phase I/IIa RPL-554 trial yields positive results
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FDA grants orphan drug designation for MediGene's EndoTAG-1
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