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BioWorld - Saturday, June 6, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 4, 2008

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Lower diabetes rate seen with voclosporin compared to tacrolimus in renal transplant patients

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Analyses reveal effects of sorafenib in hepatocellular carcinoma

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Novel agents for bone disorders disclosed in recent Sungkyunkwan University patent

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TorreyPines' NGX-267 meets primary endpoint in xerostomia phase II trial

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Phase II study results reported for cardiovascular disease candidate VIA-2291

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Questcor resubmits sNDA to FDA for H.P. Acthar Gel for infantile spasms

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TransMolecular reaches SPA agreement with FDA for 131I-TM-601 phase III trial

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Two pivotal HZT-501 phase III trials meet primary endpoints

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NMRC submits revised IND to FDA to conduct Op RESUS trial of Biopure's Hemopure

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Morphotek initiates phase II study of farletuzumab in platinum-resistant ovarian cancer

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NPS initiates enrollment in phase III STEPS study of Gattex in short bowel syndrome

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Mechanistically distinct drugs developed by PainCeptor, effective in pain models

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New positive modulator of GABA-B receptors identified at Novartis

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Recent Eisai and Scripps patents report novel antiinfective agents

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Novel diagnostic agents imparted in recent patents

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Twice-daily dosing of enzastaurin not feasible in glioma patients

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Gene transfer of VEGF and HGF improves limb ischemia

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HIV candidate VCH-286 safe, well tolerated in phase I study

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Atorvastatin/fenofibrate tablet more effective than components in dyslipidemia

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Azarga approved by EMEA for glaucoma or ocular hypertension

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FDA grants orphan drug designation for antineoplaston treatment for gliomas

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Geron initiates phase I vaccine candidate trial targeting telomerase

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Genta receives FDA complete response letter for Genasense in CLL

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Sucampo completed enrollment and initial dosing in two phase III trials of Amitiza in OBD

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Eisai to initiate head-to-head clinical trial of Dacogen and Vidaza in MDS

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FDA grants approval to PharmaEngine's IND for phase II study of PEP-02 in pancreatic cancer

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Wyeth submits MAA in Europe for13-valent vaccine for pneumococcal disease

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