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BioWorld - Sunday, December 7, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Aug. 7, 2009

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Novel anticancer compounds in early development at Pharminox

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Dainippon Sumitomo Pharma discovers new renin inhibitors for the treatment of hypertension

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HDAC inhibitors claimed by CrystaX Pharmaceuticals for cancer treatment

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Debiopharm and Mercury sign exclusive license agreement for Debio-0930

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Novartis initiates shipments of seasonal flu vaccine Fluvirin to U. S. for 2009-2010 season

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FDA extends PDUFA date for Pennsaid NDA to November 2009

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FDA accepts for review Kamada's BLA for IV-AAT for alpha-1 antitrypsin deficiency

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FDA approves Firmagon name for Ferring's prostate cancer treatment degarelix

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Progenics and Wyeth submit applications to FDA and EMEA for Relistor prefilled syringes

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Phase Ib data show antitumor activity of low-dose NGR-hTNF in advanced solid tumors

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Carisbamate reduces alcohol preference and intake in alcohol-preferring rats

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No difference in viral dynamics in ABC/3TC and TDF/FTC in ART-naive HIV-1 subjects

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Mirabegron does not affect PK, PD and safety profiles of metformin in healthy adults

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EMEA withdraws marketing authorization for Posaconazole SP

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Cilostazol confers neuroprotection in rat model of cerebral hypoperfusion

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TRPV1 vanilloid receptor antagonists disclosed by Glenmark Pharmaceuticals

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Vereniging VU-Windesheim presents H4 receptor ligands for the treatment of inflammatory disorders

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PPAR agonists synthesized for the treatment or prevention of diabetes at sanofi-aventis

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Labopharm files NDS with Health Canada for formulation of antidepressant trazodone

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NicOx to reacquire development and commercialization rights to PF-03187207 from Pfizer

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Bellicum initiates dosing in phase I/II clinical trial of BP-GMAX-CD1 in prostate cancer

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EMEA grants orphan drug designation to Aradigm's inhaled liposomal ciprofloxacin in CF

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European Commission grants marketing authorization to Genzyme's Mozobil

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ProStrakan submits Abstral NDA to FDA for breakthrough cancer pain

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Galapagos reports results from phase I trial of GLPG-0259 in rheumatoid arthritis

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FDA extends PDUFA date from August to November 2009 for NeurogesX's Qutenza NDA

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