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Home » Newsletters » BioWorld Science

BioWorld Science

March 5, 2008

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Preliminary study shows efficacy of aflibercept in diabetic macular edema

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Phase II study data detail responses to tarenflurbil in mild Alzheimer's disease patients

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Wyeth Pharmaceuticals terminates collaboration agreements with Solvay for bifeprunox

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Pfizer receives approval for sustained-release Norvasc in Japan for hypertension and angina

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GSK launches Imigran subcutaneous self-injection in Japan for migraine and cluster headache

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Crucell enters vaccine development agreement with Wyeth

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Data Safety Monitoring Board recommends continuation of HF-0220 phase II trial

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LifeCycle reports positive top-line results for phase II LCP-Tacro trial

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Paladin files new drug submission for Seasonique in Canada

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Alexza's AZ-104 phase IIa trial meets primary endpoint

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ALK-Abello announces positive third year results from Grazax trial

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Array BioPharma reports positive phase II top-line results for ARRY-797

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Novel agents for glaucoma disclosed in recent Pfizer patents

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NeuroSearch reports positive and confirmatory results from TIPO-2 trial

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Recent Organon and Activesite patents report novel antithrombotic agents

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Novel therapeutic agents for respiratory disorders described in recent Boehringer Ingelheim patent

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Reliable Abeta burden detection with Bayer's novel PET tracer

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New beta3 adrenoceptor agonists may be useful in overactive bladder

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Phase IIa multiple dose AVT-01 study shows safety but does not confirm efficacy

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Results reported for phase II Juvista trial in scar revision and breast augmentation

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FDA approves new dosage strengths of Endo's Opana

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Pfizer to acquire Serenex and the rights to SNX-5422

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Pharmacopeia initiates phase II clinical study of PS-433540 for hypertension

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Data Safety Monitoring Board recommends continuation of Debio-9902 SR trial

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GSK terminates development of Dacart in the treatment of malaria

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MP-376 granted U.S. orphan drug status for the treatment of cystic fibrosis

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Vermillion and Stanford University enter agreement for novel biomarker panel for PAD

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CHMP recommends 300 mg tablet of sanofi-aventis and Bristol-Myers Squibb's Plavix

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FDA grants fast track designation to Bioniche for Urocidin

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