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

BioWorld Science

Dec. 21, 2004

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Direct antiplatelet effects of the novel engineered human apyrase APT-102

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Preclinical characterization of the orally active factor Xa inhibitor, DU-176b

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Preclinical effects of the novel thrombopoietin receptor agonist, SB-559457, on hematopoietic cells

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Acusphere enrolls 300 in pivotal program for AI-700

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Alcon completes NDA filing for Retaane

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Avanir commences NDA submission for Neurodex

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Updates on Xyotax pivotal studies

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No overall survival benefit with Iressa in ISEL study

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Clevelox ESCAPE-1 study meets objectives

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Positive data from ongoing studies of rhC1INH for hereditary angioedema

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Exelixis plans phase I study of XL-880 for 2005

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Abbott seeks U.S., European approvals of Humira for psoriatic arthritis

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Allos Therapeutics acquires license to chemotherapeutic agent RH1

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CXCR inhibition as a therapeutic strategy in leukemia

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Potential neuroprotective effects for rifampicin in Parkinson's disease

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Fast track designation for Remicade for ulcerative colitis

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Scientists at Pfizer describe a novel series of PDE9 inhibitors

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Abbott discloses MCH receptor antagonists in a recent patent

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Compounds for the treatment of ischemic diseases described in patent literature

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Sankyo patent claims chromane analogues and their use in diabetes, hyperlipidemia, etc.

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A new series of beta3 receptor agonists in early development at Dainippon

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Kyowa Hakko isolates antiinflammatory compound from a natural source

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SB-715992 enters new phase II study for advanced ovarian cancer

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INS-50589 Cardiovascular tested in new phase I study

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Perifosine shows promise in the treatment of metastatic breast cancer

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667-Coumate enters phase I development for breast cancer

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Therapeutic benefits reported for modafinil in cocaine dependence and MDD

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Cardiovascular risks halt use of celecoxib in study/News in Context

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Lundbeck files for E.U. approval of Cipralex for generalized anxiety disorder

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Avastin approved in Switzerland

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New Invirase 500 mg receives FDA approval

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Macugen approved for neovascular AMD

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Myozyme MAA accepted in Europe for Pompe disease

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TAK-559 placed on hold

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