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BioWorld - Monday, December 8, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Feb. 18, 2002

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Emisphere reports on pipeline progress in 2001

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Rho kinase as a target for drug discovery in Japan

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Preclinical data support development of CS-758 for therapeutic use in fungal infections

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Des-fluoroquinolone exerts potent activity against respiratory and genital Chlamydia

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NO-flurbiprofen more effective and safer than flurbiprofen in accelerating tendon healing

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Teicoplanin-loaded PLGA microspheres potentially useful in musculoskeletal infections

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Novartis licenses AC-5216 from Dainippon

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New antibiotic with selective activity against H. pylori

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Preliminary phase IIIb results reported for transdermal oxybutynin in overactive bladder

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ViroLogic technology used to evaluate Panacos HIV drug candidates

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Phytomedics and Eisai collaborate to discover cancer therapeutics

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Positive preclinical and clinical results for NCX-1015 in IBD and arthritis

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Hollis-Eden signs CRADA for joint development of HE-2100 for radiation damage

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Tranzyme and Gemin X enter neurological drug discovery collaboration

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COLAL-PRED enters late-stage trials for ulcerative colitis

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OP-1 Implant receives Canadian approval

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NeoGenesis and Aventis collaborate on infectious disease drug discovery

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F-12511 reduces hypercholesterolemia and progression of atherosclerotic lesions in rabbit model

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Initiation of phase III trial of secretin in autism; further data analysis from phase II trial

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Mutant heat-labile enterotoxin as a potent adjuvant for oral influenza vaccination

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Results from the TIMI-8 trial confirm unique risk/benefit profile of bivalirudin

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Taisho claims compounds that inhibit the production of 20-HETE

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Compounds that enhance transcription factor AP-1 designed at Active Biotech

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Cyclopentyl carboxamides with potential in female sexual dysfunction

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Merck claims preparation of macrocyclic compounds for treatment of cancer, etc.

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Abbott/Ligand jointly identify selective glucocorticoid modulators

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Ortho-McNeil identifies nonpeptide vasopressin receptor antagonists

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