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BioWorld - Saturday, December 20, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 1, 1999

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Progen receives provisional approval to undertake clinical studies of PI-88 at second site

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KeraVision receives FDA approval to complete enrollment for phase IIIb Intacs trial

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Company Profile: Immucon

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CytRx initiates phase I/II study of Flocor for treatment of acute lung injury

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New anticancer compound from Diatide shown to arrest tumor growth

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Eisai's proton pump inhibitor approved in E.U. for GERD maintenance

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New glycine antagonist added to Glaxo Wellcome's research program

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New cyclopentenopyridine derivatives from Banyu active as ETA antagonists

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Antibacterial quinolines developed at SmithKline Beecham

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Inhibitors of matrix metalloproteinases reported in patent literature by American Cyanamid

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Lotronex NDA gets priority review from FDA

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AGN-194310, a high-affinity RAR antagonist for treating retinoid-induced toxicities

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Dual M2 antagonism/AChE inhibition: an effective approach to treating memory disorders

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Spironolactone continues to provide benefits in patients with heart failure

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Oxazolidinone antibacterial agents synthesized at Bayer

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MS&D's new GABA-A receptor ligands expected to be effective and safe for anxiety, etc.

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Ouabain analogue LND-623 is a more effective and less toxic inotropic agent

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Cerebrus presents new NMDA receptor antagonists with selectivity for cerebellum

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Scotia's Foscan achieves positive results in phase III clinical trial

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Non-halogen-containing PDHK inhibitors designed at Novartis

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RESPECT trial will evaluate effects of lipid reduction on stroke prevention

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More on Lilly's GH secretagogue program, including clinical candidate

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Sulfamide inhibitors of MMPs: synthesis and pharmacological data presented at ACS meeting

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p38 inhibitor RPR-200765A designated candidate for development in arthritis Rx

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Nortran and Hoechst Marion Roussel to develop new antiarrhythmic compounds

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New ulcer drug approved for the first time in Japan

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ACS news: new compounds from Merck & Co. potently and selectively inhibit 5alpha-reductase type 1

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