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BioWorld - Monday, April 20, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 14, 2007

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Zevalin meets primary endpoint in follicular non-Hodgkin's lymphoma trial

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Plasmid-mediated delivery of IGF-1 gene useful in mouse model of ALS

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GSK and Oncomed form strategic alliance to develop cancer stem cell antibodies

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Weight loss seen with taranabant in obese subjects

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KW-2449 safe and well tolerated in phase I study in hematologic malignancies

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Platelet counts, safety assessed in phase I trial of LGD-4665 in healthy males

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Responses seen in immune thrombocytopenic purpura patients given R-788

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Genesis Bioventures changes name to Abviva

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Reckitt Benckiser acquires Adams Respiratory for approximately USD 2.3 billion

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Recent patents disclose novel agents for obesity and disorders of lipoprotein metabolism

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Gene Logic will be renamed Ore Pharmaceuticals

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Bristol-Myers and Gilead enter agreement to commercialize Atripla in Europe

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TorreyPines Therapeutics reports positive results from phase I clinical trial of NGX-426

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Novel immunosuppressant agents disclosed in recent Actelion patent

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Novel therapeutic agents for glaucoma reported in recent Allergan patents

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UCB reports positive results from phase III trial of Vimpat for diabetic neuropathic pain

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Panacos reports positive results from 350 mg cohort of phase IIb study of bevirimat

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Avax reports positive results from phase I/II study of MVax for stage 3 and 4 melanoma

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SIRT1 activators show therapeutic potential in animal models of type 2 diabetes

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Orexigen initiates phase III trial of Contrave for obesity

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Data Safety Monitoring Board recommends continuation of MAESTRO-03 trial of MBP-8298

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Roche files IND application with FDA for Genmab antibody for asthma

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FDA accepts EntreMed's IND application for Panzem for rheumatoid arthritis

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Vivus initiates EQUATE phase III trial of Qnexa in obese patients with co-morbidities

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FDA accepts for filing two sNDA for Neupro for restless legs syndrome and PD

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FDA deems Neurocrine's NDA for indiplon approvable pending additional safety and efficacy data

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FDA approves BioMarin therapy for PKU

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