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BioWorld - Tuesday, June 9, 2026
Home » Newsletters » BioWorld Science

BioWorld Science

Oct. 14, 2009

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In vivo data suggest high drug load delivery of 259C/MBX-500 via emulsion formulation

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Antibacterial activity of razupenem further detailed in vitro and in vivo

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Data show Afresa efficacy in diabetes with no significant effects on lung function

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Dalcetrapib effective and well tolerated in diabetes and metabolic syndrome patients

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Recent clinical data show advantages of alogliptin plus pioglitazone combination

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Liraglutide shows advantages over glimepiride in LEAD-2 type 2 diabetes study

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Repeat-dosing toxicology studies of ATL-1103 are completed in mice and primates

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The FDA has granted marketing approval to CSL Behring's Berinert in HAE

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EMEA grants orphan drug designation to AMT-080 for Duchenne dystrophy

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Debiopharm completes European decentralized registration procedure for Decapeptyl

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FDA grants orphan drug designation to MolMed's NGR-hTNF in liver cancer

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ActoGeniX completes phase IIa trial of AG-011 in moderate ulcerative colitis

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BioAlliance granted approval in France to initiate phase I clinical trial of fentanyl

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ImaginAb signs licensing agreement for BZL Biologics' PSMA technology

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Provectus completes patient accrual and initial treatment in phase II trial of PH-10

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Schering-Plough initiates proof-of-concept phase I trial of SCH-900795 influenza vaccine

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Dilafor completes phase I clinical study of DF-02 for the treatment of severe malaria

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MSDC receives grant to study PPAR-sparing insulin sensitizers in AD

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Re-engineered ABY-025 shows specific HER2 binding, favorable biodistribution

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Sulindac exhibits protection against myocardial ischemic damage in preclinical study

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CGI Pharmaceuticals reports Syk inhibitors for the treatment of asthma

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Novel tubulin polymerization inhibitors discovered by Pierre Fabre

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Novel dopamine D2 receptor partial agonists in development at AstraZeneca

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Alkermes reports results from clinical trials of ALKS-33

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Metabolex reports results from two phase I clinical trials of MBX-2982

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FDA and EMEA grant orphan drug status to Antisoma's AS-1411 in AML

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Onyx to acquire Proteolix, along with carfilzomib for multiple myeloma

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