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BioWorld - Sunday, December 14, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Oct. 30, 2007

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Response rates not reduced by neutralizing antibodies to certolizumab pegol

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Targacept to develop TC-5214 as augmentation therapy for depression

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Novel dual adenosine A1 and A2A antagonist improves motor and cognitive function in PD models

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Combination of morphine and new TRPV1 antagonist shows promise in bone cancer pain

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Unigene successfully completes oral calcitonin study

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Positive interim phase II results reported for the immunosuppressant LCP-Tacro

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Genta files appeal to FDA over non-approval of Genasense for chronic lymphocytic leukemia

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VIA Pharmaceuticals plans third phase II trial of VIA-2291 for acute coronary syndrome

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Recent Novo Nordisk patent discloses novel antiobesity agents

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FDA approves ANG-1005 for phase I/II clinical development

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Recent Synta and Novartis patents divulge novel immunomodulatory agents

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New therapeutic agents for cancer covered in recent patent literature

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Isis to receive funding for IND-enabling studies on antisense drug for Huntington's disease

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UCB initiates phase III clinical trials of brivaracetam for partial-onset epilepsy

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Panacos announces preliminary results from the 300 mg cohort in a phase IIb trial of bevirimat

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Clinical data on apoE-mimetic peptides in neurological injury

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Positive phase III results for difluprednate for eye inflammation following ocular surgery

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Positive phase III trial results announced for The Medicine Company's Cleviprex

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Flamel Technologies announces positive results from clinical trial of IFN-alpha-XL

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Chugai reports third quarter 2007 results

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Preclinical antidepressant/anxiolytic effects of the neuronal nicotinic receptor antagonist TC-5214

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SSR-103800, a GlyT1 inhibitor, alleviates hyperactivity in a transgenic mouse model of schizophrenia

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Novel platinum-based compounds with improved in vivo activity on human xenograft models

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Onconova presents new JAK2 inhibitor for the treatment of leukemia

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Johnson & Johnson Pharmaceutical submits NDA for paliperidone palmitate

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FDA approves Tasigna for CML patients with resistance/intolerance to current therapy

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