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August 2013 Volume 12 Number 8 | Advertisement | ||||||||||||||||||||||||||||||||||||
In this issue Comment News and Analysis Research Highlights Reviews Correspondence
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In this issue p561 | doi:10.1038/nrd4076 Full Text | |||||||||||||||||||||||||||||||||||||
Comment: Towards a prevention model of health care Alasdair Breckenridge & Hans-Georg Eichler p563 | doi:10.1038/nrd4077 Health-care budgets are largely spent on treating the complications of chronic diseases, many of which have preventable risk factors. Here, we discuss some of the key issues in the necessary move towards a 'prevention model' of health care. Full Text | PDF | |||||||||||||||||||||||||||||||||||||
NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
Revolution dawning in cardiotoxicity testing Kelly Rae Chi p565 | doi:10.1038/nrd4083 Stem cell technology and computational modelling offer the promise of reducing the current burden of cardiotoxicity assessment. | |||||||||||||||||||||||||||||||||||||
NEWS IN BRIEF EMA backs approval of first biosimilar monoclonal antibodies p568 | doi:10.1038/nrd4096 | |||||||||||||||||||||||||||||||||||||
FDA approvals for first half of 2013 p568 | doi:10.1038/nrd4097 | |||||||||||||||||||||||||||||||||||||
End of the line for PPAR modulators? p568 | doi:10.1038/nrd4098 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Trial Watch: Phase II and Phase III attrition rates 2011-2012 John Arrowsmith & Philip Miller p569 | doi:10.1038/nrd4090 | |||||||||||||||||||||||||||||||||||||
PATENT WATCH Isolated DNA patent ban creates muddy waters for biomarkers and natural products Charlotte Harrison p570 | doi:10.1038/nrd4084 | |||||||||||||||||||||||||||||||||||||
AN AUDIENCE WITH Lee M. Ellis p572 | doi:10.1038/nrd4085 The lead author of the ASCO's draft guidelines to "raise the bar" for cancer clinical trials discusses the aims and potential impact of the guidelines on anticancer drug development. | |||||||||||||||||||||||||||||||||||||
FROM THE ANALYST'S COUCH Novelty in the target landscape of the pharmaceutical industry Pankaj Agarwal, Philippe Sanseau & Lon R. Cardon p575 | doi:10.1038/nrd4089 Agarwal and colleagues present an analysis of the overlap in the drug targets that are being pursued across the industry, which indicates that more than half of the novel drug targets in current pipelines are being pursued by only one company. | |||||||||||||||||||||||||||||||||||||
REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Article series: A guide to drug discovery Validating therapeutic targets through human genetics Robert M. Plenge, Edward M. Scolnick & David Altshuler p581 | doi:10.1038/nrd4051 Many clinical trial failures can be traced back to the limited predictive value of preclinical models of disease. Plenge and colleagues discuss how knowledge from human genetics, such as naturally occurring mutations in humans that affect the activity of particular proteins, can be used as a tool to more effectively prioritize molecular targets in drug development. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Novel therapies for hepatitis C — one pill fits all? Michael P. Manns & Thomas von Hahn p595 | doi:10.1038/nrd4050 It has been 25 years since the hepatitis C virus (HCV) was discovered. Now, pipelines are bristling with exciting new direct-acting antiviral drugs, many of which are in late-stage clinical trials. In this Review, Manns and von Hahn examine the future of anti-HCV therapy, the prospect of all-oral interferon-free treatment regimens, and discuss the key challenges faced by clinicians and drug developers. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Therapeutic modulators of STAT signalling for human diseases Gabriella Miklossy, Tyvette S. Hilliard & James Turkson p611 | doi:10.1038/nrd4088 Members of the signal transducer and activator of transcription (STAT) protein family are implicated in a variety of diseases. In particular, aberrant activation of STAT3 is known to promote malignant transformation. In this Review, Turkson and colleagues discuss the various therapeutic approaches used to modulate the activation of the different STAT family members, which include dimerization inhibitors, tyrosine kinase inhibitors and DNA decoys. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Emerging paradigms in GPCR allostery: implications for drug discovery Denise Wootten, Arthur Christopoulos & Patrick M. Sexton p630 | doi:10.1038/nrd4052 Allosteric ligands bind to G protein-coupled receptors at a site distinct from the endogenous ligand. This Review discusses the potential advantages that allosteric ligands could hold, and highlights how the complexity of their actions provides both challenges and opportunities for drug screening. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
CORRESPONDENCE | Top | ||||||||||||||||||||||||||||||||||||
Correspondence: The 'rule of three' for fragment-based drug discovery: where are we now? Harren Jhoti, Glyn Williams, David C. Rees & Christopher W. Murray p644 | doi:10.1038/nrd3926-c1 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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*2012 Journal Citation Report (Thomson Reuters, 2013) |
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