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TABLE OF CONTENTS | |||||||||||||||||||||||||||||||||||||
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July 2012 Volume 11 Number 7 | |||||||||||||||||||||||||||||||||||||
| In this issue![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]()
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In this issue p499 | doi:10.1038/nrd3786 Full Text | |||||||||||||||||||||||||||||||||||||
Comment: New horizons in pharmaceutical regulation Alasdair Breckenridge, Michelle Mello & Bruce M. Psaty p501 | doi:10.1038/nrd3787 Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
Anticancer TLR agonists on the ropes Malini Guha p503 | doi:10.1038/nrd3775 Toll-like receptor agonists have hit another setback with the Phase II failure of Idera's IMO-2055, but these immunotherapies may still make a comeback if appropriate combinations with vaccine antigens or anticancer drugs can be identified. | |||||||||||||||||||||||||||||||||||||
Drug repurposing programmes get lift off Asher Mullard p505 | doi:10.1038/nrd3776 What will schemes designed to get industry's discarded drug candidates into the hands of academic researchers deliver? | |||||||||||||||||||||||||||||||||||||
NEWS IN BRIEF Antibiotic R&D gets a dose of funding | FDA on track with first-half approvals | SGLT2, take two? p507 | doi:10.1038/nrd3784 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Deal watch: Epizyme–Celgene deal signals interest in new class of epigenetic drugs Alexandra Flemming p508 | doi:10.1038/nrd3772 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Market watch: Upcoming market catalysts in Q3 2012 Robert Jeng p508 | doi:10.1038/nrd3773 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Regulatory watch: Crossing the regulatory finish line p509 | doi:10.1038/nrd3774 | |||||||||||||||||||||||||||||||||||||
PATENT WATCH China aims to enhance IP laws | Two routes to patent challenge can give different results | 23andMe patent creates a stir | Toll-like receptor agonists and cancer Charlotte Harrison p510 | doi:10.1038/nrd3785 | |||||||||||||||||||||||||||||||||||||
AN AUDIENCE WITH Alan Trounson p512 | doi:10.1038/nrd3769 Alan Trounson, President of the California Institute for Regenerative Medicine, discusses his plans to get more stem cell therapeutics into trials. | |||||||||||||||||||||||||||||||||||||
FROM THE ANALYST'S COUCH FDA advisory committee meeting outcomes Jeffrey F. Smith, Seth A. Townsend, Navjot Singh & Philip Ma p513 | doi:10.1038/nrd3747 This analysis of the outcomes of advisory committee meetings held by the US Food and Drug Administration (FDA) over the past decade investigates issues such as the consistency between advisory committee votes and FDA approval decisions. | |||||||||||||||||||||||||||||||||||||
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PERSPECTIVES | Top | ||||||||||||||||||||||||||||||||||||
OPINION Antibody-enabled small-molecule drug discovery Alastair D. G. Lawson p519 | doi:10.1038/nrd3756 Here, Lawson proposes that the use of antibodies as tools in small-molecule drug discovery — for example, to validate targets, enable crystallography and to constrain proteins for screening — could reduce risks and facilitate the modulation of traditionally intractable targets, such as protein–protein interactions. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Analytical tools for characterizing biopharmaceuticals and the implications for biosimilars Steven A. Berkowitz, John R. Engen, Jeffrey R. Mazzeo & Graham B. Jones p527 | doi:10.1038/nrd3746 Biopharmaceuticals are much more complex than small-molecule drugs, which raises challenging questions for the development and regulatory evaluation of follow-on versions (also known as biosimilars). Jones and colleagues discuss the current state of the art in analytical technologies to assess three characteristics of protein biopharmaceuticals that regulatory authorities have identified as being important for biosimilars: post-translational modifications, three-dimensional structures and protein aggregation. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Ophthalmic drug discovery: novel targets and mechanisms for retinal diseases and glaucoma Kang Zhang, Liangfang Zhang & Robert N. Weinreb p541 | doi:10.1038/nrd3745 During the past decade, there have been substantial advances in our understanding of the pathogenesis and genetics of eye diseases. Focusing on glaucoma and retinal disorders, Zhang and colleagues review the current status of ocular drug therapy, discuss novel agents currently in development and clinical trials and highlight recent advances in drug delivery. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Advancing schizophrenia drug discovery: optimizing rodent models to bridge the translational gap Judith Pratt, Catherine Winchester, Neil Dawson & Brian Morris p560 | doi:10.1038/nrd3649 The paucity of treatments for schizophrenia might be partly due to the lack of suitable animal models in which to assess potential new drugs. Here, the authors highlight how new rodent models that are based on a better understanding of the genetics and neural circuitry underlying schizophrenia could lead to the development of more effective drugs. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Erratum: Busy panels recommend Pfizer's tofacitinib, Arena's lorcaserin and more Asher Mullard p579 | doi:10.1038/nrd3778 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Erratum: Amgen builds secondary hyperparathyroidism pipeline Man Tsuey Tse p579 | doi:10.1038/nrd3791 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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*2010 Journal Citation Report (Thomson Reuters, 2011) |
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