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| September 2014 Volume 13 Number 9 | Advertisement | ||||||||||||||||||||||||||||||||||||
| In this issue
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| Comment: Getting real in clinical trials John Parkinson p639 | doi:10.1038/nrd4415 How can real-world data from electronic health records be harnessed to improve the effectiveness and efficiency of clinical trials? Full Text | PDF | |||||||||||||||||||||||||||||||||||||
| NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
| Massive schizophrenia genomics study offers new drug directions Elie Dolgin p641 | doi:10.1038/nrd4411 But much more basic research on disease pathways is needed to entice more pharmaceutical companies back to the field. | |||||||||||||||||||||||||||||||||||||
| Bank tests drug development waters Asher Mullard p643 | doi:10.1038/nrd4412 The European Investment Bank has invested €75 million in a risk-sharing drug development deal with the pharmaceutical company UCB, potentially opening up a new source of research and development (R&D) funding. | |||||||||||||||||||||||||||||||||||||
| NEWS IN BRIEF Ebola outbreak triggers new development programmes p644 | doi:10.1038/nrd4424 | |||||||||||||||||||||||||||||||||||||
| FDA approves first PI3K inhibitor p644 | doi:10.1038/nrd4425 | |||||||||||||||||||||||||||||||||||||
| FDA approves second transgenic milk drug p645 | doi:10.1038/nrd4426 | |||||||||||||||||||||||||||||||||||||
| BIOBUSINESS BRIEFS Trial watch: Atopic dermatitis therapy breakthrough on the horizon? Megan Cully p645 | doi:10.1038/nrd4414 | |||||||||||||||||||||||||||||||||||||
| Market watch: A framework for biomedical innovation in emerging markets Ajay Gautam & Steve Yang p646 | doi:10.1038/nrd4413 | |||||||||||||||||||||||||||||||||||||
| PATENT WATCH Stelara safe after IL-12 antibody dispute Charlotte Harrison p647 | doi:10.1038/nrd4423 | |||||||||||||||||||||||||||||||||||||
| AN AUDIENCE WITH Bob More p648 | doi:10.1038/nrd4421 Bob More, venture capitalist with the Bill and Melinda Gates Foundation, discusses the challenges of aligning financial and philanthropic interests. | |||||||||||||||||||||||||||||||||||||
| FROM THE ANALYST'S COUCH The HIV pipeline Angel Wong p649 | doi:10.1038/nrd4364 The developmental pipeline of HIV antiretroviral therapies is large and diverse, spanning a number of different drug classes. This article provides an overview of the agents in development, including combination therapies, and an analysis of the market for current and future HIV treatments. | |||||||||||||||||||||||||||||||||||||
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| REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
| Overcoming the challenges in administering biopharmaceuticals: formulation and delivery strategies Samir Mitragotri, Paul A. Burke & Robert Langer p655 | doi:10.1038/nrd4363 Biological drugs offer high specificity and potency, but their formulation and delivery pose substantial challenges. Here, the authors highlight recent advances in formulation strategies, describe current and emerging delivery routes and review the potential of targeted and intracellular delivery of biologics. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
| Histone deacetylases and their inhibitors in cancer, neurological diseases and immune disorders Katrina J. Falkenberg & Ricky W. Johnstone p673 | doi:10.1038/nrd4360 Histone deacetylases (HDACs) are a class of epigenetic enzymes that remove acetyl groups from lysine residues on histones and other proteins. In this Review, the authors highlight the role of HDACs in cancer, neurological diseases and immune disorders, and discuss the development of small-molecule inhibitors. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
| Opportunities and challenges in the discovery of allosteric modulators of GPCRs for treating CNS disorders P. Jeffrey Conn, Craig W. Lindsley, Jens Meiler & Colleen M. Niswender p692 | doi:10.1038/nrd4308 G protein-coupled receptors (GPCRs) are highly successful drug targets, particularly for central nervous system (CNS) disorders. Compared to traditional drugs that target the orthosteric ligand-binding site of GPCRs, allosteric modulators have the potential to achieve greater subtype selectivity and allow the normal function of endogenous ligands to be preserved. Conn and colleagues reflect on the key principles for successful optimization of GPCR allosteric modulators. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
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| Erratum: Harnessing the informatics revolution for neuroscience drug R&D Husseini K. Manji, Thomas R. Insel & Vaibhav A. Narayan p709 | doi:10.1038/nrd4431 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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| *2013 Journal Citation Report (Thomson Reuters, 2014) |
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