Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| TABLE OF CONTENTS | |||||||||||||||||||||||||||||||||||||||||
| September 2016 Volume 15 Number 9 | Advertisement | ||||||||||||||||||||||||||||||||||||||||
In this issue
|
| ||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Comment: Accelerating global innovation to address antibacterial resistance: introducing CARB-X Kevin Outterson, John H. Rex, Tim Jinks, Peter Jackson, John Hallinan, Steve Karp, Deborah T. Hung, Francois Franceschi, Tyler Merkeley, Christopher Houchens, Dennis M. Dixon, Michael G. Kurilla, Rosemarie Aurigemma & Joseph Larsen p589 | doi:10.1038/nrd.2016.155 A global response to the chronic shortfall in antibiotic innovation is urgently needed to combat antimicrobial resistance. Here, we introduce CARB-X, a new global public-private partnership that will invest more than US$350 million in the next 5 years to accelerate the progression of a diverse portfolio of innovative antibacterial products into clinical trials. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||||||
| Pharma pumps up anti-tau Alzheimer pipeline despite first Phase III failure Asher Mullard p591 | doi:10.1038/nrd.2016.176 AbbVie, Bristol-Myers Squibb, Genentech, Janssen and Merck & Co. have all advanced anti-tau candidates into Phase I trials in the hunt for drugs that can modify the course of Alzheimer disease. | |||||||||||||||||||||||||||||||||||||||||
| Sickle cell solutions in sight Katie Kingwell p593 | doi:10.1038/nrd.2016.177 New targets, new drug modalities and new business strategies are drawing long-awaited attention to sickle cell disease. | |||||||||||||||||||||||||||||||||||||||||
| NEWS IN BRIEF Leading microbiome-based therapeutic falters in Phase II trial Asher Mullard p595 | doi:10.1038/nrd.2016.181 | |||||||||||||||||||||||||||||||||||||||||
| mRNA-based drug approaches Phase I milestone Asher Mullard p595 | doi:10.1038/nrd.2016.182 | |||||||||||||||||||||||||||||||||||||||||
| EMA rewrites Phase I guidelines in aftermath of FAAH tragedy Asher Mullard p595 | doi:10.1038/nrd.2016.183 | |||||||||||||||||||||||||||||||||||||||||
| BIOBUSINESS BRIEFS Trial watch: Impact of genetically supported target selection on R&D productivity Mark R. Hurle, Matthew R. Nelson, Pankaj Agarwal & Lon R. Cardon p596 | doi:10.1038/nrd.2016.164 | |||||||||||||||||||||||||||||||||||||||||
| BIOBUSINESS BRIEFS Deal watch: Galderma pursues 'itchy cytokine' by licensing antibody from Roche's Chugai Megan Cully p597 | doi:10.1038/nrd.2016.165 | |||||||||||||||||||||||||||||||||||||||||
| AN AUDIENCE WITH Melissa Paoloni p598 | doi:10.1038/nrd.2016.174 Melissa Paoloni, an architect of the I-SPY 2 trial at QuantumLeap Healthcare Collaborative, discusses the evolution of one of the first adaptive, umbrella trials. | |||||||||||||||||||||||||||||||||||||||||
| FROM THE ANALYST'S COUCH The bladder cancer drug market Khurram Nawaz & Rachel M. Webster p599 | doi:10.1038/nrd.2016.141 Traditional cytotoxic chemotherapies have been the mainstay of treatment for bladder cancer for decades, but targeted biologics are now becoming available. This article analyses the late-stage pipeline for bladder cancer and the impact of new drugs in this rapidly growing market. | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| REVIEWS | Top | ||||||||||||||||||||||||||||||||||||||||
| Twenty years on: the impact of fragments on drug discovery Daniel A. Erlanson, Stephen W. Fesik, Roderick E. Hubbard, Wolfgang Jahnke & Harren Jhoti p605 | doi:10.1038/nrd.2016.109 Fragment-based methods have made substantial contributions to drug discovery in the past 20 years, particularly for challenging targets. Erlanson and colleagues discuss progress in the field, key aspects such as the design of fragment libraries and the choice of screening technique, and how current challenges in fragment-based drug discovery might be overcome. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| Novel therapeutic strategies targeting fibroblasts and fibrosis in heart disease Robert G. Gourdie, Stefanie Dimmeler & Peter Kohl p620 | doi:10.1038/nrd.2016.89 The focus of cardiovascular research has changed over the decades, and non-myocytes, including fibroblasts, are becoming increasingly central to our understanding of cardiac function. Kohl and colleagues discuss cardiac fibroblasts, their origins and their expanding roles in homeostasis and tissue repair, and highlight opportunities for therapeutic intervention. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| Targeting adipose tissue in the treatment of obesity-associated diabetes Christine M. Kusminski, Perry E. Bickel & Philipp E. Scherer p639 | doi:10.1038/nrd.2016.75 Adipose tissue may become severely dysfunctional during obesity, resulting in disrupted metabolic homeostasis and ultimately type 2 diabetes. Here, Scherer and colleagues provide an overview of adipose tissue development, function and homeostasis, focusing on emerging potential strategies for targeting this organ in the treatment of obesity-associated diabetes. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| Corrigendum: Remyelination researchers regroup after proof-of-concept setback in multiple sclerosis Asher Mullard p660 | doi:10.1038/nrd.2016.172 Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| Corrigendum: Oncolytic viruses: a new class of immunotherapy drugs Howard L. Kaufman, Frederick J. Kohlhapp & Andrew Zloza p660 | doi:10.1038/nrd.2016.178 Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
| Advertisement | |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
| *2015 Journal Citation Report (Thomson Reuters, 2015) |
You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/myaccount For further technical assistance, please contact our registration department For print subscription enquiries, please contact our subscription department For other enquiries, please contact our feedback department Nature Publishing Group | One New York Plaza, Suite 4500 | New York | NY 10004-1562 | USA Nature Publishing Group's worldwide offices: Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at The Campus, 4 Crinan Street, London, N1 9XW. © 2016 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. |
No comments:
Post a Comment