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October 2014 Volume 13 Number 10 | Advertisement | ||||||||||||||||||||||||||||||||||||
In this issue Comment News and Analysis Research Highlights Perspectives Reviews
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Comment: Antimicrobial innovation: combining commitment, creativity and coherence Jos W. M. van der Meer, Robin Fears, Dame Sally C. Davies & Volker ter Meulen p709 | doi:10.1038/nrd4448 Urgent action to tackle antimicrobial resistance must take account of all the scientific opportunities available, find new resources to support academia and emphasize the importance of innovation to policy-makers and to the general public.Full Text | PDF | |||||||||||||||||||||||||||||||||||||
NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
Momentum builds around new antibiotic business models Asher Mullard p711 | doi:10.1038/nrd4455 The Innovative Medicines Initiative's DRIVE-AB project joins the fray of task forces working to reinvigorate interest in antibiotics by developing reimbursement models that delink revenue from sales volume. | |||||||||||||||||||||||||||||||||||||
False dawn for cystic fibrosis disease modifiers? David Holmes p713 | doi:10.1038/nrd4456 Recent results have cast doubt over how effective a breakthrough class of cystic fibrosis drugs can be in patients with the most common form of the disease. | |||||||||||||||||||||||||||||||||||||
NEWS IN BRIEF Merck wins first PD1 sprint in US p715 | doi:10.1038/nrd4458 | |||||||||||||||||||||||||||||||||||||
Illuminating interleukin-5 data p715 | doi:10.1038/nrd4459 | |||||||||||||||||||||||||||||||||||||
Reanalyse this p715 | doi:10.1038/nrd4460 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Market watch: Upcoming catalysts in Q4 2014 Andrew Ang p716 | doi:10.1038/nrd4449 | |||||||||||||||||||||||||||||||||||||
Trial watch: Next-generation antimalarial from phenotypic screen shows clinical promise Megan Cully p717 | doi:10.1038/nrd4457 | |||||||||||||||||||||||||||||||||||||
AN AUDIENCE WITH Story Landis p718 | doi:10.1038/nrd4454 Story Landis, ex-Director of the US National Institute of Neurological Disorders and Stroke, discusses how she has worked to address a crisis of basic research funding at the Institute. | |||||||||||||||||||||||||||||||||||||
FROM THE ANALYST'S COUCH The cystic fibrosis drug market Basharut A. Syed & Bashar Hamad p721 | doi:10.1038/nrd4434 Current treatments for cystic fibrosis are largely symptomatic, but the first disease-modifying drug has recently been approved and others are progressing. This article examines the multitude of agents in the clinical pipeline and their potential market impact in the next 5 years. | |||||||||||||||||||||||||||||||||||||
PERSPECTIVES | Top | ||||||||||||||||||||||||||||||||||||
OPINION Caloric restriction mimetics: towards a molecular definition Frank Madeo, Federico Pietrocola, Tobias Eisenberg & Guido Kroemer p727 | doi:10.1038/nrd4391 Caloric restriction can promote health and extend the lifespan of model organisms, and diverse classes of compounds that mimic the biochemical and functional effects of caloric restriction have attracted considerable interest as potential pharmacotherapies for diseases such as diabetes and obesity. Kroemer, Madeo and colleagues propose a unifying definition of caloric restriction mimetics as agents that induce autophagy by promoting protein deacetylation, which could have implications for their development as drugs. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Strategies to improve drug development for sepsis Mitchell P. Fink & H. Shaw Warren p741 | doi:10.1038/nrd4368 Sepsis is a potentially fatal systemic disease that is caused by microbial infection. Despite numerous clinical trials, no specific therapeutic agent has yet been approved for this indication. Here, Fink and Warren consider potential reasons for such failures and suggest possible strategies to overcome ongoing challenges, such as improving clinical trial design. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
mRNA-based therapeutics — developing a new class of drugs Ugur Sahin, Katalin Karikó & Özlem Türeci p759 | doi:10.1038/nrd4278 The therapeutic potential of in vitro-transcribed mRNA (IVT mRNA) extends from prophylactic and therapeutic vaccines to applications such as protein replacement and genome engineering. In this Review, the authors describe the recent developments in the IVT mRNA field, discuss the class-specific challenges with regards to translating IVT mRNA into a biopharmaceutical, and provide an overview of IVT mRNA drugs in development for different indications. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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*2013 Journal Citation Report (Thomson Reuters, 2014) |
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