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April 2013 Volume 12 Number 4 | |||||||||||||||||||||||||||||||||||||
In this issue Comment News and Analysis Research Highlights Reviews Correspondence
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In this issue p245 | doi:10.1038/nrd3997 Full Text | |||||||||||||||||||||||||||||||||||||
Comment: Susan R. Forda, Richard Bergström, Magda Chlebus, Richard Barker & Peter Høngaard Andersen p247 | doi:10.1038/nrd3981 Improved R&D models, supported by appropriate regulatory pathways, are needed to provide new drugs with greater efficiency, in a framework that is financially viable for all stakeholders. Here, we present the perspective of the European Federation of Pharmaceutical Industries and Associations on the key areas on which to focus to achieve this. Full Text | PDF Priorities for improving drug research, development and regulation | |||||||||||||||||||||||||||||||||||||
NEWS AND ANALYSIS | Top | ||||||||||||||||||||||||||||||||||||
Antibody drugs set to revive flagging migraine target Elie Dolgin p249 | doi:10.1038/nrd3991 CGRP makes a comeback as antibodies advance into Phase II trials. | |||||||||||||||||||||||||||||||||||||
Anticancer IGF1R classes take more knocks Malini Guha p250 | doi:10.1038/nrd3992 Disappointing developments with Amgen's ganitumab and Bristol-Myers Squibb's BMS-754807 highlight the need for rational combinations and predictive biomarkers to rescue IGF1R pathway antagonists. | |||||||||||||||||||||||||||||||||||||
Molecular imaging as a de-risking tool: coming into focus? Asher Mullard p251 | doi:10.1038/nrd3993 Molecular imaging is already engrained in early-stage trials for central nervous system disorders, but used infrequently in other therapeutic areas. What will it take to make it standard practice across the pipeline? | |||||||||||||||||||||||||||||||||||||
NEWS IN BRIEF Rare disease bonanza | Eye on ibrutinib | Resolving sirtuin uncertainty? p253 | doi:10.1038/nrd3994 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Market watch: Upcoming market catalysts in Q2 2013 Karen Nguyen p254 | doi:10.1038/nrd3990 | |||||||||||||||||||||||||||||||||||||
BIOBUSINESS BRIEFS Deal watch: Chiasma and Roche partner in oral peptide drug delivery Charlotte Harrison p255 | doi:10.1038/nrd3989 | |||||||||||||||||||||||||||||||||||||
PATENT WATCH Australia allows isolated gene patents | United States rings in 'first to file' changes | Animal models Charlotte Harrison p256 | doi:10.1038/nrd3995 | |||||||||||||||||||||||||||||||||||||
AN AUDIENCE WITH Paul Stoffels p258 | doi:10.1038/nrd3996 Paul Stoffels, Johnson & Johnson's Chief Scientific Officer, discusses the company's approach to partnering. | |||||||||||||||||||||||||||||||||||||
FROM THE ANALYST'S COUCH Antibody-drug conjugates Rachel S. Zolot, Satarupa Basu & Ryan P. Million p259 | doi:10.1038/nrd3980 Antibody-drug conjugates (ADCs), which allow cytotoxic drugs to be selectively targeted to cancer cells, are attracting considerable interest. This article analyses the pipeline of ADCs, as well as trends in collaborations and deals related to ADC platforms. | |||||||||||||||||||||||||||||||||||||
REVIEWS | Top | ||||||||||||||||||||||||||||||||||||
Adenosine receptors as drug targets — what are the challenges? Jiang-Fan Chen, Holger K. Eltzschig & Bertil B. Fredholm p265 | doi:10.1038/nrd3955 Adenosine signalling has a functional role in many diseases and has long been a target for drug development. However, only one adenosine receptor-specific agent has so far gained approval. Here, Fredholm and colleagues provide an overview of the physiological and pathological functions of adenosine and consider the challenges in the development of compounds targeting adenosine receptors. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
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Article series: A guide to drug discovery Animal models for metabolic, neuromuscular and ophthalmological rare diseases >Guillaume Vaquer, Frida Rivière, Maria Mavris, Fabrizia Bignami, Jordi Llinares-Garcia, Kerstin Westermark & Bruno Sepodes p287 | doi:10.1038/nrd3831 Animal models are vital tools in the development of therapies for orphan diseases, given the small populations of patients available to evaluate the therapies. Here, Sepodes and colleagues from the European Medicines Agency's Committee for Orphan Medicinal Products harness their experience to provide an overview of the animal models used to support regulatory applications for metabolic, neuromuscular and ophthalmological rare diseases. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||
Challenges and approaches for the development of safer immunomodulatory biologics Jean G. Sathish, Swaminathan Sethu, Marie-Christine Bielsky, Lolke de Haan, Neil S. French, Karthik Govindappa, James Green, Christopher E. M. Griffiths, Stephen Holgate, David Jones, Ian Kimber, Jonathan Moggs, Dean J. Naisbitt, Munir Pirmohamed, Gabriele Reichmann, Jennifer Sims, Meena Subramanyam, Marque D. Todd, Jan Willem Van Der Laan, Richard J. Weaver & B. Kevin Park p306 | doi:10.1038/nrd3974 Owing to their specificity, immunomodulatory biologics generally have better safety profiles than small-molecule drugs. However, adverse effects such as an increased risk of infections or cytokine release syndrome are of concern. Here, Park and colleagues discuss the current strategies used to predict and mitigate these adverse effects and consider how they can be used to inform the development of safer immunomodulatory biologics. Abstract | Full Text | PDF | Supplementary information | |||||||||||||||||||||||||||||||||||||
CORRESPONDENCE | Top | ||||||||||||||||||||||||||||||||||||
Correspondence: Moving towards early clinical trials for amyloid-targeted therapy in Alzheimer's disease Paul S. Aisen, Bruno Vellas & Harald Hampel p324 | doi:10.1038/nrd3842-c1 Full Text | PDF | |||||||||||||||||||||||||||||||||||||
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*2011 Journal Citation Report (Thomson Reuters, 2012) |
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