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<title>APT drug R&amp;D: the right active ingredient in the right presentation for the right therapeutic use</title>
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<p>
<b>APT drug R&amp;D: the right active ingredient in the right presentation for the right therapeutic use</b>
</p>
<p>Nature Reviews Drug Discovery 8, 849 (2009). <a href="http://dx.doi.org/10.1038/nrd2981">doi:10.1038/nrd2981</a>
</p>
<p>Author: David Cavalla</p>
<p>Drug repurposing, in which an established active pharmaceutical ingredient is applied in a new way &#8212; for example, for a new indication, and often combined with an alternative method of presentation, such as a novel delivery route &#8212; is an evolving strategy for pharmaceutical R&amp;D. </p>
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<title>New medicines to improve control and contribute to the eradication of malaria</title>
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<description>Despite being one of the most prevalent tropical diseases, for many years malaria was not a commercial priority for the pharmaceutical industry. However, in response to the emergence and spread of resistance to the available antimalarial drugs, there has been a renaissance in the discovery </description>
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<p>
<b>New medicines to improve control and contribute to the eradication of malaria</b>
</p>
<p>Nature Reviews Drug Discovery 8, 879 (2009). <a href="http://dx.doi.org/10.1038/nrd2972">doi:10.1038/nrd2972</a>
</p>
<p>Authors: Timothy N. C. Wells, Pedro L. Alonso &amp; Winston E. Gutteridge</p>
<p>Despite being one of the most prevalent tropical diseases, for many years malaria was not a commercial priority for the pharmaceutical industry. However, in response to the emergence and spread of resistance to the available antimalarial drugs, there has been a renaissance in the discovery </p>
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<dc:title>New medicines to improve control and contribute to the eradication of malaria</dc:title>
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<dc:creator>Winston E. Gutteridge</dc:creator>
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<title>A pre-emptive strike against malaria's stealthy hepatic forms</title>
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<description>Almost all the drugs that are widely used today against Plasmodium spp., the causative agent of malaria, target the asexual blood stages of the parasite. Widespread drug resistance severely restricts our ability to control malaria and makes it necessary to seek novel antimalarial compounds. </description>
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<p>
<b>A pre-emptive strike against malaria's stealthy hepatic forms</b>
</p>
<p>Nature Reviews Drug Discovery 8, 854 (2009). <a href="http://dx.doi.org/10.1038/nrd2960">doi:10.1038/nrd2960</a>
</p>
<p>Authors: Dominique Mazier, Laurent R&#233;nia &amp; Georges Snounou</p>
<p>Almost all the drugs that are widely used today against Plasmodium spp., the causative agent of malaria, target the asexual blood stages of the parasite. Widespread drug resistance severely restricts our ability to control malaria and makes it necessary to seek novel antimalarial compounds. </p>
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<dc:title>A pre-emptive strike against malaria's stealthy hepatic forms</dc:title>
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<title>Can literature analysis identify innovation drivers in drug discovery?</title>
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<description>Drug discovery must be guided not only by medical need and commercial potential, but also by the areas in which new science is creating therapeutic opportunities, such as target identification and the understanding of disease mechanisms. To systematically identify such areas of high scientific activity, </description>
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<p>
<b>Can literature analysis identify innovation drivers in drug discovery?</b>
</p>
<p>Nature Reviews Drug Discovery 8, 865 (2009). <a href="http://dx.doi.org/10.1038/nrd2973">doi:10.1038/nrd2973</a>
</p>
<p>Authors: Pankaj Agarwal &amp; David B. Searls</p>
<p>Drug discovery must be guided not only by medical need and commercial potential, but also by the areas in which new science is creating therapeutic opportunities, such as target identification and the understanding of disease mechanisms. To systematically identify such areas of high scientific activity, </p>
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<dc:title>Can literature analysis identify innovation drivers in drug discovery?</dc:title>
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<dc:creator>David B. Searls</dc:creator>
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<title>Targeting protein kinases in central nervous system disorders</title>
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<description>Protein kinases are a growing drug target class in disorders in peripheral tissues, but the development of kinase-targeted therapies for central nervous system (CNS) diseases remains a challenge, largely owing to issues associated specifically with CNS drug discovery. However, several candidate therapeutics that target CNS </description>
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<p>
<b>Targeting protein kinases in central nervous system disorders</b>
</p>
<p>Nature Reviews Drug Discovery 8, 892 (2009). <a href="http://dx.doi.org/10.1038/nrd2999">doi:10.1038/nrd2999</a>
</p>
<p>Authors: Laura K. Chico, Linda J. Van Eldik &amp; D. Martin Watterson</p>
<p>Protein kinases are a growing drug target class in disorders in peripheral tissues, but the development of kinase-targeted therapies for central nervous system (CNS) diseases remains a challenge, largely owing to issues associated specifically with CNS drug discovery. However, several candidate therapeutics that target CNS </p>
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<dc:title>Targeting protein kinases in central nervous system disorders</dc:title>
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<title>Influenza vaccine market dynamics</title>
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<description>The market for seasonal influenza vaccines, sized at US$2.8 billion in 2008–2009 across the seven major markets (United States, Japan, France, Germany, Italy, Spain and UK), has had a strong compound annual growth rate of 12.6% since 2005–2006 (Ref. 1). In recent years, the </description>
<content:encoded><![CDATA[

<p>
<b>Influenza vaccine market dynamics</b>
</p>
<p>Nature Reviews Drug Discovery 8, 841 (2009). <a href="http://dx.doi.org/10.1038/nrd3026">doi:10.1038/nrd3026</a>
</p>
<p>Authors: Hedwig Kresse &amp; Holger Rovini</p>
<p>The market for seasonal influenza vaccines, sized at US&#36;2.8 billion in 2008&#8211;2009 across the seven major markets (United States, Japan, France, Germany, Italy, Spain and UK), has had a strong compound annual growth rate of 12.6% since 2005&#8211;2006 (Ref. 1). In recent years, the </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/jSauMbuUh7Y" height="1" width="1"/>]]></content:encoded>
<dc:title>Influenza vaccine market dynamics</dc:title>
<dc:creator>Hedwig Kresse</dc:creator>
<dc:creator>Holger Rovini</dc:creator>
<dc:identifier>doi:10.1038/nrd3026</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 841 (2009)</dc:source>
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<title>Asenapine</title>
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<description>In August 2009, asenapine (Saphris; Schering–Plough) was approved by the US FDA for the acute treatment of schizophrenia and manic or mixed episodes associated with bipolar I disorder in adults.</description>
<content:encoded><![CDATA[

<p>
<b>Asenapine</b>
</p>
<p>Nature Reviews Drug Discovery 8, 843 (2009). <a href="http://dx.doi.org/10.1038/nrd3027">doi:10.1038/nrd3027</a>
</p>
<p>Authors: Herbert Y. Meltzer, Argyris Dritselis, Uma Yasothan &amp; Peter Kirkpatrick</p>
<p>In August 2009, asenapine (Saphris; Schering&#8211;Plough) was approved by the US FDA for the acute treatment of schizophrenia and manic or mixed episodes associated with bipolar I disorder in adults.</p>
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<dc:title>Asenapine</dc:title>
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<dc:creator>Argyris Dritselis</dc:creator>
<dc:creator>Uma Yasothan</dc:creator>
<dc:creator>Peter Kirkpatrick</dc:creator>
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<title>Nanotechnology</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/A938e79xaTs/nrd3029</link>
<description>The translation of nanotechnology-based therapies and products from the laboratory to the clinic requires a multidisciplinary approach. Our two interviewees this month discuss their roles in bringing together diverse groups of scientists to achieve this goal.</description>
<content:encoded><![CDATA[

<p>
<b>Nanotechnology</b>
</p>
<p>Nature Reviews Drug Discovery 8, 911 (2009). <a href="http://dx.doi.org/10.1038/nrd3029">doi:10.1038/nrd3029</a>
</p>
<p>The translation of nanotechnology-based therapies and products from the laboratory to the clinic requires a multidisciplinary approach. Our two interviewees this month discuss their roles in bringing together diverse groups of scientists to achieve this goal.</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/A938e79xaTs" height="1" width="1"/>]]></content:encoded>
<dc:title>Nanotechnology</dc:title>
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<dc:source>Nature Reviews Drug Discovery 8, 911 (2009)</dc:source>
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<title>Metabolic disease: Dual benefit of bile acid receptor agonist</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/J-0qyqHxbDk/nrd3032</link>
<description>Bile acids, which contribute to the emulsification and digestion of lipid-soluble nutrients following a meal, are increasingly appreciated as also having important roles in metabolic signalling pathways. Writing in Cell Metabolism, Thomas and colleagues identify an agonist of G protein-coupled bile acid receptor 1 </description>
<content:encoded><![CDATA[

<p>
<b>Metabolic disease: Dual benefit of bile acid receptor agonist</b>
</p>
<p>Nature Reviews Drug Discovery 8, 848 (2009). <a href="http://dx.doi.org/10.1038/nrd3032">doi:10.1038/nrd3032</a>
</p>
<p>Author: Sarah Crunkhorn</p>
<p>Bile acids, which contribute to the emulsification and digestion of lipid-soluble nutrients following a meal, are increasingly appreciated as also having important roles in metabolic signalling pathways. Writing in Cell Metabolism, Thomas and colleagues identify an agonist of G protein-coupled bile acid receptor 1 </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/J-0qyqHxbDk" height="1" width="1"/>]]></content:encoded>
<dc:title>Metabolic disease: Dual benefit of bile acid receptor agonist</dc:title>
<dc:creator>Sarah Crunkhorn</dc:creator>
<dc:identifier>doi:10.1038/nrd3032</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 848 (2009)</dc:source>
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<title>Antibacterial drugs: Proteasome target to tackle non-replicating TB</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/1F92Gr6xuuA/nrd3033</link>
<description>The ability of Mycobacterium tuberculosis to enter into a non-replicating state that is not strongly affected by standard antibiotics necessitates long treatment regimens, leading to poor patient compliance that can promote the emergence of drug-resistant strains. Reporting in Nature, Lin and colleagues show </description>
<content:encoded><![CDATA[

<p>
<b>Antibacterial drugs: Proteasome target to tackle non-replicating TB</b>
</p>
<p>Nature Reviews Drug Discovery 8, 845 (2009). <a href="http://dx.doi.org/10.1038/nrd3033">doi:10.1038/nrd3033</a>
</p>
<p>Author: Katie Kingwell</p>
<p>The ability of Mycobacterium tuberculosis to enter into a non-replicating state that is not strongly affected by standard antibiotics necessitates long treatment regimens, leading to poor patient compliance that can promote the emergence of drug-resistant strains. Reporting in Nature, Lin and colleagues show </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/1F92Gr6xuuA" height="1" width="1"/>]]></content:encoded>
<dc:title>Antibacterial drugs: Proteasome target to tackle non-replicating TB</dc:title>
<dc:creator>Katie Kingwell</dc:creator>
<dc:identifier>doi:10.1038/nrd3033</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 845 (2009)</dc:source>
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<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>845</prism:startingPage>
<prism:endingPage>845</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3033</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3034">
<title>Cancer: CpG–siRNA deals double blow to tumours</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/qNv1pTTgTzc/nrd3034</link>
<description>Tumours can avert an immune response and boost their own growth by inducing the expression of immunosuppressive, angiogenic and growth factors in neighbouring cells. Reporting in Nature Biotechnology, Kortylewski and colleagues now present a new strategy to alter the balance in the tumour microenvironment </description>
<content:encoded><![CDATA[

<p>
<b>Cancer: CpG&#8211;siRNA deals double blow to tumours</b>
</p>
<p>Nature Reviews Drug Discovery 8, 847 (2009). <a href="http://dx.doi.org/10.1038/nrd3034">doi:10.1038/nrd3034</a>
</p>
<p>Author: Alexandra Flemming</p>
<p>Tumours can avert an immune response and boost their own growth by inducing the expression of immunosuppressive, angiogenic and growth factors in neighbouring cells. Reporting in Nature Biotechnology, Kortylewski and colleagues now present a new strategy to alter the balance in the tumour microenvironment </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/qNv1pTTgTzc" height="1" width="1"/>]]></content:encoded>
<dc:title>Cancer: CpG–siRNA deals double blow to tumours</dc:title>
<dc:creator>Alexandra Flemming</dc:creator>
<dc:identifier>doi:10.1038/nrd3034</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 847 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3034</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3034</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>847</prism:startingPage>
<prism:endingPage>847</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3034</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3035">
<title>HIV: A new starting point for HIV vaccine design</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/Y5hg8181DhQ/nrd3035</link>
<description>Identifying broadly neutralizing antibodies (BNAbs) against HIV, which recognize most manifestations of this highly mutable virus, is important in achieving the elusive goal of developing a viable HIV vaccine. However, although the BNAbs that have been identified are effective in primate models of HIV, they </description>
<content:encoded><![CDATA[

<p>
<b>HIV: A new starting point for HIV vaccine design</b>
</p>
<p>Nature Reviews Drug Discovery 8, 846 (2009). <a href="http://dx.doi.org/10.1038/nrd3035">doi:10.1038/nrd3035</a>
</p>
<p>Author: Monica Hoyos Flight</p>
<p>Identifying broadly neutralizing antibodies (BNAbs) against HIV, which recognize most manifestations of this highly mutable virus, is important in achieving the elusive goal of developing a viable HIV vaccine. However, although the BNAbs that have been identified are effective in primate models of HIV, they </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/Y5hg8181DhQ" height="1" width="1"/>]]></content:encoded>
<dc:title>HIV: A new starting point for HIV vaccine design</dc:title>
<dc:creator>Monica Hoyos Flight</dc:creator>
<dc:identifier>doi:10.1038/nrd3035</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 846 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3035</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3035</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>846</prism:startingPage>
<prism:endingPage>847</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3035</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3036">
<title>Mood disorders: Antidepressant action through gene regulation</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/l9ZgCYUgk6c/nrd3036</link>
<description>A recent paper in the Journal of Neuroscience has shown that inhibitors of histone deacetylases (HDACs) — enzymes that affect the acetylation status of histones and regulate the remodelling of chromatin — have antidepressant actions.Although currently used antidepressants rapidly modulate monoaminergic systems in </description>
<content:encoded><![CDATA[

<p>
<b>Mood disorders: Antidepressant action through gene regulation</b>
</p>
<p>Nature Reviews Drug Discovery 8, 847 (2009). <a href="http://dx.doi.org/10.1038/nrd3036">doi:10.1038/nrd3036</a>
</p>
<p>Author: Charlotte Harrison</p>
<p>A recent paper in the Journal of Neuroscience has shown that inhibitors of histone deacetylases (HDACs) &#8212; enzymes that affect the acetylation status of histones and regulate the remodelling of chromatin &#8212; have antidepressant actions.Although currently used antidepressants rapidly modulate monoaminergic systems in </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/l9ZgCYUgk6c" height="1" width="1"/>]]></content:encoded>
<dc:title>Mood disorders: Antidepressant action through gene regulation</dc:title>
<dc:creator>Charlotte Harrison</dc:creator>
<dc:identifier>doi:10.1038/nrd3036</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 847 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3036</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3036</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>847</prism:startingPage>
<prism:endingPage>847</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3036</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3037">
<title>In brief</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/nmKKEpHcRPg/nrd3037</link>
<description>Antibacterial drugs</description>
<content:encoded><![CDATA[

<p>
<b>In brief</b>
</p>
<p>Nature Reviews Drug Discovery 8, 848 (2009). <a href="http://dx.doi.org/10.1038/nrd3037">doi:10.1038/nrd3037</a>
</p>
<p>Antibacterial drugs</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/nmKKEpHcRPg" height="1" width="1"/>]]></content:encoded>
<dc:title>In brief</dc:title>
<dc:identifier>doi:10.1038/nrd3037</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 848 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3037</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3037</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>848</prism:startingPage>
<prism:endingPage>848</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3037</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3038">
<title>Deal watch:  Nektar in US$1.5 billion licensing deal with AstraZeneca</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/sVUl0KZBbPY/nrd3038</link>
<description>Nektar Therapeutics — a company focused on drug development based on advanced polymer conjugate technology — has announced a licensing deal with AstraZeneca for two compounds to combat opioid-induced constipation. Under the deal, Nektar will receive an upfront payment of US$125 million and up to </description>
<content:encoded><![CDATA[

<p>
<b>Deal watch:  Nektar in US&#36;1.5 billion licensing deal with AstraZeneca</b>
</p>
<p>Nature Reviews Drug Discovery 8, 836 (2009). <a href="http://dx.doi.org/10.1038/nrd3038">doi:10.1038/nrd3038</a>
</p>
<p>Nektar Therapeutics &#8212; a company focused on drug development based on advanced polymer conjugate technology &#8212; has announced a licensing deal with AstraZeneca for two compounds to combat opioid-induced constipation. Under the deal, Nektar will receive an upfront payment of US&#36;125 million and up to </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/sVUl0KZBbPY" height="1" width="1"/>]]></content:encoded>
<dc:title>Deal watch:  Nektar in US$1.5 billion licensing deal with AstraZeneca</dc:title>
<dc:identifier>doi:10.1038/nrd3038</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 836 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3038</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3038</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>836</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3038</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3039">
<title>Trial watch:  CGRP receptor antagonist meets Phase III migraine end points</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/p7DZTCkfSkk/nrd3039</link>
<description>Merck has announced that the antagonist of the calcitonin gene-related peptide (CGRP) receptor telcagepant has met the primary end points in two Phase III trials to treat migraine, which is characterized by attacks of intense throbbing head pain that can last from 4 to 72 </description>
<content:encoded><![CDATA[

<p>
<b>Trial watch:  CGRP receptor antagonist meets Phase III migraine end points</b>
</p>
<p>Nature Reviews Drug Discovery 8, 836 (2009). <a href="http://dx.doi.org/10.1038/nrd3039">doi:10.1038/nrd3039</a>
</p>
<p>Merck has announced that the antagonist of the calcitonin gene-related peptide (CGRP) receptor telcagepant has met the primary end points in two Phase III trials to treat migraine, which is characterized by attacks of intense throbbing head pain that can last from 4 to 72 </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/p7DZTCkfSkk" height="1" width="1"/>]]></content:encoded>
<dc:title>Trial watch:  CGRP receptor antagonist meets Phase III migraine end points</dc:title>
<dc:identifier>doi:10.1038/nrd3039</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 836 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3039</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3039</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>836</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3039</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3040">
<title>Market watch:  Sales of biologics to show robust growth through to 2013</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/GYKy_6lDFu0/nrd3040</link>
<description>AVOS Life Sciences has analysed the revenue contributions of biologics and small-molecule drugs to the major Rx drug portfolios (MRDP) of the 14 large-cap pharmaceutical companies. MRDP is the collection of branded drugs that are each predicted to achieve at least US$500 million in annual </description>
<content:encoded><![CDATA[

<p>
<b>Market watch:  Sales of biologics to show robust growth through to 2013</b>
</p>
<p>Nature Reviews Drug Discovery 8, 837 (2009). <a href="http://dx.doi.org/10.1038/nrd3040">doi:10.1038/nrd3040</a>
</p>
<p>Author: Michael Goodman</p>
<p>AVOS Life Sciences has analysed the revenue contributions of biologics and small-molecule drugs to the major Rx drug portfolios (MRDP) of the 14 large-cap pharmaceutical companies. MRDP is the collection of branded drugs that are each predicted to achieve at least US&#36;500 million in annual </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/GYKy_6lDFu0" height="1" width="1"/>]]></content:encoded>
<dc:title>Market watch:  Sales of biologics to show robust growth through to 2013</dc:title>
<dc:creator>Michael Goodman</dc:creator>
<dc:identifier>doi:10.1038/nrd3040</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 837 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3040</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3040</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>837</prism:startingPage>
<prism:endingPage>837</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3040</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3041">
<title>In this issue</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/8ng57Plmdls/nrd3041</link>
<description>Unmet medical need and commercial potential are considered to be key drivers of novel drug discovery, but identifying disease areas for which scientific understanding is improving substantially could also have a valuable role in guiding the focus of R&amp;D investment. In their Analysis article, Agarwal </description>
<content:encoded><![CDATA[

<p>
<b>In this issue</b>
</p>
<p>Nature Reviews Drug Discovery 8, 827 (2009). <a href="http://dx.doi.org/10.1038/nrd3041">doi:10.1038/nrd3041</a>
</p>
<p>Unmet medical need and commercial potential are considered to be key drivers of novel drug discovery, but identifying disease areas for which scientific understanding is improving substantially could also have a valuable role in guiding the focus of R&amp;D investment. In their Analysis article, Agarwal </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/8ng57Plmdls" height="1" width="1"/>]]></content:encoded>
<dc:title>In this issue</dc:title>
<dc:identifier>doi:10.1038/nrd3041</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 827 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3041</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3041</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>In This Issue</prism:section>
<prism:startingPage>827</prism:startingPage>
<prism:endingPage>827</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3041</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3042">
<title>Steering for success</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/syUf90tm24s/nrd3042</link>
<description>An FDA initiative to enable companies to discuss options for future trial design following completion of early-stage trials could have an important role in addressing the high costs and failure rates of pivotal clinical trials.</description>
<content:encoded><![CDATA[

<p>
<b>Steering for success</b>
</p>
<p>Nature Reviews Drug Discovery 8, 829 (2009). <a href="http://dx.doi.org/10.1038/nrd3042">doi:10.1038/nrd3042</a>
</p>
<p>An FDA initiative to enable companies to discuss options for future trial design following completion of early-stage trials could have an important role in addressing the high costs and failure rates of pivotal clinical trials.</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/syUf90tm24s" height="1" width="1"/>]]></content:encoded>
<dc:title>Steering for success</dc:title>
<dc:identifier>doi:10.1038/nrd3042</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 829 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3042</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3042</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>Editorial</prism:section>
<prism:startingPage>829</prism:startingPage>
<prism:endingPage>829</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3042</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3043">
<title>First oral therapies for multiple sclerosis anticipated</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/Evh6D6Ciik8/nrd3043</link>
<description>With five novel oral therapies in late-stage development, there could soon be a wide range of treatment options for relapsing–remitting multiple sclerosis, but better biomarkers are needed to more effectively address the challenge of treating progressive forms of the disease.</description>
<content:encoded><![CDATA[

<p>
<b>First oral therapies for multiple sclerosis anticipated</b>
</p>
<p>Nature Reviews Drug Discovery 8, 831 (2009). <a href="http://dx.doi.org/10.1038/nrd3043">doi:10.1038/nrd3043</a>
</p>
<p>Author: Bethan Hughes</p>
<p>With five novel oral therapies in late-stage development, there could soon be a wide range of treatment options for relapsing&#8211;remitting multiple sclerosis, but better biomarkers are needed to more effectively address the challenge of treating progressive forms of the disease.</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/Evh6D6Ciik8" height="1" width="1"/>]]></content:encoded>
<dc:title>First oral therapies for multiple sclerosis anticipated</dc:title>
<dc:creator>Bethan Hughes</dc:creator>
<dc:identifier>doi:10.1038/nrd3043</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 831 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3043</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3043</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>831</prism:startingPage>
<prism:endingPage>833</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3043</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3044">
<title>Novel pharmacotherapies for obesity poised to enter market</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/oIvM3bqyWa8/nrd3044</link>
<description>Phase III trial results for three anti-obesity therapies suggest that they meet at least some of the efficacy benchmarks for regulatory approval, although questions remain about the value of the benefits offered.</description>
<content:encoded><![CDATA[

<p>
<b>Novel pharmacotherapies for obesity poised to enter market</b>
</p>
<p>Nature Reviews Drug Discovery 8, 833 (2009). <a href="http://dx.doi.org/10.1038/nrd3044">doi:10.1038/nrd3044</a>
</p>
<p>Author: Dan Jones</p>
<p>Phase III trial results for three anti-obesity therapies suggest that they meet at least some of the efficacy benchmarks for regulatory approval, although questions remain about the value of the benefits offered.</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/oIvM3bqyWa8" height="1" width="1"/>]]></content:encoded>
<dc:title>Novel pharmacotherapies for obesity poised to enter market</dc:title>
<dc:creator>Dan Jones</dc:creator>
<dc:identifier>doi:10.1038/nrd3044</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 833 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3044</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3044</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>833</prism:startingPage>
<prism:endingPage>834</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3044</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3045">
<title>News in brief</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/JxGsMyDfn3A/nrd3045</link>
<description>Mixed results for first delayed-start trial in Parkinson's diseaseA clinical trial that was designed to examine the possibility that rasagiline (Azilect/Agilect; Teva/Lundbeck) has disease-modifying effects in Parkinson's disease has shown varying results.The lowdown: To date, no treatments for Parkinson's disease have been </description>
<content:encoded><![CDATA[

<p>
<b>News in brief</b>
</p>
<p>Nature Reviews Drug Discovery 8, 835 (2009). <a href="http://dx.doi.org/10.1038/nrd3045">doi:10.1038/nrd3045</a>
</p>
<p>Mixed results for first delayed-start trial in Parkinson's diseaseA clinical trial that was designed to examine the possibility that rasagiline (Azilect/Agilect; Teva/Lundbeck) has disease-modifying effects in Parkinson's disease has shown varying results.The lowdown: To date, no treatments for Parkinson's disease have been </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/JxGsMyDfn3A" height="1" width="1"/>]]></content:encoded>
<dc:title>News in brief</dc:title>
<dc:identifier>doi:10.1038/nrd3045</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 835 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3045</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3045</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>835</prism:startingPage>
<prism:endingPage>835</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrd3045</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrd3046">
<title>Patent Watch</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/3jka64uV7Ts/nrd3046</link>
<description>Drug metabolite claims are patentableLaws of nature and natural phenomena are not patentable, but new useful processes or compositions are. So, where does a test that includes methods based on the measurement of drug metabolites fit in? Is drug metabolism a natural process? These </description>
<content:encoded><![CDATA[

<p>
<b>Patent Watch</b>
</p>
<p>Nature Reviews Drug Discovery 8, 838 (2009). <a href="http://dx.doi.org/10.1038/nrd3046">doi:10.1038/nrd3046</a>
</p>
<p>Author: Charlotte Harrison</p>
<p>Drug metabolite claims are patentableLaws of nature and natural phenomena are not patentable, but new useful processes or compositions are. So, where does a test that includes methods based on the measurement of drug metabolites fit in? Is drug metabolism a natural process? These </p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/3jka64uV7Ts" height="1" width="1"/>]]></content:encoded>
<dc:title>Patent Watch</dc:title>
<dc:creator>Charlotte Harrison</dc:creator>
<dc:identifier>doi:10.1038/nrd3046</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 838 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3046</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3046</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>838</prism:startingPage>
<prism:endingPage>839</prism:endingPage>
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<title>Frank Douglas</title>
<link>http://feeds.nature.com/~r/nrd/rss/current/~3/mlX2vcWW2g8/nrd3047</link>
<description>The President and Chief Executive Officer of the Austen BioInnovation Institute in Akron discusses the institute's multidisciplinary approach to innovation.</description>
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<p>
<b>Frank Douglas</b>
</p>
<p>Nature Reviews Drug Discovery 8, 840 (2009). <a href="http://dx.doi.org/10.1038/nrd3047">doi:10.1038/nrd3047</a>
</p>
<p>The President and Chief Executive Officer of the Austen BioInnovation Institute in Akron discusses the institute's multidisciplinary approach to innovation.</p>
<img src="http://feeds.feedburner.com/~r/nrd/rss/current/~4/mlX2vcWW2g8" height="1" width="1"/>]]></content:encoded>
<dc:title>Frank Douglas</dc:title>
<dc:identifier>doi:10.1038/nrd3047</dc:identifier>
<dc:source>Nature Reviews Drug Discovery 8, 840 (2009)</dc:source>
<prism:publicationName>Nature Reviews Drug Discovery</prism:publicationName>
<prism:doi>10.1038/nrd3047</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrd3047</prism:url>
<prism:volume>8</prism:volume>
<prism:number>11</prism:number>
<prism:section>News and Analysis</prism:section>
<prism:startingPage>840</prism:startingPage>
<prism:endingPage>840</prism:endingPage>
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