Table of contents
In This Issue
p801 | doi:10.1038/nrd2166
Editorial: A tale of two drugs
p803 | doi:10.1038/nrd2167
News and Analysis
New bill aims to reform US patent system | PDF (145 KB)
p805 | doi:10.1038/nrd2168
HIV prevention trials in danger of grinding to a standstill | PDF (127 KB)
p806 | doi:10.1038/nrd2169
Origins of ecstasy an urban myth | PDF (91 KB)
p806 | doi:10.1038/nrd2172
News in Brief
News in brief | PDF (287 KB)
p808 | doi:10.1038/nrd2170
Patent watch
Ariad's claims to NF-
B pathway rejected | Apotex appeal Plavix injunction | Oxybutynin too 'obvious' | Interleukin-1 receptor inhibition | PDF
(169 KB)
p810 | doi:10.1038/nrd2171
Career Path
William R. Keller | PDF (80 KB)
p812 | doi:10.1038/nrd2158
From the analyst's couch
Life after statin patent expiries | PDF (169 KB)
p813 | doi:10.1038/nrd2156
From the analyst's couch
Life after statin patent expiries | PDF (0KB)
p813 | doi:10.1038/nrd2156
Fresh from the Pipeline
Ranibizumab | PDF (173 KB)
p815 | doi:10.1038/nrd2157
Research Highlights
Psychiatric disorders: ProTREKtion against depression | PDF (106 KB)
p817 | doi:10.1038/nrd2162
Angiogenesis: Familiar faces and new connections | PDF (67 KB)
p818 | doi:10.1038/nrd2160
Anticancer drugs: Activating the executioner | PDF (88 KB)
p818 | doi:10.1038/nrd2164
Biomarkers: Signatures of schizophrenia | PDF (84 KB)
p819 | doi:10.1038/nrd2161
Lung cancer: Strengthening the link to adenosine | PDF (98 KB)
p820 | doi:10.1038/nrd2163
In brief
High-throughput screening | Therapeutic angiogenesis | Metabolic disorders | Cancer | PDF (73 KB)
p820 | doi:10.1038/nrd2165
Perspectives
Opinion
Drugs, their targets and the nature and number of drug targets
Peter Imming, Christian Sinning & Achim Meyer
p821 | doi:10.1038/nrd2132
What constitutes a drug target? Imming and colleagues consider this question, and by classifying known drug substances on the basis of the discussed principles, provide an estimation of the total number of current drug targets.
Reviews
Article series: Case Histories
Discovery and development of sorafenib: a multikinase inhibitor for treating cancer
Scott Wilhelm, Christopher Carter, Mark Lynch, Timothy Lowinger, Jacques Dumas, Roger A. Smith, Brian Schwartz, Ronit Simantov & Susan Kelley
p835 | doi:10.1038/nrd2130
In December 2005, sorafenib became the first new treatment to be approved for advanced renal cancer in more than a decade. Wilhelm and colleagues provide the history of this drug, which inhibits several kinases involved in tumour signalling and angiogenesis.
Novel pharmacological targets for the treatment of Parkinson's disease
Anthony H. V. Schapira, Erwan Bezard, Jonathan Brotchie, Frédéric Calon, Graham L. Collingridge, Borris Ferger, Bastian Hengerer, Etienne Hirsch, Peter Jenner, Nicolas Le Novère, José A. Obeso, Michael A. Schwarzschild, Umberto Spampinato & Giora Davidai
p845 | doi:10.1038/nrd2087
Schapira and colleagues describe recent advances in the development of novel doperminergic and non-doperminergic drugs for the treatment of Parkinson's disease and related motor complications.
Article series: Case Histories
Discovery and development of clofarabine: a nucleoside analogue for treating cancer
Peter L. Bonate, Larry Arthaud, William R. Cantrell, Jr., Katherine Stephenson, John A. Secrist, III & Steve Weitman
p855 | doi:10.1038/nrd2055
Despite considerable progress in the treatment of paediatric leukaemias, a major need still exists for therapies for patients who relapse. Bonate and colleagues describe the discovery and development of the nucleoside analogue clofarabine, which is the first such drug approved for paediatric leukaemia in more than a decade, and the first to receive approval for paediatric use before adult use.
Signalling platforms that modulate the inflammatory response: new targets for drug development
Christopher. A. McCulloch, Gregory P. Downey & Hani El-Gabalawy
p864 | doi:10.1038/nrd2109
Inflammatory diseases of lung, liver, heart, joints and periodontium have high prevalence, but many current treatments have limited efficacy and are expensive. McCulloch and colleagues consider new anti-inflammatory drug targets based on the clustering of interleukin- 1 receptors into multi-protein aggregates associated with cell adhesions.



