Problems and solutions to filling the drying drug pipeline for psychiatric disorders: a report from the inaugural 2012 CINP Think Tank

被引:10
作者
Dean, Brian [1 ,2 ]
Moller, Hans-Juergen [3 ]
Svensson, Torgny H. [4 ]
Geyer, Mark A. [5 ,6 ]
Rujescu, Dan [7 ]
Scarr, Elizabeth [1 ,2 ]
Millan, Mark J. [8 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Mol Psychiat Lab, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Dept Psychiat, Parkville, Vic 3010, Australia
[3] Univ Munich, Dept Psychiat, D-80539 Munich, Germany
[4] Karolinska Inst, Dept Physiol & Pharmacol, Sect Neuropsychopharmacol, Stockholm, Sweden
[5] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[6] VA San Diego Healthcare Syst, Res Serv, San Diego, CA USA
[7] Univ Halle Wittenberg, Dept Psychiat, D-06108 Halle, Germany
[8] Inst Rech Servier, Unite Rech & Decouverte, Croissy Sur Seine, France
关键词
CINP Think Tank; drug development; neuropsychopharmacology; RECEPTOR AGONIST XANOMELINE; MAJOR DEPRESSIVE DISORDER; PRE-MESSENGER-RNA; ANIMAL-MODELS; ALLOSTERIC MODULATORS; PERSONALIZED MEDICINE; MUSCARINIC RECEPTORS; PREFRONTAL CORTEX; GENE-EXPRESSION; DSM-IV;
D O I
10.1017/S1461145713001077
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The inaugural Collegium Internationale Neuro-Psychopharmacologicum (CINP) Think Tank, a small open meeting sponsored by the CINP, discussed impediments to developing new drugs for psychiatric disorders and approaches to overcome these impediments. Whilst neuropsycharmacology has a rich pharmacopeia (current treatments benefiting many individuals), issues of treatment resistance, sub-optimal response and unwanted side effects remain problematic. Many scientific, economic and social issues are impeding the development of drugs (e.g. higher risk of failure, placebo effects, problematic regulatory environments, pressures imposed by patent protection, downward pressure on reimbursements and financial, legal and social risk aversion). A consensus of the meeting was that efforts to understanding the core pathophysiology of psychiatric disorders are fundamental to increasing the chance of developing new drugs. However, findings from disorders such as Huntington's chorea, have shown that knowing the cause of a disorder may not reveal new drug targets. By contrast, clinically useful biomarkers that define target populationsrom animals to humans will increase the likelihood of developing new drugs. I for new drugs and models that allow findings to be accurately translated fn addition, a greater accent on experimental medicine, creative clinical investigations and improved communication between preclinical neuropsychopharmacologists, clinicians committed to neuropsychopharmacological research, industry and the regulators would also be a driver to the development of new treatments. Finally, it was agreed that the CINP must continue its role as a conduit facilitating vibrant interactions between industry and academia as such communications are a central component in identifying new drug targets, developing new drugs and transitioning new drugs into the clinic.
引用
收藏
页码:137 / 148
页数:12
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