The FDA-NIMH-MATRICS Guidelines for Clinical Trial Design of Cognitive-Enhancing Drugs: What Do We Know 5 Years Later?

被引:100
作者
Buchanan, Robert W. [1 ]
Keefe, Richard S. E. [2 ]
Umbricht, Daniel [3 ]
Green, Michael F. [4 ,5 ]
Laughren, Thomas [6 ]
Marder, Stephen R. [4 ,5 ]
机构
[1] Univ Maryland, Sch Med, Dept Psychiat, Maryland Psychiat Res Ctr, Baltimore, MD 21228 USA
[2] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC 27710 USA
[3] F Hoffmann La Roche Ltd, PDEN CRED Neurosci, CH-4070 Basel, Switzerland
[4] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90095 USA
[5] Vet Adm Vet Integrated Serv Network, Mental Illness Res Educ & Clin Ctr 22, Los Angeles, CA 90073 USA
[6] Ctr Drug Evaluat & Res, Psychiat Prod Div, Food & Drug Adm, Silver Spring, MD 20993 USA
基金
英国医学研究理事会;
关键词
study design; drug development; cognitive impairments; substance abuse; neuropsychological test battery; 1ST-EPISODE SCHIZOPHRENIA; ANTIPSYCHOTIC-DRUGS; NEGATIVE SYMPTOMS; EARLY PSYCHOSIS; CATIE TRIAL; BATTERY; HALOPERIDOL; RELIABILITY; MEDICATIONS; RISPERIDONE;
D O I
10.1093/schbul/sbq038
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
The Food and Drug Administration (FDA)-National Institute of Mental Health (NIMH)-Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) clinical trial guidelines for cognitive-enhancing drugs in schizophrenia and the MATRICS Consensus Cognitive Battery (MCCB) were designed to facilitate novel compound development in the treatment of cognitive impairments. Several studies have recently utilized the FDA-NIMH-MATRICS guidelines and MCCB and allow an evaluation of the feasibility of guideline implementation and MCCB performance. In light of the study results, we would recommend the following inclusion criteria revisions-(1) clinical status and symptom inclusion criteria: maximum allowed score for hallucinations and delusions should be increased from moderate to moderately severe and the negative symptom criterion should be dropped in phase 2 studies; (2) antipsychotic medication inclusion criteria: first-generation antipsychotics should be allowed, but only in the context of no concomitant anticholinergic agents and minimal extrapyramidal symptoms, and antipsychotic polypharmacy should be allowed in the absence of pertinent pharmacokinetic or pharmacodynamic considerations; and (3) people who use illicit substances should not be allowed in phase 1B or 2A proof-of-concept studies but may be included in phase 2B and 3 studies in which proof of effectiveness and generalizability of results become more important goals. These revisions are recommended to enhance recruitment while maintaining sufficient methodological rigor to ensure the validity of study results. The MCCB has been shown to have excellent psychometric characteristics, including reliability for multisite clinical trials, clinical relevance for real-world functioning, and possible sensitivity to behavioral treatment, and should continue to serve as the standard outcome measure for cognitive enhancement studies in schizophrenia.
引用
收藏
页码:1209 / 1217
页数:9
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