A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy, Safety, and Tolerability of Extended-Release Metadoxine in Adults With Attention-Deficit/Hyperactivity Disorder

被引:24
作者
Manor, Iris [1 ,2 ]
Ben-Hayun, Rachel [3 ]
Aharon-Peretz, Judith [3 ]
Salomy, Dana [1 ]
Weizman, Abraham [1 ,2 ]
Daniely, Yaron [4 ]
Megiddo, Dalia [4 ]
Newcorn, Jeffrey H. [5 ]
Biederman, Joseph [9 ,10 ]
Adler, Lenard A. [6 ,7 ,8 ]
机构
[1] Geha Mental Hlth Ctr, Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Rambam Hlth Care Campus, Haifa, Israel
[4] Alcobra Ltd, Tel Aviv, Israel
[5] Mt Sinai Med Ctr, New York, NY 10029 USA
[6] NYU, Med Ctr, Dept Psychiat, New York, NY 10016 USA
[7] NYU, Med Ctr, Dept Child & Adolescent Psychiat, New York, NY 10016 USA
[8] New York VA Harbor Healthcare Syst, Psychiat Serv, New York, NY USA
[9] Massachusetts Gen Hosp, Boston, MA 02114 USA
[10] Harvard Univ, Sch Med, Boston, MA USA
关键词
ADHD; PREVALENCE; PERSISTENT; PREDICTORS; SYMPTOMS; VALIDITY;
D O I
10.4088/JCP.12m07767
中图分类号
B849 [应用心理学];
学科分类号
040203 [应用心理学];
摘要
Objective: To evaluate the efficacy, safety, and tolerability of an oral extended-release (ER) formulation of the nonstimulant metadoxine in the treatment of adult attention-deficit/hyperactivity disorder (ADHD). Method:This was a 1:1 randomized, double-blind, placebo-controlled, parallel-design, phase 2 study of metadoxine ER 1,400 mg/d treatment for 6 weeks, following a 2-week baseline/screening period, involving 120 adults with DSM-IV defined ADHD. A follow-up assessment occurred 2 weeks after the trial was completed. Efficacy measures included changes in Conners'Adult ADHD Rating Scale-Investigator Rated (CAARS-INV) total ADHD symptoms score with adult ADHD prompts (primary measure), response rates (>= 25% or 40% improvement in CAARS-INV total ADHD symptom score),Test of Variables of Attention (TOVA) performance, and Adult ADHD Quality of Life (AAQoL) total score. The study was conducted from March 15, 2011, to August 21, 2011. Results: Intent-to-treat analysis revealed that subjects receiving metadoxine ER showed statistically significant improvement in CAARS-INV total ADHD symptoms score (P = .02), higher rate of response (>= 25% [P = .03] or >= 40% [P = .04] improvement) on the CAARS-INV total ADHD symptoms score, and improvement in TOVA score (P = .02) and AAQoL score (P = .01) compared with the placebo group. Improvements in ADHD symptoms (scored by CAARS-INV) were significantly different in subjects treated with metadoxine ER versus placebo as early as 2 weeks following treatment initiation. Metadoxine ER was generally well tolerated, with nausea (17% [10/58] vs 0% [0/59]), fatigue (31% [18/58] vs 27% [16/59]), and headaches (29% [17/58] vs 39% [23/59]) being the most frequently reported adverse effects for the metadoxine ER and placebo groups, respectively. Conclusions: Findings suggest that metadoxine ER is a well-tolerated and effective treatment for adults with ADHD.
引用
收藏
页码:1517 / 1523
页数:7
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