Post hoc Responder and Remission Analyses from Two Studies of SHP465 Mixed Amphetamine Salts Extended-Release Among Adults with Attention-Deficit/Hyperactivity Disorder

被引:3
|
作者
Adler, Lenard A. [1 ,2 ]
Robertson, Brigitte [3 ,6 ]
Chen, Jie [4 ]
Sarkis, Elias [5 ]
机构
[1] NYU Langone Med Ctr, Dept Psychiat, New York, NY 10016 USA
[2] NYU Langone Med Ctr, Dept Child & Adolescent Psychiat, New York, NY 10016 USA
[3] Shire, Global Clin Dev, Lexington, MA USA
[4] Shire, Biostat, Lexington, MA USA
[5] Sarkis Family Psychiat, Gainesville, FL USA
[6] Yumanity Therapeut Inc, Cambridge, MA USA
关键词
adult; attention-deficit; hyperactivity disorder (ADHD); remission; response; SHP465 mixed amphetamine salts (SHP465 MAS); DEFICIT HYPERACTIVITY DISORDER; DOUBLE-BLIND; LISDEXAMFETAMINE DIMESYLATE; FUNCTIONAL IMPROVEMENT; OROS METHYLPHENIDATE; EFFICACY; SAFETY; ADHD; FORMULATION;
D O I
10.1089/cap.2020.0012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives: In two studies of adult attention-deficit/hyperactivity disorder (ADHD), SHP465 mixed amphetamine salts (MAS) extended-release significantly reduced ADHD-Rating Scale, 4th Edition total score (ADHD-RS-IV-TS) versus placebo (PBO). This report describes post hoc analyses of SHP465 MAS treatment response and remission rates from those studies. Methods: Adults with Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision-defined ADHD were randomized to SHP465 MAS (12.5-75 mg) or PBO in a 7-week dose-optimization study and to SHP465 MAS (25, 50, or 75 mg) or PBO in a 6-week fixed-dose study. Response was examined using three definitions (definition 1: >= 30% ADHD-RS-IV-TS reduction + Clinical Global Impressions-Improvement [CGI-I] rating of 1 or 2; definition 2: >= 50% ADHD-RS-IV-TS reduction + CGI-I rating of 1 or 2; definition 3: ADHD-RS-IV-TS <= 18). Remission was defined as ADHD-RS-IV-TS <= 12. The Kaplan-Meier analyses assessed time to response or remission. Results: The intent-to-treat populations included 136 SHP465 MAS and 132 PBO participants in the dose-optimization study and 302 SHP465 MAS and 103 PBO participants in the fixed-dose study. Percentages of participants meeting response criteria (SHP465 MAS vs. PBO) at the final treatment week in the dose-optimization and fixed-dose studies, respectively, were 66.0% versus 31.6% and 72.7% versus 28.3% (definition 1); 47.9% versus 27.6% and 60.6% versus 16.7% (definition 2); and 54.3% versus 30.3% and 52.6% versus 18.3% (definition 3). The remission criterion (SHP465 MAS vs. PBO) at the final treatment week was met by 37.2% versus 19.7% of participants in the dose-optimization study and 39.7% versus 10.0% of participants in the fixed-dose study. Times to response and remission favored SHP465 MAS over PBO in both studies (all nominal log-rank p < 0.0001). Conclusion: These post hoc analyses indicate that SHP465 MAS was associated with greater response and remission rates than PBO in adults with ADHD, with times to response and remission also nominally favoring SHP465 MAS.
引用
收藏
页码:427 / 438
页数:12
相关论文
共 50 条
  • [31] Extended-Release Mixed Amphetamine Salts for Comorbid Adult Attention-Deficit/Hyperactivity Disorder and Cannabis Use Disorder: A Pilot, Randomized Double-Blind, Placebo-Controlled Trial
    Levin, Frances R.
    Mariani, John J.
    Pavlicova, Martina
    Choi, C. Jean
    Basaraba, Cale
    Mahony, Amy L.
    Brooks, Daniel J.
    Brezing, Christina A.
    Naqvi, Nasir
    JOURNAL OF ATTENTION DISORDERS, 2024, 28 (11) : 1467 - 1481
  • [32] Safety and efficacy of guanfacine extended-release in adults with attention-deficit/hyperactivity disorder: an open-label, long-term, phase 3 extension study
    Iwanami, Akira
    Saito, Kazuhiko
    Fujiwara, Masakazu
    Okutsu, Daiki
    Ichikawa, Hironobu
    BMC PSYCHIATRY, 2020, 20 (01)
  • [33] Atomoxetine Treatment Outcomes in Adolescents and Young Adults With Attention-Deficit/Hyperactivity Disorder: Results From a Post Hoc, Pooled Analysis
    Adler, Lenard A.
    Wilens, Timothy
    Zhang, Shuyu
    Dittmann, Ralf W.
    D'Souza, Deborah N.
    Schuh, Leslie
    Durell, Todd M.
    CLINICAL THERAPEUTICS, 2012, 34 (02) : 363 - 373
  • [34] Relative benefits of stimulant therapy with OROS methylphenidate versus mixed amphetamine salts extended release in improving the driving performance of adolescent drivers with attention-deficit/hyperactivity disorder
    Cox, Daniel J.
    Merkel, R. Lawrence
    Moore, Melissa
    Thorndike, Frances
    Muller, Carrie
    Kovatchev, Boris
    PEDIATRICS, 2006, 118 (03) : E704 - E710
  • [35] Executive Function Outcome of Treatment with Viloxazine Extended-Release Capsules in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Post-Hoc Analysis of Four Randomized Clinical Trials
    Faraone, Stephen, V
    Gomeni, Roberto
    Hull, Joseph T.
    Busse, Gregory D.
    Melyan, Zare
    Rubin, Jonathan
    Nasser, Azmi
    PEDIATRIC DRUGS, 2021, 23 (06) : 583 - 589
  • [36] A post hoc subgroup analysis of an 18-day randomized controlled trial comparing the tolerability and efficacy of mixed amphetamine salts extended release and atomoxetine in school-age girls with attention-deficit/hyperactivity disorder
    Biederman, J
    Wigal, SB
    Spencer, TJ
    McGough, JJ
    Mays, DA
    CLINICAL THERAPEUTICS, 2006, 28 (02) : 280 - 293
  • [37] Single-Dose Pharmacokinetics of HLD200, a Delayed-Release and Extended-Release Methylphenidate Formulation, in Healthy Adults and in Adolescents and Children with Attention-Deficit/Hyperactivity Disorder
    Childress, Ann
    Mehrotra, Shailly
    Gobburu, Jogarao
    McLean, Angus
    DeSousa, Norberto J.
    Incledon, Bev
    JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY, 2018, 28 (01) : 10 - 18
  • [38] Mixed-amphetamine salts increase abstinence from marijuana in patients with co-occurring attention-deficit/hyperactivity disorder and cocaine dependence
    Notzon, Daniel P.
    Mariani, John J.
    Pavlicova, Martina
    Glass, Andrew
    Mahony, Amy L.
    Brooks, Daniel J.
    Grabowski, John
    Levin, Frances R.
    AMERICAN JOURNAL ON ADDICTIONS, 2016, 25 (08) : 666 - 672
  • [39] A randomised, placebo-controlled, 24-week, study of low-dose extended-release methylphenidate in adults with attention-deficit/hyperactivity disorder
    Michael Rösler
    Roland Fischer
    Richard Ammer
    Claudia Ose
    Wolfgang Retz
    European Archives of Psychiatry and Clinical Neuroscience, 2009, 259 : 120 - 129
  • [40] Response of peer relations and social activities to treatment with viloxazine extended-release capsules (Qelbree®): A post hoc analysis of four randomized clinical trials of children and adolescents with attention-deficit/hyperactivity disorder
    Faraone, Stephen V.
    Gomeni, Roberto
    Hull, Joseph T.
    Busse, Gregory D.
    Lujan, Brendan
    Rubin, Jonathan
    Nasser, Azmi
    BRAIN AND BEHAVIOR, 2023, 13 (04):