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
  • [41] Efficacy and Safety of Guanfacine Extended-Release in the Treatment of Attention-Deficit/Hyperactivity Disorder in Adults: Results of a Randomized, Double-Blind, Placebo-Controlled Study
    Iwanami, Akira
    Saito, Kazuhiko
    Fujiwara, Masakazu
    Okutsu, Daiki
    Ichikawa, Hironobu
    JOURNAL OF CLINICAL PSYCHIATRY, 2020, 81 (03)
  • [42] Randomized, Double-Blind, Placebo-Controlled, Fixed-Dose Study to Evaluate the Efficacy and Safety of Amphetamine Extended-Release Tablets in Adults With Attention-Deficit/Hyperactivity Disorder
    Cutler, Andrew J.
    Childress, Ann C.
    Pardo, Antonio
    Duhoux, Stephanie
    Gomeni, Roberto
    Rafla, Eman
    King, Thomas R.
    Kando, Judith C.
    JOURNAL OF CLINICAL PSYCHIATRY, 2022, 83 (05) : 60 - 68
  • [43] Single Dose Pharmacokinetics of Amphetamine Extended-Release Oral Suspension (AMPH EROS) in Children Aged 4 to 5 Years Old With Attention-Deficit/Hyperactivity Disorder
    Herman, Barry
    Cutler, Andrew J.
    Kando, Judith
    King, Thomas
    Pardo, Antonio
    Marraffino, Andrea
    NEUROPSYCHOPHARMACOLOGY, 2018, 43 : S274 - S275
  • [44] Randomized, Double-Blind, Placebo-Controlled, Crossover Study of the Effects of Lisdexamfetamine Dimesylate and Mixed Amphetamine Salts on Cognition Throughout the Day in Adults with Attention-Deficit/Hyperactivity Disorder
    Martin, Patrick T.
    Corcoran, Mary
    Zhang, Pinggao
    Katic, Alain
    CLINICAL DRUG INVESTIGATION, 2014, 34 (02) : 147 - 157
  • [45] 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
    Manor, Iris
    Ben-Hayun, Rachel
    Aharon-Peretz, Judith
    Salomy, Dana
    Weizman, Abraham
    Daniely, Yaron
    Megiddo, Dalia
    Newcorn, Jeffrey H.
    Biederman, Joseph
    Adler, Lenard A.
    JOURNAL OF CLINICAL PSYCHIATRY, 2012, 73 (12) : 1517 - 1523
  • [46] A Phase III, Randomized, Double-Blind, Placebo-Controlled Trial Assessing the Efficacy and Safety of Viloxazine Extended-Release Capsules in Adults with Attention-Deficit/Hyperactivity Disorder
    Nasser, Azmi
    Hull, Joseph T.
    Chaturvedi, Soumya A.
    Liranso, Tesfaye
    Odebo, Oyinkansola
    Kosheleff, Alisa R.
    Fry, Nicholas
    Cutler, Andrew J.
    Rubin, Jonathan
    Schwabe, Stefan
    Childress, Ann
    CNS DRUGS, 2022, 36 (08) : 897 - 915
  • [47] Effect of Delayed-Release and Extended-Release Methylphenidate on Caregiver Strain and Validation of Psychometric Properties of the Caregiver Strain Questionnaire: Results from a Phase 3 Trial in Children with Attention-Deficit/Hyperactivity Disorder
    Lopez, Frank A.
    Faraone, Stephen V.
    Newcorn, Jeffrey H.
    Doll, Helen A.
    Rhoten, Stephanie
    Lewis, Hannah B.
    Khan, Tayyaba F.
    DeSousa, Norberto J.
    Sallee, Floyd R.
    Incledon, Bev
    JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY, 2021, 31 (03) : 179 - 186
  • [48] Efficacy and safety of mixed amphetamine salts extended release (Adderall XR) in the management of attention-deficit/hyperactivity disorder in adolescent patients: A 4-week, randomized, double-blind, placebo-controlled, parallel-group study
    Spencer, TJ
    Wilens, TE
    Biederman, J
    Weisler, RH
    Read, SC
    Pratt, R
    CLINICAL THERAPEUTICS, 2006, 28 (02) : 266 - 279
  • [49] Medication Persistence, Duration of Treatment, and Treatment-switching Patterns Among Canadian Patients Taking Once-daily Extended-release Methylphenidate Medications for Attention-Deficit/Hyperactivity Disorder: A Population-based Retrospective Cohort Study
    Park-Wyllie, Laura
    Van Stralen, Judy
    Almagor, Doron
    Dobson-Belaire, Wendy
    Charland, Katia
    Smith, Andrew
    Le Lorier, Jacques
    CLINICAL THERAPEUTICS, 2016, 38 (08) : 1789 - 1802
  • [50] Efficacy and safety of mixed amphetamine salts extended release (Adderall XR) in the management of oppositional defiant disorder with or without comorbid attention-deficit/hyperactivity disorder in school-aged children and adolescents: A 4-week, multicenter, randomized, double-blind, parallel-group, placebo-controlled, forced-dose-escalation study
    Spencer, TJ
    Abikoff, HB
    Connor, DF
    Biederman, J
    Pliszka, SR
    Boellner, S
    Read, SC
    Pratt, R
    CLINICAL THERAPEUTICS, 2006, 28 (03) : 402 - 418