Attention Deficit Hyperactivity Disorder
Conditions
Keywords
ADHD, Adult, long term, maintenance of response, Attention Deficit Hyperactivity Disorder
Brief summary
LYDO is a multi-center study that will enroll approximately 1925 adult outpatients with Attention Deficit/Hyperactivity Disorder (ADHD). Patients will receive, under open label conditions, atomoxetine up to 100 mg/day during the acute, open-label part of the study. Those patients that meet the response criteria will continue the blind phase of the study up to a year. During that period, patients that respond to atomoxetine will be randomized to continue the treatment with atomoxetine or with placebo (neither the patients nor investigators know if patients receive atomoxetine or placebo).
Interventions
Oral 40-100 mg/day
Oral delivery of matching placebo
Sponsors
Study design
Eligibility
Inclusion criteria
* Adults * Male or female * Must meet Attention-Deficit/Hyperactivity Disorder (ADHD) according to Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition Text Revision™ (DSM-IV-TR™) criteria
Exclusion criteria
* Comorbidity with major psychiatric disorder * Clinically significant depression or anxiety * Patients with significant medical conditions * Current alcohol/drugs abuse/dependence * Concomitant excluded medications
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period | Baseline (Week 24) up to Week 49 | Conners' Adult ADHD Rating Scale-Investigator Rated:Screening Version (CAARS-Inv:SV); 30-item scale (3 subscales): inattention, hyperactivity/impulsivity (9 items each), ADHD Index (12 items). Each item is scored 0 (not at all/never) to 3 (very much/very frequently). Total ADHD symptoms score (SS)=inattention+hyperactivity/impulsivity (range:0-54). Higher score=more impairment. Clinical Global Impressions-ADHD-Severity (CGI-ADHD-S) measures participant's overall severity of ADHD symptoms and scores range from 1 (normal, not at all ill) to 7 (among the most extremely ill participants). Maintenance of response during the randomized withdrawal phase was a reduction of ≥30% in the baseline CAARS-Inv:SV Total ADHD SS and a CGI-ADHD-S score ≤3. Participants had to continuously meet the response criteria, except for 1 excursion after assessment at Week 24 through Week 37 and 1 other excursion after assessment at Week 37 through Week 49. Excursions were not permitted at 2 consecutive visits. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 49 | Baseline (Week 24), Week 49 | The AAQoL is a self-reported, 29-item scale assessing functional impairments in adults with ADHD. Each item is rated on a 5-point Likert scale; range: 1 (Not at all/ Never) to 5 (Extremely/Very Often). 5-domains of scale include: work functioning, family relationships, social functioning, activities of daily living (driving, managing finances), and psychological adaptation (life satisfaction, self-esteem). These scores are transformed to a 0-100 point scale (1=0; 2=25; 3=50; 4=75; 5=100), and then the item scores are summed and divided by item count to generate overall scores. The overall scores have the same total range of scores of 0-100, with higher scores indicating better quality of life. Least Squares (LS) Mean values were adjusted for baseline AAQoL score and Investigator/site. |
| Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Baseline (Week 24), Week 49 | The CAARS-O:SV is a 30-item observer (typically a significant other or close friend) completed scale containing 3 subscales: inattention (9 items), hyperactivity/impulsivity (9 items), and ADHD Index (12 items). Each item is scored 0-3 (0=not at all/never; 1=just a little/once in a while; 2=pretty much/often; 3=very much/very frequently). Inattention and hyperactivity subscales range from 0-27; ADHD index subscale range is 0-36 with higher scores indicating more impaired participants. Total ADHD symptoms score=sum of the inattention and hyperactivity/impulsivity subscales, ranging from 0-54, with higher scores indicating more impaired participants. Least Squares (LS) Mean values adjusted for treatment, pooled Investigator, and baseline. |
| Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Baseline (Week 24), Week 49 | CAARS-S:SV is a 30-item participant completed scale containing 3 subscales: inattention (9 items), hyperactivity/impulsivity (9 items), ADHD Index (12 items). 0-3 (0=not at all/never; 1=just a little/once in a while; 2=pretty much/often; 3=very much/very frequently). Inattention and hyperactivity subscales range from 0-27; ADHD index subscale range is 0-36 with higher scores indicating more impaired participants. Total ADHD symptoms score=sum of the inattention and hyperactivity/impulsivity subscales; range: 0-54 with higher scores indicating more impaired participants. Least Squares (LS) Mean values adjusted for treatment, pooled Investigator, and baseline. |
| Number of Days Until Relapse | Baseline (Week 24) up to Week 49 | Relapse was defined as 2 consecutive visits with a CGI-ADHD-S score ≥4 points and a return to ≥80% of participant's baseline (Visit 2) CAARS-Inv:SV Total ADHD Symptom Score (SS). If the participant showed evidence of a return of symptoms at a single visit that met severity criteria described above, and because of worsening symptoms, was unwilling to remain in the study or did not return for a second visit, the participant was also considered to have relapsed. CAARS-Inv:SV is a 30-item scale (3 subscales): Inattention, Hyperactivity/Impulsivity (9 items each), ADHD Index (12 items). Each item is scored 0 (0=not at all/never) to 3 (very much/very frequently). Total ADHD SS=inattention+hyperactivity/impulsivity (range: 0-54). Higher score=more impairment. CGI-ADHD-S measures participant's overall severity of ADHD symptoms and scores range from 1 (normal, not at all ill) to 7 (among the most extremely ill participants). |
| Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version:Informant Report (BRIEF-A:Informant) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | Baseline (Week 24), Week 49 | BRIEF-A:Informant is a 75-item third-party observer's view of the participants' executive functions/self-regulation in their everyday environment. Items include: Inhibit, Shift, Emotional Control, Self Monitor, Initiate, Working Memory, Plan/Organize, Task Monitor, and Organization of Materials. Behavior is rated on a 3-point scale: 1 (behavior is never observed) to 3 (behavior is often observed). GEC Index Score is a subscore of the 75-item BRIEF-A score, reflects overall functioning and was calculated based on 70 items. Total scores range: 70-210. Lower scores = less perceived impairment. Least Squares (LS) Mean values were adjusted for treatment, pooled Investigator, and baseline. |
| Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | Baseline (Week 24), Week 49 | The EQ-5D is a Self-reported, 5-item scale to assess health utility (mobility, self-care, usual activities, pain and discomfort, and depression/anxiety). Scoring is on a 3-point scale (1=no health problems, 2=some or moderate problems, 3=major health problems). A preference value Index score is calculated using societal preference developed from a general population-based valuation studies. Index score ranges: United Kingdom (UK): -0.59 to 1.0, United States (US): -0.11 to 1.0, where 1 represents best possible health and 0 represents dead, with \<0 interpreted as a health state worse than dead. A Quality of Life Health State Score visual analog scale (VAS) was assessed, scores range from 0 to 100. Higher scores indicate better health state. Least Square (LS) Mean values were adjusted for treatment, pooled Investigator, baseline. |
| Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version: Self Report (BRIEF-A:Self Report) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | Baseline (Week 24), Week 49 | The BRIEF-A:Self Report is a 75-item self-reported measure captures adults' views of their own executive functions/self-regulation in their everyday environment. Items include: Inhibit, Shift, Emotional Control, Self Monitor, Initiate, Working Memory, Plan/Organize, Task Monitor, and Organization of Materials. Behavior is rated on a 3-point scale: 1 (behavior is never observed) to 3 (behavior is often observed). GEC Index Score is a subscore of the 75-item BRIEF-A score, reflects overall functioning and was calculated based on 70 items. Total scores range: 70-210. Lower scores = less perceived impairment. Least Squares (LS) Mean values were adjusted for treatment, pooled Investigator, and baseline. |
Countries
Austria, Belgium, Finland, France, Germany, Italy, Netherlands, Portugal, Spain, Sweden, Switzerland, United Kingdom
Participant flow
Pre-assignment details
The study consisted of 4 treatment periods: 12 weeks open-label, acute-treatment (trx) phase (Study Period 2), 12 weeks double-blind maintenance phase of Study Period 3 (Study Period 3A), 25 weeks double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B) and an Open-Label Extension Period (Study Period 4) lasting up to 2.3 years.
Participants by arm
| Arm | Count |
|---|---|
| Atomoxetine (40-100 mg) 40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment period (Study Period 2). | 2,017 |
| Total | 2,017 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 | FG004 |
|---|---|---|---|---|---|---|
| Study Period 2 (Open-Label Acute Trx) | Adverse Event | 298 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Clinical Relapse | 7 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Entry Criteria Not Met | 2 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Lack of Efficacy | 90 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Lost to Follow-up | 108 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Physician Decision | 8 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Protocol Interim Criteria Not Met | 161 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Protocol Violation | 173 | 0 | 0 | 0 | 0 |
| Study Period 2 (Open-Label Acute Trx) | Withdrawal by Subject | 164 | 0 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Adverse Event | 0 | 50 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Clinical Relapse | 0 | 49 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Lack of Efficacy | 0 | 32 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Lost to Follow-up | 0 | 41 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Missing - Not Otherwise Defined | 0 | 5 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Physician Decision | 0 | 2 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Protocol Interim Criteria Not Met | 0 | 162 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Protocol Violation | 0 | 56 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Sponsor Decision | 0 | 3 | 0 | 0 | 0 |
| Study Period 3A (Blinded Maintenance) | Withdrawal by Subject | 0 | 81 | 0 | 0 | 0 |
| Study Period 3B (Randomized Withdrawal) | Adverse Event | 0 | 0 | 8 | 5 | 0 |
| Study Period 3B (Randomized Withdrawal) | Clinical Relapse | 0 | 0 | 0 | 3 | 0 |
| Study Period 3B (Randomized Withdrawal) | Death | 0 | 0 | 1 | 0 | 0 |
| Study Period 3B (Randomized Withdrawal) | Lack of Efficacy | 0 | 0 | 3 | 11 | 0 |
| Study Period 3B (Randomized Withdrawal) | Lost to Follow-up | 0 | 0 | 19 | 9 | 0 |
| Study Period 3B (Randomized Withdrawal) | Missing | 0 | 0 | 1 | 1 | 0 |
| Study Period 3B (Randomized Withdrawal) | Physician Decision | 0 | 0 | 2 | 0 | 0 |
| Study Period 3B (Randomized Withdrawal) | Protocol Interim Criteria Not Met | 0 | 0 | 0 | 5 | 0 |
| Study Period 3B (Randomized Withdrawal) | Protocol Violation | 0 | 0 | 23 | 25 | 0 |
| Study Period 3B (Randomized Withdrawal) | Withdrawal by Subject | 0 | 0 | 25 | 34 | 0 |
| Study Period 4 (Open-Label Extension) | Adverse Event | 0 | 0 | 0 | 0 | 16 |
| Study Period 4 (Open-Label Extension) | Clinical Relapse | 0 | 0 | 0 | 0 | 1 |
| Study Period 4 (Open-Label Extension) | Death | 0 | 0 | 0 | 0 | 1 |
| Study Period 4 (Open-Label Extension) | Lack of Efficacy | 0 | 0 | 0 | 0 | 1 |
| Study Period 4 (Open-Label Extension) | Lost to Follow-up | 0 | 0 | 0 | 0 | 11 |
| Study Period 4 (Open-Label Extension) | Physician Decision | 0 | 0 | 0 | 0 | 2 |
| Study Period 4 (Open-Label Extension) | Protocol Violation | 0 | 0 | 0 | 0 | 12 |
| Study Period 4 (Open-Label Extension) | Sponsor Decision | 0 | 0 | 0 | 0 | 2 |
| Study Period 4 (Open-Label Extension) | Withdrawal by Subject | 0 | 0 | 0 | 0 | 38 |
Baseline characteristics
| Characteristic | Atomoxetine (40-100 mg) |
|---|---|
| Age, Continuous | 33.15 years STANDARD_DEVIATION 9.09 |
| Race/Ethnicity, Customized African | 56 participants |
| Race/Ethnicity, Customized Caucasian | 1765 participants |
| Race/Ethnicity, Customized East Asian | 14 participants |
| Race/Ethnicity, Customized Hispanic | 159 participants |
| Race/Ethnicity, Customized Missing | 2 participants |
| Race/Ethnicity, Customized Native American | 6 participants |
| Race/Ethnicity, Customized West Asian | 15 participants |
| Region of Enrollment Argentina | 27 participants |
| Region of Enrollment Austria | 109 participants |
| Region of Enrollment Belgium | 137 participants |
| Region of Enrollment Canada | 60 participants |
| Region of Enrollment Denmark | 15 participants |
| Region of Enrollment Finland | 52 participants |
| Region of Enrollment France | 65 participants |
| Region of Enrollment Germany | 434 participants |
| Region of Enrollment Italy | 32 participants |
| Region of Enrollment Mexico | 53 participants |
| Region of Enrollment Netherlands | 71 participants |
| Region of Enrollment Portugal | 3 participants |
| Region of Enrollment Puerto Rico | 52 participants |
| Region of Enrollment Russian Federation | 6 participants |
| Region of Enrollment Spain | 153 participants |
| Region of Enrollment Sweden | 112 participants |
| Region of Enrollment Switzerland | 7 participants |
| Region of Enrollment United Kingdom | 27 participants |
| Region of Enrollment United States | 602 participants |
| Sex: Female, Male Female | 833 Participants |
| Sex: Female, Male Male | 1184 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — | — / — |
| other Total, other adverse events | 1,611 / 2,011 | 120 / 266 | 96 / 258 | 119 / 180 |
| serious Total, serious adverse events | 29 / 2,011 | 7 / 266 | 3 / 258 | 14 / 180 |
Outcome results
Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period
Conners' Adult ADHD Rating Scale-Investigator Rated:Screening Version (CAARS-Inv:SV); 30-item scale (3 subscales): inattention, hyperactivity/impulsivity (9 items each), ADHD Index (12 items). Each item is scored 0 (not at all/never) to 3 (very much/very frequently). Total ADHD symptoms score (SS)=inattention+hyperactivity/impulsivity (range:0-54). Higher score=more impairment. Clinical Global Impressions-ADHD-Severity (CGI-ADHD-S) measures participant's overall severity of ADHD symptoms and scores range from 1 (normal, not at all ill) to 7 (among the most extremely ill participants). Maintenance of response during the randomized withdrawal phase was a reduction of ≥30% in the baseline CAARS-Inv:SV Total ADHD SS and a CGI-ADHD-S score ≤3. Participants had to continuously meet the response criteria, except for 1 excursion after assessment at Week 24 through Week 37 and 1 other excursion after assessment at Week 37 through Week 49. Excursions were not permitted at 2 consecutive visits.
Time frame: Baseline (Week 24) up to Week 49
Population: Primary outcome measure analysis was conducted using all randomized participants in the Double-Blind Maintenance/Randomized Withdrawal Period (Study Period 3B).
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Atomoxetine | Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period | 64.3 percentage of responders |
| Placebo | Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period | 50.0 percentage of responders |
Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49
CAARS-S:SV is a 30-item participant completed scale containing 3 subscales: inattention (9 items), hyperactivity/impulsivity (9 items), ADHD Index (12 items). 0-3 (0=not at all/never; 1=just a little/once in a while; 2=pretty much/often; 3=very much/very frequently). Inattention and hyperactivity subscales range from 0-27; ADHD index subscale range is 0-36 with higher scores indicating more impaired participants. Total ADHD symptoms score=sum of the inattention and hyperactivity/impulsivity subscales; range: 0-54 with higher scores indicating more impaired participants. Least Squares (LS) Mean values adjusted for treatment, pooled Investigator, and baseline.
Time frame: Baseline (Week 24), Week 49
Population: Participants with a non-missing baseline and at least 1 post-baseline CAARS-S:SV result within each treatment group, Last Observation Carried Forward (LOCF).
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|---|
| Atomoxetine | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Inattention Subscale Imputed Score | -0.70 units on a scale | Standard Error 0.38 |
| Atomoxetine | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | ADHD Symptom Imputed Index Score | -1.20 units on a scale | Standard Error 0.44 |
| Atomoxetine | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Total ADHD Symptom Imputed Score | -1.60 units on a scale | Standard Error 0.65 |
| Atomoxetine | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Hyperactivity-Impulsivity Subscale Imputed Score | -0.90 units on a scale | Standard Error 0.33 |
| Placebo | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Total ADHD Symptom Imputed Score | 1.70 units on a scale | Standard Error 0.64 |
| Placebo | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | ADHD Symptom Imputed Index Score | 0.90 units on a scale | Standard Error 0.43 |
| Placebo | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Inattention Subscale Imputed Score | 1.20 units on a scale | Standard Error 0.37 |
| Placebo | Change From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49 | Hyperactivity-Impulsivity Subscale Imputed Score | 0.50 units on a scale | Standard Error 0.32 |
Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49
The CAARS-O:SV is a 30-item observer (typically a significant other or close friend) completed scale containing 3 subscales: inattention (9 items), hyperactivity/impulsivity (9 items), and ADHD Index (12 items). Each item is scored 0-3 (0=not at all/never; 1=just a little/once in a while; 2=pretty much/often; 3=very much/very frequently). Inattention and hyperactivity subscales range from 0-27; ADHD index subscale range is 0-36 with higher scores indicating more impaired participants. Total ADHD symptoms score=sum of the inattention and hyperactivity/impulsivity subscales, ranging from 0-54, with higher scores indicating more impaired participants. Least Squares (LS) Mean values adjusted for treatment, pooled Investigator, and baseline.
Time frame: Baseline (Week 24), Week 49
Population: Participants with a non-missing baseline and at least 1 post-baseline CAARS-O:SV result within each group, Last Observation Carried Forward (LOCF) were included in the analysis.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|---|
| Atomoxetine | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | ADHD Imputed (Attributed) Index Score (N=164, 153) | -2.60 units on a scale | Standard Error 0.56 |
| Atomoxetine | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Hyperactivity/Impulsivity Subscale Imputed Score | -1.90 units on a scale | Standard Error 0.44 |
| Atomoxetine | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Inattention Subscale Imputed Score | -1.60 units on a scale | Standard Error 0.46 |
| Atomoxetine | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Total ADHD Symptom Imputed Score | -3.50 units on a scale | Standard Error 0.83 |
| Placebo | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Total ADHD Symptom Imputed Score | -0.40 units on a scale | Standard Error 0.83 |
| Placebo | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | ADHD Imputed (Attributed) Index Score (N=164, 153) | -0.10 units on a scale | Standard Error 0.57 |
| Placebo | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Inattention Subscale Imputed Score | -0.10 units on a scale | Standard Error 0.46 |
| Placebo | Change From Baseline in Conner's Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Rating Scale (Observer Rated [CAARS-O:SV]) Total ADHD Symptom Score From Week 24 to Week 49 | Hyperactivity/Impulsivity Subscale Imputed Score | -0.10 units on a scale | Standard Error 0.44 |
Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49
The EQ-5D is a Self-reported, 5-item scale to assess health utility (mobility, self-care, usual activities, pain and discomfort, and depression/anxiety). Scoring is on a 3-point scale (1=no health problems, 2=some or moderate problems, 3=major health problems). A preference value Index score is calculated using societal preference developed from a general population-based valuation studies. Index score ranges: United Kingdom (UK): -0.59 to 1.0, United States (US): -0.11 to 1.0, where 1 represents best possible health and 0 represents dead, with \<0 interpreted as a health state worse than dead. A Quality of Life Health State Score visual analog scale (VAS) was assessed, scores range from 0 to 100. Higher scores indicate better health state. Least Square (LS) Mean values were adjusted for treatment, pooled Investigator, baseline.
Time frame: Baseline (Week 24), Week 49
Population: Participants with a non-missing baseline and at least 1 post-baseline EQ-5D Index Score or VAS score within each group, Last Observation Carried Forward (LOCF) were included in the analysis.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|---|
| Atomoxetine | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | UK population-based Index Score (n=194, 180) | 0.00 units on a scale | Standard Error 0.01 |
| Atomoxetine | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | US population-based Index Score (n=194, 180) | 0.00 units on a scale | Standard Error 0.01 |
| Atomoxetine | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | Health State Score (N=197, 179) | 4.60 units on a scale | Standard Error 1.21 |
| Placebo | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | UK population-based Index Score (n=194, 180) | 0.00 units on a scale | Standard Error 0.01 |
| Placebo | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | US population-based Index Score (n=194, 180) | 0.00 units on a scale | Standard Error 0.01 |
| Placebo | Change From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49 | Health State Score (N=197, 179) | 3.20 units on a scale | Standard Error 1.19 |
Change From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 49
The AAQoL is a self-reported, 29-item scale assessing functional impairments in adults with ADHD. Each item is rated on a 5-point Likert scale; range: 1 (Not at all/ Never) to 5 (Extremely/Very Often). 5-domains of scale include: work functioning, family relationships, social functioning, activities of daily living (driving, managing finances), and psychological adaptation (life satisfaction, self-esteem). These scores are transformed to a 0-100 point scale (1=0; 2=25; 3=50; 4=75; 5=100), and then the item scores are summed and divided by item count to generate overall scores. The overall scores have the same total range of scores of 0-100, with higher scores indicating better quality of life. Least Squares (LS) Mean values were adjusted for baseline AAQoL score and Investigator/site.
Time frame: Baseline (Week 24), Week 49
Population: All randomized participants with a baseline and at least 1 post-baseline AAQoL score were included in the analysis.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Atomoxetine | Change From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 49 | 0.4 units on a scale | Standard Error 1.12 |
| Placebo | Change From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 49 | -4.0 units on a scale | Standard Error 1.1 |
Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version:Informant Report (BRIEF-A:Informant) Global Executive Composite (GEC) Index Score From Week 24 to Week 49
BRIEF-A:Informant is a 75-item third-party observer's view of the participants' executive functions/self-regulation in their everyday environment. Items include: Inhibit, Shift, Emotional Control, Self Monitor, Initiate, Working Memory, Plan/Organize, Task Monitor, and Organization of Materials. Behavior is rated on a 3-point scale: 1 (behavior is never observed) to 3 (behavior is often observed). GEC Index Score is a subscore of the 75-item BRIEF-A score, reflects overall functioning and was calculated based on 70 items. Total scores range: 70-210. Lower scores = less perceived impairment. Least Squares (LS) Mean values were adjusted for treatment, pooled Investigator, and baseline.
Time frame: Baseline (Week 24), Week 49
Population: Participants with a non-missing baseline and at least 1 post-baseline BRIEF-A:Informant result within each group, Last Observation Carried Forward (LOCF) were included in the analysis.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Atomoxetine | Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version:Informant Report (BRIEF-A:Informant) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | -8.4 units on a scale | Standard Error 2.16 |
| Placebo | Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version:Informant Report (BRIEF-A:Informant) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | -0.6 units on a scale | Standard Error 2.17 |
Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version: Self Report (BRIEF-A:Self Report) Global Executive Composite (GEC) Index Score From Week 24 to Week 49
The BRIEF-A:Self Report is a 75-item self-reported measure captures adults' views of their own executive functions/self-regulation in their everyday environment. Items include: Inhibit, Shift, Emotional Control, Self Monitor, Initiate, Working Memory, Plan/Organize, Task Monitor, and Organization of Materials. Behavior is rated on a 3-point scale: 1 (behavior is never observed) to 3 (behavior is often observed). GEC Index Score is a subscore of the 75-item BRIEF-A score, reflects overall functioning and was calculated based on 70 items. Total scores range: 70-210. Lower scores = less perceived impairment. Least Squares (LS) Mean values were adjusted for treatment, pooled Investigator, and baseline.
Time frame: Baseline (Week 24), Week 49
Population: Participants with a non-missing baseline and at least 1 post-baseline BRIEF-A:Self Report result within each group, Last Observation Carried Forward (LOCF) were included in the analysis.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) | Dispersion |
|---|---|---|---|
| Atomoxetine | Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version: Self Report (BRIEF-A:Self Report) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | -5.70 units on a scale | Standard Error 1.88 |
| Placebo | Change From Baseline in the Behavior Rating Inventory of Executive Function-Adult Version: Self Report (BRIEF-A:Self Report) Global Executive Composite (GEC) Index Score From Week 24 to Week 49 | 0.90 units on a scale | Standard Error 1.81 |
Number of Days Until Relapse
Relapse was defined as 2 consecutive visits with a CGI-ADHD-S score ≥4 points and a return to ≥80% of participant's baseline (Visit 2) CAARS-Inv:SV Total ADHD Symptom Score (SS). If the participant showed evidence of a return of symptoms at a single visit that met severity criteria described above, and because of worsening symptoms, was unwilling to remain in the study or did not return for a second visit, the participant was also considered to have relapsed. CAARS-Inv:SV is a 30-item scale (3 subscales): Inattention, Hyperactivity/Impulsivity (9 items each), ADHD Index (12 items). Each item is scored 0 (0=not at all/never) to 3 (very much/very frequently). Total ADHD SS=inattention+hyperactivity/impulsivity (range: 0-54). Higher score=more impairment. CGI-ADHD-S measures participant's overall severity of ADHD symptoms and scores range from 1 (normal, not at all ill) to 7 (among the most extremely ill participants).
Time frame: Baseline (Week 24) up to Week 49
Population: Analyses were conducted using all randomized participants in the Double-Blind Period (Study Period 3B).
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Atomoxetine | Number of Days Until Relapse | NA days |
| Placebo | Number of Days Until Relapse | NA days |