Skip to content

A Long Term Study of a Medication for Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)

Maintenance of Response After Open-Label Treatment With Atomoxetine Hydrochloride in Adult Outpatients With Attention-Deficit/Hyperactivity Disorder (ADHD): A Placebo-Controlled, Randomized Withdrawal Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00700427
Enrollment
2017
Registered
2008-06-18
Start date
2008-06-30
Completion date
2013-10-31
Last updated
2014-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder

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

DRUGatomoxetine hydrochloride

Oral 40-100 mg/day

DRUGPlacebo

Oral delivery of matching placebo

Sponsors

Eli Lilly and Company
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

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

MeasureTime frameDescription
Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal PeriodBaseline (Week 24) up to Week 49Conners' 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

MeasureTime frameDescription
Change From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 49Baseline (Week 24), Week 49The 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 49Baseline (Week 24), Week 49The 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 49Baseline (Week 24), Week 49CAARS-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 RelapseBaseline (Week 24) up to Week 49Relapse 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 49Baseline (Week 24), Week 49BRIEF-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 49Baseline (Week 24), Week 49The 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 49Baseline (Week 24), Week 49The 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

ArmCount
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
Total2,017

Withdrawals & dropouts

PeriodReasonFG000FG001FG002FG003FG004
Study Period 2 (Open-Label Acute Trx)Adverse Event2980000
Study Period 2 (Open-Label Acute Trx)Clinical Relapse70000
Study Period 2 (Open-Label Acute Trx)Entry Criteria Not Met20000
Study Period 2 (Open-Label Acute Trx)Lack of Efficacy900000
Study Period 2 (Open-Label Acute Trx)Lost to Follow-up1080000
Study Period 2 (Open-Label Acute Trx)Physician Decision80000
Study Period 2 (Open-Label Acute Trx)Protocol Interim Criteria Not Met1610000
Study Period 2 (Open-Label Acute Trx)Protocol Violation1730000
Study Period 2 (Open-Label Acute Trx)Withdrawal by Subject1640000
Study Period 3A (Blinded Maintenance)Adverse Event050000
Study Period 3A (Blinded Maintenance)Clinical Relapse049000
Study Period 3A (Blinded Maintenance)Lack of Efficacy032000
Study Period 3A (Blinded Maintenance)Lost to Follow-up041000
Study Period 3A (Blinded Maintenance)Missing - Not Otherwise Defined05000
Study Period 3A (Blinded Maintenance)Physician Decision02000
Study Period 3A (Blinded Maintenance)Protocol Interim Criteria Not Met0162000
Study Period 3A (Blinded Maintenance)Protocol Violation056000
Study Period 3A (Blinded Maintenance)Sponsor Decision03000
Study Period 3A (Blinded Maintenance)Withdrawal by Subject081000
Study Period 3B (Randomized Withdrawal)Adverse Event00850
Study Period 3B (Randomized Withdrawal)Clinical Relapse00030
Study Period 3B (Randomized Withdrawal)Death00100
Study Period 3B (Randomized Withdrawal)Lack of Efficacy003110
Study Period 3B (Randomized Withdrawal)Lost to Follow-up001990
Study Period 3B (Randomized Withdrawal)Missing00110
Study Period 3B (Randomized Withdrawal)Physician Decision00200
Study Period 3B (Randomized Withdrawal)Protocol Interim Criteria Not Met00050
Study Period 3B (Randomized Withdrawal)Protocol Violation0023250
Study Period 3B (Randomized Withdrawal)Withdrawal by Subject0025340
Study Period 4 (Open-Label Extension)Adverse Event000016
Study Period 4 (Open-Label Extension)Clinical Relapse00001
Study Period 4 (Open-Label Extension)Death00001
Study Period 4 (Open-Label Extension)Lack of Efficacy00001
Study Period 4 (Open-Label Extension)Lost to Follow-up000011
Study Period 4 (Open-Label Extension)Physician Decision00002
Study Period 4 (Open-Label Extension)Protocol Violation000012
Study Period 4 (Open-Label Extension)Sponsor Decision00002
Study Period 4 (Open-Label Extension)Withdrawal by Subject000038

Baseline characteristics

CharacteristicAtomoxetine (40-100 mg)
Age, Continuous33.15 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 typeEG000
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 / 2,011120 / 26696 / 258119 / 180
serious
Total, serious adverse events
29 / 2,0117 / 2663 / 25814 / 180

Outcome results

Primary

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).

ArmMeasureValue (NUMBER)
AtomoxetinePercentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period64.3 percentage of responders
PlaceboPercentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period50.0 percentage of responders
p-value: 0.001Fisher Exact
Secondary

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).

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Inattention Subscale Imputed Score-0.70 units on a scaleStandard Error 0.38
AtomoxetineChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49ADHD Symptom Imputed Index Score-1.20 units on a scaleStandard Error 0.44
AtomoxetineChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Total ADHD Symptom Imputed Score-1.60 units on a scaleStandard Error 0.65
AtomoxetineChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Hyperactivity-Impulsivity Subscale Imputed Score-0.90 units on a scaleStandard Error 0.33
PlaceboChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Total ADHD Symptom Imputed Score1.70 units on a scaleStandard Error 0.64
PlaceboChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49ADHD Symptom Imputed Index Score0.90 units on a scaleStandard Error 0.43
PlaceboChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Inattention Subscale Imputed Score1.20 units on a scaleStandard Error 0.37
PlaceboChange From Baseline in Conner's Adult ADHD Rating Scale-Self Rated (CARRS-S:SV) Total ADHD Symptom Score From Week 24 to Week 49Hyperactivity-Impulsivity Subscale Imputed Score0.50 units on a scaleStandard Error 0.32
p-value: <0.001ANCOVA
p-value: <0.001ANCOVA
p-value: <0.001ANCOVA
p-value: <0.001ANCOVA
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange 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 49ADHD Imputed (Attributed) Index Score (N=164, 153)-2.60 units on a scaleStandard Error 0.56
AtomoxetineChange 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 49Hyperactivity/Impulsivity Subscale Imputed Score-1.90 units on a scaleStandard Error 0.44
AtomoxetineChange 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 49Inattention Subscale Imputed Score-1.60 units on a scaleStandard Error 0.46
AtomoxetineChange 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 49Total ADHD Symptom Imputed Score-3.50 units on a scaleStandard Error 0.83
PlaceboChange 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 49Total ADHD Symptom Imputed Score-0.40 units on a scaleStandard Error 0.83
PlaceboChange 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 49ADHD Imputed (Attributed) Index Score (N=164, 153)-0.10 units on a scaleStandard Error 0.57
PlaceboChange 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 49Inattention Subscale Imputed Score-0.10 units on a scaleStandard Error 0.46
PlaceboChange 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 49Hyperactivity/Impulsivity Subscale Imputed Score-0.10 units on a scaleStandard Error 0.44
p-value: <0.001ANCOVA
p-value: 0.002ANCOVA
p-value: 0.009ANCOVA
p-value: 0.003ANCOVA
Secondary

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.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49UK population-based Index Score (n=194, 180)0.00 units on a scaleStandard Error 0.01
AtomoxetineChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49US population-based Index Score (n=194, 180)0.00 units on a scaleStandard Error 0.01
AtomoxetineChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49Health State Score (N=197, 179)4.60 units on a scaleStandard Error 1.21
PlaceboChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49UK population-based Index Score (n=194, 180)0.00 units on a scaleStandard Error 0.01
PlaceboChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49US population-based Index Score (n=194, 180)0.00 units on a scaleStandard Error 0.01
PlaceboChange From Baseline in European Quality of Life (EuroQoL) Questionnaire-5 Dimensions (EQ-5D) Index Score From Week 24 to Week 49Health State Score (N=197, 179)3.20 units on a scaleStandard Error 1.19
Secondary

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.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange From Baseline in the Adult Attention-Deficit/Hyperactivity Disorder (ADHD) Quality of Life (AAQoL) Scale From Week 24 to Week 490.4 units on a scaleStandard Error 1.12
PlaceboChange 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 scaleStandard Error 1.1
p-value: 0.002ANCOVA
Secondary

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.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange 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 scaleStandard Error 2.16
PlaceboChange 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 scaleStandard Error 2.17
p-value: 0.006ANCOVA
Secondary

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.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
AtomoxetineChange 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 scaleStandard Error 1.88
PlaceboChange 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 490.90 units on a scaleStandard Error 1.81
p-value: 0.006ANCOVA
Secondary

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).

ArmMeasureValue (MEAN)
AtomoxetineNumber of Days Until RelapseNA days
PlaceboNumber of Days Until RelapseNA days

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026