Trial Outcomes & Findings for A Long Term Study of a Medication for Adults With Attention-Deficit/Hyperactivity Disorder (ADHD) (NCT NCT00700427)

NCT ID: NCT00700427

Last Updated: 2014-06-26

Results Overview

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.

Recruitment status

COMPLETED

Study phase

PHASE3

Target enrollment

2017 participants

Primary outcome timeframe

Baseline (Week 24) up to Week 49

Results posted on

2014-06-26

Participant Flow

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.

Participant milestones

Participant milestones
Measure
Atomoxetine (Study Period 2)
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2).
Atomoxetine (Study Period 3A)
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during double-blind randomized withdrawal phase (Study Period 3).
Atomoxetine (Study Period 3B)
80-100 mg/day atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo (Study Period 3B)
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Atomoxetine (Study Period 4)
Participants who received either atomoxetine or placebo and completed the last visit of Study Period 3 who were in countries where the adult ADHD indication for atomoxetine was not approved were allowed to participant in Study Period 4 (Open-label Extension). Participants received 40 mg/day atomoxetine orally for at least 7 days after which it was increased to 80-100 mg/day atomoxetine orally for up to 2.3 years.
Study Period 2 (Open-Label Acute Trx)
STARTED
2017
0
0
0
0
Study Period 2 (Open-Label Acute Trx)
Received at Least One Dose of Study Drug
2011
0
0
0
0
Study Period 2 (Open-Label Acute Trx)
COMPLETED
1006
0
0
0
0
Study Period 2 (Open-Label Acute Trx)
NOT COMPLETED
1011
0
0
0
0
Study Period 3A (Blinded Maintenance)
STARTED
0
1005
0
0
0
Study Period 3A (Blinded Maintenance)
COMPLETED
0
524
0
0
0
Study Period 3A (Blinded Maintenance)
NOT COMPLETED
0
481
0
0
0
Study Period 3B (Randomized Withdrawal)
STARTED
0
0
266
258
0
Study Period 3B (Randomized Withdrawal)
COMPLETED
0
0
184
165
0
Study Period 3B (Randomized Withdrawal)
NOT COMPLETED
0
0
82
93
0
Study Period 4 (Open-Label Extension)
STARTED
0
0
0
0
180
Study Period 4 (Open-Label Extension)
COMPLETED
0
0
0
0
96
Study Period 4 (Open-Label Extension)
NOT COMPLETED
0
0
0
0
84

Reasons for withdrawal

Reasons for withdrawal
Measure
Atomoxetine (Study Period 2)
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2).
Atomoxetine (Study Period 3A)
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during double-blind randomized withdrawal phase (Study Period 3).
Atomoxetine (Study Period 3B)
80-100 mg/day atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo (Study Period 3B)
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Atomoxetine (Study Period 4)
Participants who received either atomoxetine or placebo and completed the last visit of Study Period 3 who were in countries where the adult ADHD indication for atomoxetine was not approved were allowed to participant in Study Period 4 (Open-label Extension). Participants received 40 mg/day atomoxetine orally for at least 7 days after which it was increased to 80-100 mg/day atomoxetine orally for up to 2.3 years.
Study Period 2 (Open-Label Acute Trx)
Adverse Event
298
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 2 (Open-Label Acute Trx)
Protocol Interim Criteria Not Met
161
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)
Lack of Efficacy
90
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)
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 3A (Blinded Maintenance)
Adverse Event
0
50
0
0
0
Study Period 3A (Blinded Maintenance)
Protocol Interim Criteria Not Met
0
162
0
0
0
Study Period 3A (Blinded Maintenance)
Withdrawal by Subject
0
81
0
0
0
Study Period 3A (Blinded Maintenance)
Protocol Violation
0
56
0
0
0
Study Period 3A (Blinded Maintenance)
Clinical Relapse
0
49
0
0
0
Study Period 3A (Blinded Maintenance)
Lost to Follow-up
0
41
0
0
0
Study Period 3A (Blinded Maintenance)
Lack of Efficacy
0
32
0
0
0
Study Period 3A (Blinded Maintenance)
Sponsor Decision
0
3
0
0
0
Study Period 3A (Blinded Maintenance)
Physician Decision
0
2
0
0
0
Study Period 3A (Blinded Maintenance)
Missing - Not Otherwise Defined
0
5
0
0
0
Study Period 3B (Randomized Withdrawal)
Adverse Event
0
0
8
5
0
Study Period 3B (Randomized Withdrawal)
Withdrawal by Subject
0
0
25
34
0
Study Period 3B (Randomized Withdrawal)
Protocol Violation
0
0
23
25
0
Study Period 3B (Randomized Withdrawal)
Lost to Follow-up
0
0
19
9
0
Study Period 3B (Randomized Withdrawal)
Lack of Efficacy
0
0
3
11
0
Study Period 3B (Randomized Withdrawal)
Protocol Interim Criteria Not Met
0
0
0
5
0
Study Period 3B (Randomized Withdrawal)
Clinical Relapse
0
0
0
3
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)
Death
0
0
1
0
0
Study Period 4 (Open-Label Extension)
Adverse Event
0
0
0
0
16
Study Period 4 (Open-Label Extension)
Death
0
0
0
0
1
Study Period 4 (Open-Label Extension)
Protocol Violation
0
0
0
0
12
Study Period 4 (Open-Label Extension)
Withdrawal by Subject
0
0
0
0
38
Study Period 4 (Open-Label Extension)
Physician Decision
0
0
0
0
2
Study Period 4 (Open-Label Extension)
Sponsor Decision
0
0
0
0
2
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)
Clinical Relapse
0
0
0
0
1

Baseline Characteristics

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

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Atomoxetine (40-100 mg)
n=2017 Participants
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).
Age, Continuous
33.15 years
STANDARD_DEVIATION 9.09 • n=99 Participants
Sex: Female, Male
Female
833 Participants
n=99 Participants
Sex: Female, Male
Male
1184 Participants
n=99 Participants
Race/Ethnicity, Customized
Caucasian
1765 participants
n=99 Participants
Race/Ethnicity, Customized
African
56 participants
n=99 Participants
Race/Ethnicity, Customized
Hispanic
159 participants
n=99 Participants
Race/Ethnicity, Customized
Native American
6 participants
n=99 Participants
Race/Ethnicity, Customized
East Asian
14 participants
n=99 Participants
Race/Ethnicity, Customized
West Asian
15 participants
n=99 Participants
Race/Ethnicity, Customized
Missing
2 participants
n=99 Participants
Region of Enrollment
Argentina
27 participants
n=99 Participants
Region of Enrollment
Austria
109 participants
n=99 Participants
Region of Enrollment
Belgium
137 participants
n=99 Participants
Region of Enrollment
Canada
60 participants
n=99 Participants
Region of Enrollment
Denmark
15 participants
n=99 Participants
Region of Enrollment
Finland
52 participants
n=99 Participants
Region of Enrollment
France
65 participants
n=99 Participants
Region of Enrollment
Germany
434 participants
n=99 Participants
Region of Enrollment
Italy
32 participants
n=99 Participants
Region of Enrollment
Mexico
53 participants
n=99 Participants
Region of Enrollment
Netherlands
71 participants
n=99 Participants
Region of Enrollment
Portugal
3 participants
n=99 Participants
Region of Enrollment
Puerto Rico
52 participants
n=99 Participants
Region of Enrollment
Russian Federation
6 participants
n=99 Participants
Region of Enrollment
Spain
153 participants
n=99 Participants
Region of Enrollment
Sweden
112 participants
n=99 Participants
Region of Enrollment
Switzerland
7 participants
n=99 Participants
Region of Enrollment
United Kingdom
27 participants
n=99 Participants
Region of Enrollment
United States
602 participants
n=99 Participants

PRIMARY outcome

Timeframe: 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).

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=266 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=258 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Percentage of Participants Who Maintain a Satisfactory Response During the Double-Blind Maintenance/Randomized Withdrawal Period
64.3 percentage of responders
50.0 percentage of responders

SECONDARY outcome

Timeframe: Baseline (Week 24) up to Week 49

Population: Analyses were conducted using all randomized participants in the Double-Blind Period (Study Period 3B).

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).

Outcome measures

Outcome measures
Measure
Atomoxetine
n=266 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=258 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Number of Days Until Relapse
NA days
Standard Deviation NA
The mean and standard deviation could not be reliably estimated because of low numbers of participants who relapsed.
NA days
Standard Deviation NA
The mean and standard deviation could not be reliably estimated because of low numbers of participants who relapsed.

SECONDARY outcome

Timeframe: 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.

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=198 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=180 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
-4.0 units on a scale
Standard Error 1.10

SECONDARY outcome

Timeframe: 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.

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=165 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=153 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
-0.10 units on a scale
Standard Error 0.57
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
-0.10 units on a scale
Standard Error 0.44
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
-0.10 units on a scale
Standard Error 0.46
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
-0.40 units on a scale
Standard Error 0.83

SECONDARY outcome

Timeframe: 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).

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=193 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=178 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
0.90 units on a scale
Standard Error 0.43
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
0.50 units on a scale
Standard Error 0.32
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
1.20 units on a scale
Standard Error 0.37
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
1.70 units on a scale
Standard Error 0.64

SECONDARY outcome

Timeframe: 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.

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=187 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=173 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
0.90 units on a scale
Standard Error 1.81

SECONDARY outcome

Timeframe: 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.

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=154 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=147 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
-0.6 units on a scale
Standard Error 2.17

SECONDARY outcome

Timeframe: 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.

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.

Outcome measures

Outcome measures
Measure
Atomoxetine
n=197 Participants
80-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo
n=180 Participants
Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
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
0.00 units on a scale
Standard Error 0.01
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
0.00 units on a scale
Standard Error 0.01
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
3.20 units on a scale
Standard Error 1.19

Adverse Events

Atomoxetine (Study Periods 2 and 3A)

Serious events: 29 serious events
Other events: 1611 other events
Deaths: 0 deaths

Atomoxetine (Study Period 3B)

Serious events: 7 serious events
Other events: 120 other events
Deaths: 0 deaths

Placebo (Study Period 3B)

Serious events: 3 serious events
Other events: 96 other events
Deaths: 0 deaths

Atomoxetine (Study Period 4; Open-Label Extension)

Serious events: 14 serious events
Other events: 119 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Atomoxetine (Study Periods 2 and 3A)
n=2011 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A).
Atomoxetine (Study Period 3B)
n=266 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A). Followed by 80-100 mg/day atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo (Study Period 3B)
n=258 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A). Followed by Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Atomoxetine (Study Period 4; Open-Label Extension)
n=180 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A) and for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B), followed by a 2 year open label extension (Study Period 4). The open-label extension was optional and only offered to participants living in countries where atomoxetine for the adult ADHD indication had not been approved who had completed the Study Period 3B and were receiving benefit from the drug.
Cardiac disorders
Myocardial infarction
0.05%
1/2011 • Number of events 1
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
0.00%
0/180
Cardiac disorders
Palpitations
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Gastrointestinal disorders
Gastrooesophageal reflux disease
0.00%
0/2011
0.00%
0/266
0.39%
1/258 • Number of events 1
0.56%
1/180 • Number of events 1
Gastrointestinal disorders
Intestinal obstruction
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Gastrointestinal disorders
Umbilical hernia
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Hepatobiliary disorders
Cholecystitis
0.00%
0/2011
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Hepatobiliary disorders
Hepatitis alcoholic
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Infections and infestations
Appendicitis
0.10%
2/2011 • Number of events 2
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Infections and infestations
Erysipelas
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Infections and infestations
Gastroenteritis
0.05%
1/2011 • Number of events 1
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Infections and infestations
Peritonsillar abscess
0.00%
0/2011
0.00%
0/266
0.39%
1/258 • Number of events 1
0.00%
0/180
Injury, poisoning and procedural complications
Accidental overdose
0.20%
4/2011 • Number of events 4
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Diaphragmatic injury
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Fall
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Foot fracture
0.05%
1/2011 • Number of events 1
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Intentional overdose
0.10%
2/2011 • Number of events 2
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Lower limb fracture
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Injury, poisoning and procedural complications
Meniscus injury
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Road traffic accident
0.00%
0/2011
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Injury, poisoning and procedural complications
Splenic injury
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Toxicity to various agents
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Musculoskeletal and connective tissue disorders
Back pain
0.10%
2/2011 • Number of events 2
0.00%
0/266
0.00%
0/258
0.00%
0/180
Musculoskeletal and connective tissue disorders
Intervertebral disc protrusion
0.10%
2/2011 • Number of events 2
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Musculoskeletal and connective tissue disorders
Pain in extremity
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Intraductal proliferative breast lesion
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Nervous system disorders
Cerebellar infarction
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Nervous system disorders
Convulsion
0.00%
0/2011
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Nervous system disorders
Headache
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Nervous system disorders
Hypoaesthesia
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Psychiatric disorders
Alcohol abuse
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Psychiatric disorders
Depressive symptom
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Psychiatric disorders
Hallucination, auditory
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Psychiatric disorders
Insomnia
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Psychiatric disorders
Restlessness
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180
Psychiatric disorders
Suicidal ideation
0.15%
3/2011 • Number of events 3
0.00%
0/266
0.00%
0/258
0.00%
0/180
Reproductive system and breast disorders
Uterine polyp
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Respiratory, thoracic and mediastinal disorders
Dyspnoea
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Skin and subcutaneous tissue disorders
Angioedema
0.00%
0/2011
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Surgical and medical procedures
Bunion operation
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Surgical and medical procedures
Hospitalisation
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Surgical and medical procedures
Skin neoplasm excision
0.00%
0/2011
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Surgical and medical procedures
Tonsillectomy
0.00%
0/2011
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Vascular disorders
Haemorrhage
0.05%
1/2011 • Number of events 1
0.00%
0/266
0.00%
0/258
0.00%
0/180

Other adverse events

Other adverse events
Measure
Atomoxetine (Study Periods 2 and 3A)
n=2011 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A).
Atomoxetine (Study Period 3B)
n=266 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A). Followed by 80-100 mg/day atomoxetine orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Placebo (Study Period 3B)
n=258 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A). Followed by Placebo orally, once daily or twice daily for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B).
Atomoxetine (Study Period 4; Open-Label Extension)
n=180 participants at risk
40-100 milligrams/day (mg/day) atomoxetine orally, once daily or twice daily for 12 weeks during open-label, acute-treatment phase (Study Period 2), and 80-100 mg/day for 12 weeks during double-blind maintenance phase of Study Period 3 (Study Period 3A) and for 25 weeks during double-blind randomized withdrawal phase of Study Period 3 (Study Period 3B), followed by a 2 year open label extension (Study Period 4). The open-label extension was optional and only offered to participants living in countries where atomoxetine for the adult ADHD indication had not been approved who had completed the Study Period 3B and were receiving benefit from the drug.
Cardiac disorders
Angina pectoris
0.10%
2/2011 • Number of events 2
0.75%
2/266 • Number of events 2
0.00%
0/258
1.7%
3/180 • Number of events 3
Cardiac disorders
Palpitations
4.1%
83/2011 • Number of events 90
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Cardiac disorders
Tachycardia
3.5%
70/2011 • Number of events 73
1.1%
3/266 • Number of events 4
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Ear and labyrinth disorders
Vertigo
1.9%
38/2011 • Number of events 46
0.00%
0/266
0.39%
1/258 • Number of events 1
1.7%
3/180 • Number of events 4
Eye disorders
Conjunctivitis
0.40%
8/2011 • Number of events 8
0.00%
0/266
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Eye disorders
Vision blurred
1.6%
32/2011 • Number of events 32
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Gastrointestinal disorders
Abdominal discomfort
1.4%
29/2011 • Number of events 30
0.38%
1/266 • Number of events 1
0.00%
0/258
0.00%
0/180
Gastrointestinal disorders
Abdominal pain
1.9%
38/2011 • Number of events 41
0.00%
0/266
0.00%
0/258
0.00%
0/180
Gastrointestinal disorders
Abdominal pain upper
3.0%
61/2011 • Number of events 73
0.75%
2/266 • Number of events 2
0.78%
2/258 • Number of events 2
1.7%
3/180 • Number of events 3
Gastrointestinal disorders
Constipation
4.6%
93/2011 • Number of events 99
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Gastrointestinal disorders
Diarrhoea
2.6%
53/2011 • Number of events 60
1.5%
4/266 • Number of events 4
1.9%
5/258 • Number of events 5
4.4%
8/180 • Number of events 10
Gastrointestinal disorders
Dry mouth
17.0%
342/2011 • Number of events 368
1.1%
3/266 • Number of events 4
0.78%
2/258 • Number of events 2
3.3%
6/180 • Number of events 6
Gastrointestinal disorders
Dyspepsia
3.2%
65/2011 • Number of events 72
0.38%
1/266 • Number of events 1
0.00%
0/258
3.3%
6/180 • Number of events 6
Gastrointestinal disorders
Gastritis
0.20%
4/2011 • Number of events 4
0.38%
1/266 • Number of events 1
0.00%
0/258
3.3%
6/180 • Number of events 6
Gastrointestinal disorders
Haemorrhoids
0.20%
4/2011 • Number of events 5
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Gastrointestinal disorders
Nausea
27.4%
552/2011 • Number of events 707
2.3%
6/266 • Number of events 6
1.2%
3/258 • Number of events 4
5.0%
9/180 • Number of events 9
Gastrointestinal disorders
Toothache
1.1%
23/2011 • Number of events 25
0.38%
1/266 • Number of events 1
0.78%
2/258 • Number of events 2
0.56%
1/180 • Number of events 2
Gastrointestinal disorders
Vomiting
4.1%
82/2011 • Number of events 96
0.38%
1/266 • Number of events 1
1.2%
3/258 • Number of events 3
0.56%
1/180 • Number of events 1
General disorders
Chills
2.8%
57/2011 • Number of events 60
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
General disorders
Fatigue
13.0%
262/2011 • Number of events 292
0.38%
1/266 • Number of events 1
1.2%
3/258 • Number of events 3
2.2%
4/180 • Number of events 5
General disorders
Influenza like illness
0.55%
11/2011 • Number of events 11
0.75%
2/266 • Number of events 3
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
General disorders
Irritability
4.0%
80/2011 • Number of events 87
0.75%
2/266 • Number of events 2
0.00%
0/258
0.00%
0/180
General disorders
Malaise
2.3%
46/2011 • Number of events 57
0.38%
1/266 • Number of events 1
0.00%
0/258
0.56%
1/180 • Number of events 1
General disorders
Pyrexia
0.80%
16/2011 • Number of events 17
1.5%
4/266 • Number of events 4
0.78%
2/258 • Number of events 2
0.56%
1/180 • Number of events 1
Infections and infestations
Bronchitis
0.90%
18/2011 • Number of events 19
1.1%
3/266 • Number of events 3
0.78%
2/258 • Number of events 2
2.8%
5/180 • Number of events 7
Infections and infestations
Cystitis
0.40%
8/2011 • Number of events 8
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
2.8%
5/180 • Number of events 8
Infections and infestations
Ear infection
0.10%
2/2011 • Number of events 2
0.75%
2/266 • Number of events 2
0.00%
0/258
1.1%
2/180 • Number of events 2
Infections and infestations
Gastroenteritis
1.2%
24/2011 • Number of events 24
1.9%
5/266 • Number of events 5
0.78%
2/258 • Number of events 2
2.8%
5/180 • Number of events 7
Infections and infestations
Gastrointestinal infection
0.20%
4/2011 • Number of events 4
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Infections and infestations
Herpes zoster
0.00%
0/2011
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Infections and infestations
Influenza
2.6%
52/2011 • Number of events 55
3.0%
8/266 • Number of events 8
2.3%
6/258 • Number of events 6
5.6%
10/180 • Number of events 10
Infections and infestations
Nasopharyngitis
6.8%
137/2011 • Number of events 153
6.8%
18/266 • Number of events 26
5.0%
13/258 • Number of events 16
12.2%
22/180 • Number of events 39
Infections and infestations
Pneumonia
0.05%
1/2011 • Number of events 1
0.75%
2/266 • Number of events 2
0.00%
0/258
1.1%
2/180 • Number of events 2
Infections and infestations
Rhinitis
0.65%
13/2011 • Number of events 13
0.38%
1/266 • Number of events 1
0.78%
2/258 • Number of events 2
2.2%
4/180 • Number of events 4
Infections and infestations
Sinusitis
1.1%
23/2011 • Number of events 24
0.75%
2/266 • Number of events 2
1.2%
3/258 • Number of events 4
2.2%
4/180 • Number of events 4
Infections and infestations
Tonsillitis
0.45%
9/2011 • Number of events 9
0.38%
1/266 • Number of events 1
0.78%
2/258 • Number of events 2
1.7%
3/180 • Number of events 4
Infections and infestations
Upper respiratory tract infection
2.8%
57/2011 • Number of events 62
4.1%
11/266 • Number of events 13
2.7%
7/258 • Number of events 7
0.56%
1/180 • Number of events 2
Infections and infestations
Urinary tract infection
0.60%
12/2011 • Number of events 12
0.38%
1/266 • Number of events 2
0.00%
0/258
1.1%
2/180 • Number of events 2
Injury, poisoning and procedural complications
Arthropod bite
0.10%
2/2011 • Number of events 2
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Injury, poisoning and procedural complications
Contusion
0.40%
8/2011 • Number of events 8
1.9%
5/266 • Number of events 5
0.00%
0/258
0.00%
0/180
Injury, poisoning and procedural complications
Post-traumatic neck syndrome
0.15%
3/2011 • Number of events 3
0.00%
0/266
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Investigations
Blood pressure increased
0.65%
13/2011 • Number of events 13
1.5%
4/266 • Number of events 6
0.00%
0/258
1.7%
3/180 • Number of events 3
Investigations
Heart rate increased
1.0%
21/2011 • Number of events 24
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Investigations
Weight decreased
1.9%
39/2011 • Number of events 39
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Investigations
Weight increased
0.65%
13/2011 • Number of events 13
1.1%
3/266 • Number of events 3
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Metabolism and nutrition disorders
Decreased appetite
14.6%
294/2011 • Number of events 319
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
0.56%
1/180 • Number of events 1
Metabolism and nutrition disorders
Increased appetite
0.50%
10/2011 • Number of events 10
0.38%
1/266 • Number of events 1
1.2%
3/258 • Number of events 3
0.00%
0/180
Musculoskeletal and connective tissue disorders
Arthralgia
0.75%
15/2011 • Number of events 15
0.75%
2/266 • Number of events 2
0.39%
1/258 • Number of events 1
4.4%
8/180 • Number of events 8
Musculoskeletal and connective tissue disorders
Back pain
1.5%
30/2011 • Number of events 30
1.1%
3/266 • Number of events 3
2.7%
7/258 • Number of events 7
3.9%
7/180 • Number of events 9
Musculoskeletal and connective tissue disorders
Intervertebral disc protrusion
0.10%
2/2011 • Number of events 2
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Musculoskeletal and connective tissue disorders
Neck pain
0.30%
6/2011 • Number of events 6
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Nervous system disorders
Carpal tunnel syndrome
0.00%
0/2011
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Nervous system disorders
Dizziness
8.5%
170/2011 • Number of events 195
0.38%
1/266 • Number of events 1
0.78%
2/258 • Number of events 2
1.7%
3/180 • Number of events 3
Nervous system disorders
Headache
17.3%
347/2011 • Number of events 482
4.9%
13/266 • Number of events 15
4.3%
11/258 • Number of events 11
9.4%
17/180 • Number of events 38
Nervous system disorders
Migraine
1.3%
26/2011 • Number of events 46
0.38%
1/266 • Number of events 3
0.39%
1/258 • Number of events 1
1.7%
3/180 • Number of events 3
Nervous system disorders
Paraesthesia
3.7%
74/2011 • Number of events 76
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Nervous system disorders
Sedation
1.3%
26/2011 • Number of events 27
0.00%
0/266
0.00%
0/258
0.00%
0/180
Nervous system disorders
Somnolence
5.6%
112/2011 • Number of events 126
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
0.56%
1/180 • Number of events 2
Nervous system disorders
Tremor
1.2%
25/2011 • Number of events 26
0.00%
0/266
0.39%
1/258 • Number of events 1
1.7%
3/180 • Number of events 3
Psychiatric disorders
Abnormal dreams
1.7%
34/2011 • Number of events 35
0.00%
0/266
0.00%
0/258
0.00%
0/180
Psychiatric disorders
Agitation
1.4%
28/2011 • Number of events 32
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Psychiatric disorders
Anxiety
3.0%
60/2011 • Number of events 62
1.1%
3/266 • Number of events 3
1.2%
3/258 • Number of events 3
1.1%
2/180 • Number of events 2
Psychiatric disorders
Depressed mood
2.8%
56/2011 • Number of events 62
0.00%
0/266
0.78%
2/258 • Number of events 2
2.2%
4/180 • Number of events 5
Psychiatric disorders
Depression
1.7%
34/2011 • Number of events 34
0.75%
2/266 • Number of events 2
1.2%
3/258 • Number of events 4
0.56%
1/180 • Number of events 1
Psychiatric disorders
Initial insomnia
1.7%
34/2011 • Number of events 40
1.5%
4/266 • Number of events 4
0.00%
0/258
0.56%
1/180 • Number of events 1
Psychiatric disorders
Insomnia
8.8%
177/2011 • Number of events 209
1.1%
3/266 • Number of events 3
0.39%
1/258 • Number of events 1
2.2%
4/180 • Number of events 6
Psychiatric disorders
Libido decreased
3.0%
61/2011 • Number of events 65
0.75%
2/266 • Number of events 2
0.78%
2/258 • Number of events 2
0.56%
1/180 • Number of events 1
Psychiatric disorders
Middle insomnia
1.6%
33/2011 • Number of events 35
0.75%
2/266 • Number of events 2
0.00%
0/258
1.7%
3/180 • Number of events 3
Psychiatric disorders
Nervousness
0.45%
9/2011 • Number of events 9
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 3
Psychiatric disorders
Restlessness
1.3%
27/2011 • Number of events 34
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 3
Psychiatric disorders
Sleep disorder
3.5%
71/2011 • Number of events 82
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
2.8%
5/180 • Number of events 5
Renal and urinary disorders
Dysuria
2.4%
49/2011 • Number of events 54
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Renal and urinary disorders
Urinary hesitation
2.1%
43/2011 • Number of events 46
0.75%
2/266 • Number of events 2
0.00%
0/258
0.56%
1/180 • Number of events 1
Renal and urinary disorders
Urinary retention
1.0%
21/2011 • Number of events 22
0.00%
0/266
0.00%
0/258
0.56%
1/180 • Number of events 1
Reproductive system and breast disorders
Dysmenorrhoea
0.94%
19/2011 • Number of events 23
0.38%
1/266 • Number of events 2
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Reproductive system and breast disorders
Ejaculation disorder
1.2%
25/2011 • Number of events 29
0.00%
0/266
0.00%
0/258
0.00%
0/180
Reproductive system and breast disorders
Erectile dysfunction
4.9%
99/2011 • Number of events 103
1.1%
3/266 • Number of events 3
0.00%
0/258
1.1%
2/180 • Number of events 2
Respiratory, thoracic and mediastinal disorders
Asthma
0.30%
6/2011 • Number of events 7
0.00%
0/266
0.00%
0/258
1.1%
2/180 • Number of events 2
Respiratory, thoracic and mediastinal disorders
Cough
1.1%
22/2011 • Number of events 23
1.9%
5/266 • Number of events 6
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Respiratory, thoracic and mediastinal disorders
Oropharyngeal pain
0.99%
20/2011 • Number of events 20
1.9%
5/266 • Number of events 5
1.6%
4/258 • Number of events 5
3.3%
6/180 • Number of events 6
Respiratory, thoracic and mediastinal disorders
Rhinitis allergic
0.25%
5/2011 • Number of events 5
0.38%
1/266 • Number of events 1
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Skin and subcutaneous tissue disorders
Hyperhidrosis
9.0%
180/2011 • Number of events 196
0.75%
2/266 • Number of events 2
0.00%
0/258
4.4%
8/180 • Number of events 8
Skin and subcutaneous tissue disorders
Piloerection
1.1%
23/2011 • Number of events 25
0.00%
0/266
0.00%
0/258
0.00%
0/180
Skin and subcutaneous tissue disorders
Rash
0.60%
12/2011 • Number of events 12
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2
Surgical and medical procedures
Tooth extraction
0.25%
5/2011 • Number of events 7
0.00%
0/266
0.39%
1/258 • Number of events 1
1.1%
2/180 • Number of events 2
Vascular disorders
Hot flush
2.8%
56/2011 • Number of events 61
1.1%
3/266 • Number of events 3
0.00%
0/258
0.56%
1/180 • Number of events 1
Vascular disorders
Hypertension
1.3%
27/2011 • Number of events 28
0.38%
1/266 • Number of events 1
0.00%
0/258
1.1%
2/180 • Number of events 2

Additional Information

Chief Medical Officer

Eli Lilly and Company

Phone: 800-545-5979

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: GT60