Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.
Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.
The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.
Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.
Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.
The following trials have been conducted for Strattera.
| Disease |
Trial ID |
Trial Title |
Trial
Phase |
Alzheimer's Disease |
7951 |
Atomoxetine Augmentation of Cholinesterase Inhibitor Therapy in Patients with
Alzheimer’s Disease
|
2 / 3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
634 |
Safety and Pharmacokinetic Study of Tomoxetine Hydrochloride in Pediatric Patients with ADHD
|
1 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
8619 |
A Study to Evaluate Single Dose and Multiple Dose Pharmacokinetics of Atomoxetine Hydrochloride in Chinese Healthy Subjects
|
1 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9586 |
An Exploratory Study, using Atomoxetine, on Central Nervous System (CNS) Biomarkers
|
1 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9916 |
The Haemodynamic Effects of Inhaled Salbutamol in the Absence and Presence of
Atomoxetine
|
1 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6425 |
A Randomized, Double-Blind, Placebo- and Comparator-Controlled Study of Atomoxetine Hydrochloride in a Drug-Abusing Population
|
1 / 2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
1585 |
A Randomized, Double-Blind Study of Tomoxetine Hydrochloride, Methylphenidate Hydrochloride, and Placebo in Pediatric Outpatients with Attention Deficit/Hyperactivity Disorder
|
2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
1586 |
A Randomized, Double-Blind Study of Tomoxetine Hydrochloride, Methylphenidate Hydrochloride, and Placebo in Pediatric Outpatients with Attention-Deficit/Hyperactivity Disorder
|
2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
1855 |
Randomized, Double-Blind, Placebo-Controlled, Variable Discontinuation Study of Tomoxetine Hydrochloride in Children with Attention-Deficit/Hyperactivity Disorder
|
2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2097 |
Long-Term, Open-Label, Safety Study of Tomoxetine Hydrochloride in Patients, 6 Years and Older |
2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5286 |
An Open-Label, Dose-Titration Safety Study of Atomoxetine Hydrochloride in Outpatient Japanese Children with Attention Deficit/Hyperactivity Disorder
|
2 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2552a |
Relapse Prevention After 10-Week and 52-Week Treatment with Tomoxetine Hydrochloride in Children with Attention-Deficit/Hyperactivity Disorder
|
2 / 3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2552b |
Relapse Prevention After 10-Week and 52-Week Treatment with Tomoxetine Hydrochloride in Children with Attention-Deficit/Hyperactivity Disorder
|
2 / 3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5285 |
A Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Comparison of Fixed-Dose Ranges of Atomoxetine Hydrochloride in Child Outpatients with Attention-Deficit/Hyperactivity Disorder
|
2 / 3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2553 |
A Randomized, Double-Blind, Placebo- and Comparator-Controlled Study of Tomoxetine Hydrochloride in Recreational Drug Users
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2556 |
A Phase III Randomized, Double-Blind Comparison of Placebo and Atomoxetine Hydrochloride in Adult Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2561 |
A Phase III Open-Label Safety and Efficacy Study of Tomoxetine Hydrochloride in Outpatients with ADHD, Ages 6 to 18 Years |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2746 |
Efficacy, Tolerability, and Safety of Once-Daily Atomoxetine Hydrochloride versus Placebo in Children with Attention-Deficit/Hyperactivity Disorder
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
3468 |
A Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Comparison of Fixed-Dose Ranges (mg/kg/day) of Tomoxetine with Placebo in Child and Adolescent Outpatients with ADHD, Aged 8 to 18 Years
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
4642 |
A Phase III Randomized, Double-Blind Comparison of Placebo and Tomoxetine Hydrochloride in Adult Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
4668 |
Safety and Efficacy of Atomoxetine or Atomoxetine Plus Fluoxetine in the Treatment of Mixed Attentional and Affective Disorders
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
4671 |
Long-Term, Open-Label Safety Study of Atomoxetine Hydrochloride in Adult Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
4908 |
A Randomized, Double-Blind Study of Tomoxetine Hydrochloride and Placebo in Pediatric Outpatients with Attention Deficit/Hyperactivity Disorder and Comorbid Tic Disorders
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5001 |
A Double-Blind Crossover Study of Tomoxetine Hydrochloride and Methylphenidate Effects on Neural Activity in Attention-Deficit/Hyperactivity Disorder
|
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5003a |
A Double-Blind, Placebo-Controlled Trial of Atomoxetine Hydrochloride to Evaluate Efficacy in the School Setting in Children Ages 8 to 12 Years with Attention- Deficit/Hyperactivity Disorder– Acute Treatment Period (Visit 1 through Visit 7) |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5004 |
A Randomized, Double-Blind, Placebo-Controlled Study of Atomoxetine Hydrochloride in Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Depressive Disorder |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5197 |
A Phase 3 Open-Label Safety and Efficacy Study of Tomoxetine Hydrochloride in Pediatric Outpatients (6 to 18 Years) with ADHD |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5670 |
A Randomized, Double-Blind, Placebo-Controlled Trial of Once Daily Atomoxetine Hydrochloride to Evaluate Efficacy in the Treatment of Attention-Deficit/Hyperactivity Disorder in Children Ages 6-12 with an Assessment of Evening Behavior |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5831 |
A Randomized, Double-Blind Comparison of Atomoxetine Hydrochloride, Extended-Release Methylphenidate Hydrochloride (Concerta), and Placebo in Pediatric Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6934 |
A Randomized, Double-Blind Comparison, Safety and Efficacy Trial of Atomoxetine Hydrochloride and Methylphenidate Hydrochloride in Pediatric Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7065 |
A Randomized, Double-Blind Comparison of Atomoxetine Hydrochloride Augmented with Either Extended-Release Methylphenidate Hydrochloride (Concerta®) or Placebo in Children with Attention-Deficit/Hyperactivity Disorder (ADHD) Who Have Not Responded to Stimulant Mono Therapy |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7233 |
An Open-label Study on Effectiveness and Tolerability of Atomoxetine as Perceived by Patients, Parents, and Physicians in Adolescents with Attention-Deficit/Hyperactivity Disorder in Germany |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7972 |
Evaluation of Continuous Symptom Treatment of ADHD: A Placebo-Controlled
Double-Blind Assessment of Morning-Dosed or Evening-Dosed Strattera |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9496 |
An Open-label Study on Effectiveness and Tolerability of Atomoxetine as Perceived by Patients, Parents, and Physicians in Children with Attention-Deficit/Hyperactivity Disorder in Germany |
3 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5671 |
Placebo-Controlled Study of the Effects of Atomoxetine Hydrochloride on Bladder Control in Children with Nocturnal Enuresis |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6477a |
A Randomized, Double-Blind, Placebo-Controlled Study of Atomoxetine Hydrochloride in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Anxiety |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6477b |
A Randomized, Double-Blind, Placebo-Controlled Study of Atomoxetine Hydrochloride in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Anxiety |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6671 |
A Randomized, Double Blind, Placebo Controlled Study of the Broader Efficacy of Atomoxetine Hydrochloride in the Treatment of Attention-Deficit/Hyperactivity Disorder in Swedish Children and Adolescents |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6962 |
A Randomized, Controlled, Open-Label Study of the Broader Efficacy of Atomoxetine Hydrochloride in the Treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in Children and Adolescents |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7649 |
A Phase IIIb Open-label Trial of Atomoxetine Hydrochloride to Evaluate Academic Outcome in Children Ages 8 to 11 Years with Attention-Deficit/Hyperactivity Disorder |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
8160 |
Efficacy, Tolerability, and Safety of Once-Daily Atomoxetine Hydrochloride versus Placebo in Taiwanese Children and Adolescents with Attention-Deficit/Hyperactivity Disorder |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9081 |
Efficacy, Tolerability, and Safety of Once-Daily Atomoxetine Hydrochloride versus Placebo in Russian Children and Adolescents with Attention-Deficit/Hyperactivity Disorder |
3B |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5002 |
Sleep and Cognitive/Neuropsychological Function in Children with Attention-Deficit/Hyperactivity Disorder Before and During Treatment with Tomoxetine Hydrochloride and Stimulants |
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5003b |
A Double-Blind, Placebo-Controlled Trial of Atomoxetine Hydrochloride to Evaluate Efficacy in the School Setting in Children Ages 8 to 12 Years with Attention- Deficit/Hyperactivity Disorder |
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6065 |
A Double-Blind Study of Treatment Optimization with Atomoxetine Hydrochloride in Adults with DSM-IV Attention Deficit/Hyperactivity Disorder
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6066 |
Noradrenergic Augmentation of SSRI Therapy in Patients with Depression Unresponsive or Incompletely Responsive to SSRI Monotherapy
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6639 |
An Open-Label Pilot Study of Atomoxetine for Attention Deficit and Hyperactive/Impulsive Behavior Problems in Children and Adolescents with Autistic Spectrum Disorders
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7066 |
A Double-Blind Study of Functional Outcomes with Atomoxetine-Hydrochloride and Placebo in Adult Outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7069 |
Atomoxetine Treatment of Adults with ADHD and Comorbid Alcohol Abuse: A
Randomized, Placebo-Controlled Trial
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7953 |
An Open-Label, Multicenter, Pilot Study of the Safety and Efficacy of Transitioning from a Stimulant Medication to Atomoxetine in Pediatric and Adolescent Outpatients with DSM IV Attention-Deficit/Hyperactivity Disorder (ADHD)
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7974 |
Maintenance of Benefit after 8-Week and 52-Week Treatment with Atomoxetine Hydrochloride in Adolescents with Attention-Deficit/Hyperactivity Disorder
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7975 |
Open-Label Treatment with Atomoxetine Hydrochloride in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder and Comorbid Dyslexia
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
8226 |
Guiding Dose Increases in Patients Incompletely Responsive to Usual Doses of Atomoxetine by Determining Plasma Atomoxetine Concentrations: A Randomized, Double-Blind Study
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9040 |
Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults with ADHD Over An Extended Period of Time (6 Months): With a Brief Evaluation of Executive Cognition
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9684 |
A 3-Month, Open-Label Study of Atomoxetine in Children with Attention-Deficit/Hyperactivity Disorder; Symptomatic and Functional Outcomes
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9721 |
An Open-Label Pilot Study of Atomoxetine Hydrochloride to Evaluate Neuropsychological Function in Children Ages 6 to 10 Years with Attention-Deficit/ Hyperactivity Disorder
|
4 |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9855 |
A Double-Blind Placebo-Controlled Study of Atomoxetine Hydrochloride in the Treatment of Adults with ADHD and Comorbid Social Anxiety Disorder
|
4 |