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 products in the mental health/neuroscience therapeutic area.
| Drug |
Disease |
Trial ID |
Trial Title |
Trial
Phase |
| Cymbalta for Generalized Anxiety Disorder |
Cymbalta |
Generalized Anxiety Disorder |
5075 |
Duloxetine Hydrochloride 60 mg or 120 mg Once Daily Compared with Placebo in Patients with Generalized Anxiety Disorder
|
3 |
Cymbalta |
Generalized Anxiety Disorder |
6089 |
Duloxetine Hydrochloride Once Daily Compared with Placebo in the Treatment of Generalized Anxiety Disorder
|
3 |
Cymbalta |
Generalized Anxiety Disorder
|
7106 |
A Comparison of Duloxetine Hydrochloride, Venlafaxine-Extended Release, and
Placebo in the Treatment of Generalized Anxiety Disorder
|
3 |
Cymbalta |
Generalized Anxiety Disorder
|
7107 |
A Comparison of Duloxetine Hydrochloride, Venlafaxine Extended Release, and Placebo in the Treatment of Generalized Anxiety Disorder
|
3 |
Cymbalta |
Generalized Anxiety Disorder
|
7108 |
"Duloxetine 60 to 120 mg Once Daily Compared with Placebo in the Prevention of Relapse
in Generalized Anxiety Disorder"
|
3 |
| Cymbalta for Major Depressive Disorder (MDD) |
Cymbalta |
Major Depressive Disorder (MDD) |
9547 |
Evaluation of the Effects of Duloxetine on Norepinephrine Transporter Inhibition in Healthy Subjects
|
1 |
Cymbalta |
Major Depressive Disorder (MDD) |
1124 |
Duloxetine/Placebo in Major Depressive Disorders
|
1b/2 |
Cymbalta |
Major Depressive Disorder (MDD) |
1096 |
A Pilot Study in Major Depressive Disorder
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
1125 |
Duloxetine 20/30 mg vs. Placebo in Major Depression
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
1126 |
A Double-Blind, Placebo- and Clomipramine-Controlled Study in Duloxetine Patients
with Major Depression
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
3327a |
Duloxetine Versus Placebo in the Treatment of Major Depression
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
3327b |
Duloxetine Versus Placebo in the Treatment of Major Depression
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
7566 |
Validation of Daily Telephone Self-Assessment in the Study of Antidepressant Treatment Outcome
|
2 |
Cymbalta |
Major Depressive Disorder (MDD) |
4091a |
Duloxetine Versus Placebo and Paroxetine in the Acute Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4091b |
Duloxetine Versus Placebo and Paroxetine in the Acute Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4092 |
Long-Term Open-Label Treatment with Duloxetine Hydrochloride for Evaluation of Safety in Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4298a |
Duloxetine Versus Placebo and Paroxetine in the Treatment of Major Depression |
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4298b |
Duloxetine Versus Placebo and Paroxetine in the Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4445 |
Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder |
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4689a |
Duloxetine Once-Daily Dosing Versus Placebo in the Acute Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
4689b |
Duloxetine Once-Daily Dosing Versus Placebo in the Acute Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
6937 |
Duloxetine Versus Paroxetine in the Acute Treatment of Major Depression
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
9548 |
Open-Label Duloxetine Extension Phase in Patients Who Have Completed the HMDG Clinical Trial
|
3 |
Cymbalta |
Major Depressive Disorder (MDD) |
6090 |
Duloxetine Versus Venlafaxine Extended Release in the Treatment of Major Depressive Disorder
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
6353 |
Duloxetine Once-Daily Dosing Versus Placebo in Patients with Major Depression and Pain
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
6475 |
Dose Escalation, Double-Blind Treatment with Duloxetine Hydrochloride Once Daily Dosing for Evaluation of Safety in Major Depression
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
6476 |
Open-Label Treatment with Duloxetine Hydrochloride Once-Daily Dosing for Evaluation of Stabilization Dose in Patients with Major Depression |
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
7978 |
Duloxetine versus Escitalopram and Placebo in the Treatment of Patients with Major Depression
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
7999 |
Duloxetine Versus Venlafaxine Extended Release in the Treatment of Major Depressive Disorder
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
8163 |
Duloxetine in the Treatment of Melancholic Depression: An 8-Week Open-Label Dose Study
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
8605 |
"A Ten-Week, Randomized, Double-Blind Study Evaluating the Efficacy of Duloxetine 60
mg Once Daily Versus Placebo in Outpatients with Major Depressive Disorder and Pain"
|
3b |
Cymbalta |
Major Depressive Disorder (MDD) |
6091 |
Duloxetine Versus Placebo in the Treatment of Elderly Patients with Major Depressive Disorder
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
7442 |
Lilly's Emotional and Physical Symptoms of Depression Study (LEAPS)
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
8299 |
Lilly's Emotional and Physical Symptoms of Depression Study (LEAPS)
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
8300 |
Lilly's Emotional and Physical Symptoms of Depression Study (LEAPS)
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
8601 |
Duloxetine versus Duloxetine plus Non-Pharmacological Intervention in the Treatment of Depression
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
8604 |
Switching to Duloxetine from Other Antidepressants: A Regional Multicentre Trial Comparing Two Switching Techniques
|
4 |
Cymbalta |
Major Depressive Disorder (MDD) |
8950 |
A Comparison of Duloxetine Dosing Strategies in the Treatment of Patients with Major Depression
|
4 |
| Permax for Parkinson's Disease |
Permax |
Parkinson's Disease |
607 |
A Randomized, Double-Blind Study of Pergolide versus Levodopa as Monotherapy in Early-Stage Parkinson’s Disease |
3 |
Permax |
Parkinson's Disease |
608
|
A Randomized, Double-Blind Study of Pergolide versus Placebo as Monotherapy in Early-Stage Parkinson's Disease
|
3 |
Permax |
Parkinson's Disease |
609
|
A Randomized, Double-Blind Study of Pergolide versus Placebo as Monotherapy in Early-Stage Parkinson's Disease
|
3 |
| Prozac for Major Depressive Disorder |
Prozac |
Major Depressive Disorder |
6334 |
Enteric-Coated Hydrochlorate Fluoxetine Administered Once Weekly during the Maintenance Treatment of the Major Depressive Disorder |
4 |
Prozac |
Major Depressive Disorder |
6706 |
Depression with Lack of Motivation; Comparison Between Fluoxetine and Trazodone
|
4 |
| Prozac for Pediatric Depression |
Prozac |
Pediatric Depression |
236 |
Fluoxetine: Fluoxetine Versus Placebo in Adolescent Depressed Patients
|
3 |
Prozac |
Pediatric Depression |
375 |
Fluoxetine Versus Placebo in the Acute Treatment of Major Depressive Disorder in Children and Adolescents |
3 |
Prozac |
Pediatric Depression |
2201 |
Fluoxetine Versus Placebo in Childhood/Adolescent Depression
|
3 |
Prozac |
Pediatric Depression |
3032 |
Fluoxetine Versus Placebo in the Treatment of Children and Adolescents with Obsessive-Compulsive Disorder
|
3 |
Prozac |
Pediatric Depression |
1545 |
Pharmacokinetic Assessment of Fluoxetine and Norfluoxetine in Preadolescent and Adolescent Patients |
4 |
| Strattera for Alzheimer's Disease |
Strattera |
Alzheimer's Disease |
7951 |
Atomoxetine Augmentation of Cholinesterase Inhibitor Therapy in Patients with
Alzheimer’s Disease |
2 / 3 |
| Strattera for Attention Deficit/Hyperactivity Disorder (ADHD) |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
634 |
Safety and Pharmacokinetic Study of Tomoxetine Hydrochloride in Pediatric Patients with ADHD
|
1 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
8619 |
A Study to Evaluate Single Dose and Multiple Dose Pharmacokinetics of Atomoxetine Hydrochloride in Chinese Healthy Subjects
|
1 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9586 |
An Exploratory Study, using Atomoxetine, on Central Nervous System (CNS) Biomarkers
|
1 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
9916 |
The Haemodynamic Effects of Inhaled Salbutamol in the Absence and Presence of
Atomoxetine
|
1 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2097 |
Long-Term, Open-Label, Safety Study of Tomoxetine Hydrochloride in Patients, 6 Years and Older |
2 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
2553 |
A Randomized, Double-Blind, Placebo- and Comparator-Controlled Study of Tomoxetine Hydrochloride in Recreational Drug Users
|
3 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
5671 |
Placebo-Controlled Study of the Effects of Atomoxetine Hydrochloride on Bladder Control in Children with Nocturnal Enuresis |
3B |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
6066 |
Noradrenergic Augmentation of SSRI Therapy in Patients with Depression Unresponsive or Incompletely Responsive to SSRI Monotherapy
|
4 |
Strattera |
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 |
Strattera |
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 |
Strattera |
Attention-Deficit/Hyperactivity Disorder (ADHD) |
7069 |
Atomoxetine Treatment of Adults with ADHD and Comorbid Alcohol Abuse: A
Randomized, Placebo-Controlled Trial
|
4 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
Strattera |
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 |
| Symbyax for Bipolar Disorder |
Symbyax |
Bipolar Disorder |
3077a |
Placebo-Controlled Olanzapine Monotherapy in the Treatment of Bipolar I Depression |
3 |
Symbyax |
Bipolar Disorder |
3077b |
Placebo-Controlled Olanzapine Monotherapy in the Treatment of Bipolar I Depression (Open-Label Phase Final Results) |
3 |
Symbyax |
Bipolar Disorder |
7980 |
Olanzapine/Fluoxetine Combination versus Lamotrigine in the Treatment of Bipolar I Depression
|
4 |
Symbyax |
Bipolar Disorder |
9370 |
Bipolar Depression Assessment Study on Treatment Response (BiDAS-TR)
|
4 |
| Symbyax Clinical Pharmacology Trial |
Symbyax |
Clinical Pharmacology Trial |
1072 |
Pharmacokinetic Interaction Study of Fluoxetine on Olanzapine after Single and Repeated Administration of Fluoxetine in Healthy Volunteers
|
1 |
| Symbyax for Major Depressive Disorder |
Symbyax |
Major Depressive Disorder |
1831 |
Olanzapine Alone and in Combination with Fluoxetine Versus Placebo in Major Depressive Disorder with Psychotic Features
|
3 |
Symbyax |
Major Depressive Disorder |
4102 |
Open-Label Combination of Olanzapine and Fluoxetine in Major Depressive Disorder
|
3 |
| Symbyax for Schizophrenia |
Symbyax |
Schizophrenia |
1577 |
Fluoxetine Augmentation in Schizophrenic or Schizoaffective Patients with Depressive or Negative Symptoms Who Are Partial or Nonresponders to Olanzapine
|
3 |
| Symbyax for Treatment-Resistant Depression |
Symbyax |
Treatment-Resistant Depression |
1034 |
Study of Olanzapine in Treatment Resistant Major Depressive Disorder Without Psychotic Features
|
2 |
Symbyax |
Treatment-Resistant Depression |
3079 |
The Combination of Olanzapine and Fluoxetine in Treatment Resistant Depression without Psychotic Features
|
2 / 3 |
Symbyax |
Treatment-Resistant Depression
|
3641 |
Olanzapine Plus Fluoxetine Combination Therapy in Treatment-Resistant Depression: A Dose Ranging Study
|
2 / 3 |
Symbyax |
Treatment-Resistant Depression
|
6272 |
The Study of Olanzapine plus Fluoxetine in Combination for Treatment-Resistant Depression Without Psychotic Features
|
3 |
| Zyprexa for Bipolar Disorder |
Zyprexa |
Bipolar Disorder |
1718 |
Olanzapine-Divalproex Sodium/Valproic Acid Interaction Trial
|
1 |
Zyprexa |
Bipolar Disorder |
1028 |
Olanzapine Versus Placebo in the Treatment of Mania Associated with Bipolar I Disorder
|
3 |
Zyprexa |
Bipolar Disorder |
1035a |
Olanzapine Added to Mood Stabilizer in the Treatment of Bipolar Disorder |
3 |
Zyprexa |
Bipolar Disorder |
1035b |
Olanzapine Added to Mood Stabilizer for Relapse Prevention in Patients With Bipolar Disorder
|
3 |
Zyprexa |
Bipolar Disorder |
1729 |
Olanzapine Versus Placebo in the Treatment of Bipolar Disorder, Manic or Mixed |
3 |
Zyprexa |
Bipolar Disorder |
2055 |
Olanzapine Versus Haloperidol in the Treatment of Acute Mania
|
3 |
Zyprexa |
Bipolar Disorder |
2354 |
Olanzapine versus Placebo in the Prevention of Relapse in Bipolar Disorder
|
3 |
Zyprexa |
Bipolar Disorder |
2551 |
Olanzapine Versus Divalproex in the Treatment of Acute Mania
|
3 |
Zyprexa |
Bipolar Disorder |
3031 |
Olanzapine versus Lithium in Relapse Prevention in Bipolar Disorder |
3 |
Zyprexa |
Bipolar Disorder |
7598 |
Olanzapine versus Lithium Carbonate in the Treatment of Bipolar Disorder, Manic or Mixed Episodes
|
3 |
Zyprexa |
Bipolar Disorder |
7031 |
Olanzapine Plus Carbamazepine Versus Carbamazepine Alone in the Treatment of Manic or Mixed Episodes Associated with Bipolar I Disorder
|
3b |
Zyprexa |
Bipolar Disorder |
4360 |
Olanzapine Versus Placebo in the Treatment of Mania in Adolescents with Bipolar I Disorder
|
3 / 4 |
Zyprexa |
Bipolar Disorder |
7029 |
Olanzapine Versus Divalproex and Placebo in the Treatment of Mild to Moderate Mania Associated with Bipolar I Disorder
|
4 |
Zyprexa |
Bipolar Disorder |
7399 |
A prospective/parallel study on induced weight gain during atypical antipsychotic treatment and its management with psychoeducational program
|
4 |
Zyprexa |
Bipolar Disorder |
8834 |
Optimal Treatment Duration with Olanzapine following Remission of Manic or Mixed Episode. An Open-Label, Randomized Trial Comparing Two Treatment Strategies
|
4 |
| Zyprexa for Borderline Personality Disorder |
Zyprexa |
Borderline Personality Disorder |
6253 |
Efficacy and Safety of Olanzapine in Patients with Borderline Personality Disorder: A Randomized Double-Blind Comparison with Placebo
|
3 |
Zyprexa |
Borderline Personality Disorder |
6257 |
Efficacy and Safety of Olanzapine in Patients with Borderline Personality Disorder: A Randomized, Flexible-Dose, Double-Blind Comparison with Placebo
|
3 |
| Zyprexa for Dementia |
Zyprexa |
Dementia |
3611 |
Safety and Efficacy of Olanzapine on Cognitive Symptoms in Subjects with Mild to Moderate Alzheimer’s Disease without Psychosis |
2 |
Zyprexa |
Dementia |
981 |
Olanzapine versus Placebo in the Treatment of Patients with Psychosis Associated with Dementia
|
3 |
Zyprexa |
Dementia |
1032 |
Olanzapine Versus Placebo in the Treatment of Psychosis and Behavioral Disturbances Associated with Alzheimer’s Disease
|
3 |
Zyprexa |
Dementia |
1701 |
Olanzapine versus Risperidone and Placebo in the Treatment of Psychosis and Associated Behavioral Disturbances in Patients with Dementia |
3 |
Zyprexa |
Dementia |
4414 |
Olanzapine versus Placebo in the Treatment of Psychosis with or without Associated Behavioral Disturbances in Patients with Alzheimer’s Disease
|
3 |
| Zyprexa for Parkinson's Disease |
Zyprexa |
Parkinson's Disease |
1036 |
Olanzapine versus Placebo for Treatment-Associated Psychosis in Patients with Parkinson’s Disease
|
3 |
Zyprexa |
Parkinson's Disease
|
1821 |
Olanzapine (LY170053) versus Placebo for Treatment-Associated Psychosis in Patients with Parkinson’s Disease
|
3 |
| Zyprexa for Schizophrenia |
Zyprexa |
Schizophrenia |
8269 |
Atypical Antipsychotics Augmented with Atomoxetine in the Treatment of Schizophrenia: A Double-Blind, Placebo-Controlled Proof-of-Concept Study of Effects on Cognitive Function
|
1b |
Zyprexa |
Schizophrenia |
917 |
A Fixed-Dose Range Safety and Efficacy Study of Olanzapine Versus Haloperidol in the Treatment of Schizophrenia
|
2 |
Zyprexa |
Schizophrenia |
978 |
Olanzapine Versus Placebo and Haloperidol in the Treatment of Schizophrenia
|
2 |
Zyprexa |
Schizophrenia |
980 |
Olanzapine Versus Haloperidol in the Treatment of Schizophrenia and Other Psychotic Disorders
|
3 |
Zyprexa |
Schizophrenia |
982 |
Fixed-Dose Olanzapine Versus Placebo in the Treatment of Schizophrenia
|
3 |
Zyprexa |
Schizophrenia |
1960 |
Olanzapine Relapse Prevention Versus Placebo in the Treatment of Schizophrenia
|
3 |
Zyprexa |
Schizophrenia |
3131 |
Open-label Study on the Efficacy and Safety of Olanzapine in Adolescent and Young Adult Patients with Schizophrenia, Schizoaffective, and Schizophreniform Disorder
|
3 |
Zyprexa |
Schizophrenia |
4066 |
Olanzapine Versus Placebo in the Treatment of Adolescents with Schizophrenia
|
3 / 4 |
Zyprexa |
Schizophrenia |
5209 |
Assessment of Cognitive Functions in Patients with a Residual Schizophrenic Disorder in Olanzapine Treatment |
3 / 4 |
Zyprexa |
Schizophrenia |
2325 |
Cost-Effectiveness and Functional Outcomes of Olanzapine in the Treatment of Schizophrenia in Usual Clinical Practice: A Randomized Clinical Study
|
4 |
Zyprexa |
Schizophrenia |
2347 |
Olanzapine Versus Ziprasidone in the Treatment of Schizophrenia |
4 |
Zyprexa |
Schizophrenia |
4278 |
Schizophrenia Care And Assessment Program |
4 |
Zyprexa |
Schizophrenia |
4945 |
Residual Symptoms And Neurological Side-Effects In Schizophrenic Patients Treated With Conventional Neuroleptics Or Olanzapine |
4 |
Zyprexa |
Schizophrenia |
5102 |
The Assessment of Sibutramine for the Treatment of Olanzapine-Associated Weight Gain in Subjects with Schizophrenia, Schizophreniform Disorder, Schizoaffective Disorder, and Bipolar I Disorder
|
4 |
Zyprexa |
Schizophrenia |
5708
|
Olanzapine Post-marketing Clinical Study - Switching from Previous Antipsychotics to Olanzapine
|
4 |
Zyprexa |
Schizophrenia |
6589
|
A Double-Blind Long-term Study Comparing the Efficacy and Safety of Olanzapine versus Haloperidol in Patients with Schizophrenia Previously Stabilized with Conventional Antipsychotic Treatment
|
4 |
Zyprexa |
Schizophrenia |
6696 |
The Assessment of a Weight Management Program for Treatment-Emergent Weight Gain in Patients with Schizophrenia, Schizophreniform Disorder, and Schizoaffective Disorder During Olanzapine Therapy
|
4 |
Zyprexa |
Schizophrenia |
6704 |
Managing Acute Schizophrenia, a Double-Blind Comparison Between Two Atypical Antipsychotics - Olanzapine and Risperidone |
4 |
Zyprexa |
Schizophrenia |
6720 |
Olanzapine For Schizophrenia: A Cost Benefit Study |
4 |
Zyprexa |
Schizophrenia |
7932 |
Weight Gain Management in Patients with Schizophrenia During Treatment with Olanzapine in Association with Nizatidine
|
4 |
Zyprexa |
Schizophrenia |
8047 |
A Randomized Double-Blind Study of Olanzapine Versus Aripiprazole in the Treatment of Schizophrenia
|
4 |
Zyprexa |
Schizophrenia |
8333 |
Efficacy of High Dose Olanzapine in a Controlled Fixed-Dose Response Trial for the Treatment of Schizophrenia and Schizoaffective Disorder
|
4 |
Zyprexa |
Schizophrenia |
8894 |
The Comparison of Efficacy and Safety of Continuing Olanzapine to Switching to Quetiapine in Overweight or Obese Patients with Schizophrenia or Schizoaffective Disorder
|
4 |
Zyprexa |
Schizophrenia |
8928 |
Olanzapine Versus Aripiprazole in the Treatment of Acutely Ill Patients with Schizophrenia
|
4 |
| Zyprexa for Schizophrenia and Bipolar Disorder |
Zyprexa |
Schizophrenia and Bipolar Disorder
|
9483 |
Population Pharmacokinetic Study in Adolescent Patients with Schizophrenia or Bipolar I Disorder Treated with Olanzapine
|
3 / 4 |
| Zyprexa Intramuscular for Agitation |
Zyprexa Intramuscular |
Agitation |
5293 |
An Exploratory Study Examining Clinical Therapeutic Dose of Rapid Acting Intra-muscular Olanzapine in Japanese Agitated Patients with Schizophrenia |
1B / 2 |
Zyprexa Intramuscular |
Agitation |
5294 |
A Double-Blind Dose-Response Study Comparing Rapid Acting Intramuscular Olanzapine and Intramuscular Placebo in Agitated Patients with Schizophrenia |
2 |
Zyprexa Intramuscular |
Agitation |
1898 |
A Double-Blind Randomized Comparison of the Efficacy and Safety of Short Acting Intramuscular Olanzapine, Short Acting Intramuscular Haloperidol and Intramuscular Placebo in Patients with Schizophrenia
|
3 |
Zyprexa Intramuscular |
Agitation |
3043 |
A Double-Blind Dose-Response Study Comparing Short Acting Intramuscular Olanzapine, Short Acting Intramuscular Haloperidol, and Intramuscular Placebo in Patients with Schizophrenia
|
3 |
Zyprexa Intramuscular |
Agitation |
3045 |
A Double-Blind Randomized Comparison of the Efficacy and Safety of Short-Acting Intramuscular Olanzapine, Short-Acting Intramuscular Lorazepam and Intramuscular Placebo in Acutely Agitated Patients Diagnosed with Mania Associated with Bipolar Disorder
|
3 |
Zyprexa Intramuscular |
Agitation |
3047 |
A Double-Blind, Placebo-Controlled Comparison of the Efficacy and Safety of Short-Acting Intramuscular Olanzapine, Short-Acting Intramuscular Lorazepam, and Intramuscular Placebo in Treating Agitation in Patients with Dementia of the Alzheimer’s Type, Vascular Dementia, and Mixed Dementia
|
3 |
Zyprexa Intramuscular |
Agitation |
6409 |
A Double-Blind Randomized Comparison of the Efficacy and Safety of Intramuscular Olanzapine and Intramuscular Haloperidol in Acutely Agitated Patients with Schizophrenia
|
4 |