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Phase 3 Completed N=495 Randomized Quadruple-blind Treatment

A Study in Adult Patients With Major Depressive Disorder

Depressive Disorder, Major
Source: ClinicalTrials.gov NCT00795821 ↗
Enrolled (actual)
495
Serious AEs
1.3%
Results posted
Mar 2018
Primary outcomePrimary: Mean Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) at Week 10 — -13.30; -9.82 units on a scale — p=<0.001
◆ Published Evidence
Emerging
5citations · ~1 / year
Is the Noradrenergic Symptom Cluster a Valid Construct in Adjunctive Treatment of Major Depressive Disorder?
The Journal of clinical psychiatry · 2017 · Likely link

Summary

The purpose of this study is to assess whether LY2216684 is superior to placebo in the treatment of adult patients with major depressive disorder.

Linked Publications

  • Is the Noradrenergic Symptom Cluster a Valid Construct in Adjunctive Treatment of Major Depressive Disorder?
    The Journal of clinical psychiatry · 2017 · 5 citations · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) at Week 10
-13.30; -9.82 <0.001 sig
SECONDARY
Mean Change From Baseline (Week 10) in Montgomery-Asberg Depression Rating Scale (MADRS) at Week 62
-7.44; -9.43
SECONDARY
Mean Change From Baseline in Sheehan Disability Scale (SDS) Global Functional Impairment at Week 10
-8.21; -5.79 <0.001 sig
SECONDARY
Mean Change From Baseline (Week 10) in Sheehan Disability Scale (SDS) Global Functional Impairment at Week 62
-3.06; -4.56
SECONDARY
Mean Change From Baseline in Clinical Global Impressions of Severity (CGI-Severity) Scale at Week 10
-1.48; -1.08 <0.001 sig
SECONDARY
Mean Change From Baseline (Week 10) in Clinical Global Impressions of Severity (CGI-Severity) Scale at Week 62
-1.03; -1.24
SECONDARY
Mean Change From Baseline in the 16-Item Quick Inventory of Depressive Symptomatology-Self Rated (QIDS-SR16) at Week 10
-6.50; -4.93 0.002 sig
SECONDARY
Mean Change From Baseline (Week 10) in the 16-Item Quick Inventory of Depressive Symptomatology-Self Rated (QIDS-SR16) at Week 62
-2.64; -3.33
SECONDARY
Mean Change From Baseline in the Massachusetts General Hospital Cognitive and Physical Functioning Questionnaire (CPFQ) at Week 10
-6.61; -5.04 0.007 sig
SECONDARY
Mean Change From Baseline (Week 10) in the Massachusetts General Hospital Cognitive and Physical Functioning Questionnaire (CPFQ) at Week 62
-2.79; -3.72
SECONDARY
Mean Change From Baseline in the EuroQol Questionnaire-5 Dimension (EQ-5D) United States (US) Index Score at Week 10
0.12; 0.09 0.056
SECONDARY
Mean Change From Baseline (Week 10) in the EuroQol Questionnaire-5 Dimension (EQ-5D) United States (US) Index Score at Week 62
0.08; 0.06
SECONDARY
Mean Change From Baseline in the Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Average Score at Week 10
-0.99; -0.74 0.002 sig
SECONDARY
Mean Change From Baseline (Week 10) in Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Average Score at Week 62
-0.51; -0.65
SECONDARY
Mean Change From Baseline in the Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Fatigue Experience Average Score at Week 10
-0.96; -0.69 <0.001 sig
SECONDARY
Mean Change From Baseline (Week 10) in Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Fatigue Experience Average Score at Week 62
-0.50; -0.70
SECONDARY
Mean Change From Baseline in the Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Fatigue Impact Average Score at Week 10
-1.02; -0.77 0.003 sig
SECONDARY
Mean Change From Baseline (Week 10) in Fatigue Associated With Depression (FAsD) Patient Reported Outcome (PRO): Fatigue Impact Average Score at Week 62
-0.51; -0.58
SECONDARY
Mean Change From Baseline in the Brief Fatigue Inventory (BFI) Global Total Score at Week 10
-2.25; -1.74 0.009 sig
SECONDARY
Mean Change From Baseline (Week 10) in Brief Fatigue Inventory (BFI) Global Total Score at Week 62
-1.28; -1.59
SECONDARY
Mean Change From Baseline in the Visual Analogue Scale for Fatigue (VAS-F) Overall Severity and Interference With Daily Activities Scores at Week 10
-23.30; -16.69; -24.48; -18.62 0.008 sig
SECONDARY
Mean Change From Baseline (Week 10) in the Visual Analogue Scale for Fatigue (VAS-F) Overall Severity and Interference With Daily Activities Scores at Week 62
-12.72; -18.69; -13.89; -17.47
SECONDARY
Percentage of Participants Reporting Resource Utilization at Week 10
13.3; 10.9; 5.8; 5.7; 6.6; 5.7 0.261
SECONDARY
Percentage of Participants Reporting Resource Utilization at Week 62
27.3; 24.4; 14.0; 13.3; 5.8; 5.6
SECONDARY
Percentage of Participants With Suicidal Ideation, Behavior, and Acts Based on The Columbia Suicide Severity Rating Scale (C-SSRS) at Week 10
7.3; 8.3; 0.0; 0.0; 0.0; 0.0 0.737
SECONDARY
Percentage of Participants With Suicidal Ideation, Behavior, and Acts Based on The Columbia Suicide Severity Rating Scale (C-SSRS) at Week 62
5.9; 6.8; 1.1; 0.5; 0.0; 0.5
SECONDARY
Mean Change From Baseline in Supine Systolic and Diastolic Blood Pressure at Week 10
1.45; -1.57; 3.54; -0.64 0.002 sig
SECONDARY
Mean Change From Baseline (Week 10) in Supine Systolic and Diastolic Blood Pressure at Week 62
0.52; 2.55; -0.68; 2.25
SECONDARY
Mean Change From Baseline in Supine Pulse at Week 10
9.72; -0.11 <0.001 sig
SECONDARY
Mean Change From Baseline (Week 10) in Supine Pulse at Week 62
-1.15; 7.33
SECONDARY
Pharmacokinetic (PK) Parameter: Plasma Concentration of LY2216684
12.3; 18.2; 26.0; 40.0

Eligibility Criteria

Inclusion Criteria

  • Adults age 18-65 years
  • Meet criteria for major depressive disorder (MDD) as defined by Diagnostic and Statistical Manual of Mental Disorders-fourth edition-text revision (DSM-IV-TR) criteria without psychotic features
  • Women of child-bearing potential must test negative for pregnancy and agree to use a reliable method of birth control
  • Grid 17-item Hamilton Rating Scale for Depression (GRID-HAMD17) total score ≥18 at Visit 1 and Visit 2
  • Clinical global impressions of severity (CGI-S) score ≥4 at Visit 1 and Visit 2

Exclusion Criteria

  • Are currently involved in or discontinued within the last 30 days from a clinical trial involving an off-label use of an investigational drug
  • Have previously completed or withdrawn from this study or any other study investigating LY2216684
  • Have had or currently have any additional ongoing DSM-IV-TR Axis 1 condition other than MDD
  • Have had any anxiety disorder preceding the onset of depression that was considered the primary diagnosis within 1 year of Visit 1
  • Have an Axis II disorder that would interfere with protocol compliance
  • Have a current or previous diagnosis of Bipolar I or II, psychotic depression, schizophrenia, or other psychotic disorder
  • Have a history of substance abuse within the past 1 year
  • Women who are pregnant or breast-feeding
  • Have had a lack of response of the current depressive episode to 2 or more adequate courses of antidepressant therapy, or in the judgment of the investigator, considered to have treatment-resistant depression
  • Participants who are judged to be at serious suicidal risk
  • Have a serious or unstable medical illness
  • Have any diagnosed medical condition which could be exacerbated by noradrenergic agents including unstable hypertension, unstable heart disease, tachycardia or tachyarrhythmia, narrow angle glaucoma, or urinary hesitation or retention
  • Have received treatment with a monoamine oxidase inhibitor (MAOI) within 14 days prior to Visit 1
  • Have a history of severe allergies to more than 1 class of medication or multiple adverse drug reactions
  • Have a history of electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS) or psychosurgery within the last year
  • Have a history of any seizure disorder (other than febrile seizures)
  • Require psychotropic medication other than sedative/hypnotic medication for sleep
  • Have a thyroid stimulating hormone (TSH) level outside the established reference range.
  • Are taking or have received treatment with any excluded medication within 7 days prior to Visit 2
  • Initiation or change in intensity of psychotherapy or other non-drug therapies within 6 weeks prior to enrollment
  • A positive urine drug screen for any substance of abuse at Visit 1
  • Have initiated or discontinued hormone therapy within the previous 3 months prior to enrollment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00795821) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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