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Safety and Efficacy of Eszopiclone in Patients With Generalized Anxiety Disorder

Primary Purpose

Insomnia, Generalized Anxiety Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Eszopiclone (Lunesta)
Sponsored by
Sumitomo Pharma America, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring Insomnia, Anxiety, Generalized Anxiety Disorder

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesDoes not accept healthy volunteers

Subjects, between the ages of 18 and 64 years inclusive Subjects with Generalized Anxiety Disorder (GAD) Subjects with insomnia related to GAD.

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Escitalopram oxalate 10 mg at bedtime

Eszopiclone 3 mg at bedtime

Outcomes

Primary Outcome Measures

The change from baseline in subjective sleep latency averaged over the double-blind treatment period.

Secondary Outcome Measures

Change from baseline in subjective total sleep time averaged over the double blind treatment period.

Full Information

First Posted
October 6, 2005
Last Updated
February 21, 2012
Sponsor
Sumitomo Pharma America, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00235508
Brief Title
Safety and Efficacy of Eszopiclone in Patients With Generalized Anxiety Disorder
Official Title
The Efficacy of Eszopiclone 3 mg as Adjunctive Therapy in Subjects With Insomnia Related to Generalized Anxiety Disorder.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
April 2006 (Actual)
Study Completion Date
April 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sumitomo Pharma America, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine the safety and efficacy of eszopiclone as adjunctive therapy in the treatment of insomnia in patients with insomnia related to Generalized Anxiety Disorder. All subjects will receive an approved anxiolytic agent and will be randomized to nightly therapy with either eszopiclone or placebo.
Detailed Description
An 8-week, randomized, double-blind, placebo-controlled, parallel-group adjunctive therapy trial. The study consists of subjects with insomnia related to Generalized Anxiety Disorder who will be treated for 10 weeks with open-label escitalopram oxalate 10 mg/day at bedtime, and randomized to receive either eszopiclone 3 mg nightly or placebo nightly for 8 weeks. This study was previously posted by Sepracor Inc. In October 2009, Sepracor Inc. was acquired by Dainippon Sumitomo Pharma., and in October 2010, Sepracor Inc's name was changed to Sunovion Pharmaceuticals Inc.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia, Generalized Anxiety Disorder
Keywords
Insomnia, Anxiety, Generalized Anxiety Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
420 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Escitalopram oxalate 10 mg at bedtime
Arm Title
2
Arm Type
Active Comparator
Arm Description
Eszopiclone 3 mg at bedtime
Intervention Type
Drug
Intervention Name(s)
Eszopiclone (Lunesta)
Other Intervention Name(s)
Lunesta
Intervention Description
Escitalopram oxalate 10 mg at bedtime; Eszopiclone 3 mg at bedtime
Primary Outcome Measure Information:
Title
The change from baseline in subjective sleep latency averaged over the double-blind treatment period.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in subjective total sleep time averaged over the double blind treatment period.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Subjects, between the ages of 18 and 64 years inclusive Subjects with Generalized Anxiety Disorder (GAD) Subjects with insomnia related to GAD.
Facility Information:
City
Birmingham
State/Province
Alabama
Country
United States
City
Mesa
State/Province
Arizona
Country
United States
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Scottsdale
State/Province
Arizona
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United States
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Irvine
State/Province
California
Country
United States
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La Mesa
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California
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United States
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National City
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California
Country
United States
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Oceanside
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California
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United States
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Orange
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California
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United States
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Pasadena
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California
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United States
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Redlands
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California
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United States
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Riverside
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California
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United States
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San Diego
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California
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United States
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Farmington
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Connecticut
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United States
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Washington
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District of Columbia
Country
United States
City
Coral Springs
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Florida
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United States
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Fort Lauderdale
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Florida
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United States
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Gainesville
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Florida
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United States
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Jacksonville
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Florida
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United States
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Orlando
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Florida
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United States
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Pembroke Pines
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Florida
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United States
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St. Petersburg
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Florida
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United States
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Atlanta
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Georgia
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United States
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Augusta
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Georgia
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United States
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Smyrna
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Georgia
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United States
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Northfield
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Illinois
Country
United States
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Indianapolis
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Indiana
Country
United States
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Owensboro
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Kentucky
Country
United States
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Baltimore
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Maryland
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United States
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Rockville
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Maryland
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United States
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Braintree
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Massachusetts
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United States
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Brighton
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Massachusetts
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United States
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Brockton
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Massachusetts
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United States
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Cambridge
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Massachusetts
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United States
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Watertown
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Massachusetts
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United States
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St. Louis
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Missouri
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United States
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Kenilworth
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New Jersey
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United States
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Piscataway
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New Jersey
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United States
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Brooklyn
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New York
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United States
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Lawrence
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New York
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United States
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New York
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New York
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United States
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Durham
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North Carolina
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United States
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Raleigh
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North Carolina
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United States
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Winston-Salem
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North Carolina
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United States
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Bismarck
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North Dakota
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United States
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Beachwood
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Ohio
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United States
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Cincinnati
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Ohio
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United States
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Dayton
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Ohio
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United States
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Middleburg Heights
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Ohio
Country
United States
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Eugene
State/Province
Oregon
Country
United States
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Portland
State/Province
Oregon
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United States
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Salem
State/Province
Oregon
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United States
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Moon Township
State/Province
Pennsylvania
Country
United States
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Philadelphia
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Pennsylvania
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United States
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Scotland
State/Province
Pennsylvania
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United States
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Columbia
State/Province
South Carolina
Country
United States
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Memphis
State/Province
Tennessee
Country
United States
City
Austin
State/Province
Texas
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United States
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Houston
State/Province
Texas
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United States
City
Richardson
State/Province
Texas
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United States
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San Antonio
State/Province
Texas
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United States
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Wichita Falls
State/Province
Texas
Country
United States
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Falls Church
State/Province
Virginia
Country
United States
City
Richmond
State/Province
Virginia
Country
United States
City
Middleton
State/Province
Wisconsin
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21208574
Citation
Fava M, Schaefer K, Huang H, Wilson A, Iosifescu DV, Mischoulon D, Wessel TC. A post hoc analysis of the effect of nightly administration of eszopiclone and a selective serotonin reuptake inhibitor in patients with insomnia and anxious depression. J Clin Psychiatry. 2011 Apr;72(4):473-9. doi: 10.4088/JCP.09m05131gry. Epub 2010 Nov 2.
Results Reference
result
PubMed Identifier
18458207
Citation
Pollack M, Kinrys G, Krystal A, McCall WV, Roth T, Schaefer K, Rubens R, Roach J, Huang H, Krishnan R. Eszopiclone coadministered with escitalopram in patients with insomnia and comorbid generalized anxiety disorder. Arch Gen Psychiatry. 2008 May;65(5):551-62. doi: 10.1001/archpsyc.65.5.551.
Results Reference
derived

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Safety and Efficacy of Eszopiclone in Patients With Generalized Anxiety Disorder

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