Status:

COMPLETED

An Efficacy Study of Compound LY2624803 in the Treatment of Patients With Chronic Insomnia

Lead Sponsor:

Eli Lilly and Company

Conditions:

Primary Insomnia

Secondary Insomnia

Eligibility:

All Genders

18-85 years

Phase:

PHASE2

Brief Summary

The purpose of this study is to compare an investigational drug (LY2624803) with placebo and with zolpidem in the treatment of outpatients with chronic insomnia.

Detailed Description

Outpatients with chronic insomnia who participate in this study will be treated in each of four 2-week treatment periods with bedtime doses of either placebo, zolpidem, LY2624803 1 mg, or LY2624803 3 ...

Eligibility Criteria

Inclusion

  • Patients must be between 18 and 85 years of age, with a stable living situation
  • Clinical diagnosis of either primary insomnia or "secondary" insomnia (comorbid with depression, anxiety, and/or medical illness)
  • Insomnia systems must be at least moderate in severity within the month prior to study entry, and must include difficulty staying asleep and/or problems with awakening earlier than desired
  • Psychiatric and medical conditions present must be stable over the 3 months prior to study entry, and not expected to worsen significantly or require hospitalization during participation in the study
  • Ongoing treatments for psychiatric and medical conditions present must have been stable for the 3 months prior to study entry, and must be expected to remain stable during participation in the study
  • Patients must be willing to abstain from taking medications (other than study drug) to help them sleep during participation in the study
  • Patients must be willing to consistently spend at least 7 hours each night either sleeping or trying to sleep during participation in the study
  • Patients must be able to speak and read English and be capable of using a computer with a web browser (computers with internet connections will be provided to patients who need them)

Exclusion

  • Unusual or unstable sleep/wake schedule, such as with rotating shift work
  • Severe or unstable psychiatric or medical illness
  • Suicidal ideation
  • Substance abuse
  • Known obstructive sleep apnea, restless leg syndrome, or periodic limb movement disorder
  • History of seizures
  • Body Mass Index \> 33
  • Clinically significant abnormality in clinical chemistry, hematology, urinalysis, and/or electrocardiogram
  • Anticipated inability to regularly use a medication which might reduce motor or cognitive functioning during sleeping hours, such as a person who might often need to be "on call", drive a car, or be responsible for the care of another person during sleeping hours
  • Contraindication to zolpidem
  • History of breast cancer
  • An estimated glomerular filtration rate (GFR; an index of renal function) that is \<30 mL/min at study entry

Key Trial Info

Start Date :

October 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2010

Estimated Enrollment :

643 Patients enrolled

Trial Details

Trial ID

NCT00784875

Start Date

October 1 2008

End Date

February 1 2010

Last Update

February 29 2012

Active Locations (49)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 13 (49 locations)

1

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Birmingham, Alabama, United States, 35213

2

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Glendale, Arizona, United States, 85306

3

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Mesa, Arizona, United States, 85210

4

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Little Rock, Arkansas, United States, 72211