A Study of LY2624803 in Participants With Transient Insomnia

January 28, 2013 updated by: Eli Lilly and Company

A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Crossover Study of Single Doses of LY2624803 in a 5-hour Phase Advance Model of Transient Insomnia in Healthy Subjects

The aim of this study is to learn how different doses of LY2624803 affect sleep in healthy people. The study has four treatment periods. Participants will receive a single dose of LY2624803, another sleeping pill, or placebo in each treatment period. The study will last approximately 1 month for each participant.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Rouffach, France
        • 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.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Overtly healthy males or females
  • Women of child-bearing potential, who test negative for pregnancy at the time of enrollment based on a urine pregnancy test and agree to use a reliable method of birth control during the study and for one month following the last dose of study drug
  • Between the Body Mass Index (BMI) of 19 and 30 kilogram per meter square (kg/m^2), inclusive
  • Normal bedtime hours, with routine time spent in bed between 6.5 hours and 9 hours each night
  • Participants whose daily caffeine intake permits maintenance of normal bed time hours
  • Non response to placebo defined as a Wake After Sleep Onset (WASO) of greater than or equal to 45 minutes, on a 5-hour phase-advanced polysomnography (PSG) screening night after bedtime single-blind placebo administration
  • Males must agree to use effective barrier contraception during the course of the trial and 3 months later
  • Participants over 65 years of age, on a stable dose of one medication for lowering cholesterol, triglycerides and/or one medication for lowering blood pressure and/or substitutive hormonal therapy in post menopausal women are allowed provided those treatments have no central effect
  • Clinical laboratory test results within normal reference range judged to be not clinically significant
  • Normal sitting blood pressure and pulse rate as determined
  • Venous access sufficient to allow blood sampling
  • Are reliable and willing to make themselves available for the duration of the study
  • Have given written informed consent approved by Lilly and the ethical review board governing the site

Exclusion Criteria:

  • Shift workers (those who shifted work within 7 days of any PSG night) or any person who has crossed (or will have crossed) more than one time zone by aircraft within 3 days prior to entry
  • Rhinoconjunctivitis, urticaria or chronic pain severe enough to interfere with sleep
  • Nocturia that would interfere with sleep assessment
  • Participants with allergic conjunctivitis or urticaria
  • Regular napping (greater than (≥) 2 daytime naps/week by history)
  • Symptoms consistent with a sleep disorder or history of same
  • Sleep disorders detected during the screening night
  • Evidence of significant active neuropsychiatric disease and in particular evidence of significant medical or psychiatric illness within the past 12 months that could contribute to insomnia
  • Irregular or altered sleep/wake schedule
  • Known history of fainting or low blood pressure. History of cranial trauma and loss of consciousness will be discussed prior to including any such participant
  • Within 3 months of the initial dose of study drug, have received treatment with a drug that has not received regulatory approval for any indication
  • Participants with postural hypotension at screening
  • Participants with a history of postural hypotension, loss of consciousness, explained or unexplained syncope or seizure episodes or a family history of seizures. History of a single febrile convulsion is acceptable
  • Known allergies to LY2624803, Zolpidem or related compounds
  • Persons who have previously completed or withdrawn from this study or any other study investigating LY2624803
  • An abnormality in the 12-lead electrocardiogram (ECG) that increases the risks associated with participating in the study
  • History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, neurocardiogenic or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; of constituting a risk when taking the study medication; or of interfering with the interpretation of data
  • Any other condition with in the opinion of the investigator would preclude participation the study
  • Regular use of known drugs of abuse and/or positive findings on urinary drug screening
  • Evidence of Human Immunodeficiency Virus (HIV) and/or positive human HIV antibodies
  • Evidence of hepatitis C and/or positive hepatitis C antibody
  • Evidence of hepatitis B and/or positive hepatitis B surface antigen
  • Women with a positive pregnancy test
  • Women who are lactating
  • Use of prescription, over the counter or herbal medications that cannot safely be discontinued within 28 days prior to enrollment
  • Blood donation of more than 500 milliliter (mL) within the last month
  • History of smoking within the previous 6 months of screening
  • Participants who have an average weekly alcohol intake that exceeds 28 units per week (males) and 21 units per week (females), or participants unwilling to stop alcohol consumption for the duration of the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: 0.3 mg LY2624803
Single dose of 0.3 mg LY2624803 administered orally in up to 2 of 4 treatment periods.
Drug: LY2624803 - Capsules
Administered orally as capsules.
Other Names:
  • Hypnion
EXPERIMENTAL: 3.0 mg LY2624803
Single dose of 3.0 mg LY2624803 administered orally in up to 2 of 4 treatment periods.
Drug: LY2624803 - Capsules
Administered orally as capsules.
Other Names:
  • Hypnion
EXPERIMENTAL: 6.0 mg LY2624803
Single dose of 6.0 mg LY2624803 administered orally in up to 2 of 4 treatment periods.
Drug: LY2624803 - Capsules
Administered orally as capsules.
Other Names:
  • Hypnion
ACTIVE_COMPARATOR: 10 mg Zolpidem
Single dose of 10 mg zolpidem administered orally in up to 1 of 4 treatment periods.
Drug: Zolpidem - Tablets
Administered orally as tablets.
PLACEBO_COMPARATOR: Placebo
Single dose of placebo administered orally in up to 1 of 4 treatment periods.
Drug: Placebo - Capsules
Administered orally as capsules.
Drug: Placebo - Tablets
Administered orally as tablets.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in Wake After Sleep Onset (WASO) With LY2624803 Compared to Placebo
Time Frame: Baseline up to Day 60
Baseline up to Day 60

Secondary Outcome Measures

Outcome Measure
Time Frame
Latency to Persistent Sleep (LPS) with LY2624803 Compared to Placebo
Time Frame: Baseline up to Day 60
Baseline up to Day 60
Total Sleep Time (TST) with LY2624803 Compared to Placebo
Time Frame: Baseline up to Day 60
Baseline up to Day 60

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Eli Lilly and Company

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2008

Primary Completion (ACTUAL)

November 1, 2008

Study Completion (ACTUAL)

November 1, 2008

Study Registration Dates

First Submitted

January 25, 2013

First Submitted That Met QC Criteria

January 28, 2013

First Posted (ESTIMATE)

January 30, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

January 30, 2013

Last Update Submitted That Met QC Criteria

January 28, 2013

Last Verified

January 1, 2013

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 12057
  • I2K-MC-ZZAA (OTHER: Eli Lilly and Company)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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