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Safety of Ramelteon in Subjects With Chronic Obstructive Pulmonary Disease

31 mei 2010 bijgewerkt door: Takeda

A Study of the Safety of Ramelteon in Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease

The purpose of this study is to determine if ramelteon has respiratory depressant effects in subjects with moderate to severe chronic obstructive pulmonary disease.

Studie Overzicht

Toestand

Voltooid

Interventie / Behandeling

Gedetailleerde beschrijving

About 30% of the adult population report sleep disturbance and 10% meet diagnostic criteria for chronic insomnia. While 20 -25% of these individuals have primary insomnia the vast majority have an additional condition such as chronic obstructive pulmonary disease. Several studies have looked at this and have estimated that 30% to 48% of the general population is affected at some time in their life with a form of insomnia that goes on for several months, and about one third of those are described as severely affected. Daytime symptoms of insomnia include tiredness, lack of energy, difficulty concentrating and irritability. Recent epidemiologic research focusing on the quality of life has identified significant insomnia related conditions or diseases that relate to work productivity, health care utilization, and risk of depression. Insomnia is associated with diminished work output, absenteeism and greater rates of accidents.

Ramelteon, is being developed as a sleep promoting agent based on agonism of melatonin receptor subtype 1 and 2. Ramelteon is marketed in the United States as Rozerem™ for the treatment of insomnia characterized by difficulty with sleep initiation.

Sleep problems are common in patients with chronic obstructive pulmonary disease. There is evidence that traditional hypnotics can cause adverse respiratory effects in insomniac populations with respiratory disorders, and so the safety and efficacy of new hypnotic agents must be ascertained in this group of patients.

This study will examine if ramelteon has respiratory depressant effects in subjects with moderate to severe chronic obstructive pulmonary disease. Study participation is anticipated to be about 6 weeks.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

25

Fase

  • Fase 4

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Alabama
      • Birmingham, Alabama, Verenigde Staten, 35213
    • California
      • Los Angeles, California, Verenigde Staten
      • Santa Monica, California, Verenigde Staten, 90404
    • Florida
      • Naples, Florida, Verenigde Staten, 34110
      • St. Petersburg, Florida, Verenigde Staten, 33707
    • Kentucky
      • Louisville, Kentucky, Verenigde Staten, 40217
    • Nebraska
      • Lincoln, Nebraska, Verenigde Staten, 68510
    • New York
      • New York, New York, Verenigde Staten, 10025

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

40 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria

  • Females of childbearing potential who are sexually active must agree to use adequate contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.
  • Body mass index between 18 and 34, inclusive.
  • Clinical history of chronic obstructive pulmonary disease and a confirmatory diagnosis based on pulmonary function tests performed at the Outpatient Screening Visit, with moderate to severe airflow limitation defined by: Moderate: forced expiratory volume in one second to forced vital capacity less than 70%; 50% less than forced expiratory volume in one second; less than 80% predicted. Severe: forced expiratory volume in one second to forced vital capacity less than 70%; forced expiratory volume in one second less than 50% predicted.
  • Post-bronchodilator forced expiratory volume in one second change from baseline of less than12% and not exceeding 200 ml at the Outpatient Screening Visit.
  • Oxygen saturation during wakefulness greater than 90% (both supine and sitting) as assessed by pulse oximetry at the Outpatient Screening Visit.
  • Oxygen saturation during sleep of greater than or equal to 80% for at least 75% of the recording period with no more than 5 continuous minutes less than 80% and with no oxygen saturation readings less than 70% as assessed by pulse oximetry at the Inpatient Screening Visit.

Exclusion Criteria

  • The health of subjects using nocturnal oxygen therapy would, in the investigator's opinion, be jeopardized by the removal of oxygen therapy during inpatient study visits.
  • Electrocardiographic evidence of right ventricular hypertrophy, or evidence of right heart failure.
  • Apnea hypopnea index (per hour of sleep) greater than 15 during polysomnography.
  • Has had an acute clinically significant illness within two weeks or has been hospitalized within four weeks of the Outpatient Screening Visit.
  • History of seizures (except childhood febrile seizures).
  • History of cancer, other than basal cell carcinoma, that has not been in remission for at least five years prior to the first dose of study drug. (This criterion does not include those subjects with basal cell or Stage 1 squamous cell carcinoma of the skin.)
  • History of drug addiction or drug abuse within the past 12 months, as defined in Diagnostic and Statistical Manual of Mental Disorders, 4th Edition Revised.
  • History of alcohol abuse within the past 12 months, as defined in
  • Diagnostic and Statistical Manual of Mental Disorders, 4th Edition Revised and/or regularly consumes more than 14 alcoholic drinks per week, or consumed any alcoholic drinks within six hours of any PSG visits.
  • Will not refrain from use of tobacco products while in the sleep laboratory.
  • Any clinically important abnormal finding, other than chronic obstructive pulmonary disease, as determined by medical history, physical examination, electrocardiogram, or clinical laboratory tests, as determined by the investigator.
  • Current significant neurological, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, hematologic, or metabolic disease, unless currently controlled and stable with protocol-allowed medication 30 days prior to the Inpatient Screening Visit.
  • Hematocrit value greater than 55% at the Outpatient Screening Visit.
  • Positive hepatitis panel including anti-hepatitis A virus (only immunoglobulin M is exclusionary), hepatitis B surface antigen, or anti-hepatitis C virus.
  • Alanine transaminase level of greater than three times the upper limit of normal, active liver disease, jaundice or any clinically significant abnormal laboratory findings as determined by the investigator.
  • Donated more than 400 mL of blood within the 90 days preceding the beginning of the study.
  • Positive urine drug screen for drugs known to alter sleep-wake function (eg, barbiturates, opiates, amphetamines, cannabinoids and alcohol) at screening, or a positive breathalyzer test for alcohol at any check-in.
  • Known hypersensitivity to ramelteon or related compounds, including melatonin.
  • Known hypersensitivity to albuterol or related compounds.
  • Participated in any other investigational study and/or taken any investigational drug within 30 days or five half-lives prior to the first dose of single-blind study medication, whichever is longer.
  • Unable to discontinue the use of hypnotics for the duration of the study.
  • Has used melatonin, or other drugs or supplements known to affect sleep-wake function, within one week (or five half-lives of the drug, whichever is longer) prior to the first dose of single-blind study medication.
  • Any additional condition(s) that in the Investigator's opinion would prohibit the subject from completing the study or not be in the best interest of the subject.
  • Is required to take or continues taking any disallowed medication, prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:

    • Within one week of single-blind medication and during the entire study.

      • Hypnotics
      • Sedating Antidepressants
      • Sedating H1 antihistamines
      • Respiratory stimulants
      • Muscle relaxants
      • The use of albuterol is acceptable during reversibility testing at the Outpatient Screening Visit.
    • Melatonin and all other drugs or supplements known to affect sleep/wake function will be prohibited within one week of the first dose of single-blind medication and during the entire study.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Ramelteon 8 mg and Placebo
Ramelteon 8 mg, tablets, orally, one night only and Ramelteon placebo-matching tablets, orally, one night only.
Andere namen:
  • TAK-375
  • Rozerem™

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Mean oxygen saturation during sleep for the entire night measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Mean oxygen saturation calculated for each hour of the night, as measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Mean oxygen saturation for rapid eye movement sleep stages, as measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Mean oxygen saturation for non- rapid eye movement sleep stages, as measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Minutes for which oxygen saturation was less than 80% as measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Minutes for which oxygen saturation was less than 90% as measured by pulse oximetry.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Apnea-hypopnea index as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Latency to persistent sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Total sleep time as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Sleep efficiency as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Wake time after persistent sleep onset as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Number of awakenings after persistent sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Percentage of time in rapid eye movement sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Percentage of time in stage 1 sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Percentage of time in stage 2 sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Percentage of time in stage 3/4 sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Latency to rapid eye movement sleep as determined by polysomnography.
Tijdsspanne: Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Crossover Period 1 Night 1 and Crossover Period 2 Night 1
Subjective sleep latency as determined by postsleep questionnaire.
Tijdsspanne: Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Subjective total sleep time as determined by postsleep questionnaire.
Tijdsspanne: Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Subjective Sleep Quality as determined by postsleep questionnaire.
Tijdsspanne: Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Subjective number of awakenings as determined by postsleep questionnaire.
Tijdsspanne: Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1
Crossover Period 1 Morning 1 and Crossover Period 2 Morning 1

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Onderzoekers

  • Studie directeur: Medical Director Clinical Science, Takeda Global Research and Development

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 april 2006

Primaire voltooiing (Werkelijk)

1 november 2006

Studie voltooiing (Werkelijk)

1 november 2006

Studieregistratiedata

Eerst ingediend

19 april 2006

Eerst ingediend dat voldeed aan de QC-criteria

19 april 2006

Eerst geplaatst (Schatting)

21 april 2006

Updates van studierecords

Laatste update geplaatst (Schatting)

2 juni 2010

Laatste update ingediend die voldeed aan QC-criteria

31 mei 2010

Laatst geverifieerd

1 mei 2010

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • 01-05-TL-375-068
  • U1111-1115-1960 (Register-ID: WHO)

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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