- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00755508
Efficacy and Safety of Ramelteon Combined With Gabapentin in Treating Patients With Insomnia
A Phase 2, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Multicenter, Proof-of-Concept Study to Evaluate the Safety and Efficacy of ROZEREM™ Taken in Combination With Gabapentin for the Treatment of Subjects With Chronic Insomnia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Approximately 60 to 70 million adults in the United States alone are affected by insomnia. Daytime symptoms of insomnia include tiredness, lack of energy, difficulty concentrating, and irritability. Recent epidemiologic research focusing on quality of life has identified significant insomnia-related morbidities that relate to work productivity, health care utilization, and risk of depression. Insomnia is also associated with diminished work output, absenteeism, and greater rates of accidents. gamma-aminobutyric acid is the major inhibitory transmitter in the central nervous system and most currently prescribed sleep agents are benzodiazepine receptor agonists, which induce sleep by binding to the benzodiazepine receptor site of the gamma-aminobutyric acid -A receptor complex. In addition to sleep, benzodiazepine receptor agonists can cause a wide range of ancillary effects not directly related to sleep, including sedative, anxiolytic, muscle-relaxant, and amnesic effects, and have risks of tolerance, dependence, and abuse potential.
Gabapentin is a novel anti-epileptic drug, which is currently used in subjects with partial seizures. Some studies have shown that gabapentin also has an effect on sleep architecture. In several studies, which included healthy subjects, epileptic subjects, and subjects with restless leg syndrome, the use of gabapentin been shown to prolong slow-wave sleep, increase total sleep time and sleep efficiency, and decrease number of awakenings.
Ramelteon is a melatonin receptor agonist with affinity for the human melatonin receptor subtype 1, melatonin receptor subtype 2 and selectivity over the melatonin receptor subtype 3 receptor. It also demonstrates agonist activity in vitro relative to melatonin in cells expressing human melatonin receptor subtype 1 or melatonin receptor subtype 2 receptors. The binding of melatonin at these receptors is thought to contribute to maintenance of the circadian rhythm underlying the normal sleep-wake cycle.
The purpose of this trial is to determine if the co-administration of Ramelteon and gabapentin may produce increased sleep efficiency through reduction of wake time after persistent sleep onset, in addition to the reduction in sleep latency and increase in sleep duration. Study participation is anticipated to be about one month.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Female patients of childbearing potential must be nonpregnant and nonlactating, and utilizing an acceptable method of contraception.
- Based on sleep history, the subject has had primary insomnia as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition Revised (DSM-IV-TR™) for at least 3 months.
- Based on sleep history, reports a subjective sleep latency greater than or equal to 45 minutes and reports wake time after persistent sleep onset of greater than or equal to 45 minutes.
- Has an average wake time after persistent sleep onset of at least 60 minutes as determined by polysomnography during Screening (Day minus 7 PM through Day minus 5 AM). Wake time after persistent sleep onset must be greater than or equal to 30 minutes each night of polysomnography Screening.
- Reports wake time after persistent sleep onset values of at least 60 minutes on at least 3 of the 7 nights during the single-blind screening period (Day minus 6 AM through Day 1 AM) as determined by post-sleep questionnaire.
- Has an average latency to persistent sleep of at least 20 minutes as determined by polysomnography during Screening (Day minus 7 PM through Day minus 5 AM).
- Based on sleep history, has an habitual bedtime between 9:00 PM and 1:00 AM.
- The subject is willing to have a fixed bedtime and agrees to go to bed within plus or minus 30 minutes of the habitual bedtime during the entire study and agrees to remain in bed for at least 8 hours each night.
- Based on sleep history, has not been using pharmacological assistance to sleep or uses pharmacological assistance no more than 4 times per week during the 3 months prior to Initial Screening.
- Has consistent access to a touch-tone phone and are willing to complete telephone questionnaires twice daily during participation in the study.
Exclusion Criteria:
- Has a known hypersensitivity to gabapentin or its ingredients, ramelteon or related compounds, including melatonin, and 5-hydroxytryptophan.
- Has participated in any other investigational study and/or taken any investigational drug within 30 days prior to the first dose of single-blind study medication.
- Has sleep schedule changes required by employment (eg, shift worker) within 3 months prior to the first dose of single-blind study medication.
- Has flown across greater than 3 time zones within 7 days prior to Initial Screening, or will travel across 2 or more time zones during the course of the study.
- Has participated in a weight loss program or has substantially altered their exercise routine within 30 days prior to the first dose of single-blind study medication.
- Has ever had a history of seizures, sleep apnea, and/or chronic obstructive pulmonary disease.
- Has a history of psychiatric disorder (including anxiety, depression, mental retardation, cognitive disorder, bipolar illness and schizophrenia) within the past 6 months of Initial Screening.
- Has a history of fibromyalgia.
- Has a history of drug addiction or drug abuse within the past 12 months of Initial Screening.
- Has a history of alcohol abuse within the past 12 months, as defined in DSM-IV-TR™ and/or regularly consumes more than 2 alcoholic drinks per day.
- Has a current significant hepatic, endocrine, cardiovascular, gastrointestinal, pulmonary, hematological, metabolic or neurological disorders, unless currently controlled and stable with protocol-allowed medication, within 30 days prior to the first dose of single-blind study medication.
- Has any diagnosed renal impairment within 30 days prior to the first dose of single-blind study medication.
- Has a previous history of cancer, other than basal cell carcinoma, that has not been in remission for at least 5 years prior to the first dose of single-blind study drug.
- Uses tobacco products or any other products that may interfere with the sleep wake cycle during nightly awakenings.
Is required to take or intends to continue taking any disallowed medication or any prescription medication or over-the counter medication that is known to affect the sleep/wake function or otherwise interfere with evaluation of the study medication, including:
- Anxiolytics central nervous system active drugs (including herbal)
- Hypnotics Narcotic analgesics
- Antidepressants Beta blockers
- Anticonvulsants St. John's Wort
- Sedating H1 antihistamines Kava-kava
- Systemic steroids Ginkgo-biloba
- Respiratory stimulants over-the counter and prescription stimulants
- Sedating decongestants over-the counter and prescription diet aids
- Antipsychotics over-the counter sleep aids
- Muscle relaxants Antacids
- Melatonin and all other drugs or supplements known to affect sleep/wake function.
- Has a positive hepatitis panel including anti- hepatitis A virus, hepatitis B surface antigen or anti-hepatitis C virus.
- Has a positive urine drug screen including alcohol at Initial Screening or a positive breathalyzer test at each polysomnography Screening check-in.
- Has an apnea hypopnea index (per hour of sleep) >15 as seen on polysomnography, on the first night of the polysomnography screening.
- Has a history of restless leg syndrome.
- The subject has a body mass index of less than 18 or greater than 34 (weight /height2).
Has any additional condition(s) that in the Investigator's opinion would:
- Affect sleep/wake function
- Prohibit the subject from completing the study
- Not be in the best interest of the subject.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Placebo
|
Ramelteon placebo-matching tablets, orally, once daily and gabapentin placebo-matching capsules, orally, once daily for up to one week.
Other Names:
|
Experimental: Ramelteon 4 mg QD and Gabapentin 400 mg QD
|
Ramelteon 4 mg, tablets, orally, once daily and gabapentin 400 mg, capsules, orally, once daily for up to one week.
Other Names:
Ramelteon 8 mg, tablets, orally, once daily and gabapentin 800 mg, capsules, orally, once daily for up to one week.
Other Names:
|
Experimental: Ramelteon 8 mg QD and Gabapentin 800 mg QD
|
Ramelteon 4 mg, tablets, orally, once daily and gabapentin 400 mg, capsules, orally, once daily for up to one week.
Other Names:
Ramelteon 8 mg, tablets, orally, once daily and gabapentin 800 mg, capsules, orally, once daily for up to one week.
Other Names:
|
Experimental: Ramelteon 8 mg QD and Gabapentin Placebo QD
|
Ramelteon 8 mg, tablets, orally, once daily and gabapentin placebo-matching capsules, orally, once daily for up to one week.
Other Names:
|
Active Comparator: Gabapentin 800 mg QD
|
Ramelteon placebo-matching tablets, orally, once daily and gabapentin 800 mg, capsules, orally, once daily for up to one week.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Mean objective wake time after persistent sleep onset in sleep lab.
Time Frame: Nights: 1 and 2.
|
Nights: 1 and 2.
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Subjective wake time after persistent sleep onset determined by the post-sleep questionnaire.
Time Frame: Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Number of awakenings after persistent sleep polysomnography.
Time Frame: Nights: 1 and 2
|
Nights: 1 and 2
|
Subjective number of awakenings as determined by post-sleep questionnaire.
Time Frame: Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Latency to persistent sleep and total sleep time as determined by polysomnography.
Time Frame: Nights: 1 and 2
|
Nights: 1 and 2
|
Subjective sleep latency, subjective total sleep time and subjective sleep quality determined by post-sleep questionnaire.
Time Frame: Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Daytime functioning determined by pre-sleep questionnaire.
Time Frame: Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Nights: 1, 2, 3, 4, 5, 6 and 7.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Sr. VP Clinical Science, Takeda
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Nervous System Diseases
- Sleep Disorders, Intrinsic
- Dyssomnias
- Sleep Wake Disorders
- Sleep Initiation and Maintenance Disorders
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Central Nervous System Depressants
- Peripheral Nervous System Agents
- Analgesics
- Sensory System Agents
- Excitatory Amino Acid Antagonists
- Excitatory Amino Acid Agents
- Tranquilizing Agents
- Psychotropic Drugs
- Anti-Anxiety Agents
- Anticonvulsants
- Antimanic Agents
- Gabapentin
Other Study ID Numbers
- 01-05-TL-375-055
- U1111-1114-3348 (Registry Identifier: WHO)
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.
Clinical Trials on Sleep Initiation and Maintenance Disorders
-
Merck Sharp & Dohme LLCCompletedDyssomnias | Sleep Disorders | Mental Disorder | Sleep Initiation and Maintenance Disorder; Elderly | Sleep Disorder, Intrinsic
-
Eisai Co., Ltd.RecruitingSleep Initiation and Maintenance DisordersKorea, Republic of
-
Shanghai Institute of Acupuncture, Moxibustion...Shanghai University of Traditional Chinese MedicineNot yet recruitingSleep Initiation and Maintenance DisordersChina
-
Saint Vincent's Hospital, KoreaCompletedSleep Initiation and Maintenance DisordersKorea, Republic of
-
Chang Gung Memorial HospitalUnknownSleep Initiation and Maintenance DisordersTaiwan
-
Seattle Children's HospitalEunice Kennedy Shriver National Institute of Child Health and Human Development...UnknownSleep Initiation and Maintenance DisordersUnited States
-
Marmara UniversityCompletedSleep Initiation and Maintenance Disorders
-
GlaxoSmithKlineCompletedSleep Initiation and Maintenance DisordersUnited States
-
Boehringer IngelheimCompletedSleep Initiation and Maintenance Disorders
-
Astellas Pharma IncCompletedSleep Initiation and Maintenance DisordersJapan
Clinical Trials on Ramelteon and gabapentin
-
Virginia Commonwealth UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Completed
-
TakedaCompletedChronic Obstructive Pulmonary Disease | COPDUnited States
-
TakedaCompletedSleep Apnea, ObstructiveUnited States
-
Southern Arizona VA Health Care SystemUnknownGastroesophageal Reflux Disease | Chronic InsomniaUnited States
-
TakedaCompletedChronic InsomniaUnited States
-
Centennial Medical CenterRecruiting
-
University of California, San DiegoActive, not recruitingDelirium | Sleep Deprivation
-
TakedaCompleted
-
Massachusetts General HospitalWithdrawnParkinson's Disease | Sleep Disorders | Dementia With Lewy Bodies | Huntington's Disease | Circadian DysregulationUnited States