Behavioral and Subjective Efficacy of Ramelteon in Subjects With a History of Polydrug Abuse

NCT ID: NCT00671632

Last Updated: 2012-02-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-06-30
• Study Completion Date: 2003-12-31

Brief Summary

The purpose of this study is to determine the relative abuse potential of ramelteon, once daily (QD), compared to triazolam in subjects with a history of drug abuse.

Detailed Description

Insomnia is characterized by a complaint of either difficulties initiating and maintaining sleep, or of nonrestorative and non-refreshing sleep. Transient insomnia affects approximately one-third to one-half of the US population, based on the results of 2 surveys of representative samples of the adult US population conducted by the Gallup Organization in which respondents were asked if they had "ever had difficulty sleeping." Based on reports of "regular" or "frequent" sleep difficulty, results from the same studies suggest that approximately one-tenth of the US population experiences chronic insomnia. The ideal treatment for insomnia would reduce the latency to onset of sleep and increase total sleep time, without a negative impact on sleep architecture and without safety concerns or next-day effects.

Ramelteon is a melatonin-1 receptor agonist under global development by Takeda Chemical Industries, Ltd., for the treatment of transient and chronic insomnia and for the treatment of Circadian Rhythm Sleep Disorders.

Participation in this study is anticipated to be about 1 month.

Conditions

Drug Abuse

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Ramelteon, triazolam, and placebo (56 poss. combinations)

Ramelteon, triazolam, and placebo (56 possible combinations total)

Group Type: EXPERIMENTAL

Ramelteon, triazolam, and placebo (56 possible combinations total)

Intervention Type: DRUG

Randomized sequence over eight consecutive days to include the following:

Ramelteon 16 mg, tablets, orally, one day only;

Ramelteon 80 mg, tablets, orally, one day only;

Ramelteon 160 mg, tablets, orally, one day only;

Triazolam 0.25 mg, capsules, orally, one day only;

Triazolam 0.50 mg, capsules, orally, one day only;

Triazolam 0.75 mg, capsules, orally, one day only;

Ramelteon placebo-matching tablets, orally, one day only, OR Triazolam placebo-matching capsules, orally, one day only;

Additional dose of study medication or placebo, tablets or capsules, orally, one day only.

Interventions

Ramelteon, triazolam, and placebo (56 possible combinations total)

Randomized sequence over eight consecutive days to include the following:

Ramelteon 16 mg, tablets, orally, one day only;

Ramelteon 80 mg, tablets, orally, one day only;

Ramelteon 160 mg, tablets, orally, one day only;

Triazolam 0.25 mg, capsules, orally, one day only;

Triazolam 0.50 mg, capsules, orally, one day only;

Triazolam 0.75 mg, capsules, orally, one day only;

Ramelteon placebo-matching tablets, orally, one day only, OR Triazolam placebo-matching capsules, orally, one day only;

Additional dose of study medication or placebo, tablets or capsules, orally, one day only.

Intervention Type: DRUG

Other Intervention Names

Rozerem™; TAK-375

Eligibility Criteria

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.
• Must be in good health as determined by a physician (ie, via medical history and physical examination).
• Clinical laboratory evaluations (including clinical chemistry, hematology, and complete urinalysis) within the reference range for the testing laboratory unless the results are deemed not clinically significant by the investigator or sponsor.
• Must have a history of substance abuse or dependence, on a commonly abuse recreational psychoactive drug (e.g., benzodiazepines, cocaine, opiates, cannabinoids).
• Must have a negative urine sample for substances of abuse and a negative breathalyzer test before the first dose of study medication is administered.
• Must be free of any signs/symptoms of withdrawal from substances after admittance to the research unit and prior to the first dose of study medication.
• Must report liking for study medication given on Day -2 and liking must be of greater magnitude that than the liking for study medication given on Day -1.

Exclusion Criteria

• Known hypersensitivity to ramelteon or related compounds including melatonin.
• Known hypersensitivity to benzodiazepines or related compounds.
• Current diagnosis of any type of physical drug dependence other than nicotine or caffeine.
• Positive HBsAg are excluded.
• Positive human immunodeficiency virus antibody at screening.
• Diastolic blood pressure greater than 90 mm Hg or a systolic pressure of greater than 140 mm Hg at screening.
• 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 study drug.
• Body weight is less than 99 or greater than 264 pounds. Subjects that are morbidly obese as defined by greater than 2 times ideal body weight
• Significant urine concentration of any drug that could interfere with the study.
• Clinically significant abnormal finding on physical examination or electrocardiogram. Subjects with a clinically significant illness in the past 30 days.
• Current Diagnostic and Statistical Manual of Mental Disorders, 4th Edition Revised diagnosis of a serious psychiatric condition (e.g. Schizophrenia, Major Depression).
• Currently is participating in another investigational study or has participated in an investigational study within the past 30 days.
• Any other serious disease or condition at screening or at randomization that might affect life expectancy or make it difficult to successfully manage and follow the subject according to the protocol.
• 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

VP Clinical Science

Role: STUDY_DIRECTOR

Takeda

Locations

Baltimore, Maryland, United States

Countries

United States

References

Johnson MW, Suess PE, Griffiths RR. Ramelteon: a novel hypnotic lacking abuse liability and sedative adverse effects. Arch Gen Psychiatry. 2006 Oct;63(10):1149-57. doi: 10.1001/archpsyc.63.10.1149.

Reference Type: RESULT

PMID: 17015817 (View on PubMed)

Related Links

http://general.takedapharm.com/content/file/pi.pdf?applicationcode=ab2d7112-8eb3-465a-8fda-35018a9eafb0&fileTypeCode=ROZEREMPI

Rozerem Package Insert

Other Identifiers

U1111-1114-3109

Identifier Type: REGISTRY

Identifier Source: secondary_id

01-02-TL-375-015

Identifier Type: -

Identifier Source: org_study_id