Efficacy and Safety Study of Adipiplon, Placebo and an Active Control in Primary Insomniacs

Stopped early · Phase 2 · Has a placebo group

Conditions studied: Primary Insomnia

In brief

This will be a multi-center, randomized, blinded, comparative, placebo-controlled, 4 arm crossover study in patients with primary insomnia.

Key facts

Study ID: NCT00683436
Run by: Neurogen Corporation
People needed: 84
Starts: 2008-05-01
Expected to finish: 2008-11-01
Last updated by the study team: 2008-07-22

Who can join

Age: 21 and older, up to 64. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Be between the ages of 21 and 64 years, inclusive;
Have a body mass index (BMI) between 21 and 34 kg/m2, inclusive;
Be a primary insomniac as defined by DSM-IV criteria; in particular difficulty with both sleep initiation and sleep maintenance;
Have subjective Latency to Sleep Onset > 45 minutes;
Have a mean habitual subjective TST of <6.5 hours;
Have a TST of 240 - 420 minutes at each of two baseline PSGs;
Have a mean LPS > 20min, with neither value <15 minutes and mean WASO > 40 minutes on baseline PSGs;
Be in good general health as determined by a thorough medical history and physical examination (including vital signs), 12-lead ECG and clinical laboratory tests;
Have clinical laboratory values within normal reference range or not clinically significantly abnormal as judged by the Principal Investigator;
Be off any investigational drug for at least 30 days prior to screening;
If the patient is a female of childbearing potential, she must be using an acceptable method of contraception, must have a negative serum pregnancy test at screening, and must have a negative urine pregnancy test before randomization.
Female patients who have been surgically sterilized or have had a hysterectomy are eligible if they have a negative pregnancy test at screening;
Be able to read, understand, and provide written/dated informed consent before enrolling in the study, and must be willing to comply with all study procedures.

You may not qualify if…

Clinically significant unstable medical illness;
Evidence or history of clinically significant allergic (except for untreated, asymptomatic, seasonal allergies at time of dosing), hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease;
History of cancer other than basal cell carcinoma, squamous cell carcinoma of the skin or cancer in situ within 5 years of screening;
Supine or sitting blood pressure > 140/90 mmHg at the screening or baseline visits;
Heart rate >100 bpm at the screening or baseline visits;
Within the past three years, clinically significant psychiatric illness, including chronic psychiatric illness or any Axis I condition;
History or presence of chronic pain;
History of epilepsy or serious head injury;
Other than primary insomnia, a history of clinically significant sleep disorder including narcolepsy, parasomnia as an adult, circadian rhythm disorder, restless leg syndrome, or on the initial baseline PSG, sleep apnea [Apnea Hypopnea Index (AHI) >10] or Periodic Limb Movement Disorder [Periodic Limb Movement Arousal Index (PLMAI) > 10];
Any condition that may affect drug absorption;
Smokers who habitually smoke more than 10 cigarettes per day or smoke during the overnight hours;
Travel across more than three time zones, an expected change in sleep schedules of 3 hours or more, or involvement in rotating shift work within 14 days prior to screening or during the study period;
Self-report of napping ≥30 minutes more than 2 times per week within the last month;
Any clinically significant abnormal finding on physical examination, vital signs, ECG, or clinical laboratory tests, as determined by the investigator. (The QTc interval must be ≤430 msec. for males and ≤450 msec for females);
Known or suspected diagnosis of Acquired Immune Deficiency Syndrome, or previous or current positive result on human immunodeficiency virus antibody or antigen testing;
History or laboratory finding of positive hepatitis B surface antigen or hepatitis C core antibody;
History of allergies, or known sensitivity, hypersensitivity, or adverse reaction to any drug similar to adipiplon, including benzodiazepines, or zolpidem, zaleplon, zopiclone, or eszopiclone;
Use of any psychotropic medications, including over-the-counter (OTC) and herbal products, that may affect sleep/wake function within one week or five half-lives (whichever is longer) prior to screening or need to use any of these medications at any time during the study;
Pregnant or lactating females;
Positive serum pregnancy test at screening or urine pregnancy test at baseline;
Recent history (≤ one year) of alcohol or drug abuse, or current evidence of substance dependence or abuse as defined by DSM-IV criteria;
Regular consumption of large amounts of xanthine-containing substances (i.e. more than 5 cups of coffee or equivalent amounts of xanthine-containing substances per day);
Have eaten grapefruit or had grapefruit juice from baseline through the completion of study dosing;
Self report of a usual consumption of more than 14 units of alcohol per week;
Requiring the concomitant usage of any 3A4 inhibitors;

Where it is running

Broward Research Group — Pembroke Pines, Florida, United States
Miami Research Associates — South Miami, Florida, United States
Neurotrials Research, Inc — Atlanta, Georgia, United States
Sleep and Behavior Medicine Institute — Vernon Hills, Illinois, United States
Vince & Associates Clinical Research — Overland Park, Kansas, United States
St. Luke's Hospital Sleep Medicine and Research Center — Chesterfield, Missouri, United States
Clinilabs, Inc. — New York, New York, United States
Tri-State Sleep Disorders Center — Cincinnati, Ohio, United States
Lynn Health Science Institute — Oklahoma City, Oklahoma, United States

Full record on ClinicalTrials.gov

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