A study to evaluate safety and efficacy of MK4305 in insomnia (StudyB)
Research type
Research Study
Full title
A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of MK4305 in Patients with Primary Insomnia- Study B
IRAS ID
47798
Contact name
Paul Robinson
Sponsor organisation
Merck Sharp & Dohme Corp.
Eudract number
2010-018414-69
ISRCTN Number
NA
Clinicaltrials.gov Identifier
N/A
Research summary
This study will assess the efficacy and safety of a new medication for the treatment of insomnia (inadequate or poor quality sleep).Chronic (long term) insomnia affects up to one-third of the adult population, with more than 50% of affected people experiencing significant daytime consequences such as reduced energy, memory problems, and difficulty concentrating.Insomnia may also be associated with negative effects on physical and mental wellbeing, reflected in higher levels of depression, anxiety, and diminished quality of life.There is a need for new treatments for insomnia as traditional treatments such as benzodiazepines (e.g. valium) can be addictive, cause drowsiness the following day and memory disturbance.The medicine being tested in this study works in a different way to currently available insomnia medicines and it is hoped that it will promote restful sleep without many of the side-effects associated with current treatments.Results from previous studies have indicated that the study medication may be effective in the treatment of insomnia, but we need to perform more studies to be sure of this.Patients will be in the study for about 4 months and will attend the clinic on about 8-10 occasions. Patients will receive either the study medicine or an inactive look-alike tablet called placebo so that we can see how the study medicine improves sleep compared to the placebo. Most patients will have to stay in the sleep centre overnight on 6 occasions so that measurements of sleep such as brainwave activity can be assessed using monitoring equipment.The study is being conducted at sleep research units at LCG-Bioscience in Cambridge and at Qinetiq in Farnborough, Hants.The research is being funded by the pharmaceutical company that's developing the study medicine.
REC name
West Midlands - Edgbaston Research Ethics Committee
REC reference
10/H1208/29
Date of REC Opinion
9 Jun 2010
REC opinion
Further Information Favourable Opinion