Overview

Efficacy an Safety of Volinanserin on Sleep Maintenance Insomnia With a Sub-study on Stable Type II Diabetes Mellitus

Status:
Terminated
Trial end date:
2009-03-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to assess efficacy and safety of volinanserin in the population of patients complaining of sleep maintenance insomnia. The objective of the substudy is to assess glycemic control in the subgroup of patients with type II diabetes mellitus.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sanofi
Treatments:
MDL 100907
Volinanserin
Criteria
Inclusion Criteria:

- Diagnosis of primary insomnia based on Diagnostic and Statistical Manual of Mental
Disorders (Fourth Edition) criteria

- Disturbances of sleep maintenance criteria based on participant's information related
to sleep pattern during the preceding month

Sub-study :

- Participants will be included if they have an established medical diagnosis of type II
Diabetes Mellitus, and have been treated either with an oral hypoglycemic agent and/or
insulin for at least three months prior to the Screening Visit (with stable regimen
for at least one month prior to screening)

Exclusion Criteria:

- Females who are lactating or who are pregnant

- Night shift workers, and individuals who nap 3 or more times per week over the
preceding month

- Consumption of xanthine-containing beverages (i.e. tea, coffee, cola) comprising more
than 5 cups/day

- Participation in another trial having received study medication within 1 month before
the screening visit

- Body Mass Index ≥ 33

- Use of over-the-counter medications such as tryptophan, valerian root, kava,
melatonin, St. John's Wort, Alluna or prescription sleep medication

- Use of any substance with psychotropic effects or properties know to affect sleep/wake

- History of primary hypersomnia, narcolepsy, breathing-related sleep disorder,
circadian rhythm sleep disorder, parasomnia, dyssomnia

- Clinically significant, severe or unstable, acute or chronically progressive medical
or surgical disorder

- Positive qualitative urine drug screen (opiates, cocaine, amphetamine…)

The above information is not intended to contain all considerations relevant to a
participant's potential participation in a clinical trial.