Armodafinil (CEP-10953) in Treatment of Excessive Sleepiness Associated With Obstructive Sleep Apnea/Hypopnea (OSA/H) Syndrome

NCT ID: NCT00079677

Last Updated: 2013-07-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 263 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-03-31
• Study Completion Date: 2004-10-31

Brief Summary

The primary objective of this study is to determine whether treatment with Armodafinil (CEP-10953) is more effective than placebo treatment for patients with residual excessive sleepiness associated with obstructive sleep apnea/hypopnea syndrome (OSAHS) by measuring mean sleep latency from the Maintenance of Wakefulness Test (MWT) (30 minute version) (average of 4 naps at 0900, 1100, 1300, and 1500) and by Clinical Global Impression of Change (CGI C) ratings (as related to general condition) at week 12 (or last postbaseline visit).

Conditions

Obstructive Sleep Apnea; Sleep Hypopnea

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

1

Armodafinil 150 mg/day

Group Type: EXPERIMENTAL

Armodafinil 150 mg/day

Intervention Type: DRUG

Armodafinil 150 mg once daily in the morning

2

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Matching placebo tablets once daily

Interventions

Armodafinil 150 mg/day

Armodafinil 150 mg once daily in the morning

Intervention Type: DRUG

Placebo

Matching placebo tablets once daily

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Written informed consent is obtained.

2. The patient is an outpatient, man or woman of any ethnic origin, 18 to 65 years of age (inclusive).

3. The patient has a complaint of excessive sleepiness despite nCPAP therapy being effective and being a regular user of nCPAP therapy.

4. The patient has a current diagnosis of OSAHS according to International Classification of Sleep Disorders (ICSD) criteria.

5. The patient meets the following nCPAP therapy requirements:

• Adequate education and intervention efforts to encourage nCPAP therapy use must be documented.
• A patient's nCPAP therapy regimen must be stable for at least 4 weeks.
• nCPAP therapy is shown to be effective, with effectiveness defined as having an apnea hypopnea index (AHI) of 10 or less during nocturnal PSG, and, in the opinion of the investigator, nCPAP is effective therapy.
• Following demonstration of effectiveness, evidence of regular nCPAP usage must be shown during a 2 week evaluation period (ie, nCPAP usage for at least 4 hours/night on at least 70% of the nights).

6. The patient is in good health as determined by a medical and psychiatric history, physical examination, ECG, and serum chemistry and hematology.

7. Women must be surgically sterile, 2 years postmenopausal, or, if of child bearing potential, using a medically accepted method of birth control (ie, barrier method with spermicide, steroidal contraceptive [oral, implanted, and Depo Provera contraceptives must be used in conjunction with a barrier method], or intrauterine device [IUD]) and agree to continued use of this method for the duration of the study.

8. The patient has a Clinical Global Impression of Severity of Illness (CGI S) rating of 4 or more.

9. The patient has an ESS score of 10 or more.

10. The patient does not have any medical or psychiatric disorders that could account for the excessive sleepiness.

11. The patient is able to complete self rating scales and computer based testing.

12. The patient is willing and able to comply with study restrictions and to attend regularly scheduled clinic visits as specified in this protocol.

Criteria for Exclusion: Patients are excluded from participating in this study if 1 or more of the following criteria are met:

1. has any clinically significant, uncontrolled medical or psychiatric conditions (treated or untreated)

2. has a probable diagnosis of a current sleep disorder other than OSAHS

3. consumes caffeine including coffee, tea and/or other caffeine containing beverages or food averaging more than 600 mg of caffeine per day

4. used any prescription drugs disallowed by the protocol or clinically significant use of over the counter (OTC) drugs within 14 days before the second screening visit

5. has a history of alcohol, narcotic, or any other drug abuse as defined by the Diagnostic and Statistical Manual of Mental Disorders of the American Psychiatric Association, 4th Edition (DSM IV)

6. has a positive urine drug screen (UDS)

7. has a clinically significant deviation from normal in the physical examination

8. is a pregnant or lactating woman. (Any woman becoming pregnant during the study will be withdrawn from the study.)

9. has used an investigational drug within 1 month before the initial screening visit

10. has any disorder that may interfere with drug absorption, distribution, metabolism, or excretion (including gastrointestinal surgery)

11. has a known clinically significant drug sensitivity to stimulants or modafinil

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cephalon

INDUSTRY

Sponsor Role: lead

Other Identifiers

C10953/3025/AP/MN

Identifier Type: -

Identifier Source: org_study_id