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

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ClinicalTrials.gov Identifier: NCT00078325
Recruitment Status : Completed
First Posted : February 25, 2004
Results First Posted : July 29, 2010
Last Update Posted : July 19, 2013
Information provided by:
Teva Pharmaceutical Industries

February 23, 2004
February 25, 2004
June 1, 2009
July 29, 2010
July 19, 2013
February 2004
November 2004   (Final data collection date for primary outcome measure)
  • Maintenance of Wakefulness Test (MWT) [ Time Frame: change from baseline at 12 weeks ]
    The MWT is an objective assessment of sleepiness that measures the ability of a subject to remain awake. Long latencies to sleep are indicative of a patient's ability to remain awake. The primary variable was the 30 minute MWT (average of 4 naps at 0900, 1100, 1300, and 1500) assessed at the last postbaseline observation.
  • Clinical Global Impression of Change (CGI-C) [ Time Frame: change from baseline at 12 weeks ]
    The CGI-C represents a subjective measure of the patient's global health (clinician's rating of disease severity as compared with a pretreatment evaluation as assessed by the CGI-S). The CGI-C scale (change from baseline)categories include:1=Very much improved; 2=Much improved; 3=Minimally improved; 4=No change; 5=Minimally worse; 6=Much worse; and 7=Very much worse. Severity of illness (CGI-S) was assessed at baseline includes categories: 1=Normal; 2=Borderline ill; 3=Mildly (Slightly) ill; 4=Moderately ill; 5=Markedly ill; 6=Severely ill; and 7=Among the most extremely ill patients.
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Complete list of historical versions of study NCT00078325 on ClinicalTrials.gov Archive Site
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Armodafinil (CEP-10953) in Treatment of Excessive Sleepiness Associated With Obstructive Sleep Apnea/Hypopnea Syndrome(OSAHS)
A 12 Week, Randomized, Double Blind, Placebo Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of CEP 10953 (150 and 250 mg/Day) as Treatment for Adults With Residual Excessive Sleepiness Associated With Obstructive Sleep Apnea/Hypopnea Syndrome
The primary objective of this study is to determine whether treatment with Armodafinil (CEP-10953) is more effective than placebo treatment for patients with 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 post-baseline visit.
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Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
  • Obstructive Sleep Apnea
  • Hypopnea
  • Drug: Armodafinil 250 mg/day
    Armodafinil 250 mg once daily in the morning
    Other Names:
    • CEP-10953
  • Drug: Armodafinil 150 mg/day
    Armodafinil 150 mg once daily in the morning
    Other Names:
    • CEP-10953
  • Drug: Placebo
    Matching placebo tablets once daily in the morning
  • Experimental: 1
    Armodafinil 250 mg/day
    Intervention: Drug: Armodafinil 250 mg/day
  • Experimental: 2
    Armodafinil 150 mg/day
    Intervention: Drug: Armodafinil 150 mg/day
  • Placebo Comparator: 3
    Intervention: Drug: Placebo
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
November 2004
November 2004   (Final data collection date for primary outcome measure)

Inclusion Criteria:

Patients are included in the study if all of the following criteria are met:

  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.

Exclusion Criteria:

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 7 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
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
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Teva Pharmaceutical Industries
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP