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Phase 4 Completed N=249 Randomized Double-blind Treatment

Efficacy and Safety of Armodafinil for Adults With Excessive Sleepiness Obstructive Sleep Apnea/Hypopnea and Depression

Source: ClinicalTrials.gov NCT00518986 ↗
Enrolled (actual)
249
Serious AEs
1.6%
Results posted
Mar 2011
Primary outcomePrimary: Change From Baseline on Maintenance of Wakefulness Test (MWT) to Endpoint (12 Weeks or Last Observation After Baseline) — 2.6; 1.1 Minutes — p=0.3043

Summary

The primary objective of the study is to evaluate whether armodafinil at a target dosage of 200 mg/day is more effective than placebo treatment in improving excessive sleepiness in patients with obstructive sleep apnea/hypopnea syndrome (OSAHS) who have comorbid major depressive disorder or dysthymic disorder.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline on Maintenance of Wakefulness Test (MWT) to Endpoint (12 Weeks or Last Observation After Baseline)
2.6; 1.1 0.3043
PRIMARY
Clinical Global Impression of Change (CGI-C) at Endpoint (12-weeks or Last Observation After Baseline)
78; 59; 35; 53 0.0120 sig
SECONDARY
Change From Baseline on the Epworth Sleepiness Scale (ESS) at Endpoint (12 Weeks or Last Measurement After Baseline)
-6.5; -4.6 0.0027 sig
SECONDARY
Change From Baseline on Maintenance of Wakefulness Test (MWT) at 4 Weeks
2.7; -0.1 0.0019 sig
SECONDARY
Change From Baseline on Maintenance of Wakefulness Test (MWT) at 8 Weeks
2.1; 1.2 0.3145
SECONDARY
Change From Baseline on Maintenance of Wakefulness Test (MWT) at 12 Weeks
2.5; 1.4 0.2196
SECONDARY
Clinical Global Impression of Change (CGI-C) at 4 Weeks
75; 64; 36; 44 0.2017
SECONDARY
Clinical Global Impression of Change (CGI-C) at 8 Weeks
76; 52; 28; 46 0.0032 sig
SECONDARY
Clinical Global Impression of Change (CGI-C) at 12 Weeks
69; 53; 27; 42 0.0207 sig
SECONDARY
Clinical Global Impression of Change (CGI C) at 4 Weeks - Full Scale
15; 11; 34; 21; 26; 32 0.0529
SECONDARY
Clinical Global Impression of Change (CGI-C) at 8 Weeks - Full Scale
16; 11; 39; 19; 21; 22 0.0011 sig
SECONDARY
Clinical Global Impression of Change (CGI-C) at 12 Weeks - Full Scale
27; 11; 20; 22; 22; 20 0.0064 sig
SECONDARY
Change From Baseline on Epworth Sleepiness Scale (ESS) at 2 Weeks
-4.8; -3.8 0.1072
SECONDARY
Change From Baseline on Epworth Sleepiness Scale (ESS) at 4 Weeks
-5.5; -4.2 0.0355 sig
SECONDARY
Change From Baseline on Epworth Sleepiness Scale (ESS) at 8 Weeks
-6.0; -4.8 0.0591
SECONDARY
Change From Baseline on Epworth Sleepiness Scale (ESS) at 12 Weeks
-6.8; -4.8 0.0025 sig
SECONDARY
Number of Responders According to the Epworth Sleepiness Scale (ESS) Total Score at 2 Weeks
54; 40; 53; 64 0.0794
SECONDARY
Number of Responders According to the Epworth Sleepiness Scale (ESS) Total Score at 4 Weeks
59; 45; 52; 63 0.0888
SECONDARY
Number of Responders According to the Epworth Sleepiness Scale (ESS) Total Score at 8 Weeks
64; 47; 39; 51 0.0433 sig
SECONDARY
Number of Responders According to the Epworth Sleepiness Scale (ESS) Total Score at 12 Weeks
65; 47; 31; 48 0.0105 sig
SECONDARY
Change From Baseline to Endpoint (Week 12 or Last Observation After Baseline) in the Brief Fatigue Inventory (BFI) Total Score
-8.9; -3.8 0.0523
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Total Score at 2 Weeks
-6.1; -0.9 0.0289 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Total Score at 4 Weeks
-9.5; -5.8 0.1272
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Total Score at 8 Weeks
-8.8; -3.0 0.0349 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Total Score at 12 Weeks
-10.5; -3.3 0.0094 sig
SECONDARY
Change From Baseline on the Brief Fatigue Inventory (BFI) Worst Daily Fatigue Score at Endpoint (12 Weeks or Last Observation After Baseline)
-1.3; -0.7 0.0754
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Worse Daily Fatigue Score at 2 Weeks
-1.1; -0.2 0.0105 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Worse Daily Fatigue Score at 4 Weeks
-1.2; -0.8 0.2888
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Worse Daily Fatigue Score at 8 Weeks
-1.2; -0.3 0.0130 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Worse Daily Fatigue Score at 12 Weeks
-1.4; -0.6 0.0354 sig
SECONDARY
Number of Responders According to Brief Fatigue Inventory (BFI) Worst Fatigue Score at Endpoint (12 Weeks or Last Observation After Baseline)
63; 56; 49; 55 0.3854
SECONDARY
Number of Responders According to the Brief Fatigue Inventory (BFI) Worst Fatigue Score at 2 Weeks
62; 43; 48; 65 0.0145 sig
SECONDARY
Number of Responders According to the Brief Fatigue Inventory (BFI) Worst Fatigue Score at 4 Weeks
62; 57; 49; 51 0.6475
SECONDARY
Number of Responders According to the Brief Fatigue Inventory (BFI) Worst Fatigue Score at 8 Weeks
63; 42; 41; 56 0.0118 sig
SECONDARY
Number of Responders According to the Brief Fatigue Inventory (BFI) Worst Fatigue Score at 12 Weeks
55; 48; 41; 47 0.3483
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Interference Score at Endpoint (12 Weeks or Last Observation After Baseline)
-0.9; -0.3 0.0879
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Interference Score at 2 Weeks
-0.6; 0.0 0.0277 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Interference Score at 4 Weeks
-1.0; -0.6 0.1245
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Interference Score at 8 Weeks
-0.9; -0.2 0.0305 sig
SECONDARY
Change From Baseline on Brief Fatigue Inventory (BFI) Interference Score at 12 Weeks (or Last Observation After Baseline)
-1.1; -0.3 0.0129 sig
SECONDARY
Change From Baseline on Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at Endpoint (12 Weeks or Last Observation After Baseline)
2.3; 1.5 0.0308 sig
SECONDARY
Change From Baseline on Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at 2 Weeks
1.7; 1.1 0.0679
SECONDARY
Change From Baseline on Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at 4 Weeks
2.2; 1.4 0.0153 sig
SECONDARY
Change From Baseline on Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at 8 Weeks
2.2; 1.4 0.0296 sig
SECONDARY
Change From Baseline on Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at 12 Weeks
2.6; 1.6 0.0107 sig
SECONDARY
Number of Responders According to the Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at Endpoint (Week 12 or Last Observation After Baseline)
49; 30; 61; 78 0.0100 sig
SECONDARY
Number of Responders According to the Functional Outcomes of Sleep Questionnaire (FOSQ) Total Score at 2 Weeks
30; 19; 75; 84 0.0854
SECONDARY
Number of Responders According to the Functional Outcomes of Sleep Questionnaire (FOSQ) at Week 4
45; 24; 60; 79 0.0027 sig
SECONDARY
Number of Responders According to the Functional Outcomes of Sleep Questionnaire (FOSQ) at Week 8
36; 20; 65; 77 0.0189 sig
SECONDARY
Number of Responders According to the Functional Outcomes of Sleep Questionnaire (FOSQ) at Week 12
43; 28; 51; 66 0.0240 sig
SECONDARY
Change From Baseline on Medical Outcomes Study 6 Item Cognitive Functioning (MOS-CF6) Scale at Endpoint (12 Weeks or Last Observation After Baseline)
3.2; 2.4 0.3320
SECONDARY
Change From Baseline on Medical Outcomes Study 6 Item Cognitive Functioning (MOS-CF6) Scale at 2 Weeks
2.0; 1.9 0.8930
SECONDARY
Change From Baseline on Medical Outcomes Study 6 Item Cognitive Functioning (MOS-CF6) Scale at 4 Weeks
3.4; 2.4 0.1774
SECONDARY
Change From Baseline on Medical Outcomes Study 6 Item Cognitive Functioning (MOS-CF6) Scale at 8 Weeks
3.3; 2.1 0.1000
SECONDARY
Change From Baseline on Medical Outcomes Study 6 Item Cognitive Functioning (MOS-CF6) Scale at 12 Weeks
3.3; 2.4 0.2428
SECONDARY
Change From Baseline in the Excessive Sleepiness (ES) Symptom Rating Form - Sleepiness Scores at Endpoint (12 Weeks or Last Observation After Baseline)
-1.8; -1.4 0.1816
SECONDARY
Change From Baseline in the Excessive Sleepiness (ES) Symptom Rating Form - Sleepiness Scores at 2 Weeks
-1.6; -1.2 0.1627
SECONDARY
Change From Baseline in the Excessive Sleepiness (ES) Symptom Rating Form - Sleepiness Scores at 4 Weeks
-2.1; -1.1 0.0018 sig
SECONDARY
Change From Baseline in the Excessive Sleepiness (ES) Symptom Rating Form - Sleepiness Scores at 8 Weeks
-1.8; -0.9 0.0096 sig
SECONDARY
Change From Baseline in the Excessive Sleepiness (ES) Symptom Rating Form - Sleepiness Scores at 12 Weeks
-2.2; -1.3 0.0126 sig

Eligibility Criteria

Inclusion Criteria

  • Current diagnosis of obstructive sleep apnea/hypopnea syndrome (OSAHS)
  • Complaint of residual excessive sleepiness despite nasal continuous positive airway pressure (nCPAP) therapy being effective
  • Current or prior diagnosis of major depressive disorder or dysthymic disorder
  • Clinically stable with regard to depressed mood and has shown a treatment response to selective serotonin reuptake inhibitor (SSRI) therapy or serotonin and norepinephrine reuptake inhibitor (SNRI) therapy
  • Patient has been on a stable monotherapy dose of an allowed SSRI or SNRI for at least 8 weeks at the time of screening
  • Women of childbearing potential must use a medically accepted method of contraception.

Exclusion Criteria

  • Confirmed or suspected diagnosis of a currently active sleep disorder other than obstructive sleep apnea/hypopnea syndrome (OSAHS)
  • Current episode of major depression that is considered to be treatment-resistant
  • A primary diagnosis of: eating disorder, psychotic disorder, delirium, dementia, substance-related disorders, or moderate to severe hypochondriasis
  • Patient has a history of bipolar disorder, psychotic depression, schizophrenia, schizoaffective disorder, any other psychotic disorder, or other clinically significant uncontrolled psychiatric condition.
  • Patient has a history of homicidal ideation or significant aggression
  • Patient has a diagnosis of severe antisocial or borderline personality disorder
  • Has a history of significant suicidal ideation, or has current active suicidal ideation, or is considered at imminent risk of self harm.
  • Patient has a history consistent with fibromyalgia or chronic fatigue syndrome
  • A high consumption of caffeinated products, approximately equivalent to 5 or more cups of coffee per day
  • Patient history of any clinically significant cutaneous drug reaction, or a history of clinically significant hypersensitivity reaction
  • Has a past or present seizure disorder
  • Patient has a history of alcohol, narcotic, or any other substance abuse or dependence (with the exception of nicotine)
  • Psychotherapeutic intervention for the patient was initiated within 8 weeks of the screening visit.
  • Patient has known human immunodeficiency virus (HIV)
  • Patient has any clinically significant uncontrolled medical condition (including illnesses related to the cardiovascular, renal, or hepatic systems) or surgical condition (treated or untreated)
  • Patient is a pregnant or lactating woman
  • Patient has previously received armodafinil; or, patient has used modafinil or any investigational product within 28 days of the baseline visit.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00518986). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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