Phase 3
Completed N=359
Effect of Liraglutide in Obese Subjects With Moderate or Severe Obstructive Sleep Apnoea: SCALE™ - Sleep Apnoea
Metabolism and Nutrition Disorder · Obesity · Obstructive Sleep Apnea
Source: ClinicalTrials.gov NCT01557166 ↗
Enrolled (actual)
359
Serious AEs
3.4%
Results posted
Feb 2015
Primary outcomePrimary: Change From Baseline in Apnoea-hypopnoea Index (AHI) — -12.22; -6.08 events/hour — p=0.015
Summary
This trial is conducted in North America. The aim of the trial is to investigate the effect of liraglutide in obese subjects with sleep apnoea.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Apnoea-hypopnoea Index (AHI) |
-12.22; -6.08 | 0.015 sig |
| SECONDARY Change From Baseline in Body Weight (kg) |
-6.73; -1.87 | — |
| SECONDARY Change From Baseline in Fasting Plasma Glucose |
-0.15; 0.17 | — |
| SECONDARY Change From Baseline in Glycosylated Haemoglobin (HbA1c) (%) |
-0.36; -0.17 | — |
Eligibility Criteria
Inclusion Criteria
- Informed consent
- Body mass index equal to or above 30 kg/m^2
- Stable body weight (less than 5% self-reported change during the previous 3 months)
- Diagnosis of moderate or severe obstructive sleep apnoea (OSA)
- Unwilling or unable to use continuous positive airway pressure (CPAP) (or other positive airway pressure) treatment. No CPAP (or other positive airway pressure) treatment for at least four weeks prior to screening
- Ability and willingness to comply with all protocol procedures e.g. correct handling of trial product, compliance to visit schedule and dietary advice and complete trial related questionnaires
Exclusion Criteria
- Treatment with glucagon-like peptide-1 (GLP-1) receptor agonists, dipeptidyl peptidase-4 inhibitors or insulin within the last 3 months prior to screening
- Diagnosis of type 1 or type 2 diabetes per judgement of the investigator
- Glycosylated haemoglobin (HbA1c) equal to or above 6.5%
- Significant craniofacial abnormalities that may cause OSA
- Respiratory and neuromuscular diseases that could interfere with the results of the trial in the opinion of the investigator
- Use of central stimulants, hypnotics, mirtazepine, opioids, trazodone within the previous 3 months prior to screening
- Obesity induced by drug treatment
- Treatment with pramlintide, sibutramine, orlistat, zonisamide, topiramate or phenteremine within the last 3 month prior to screening
- Previous surgical treatment for obesity
- Screening calcitonin equal to or above 50 ng/L
- Familial or personal history of Multiple Endocrine Neoplasia type 2 or familial Medullary Thyroid Carcinoma
- Personal history of non-familial Medullary Thyroid Carcinoma
- History of chronic pancreatitis or idiopathic acute pancreatitis
- History of Major Depressive Disorder or suicide attempts
- Systolic blood pressure equal to or above 160 mmHg and/or diastolic blood pressure equal to or above 100 mmHg
Data sourced from ClinicalTrials.gov (NCT01557166). 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.