AMAZE 3: A Research Study Investigating How Well the Medicine NNC0487-0111 Helps People With Excess Body Weight and Obstructive Sleep Apnoea Not Treated With Positive Airway Pressure Lose Weight and Improve Sleep Apnoea
Efficacy and Safety of NNC0487-0111 s.c. Once-weekly in Participants With Overweight or Obesity, and Obstructive Sleep Apnoea Not Treated With Positive Airway Pressure (AMAZE 3)
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Key Inclusion Criteria: * Male or female (sex at birth) * Age 18 years or above at the time of signing informed consent * Previously diagnosed moderate-to-severe OSA with an AHI ≥ 15, as diagnosed with polysomnography (PSG), home sleep apnoea test (HSAT), or other method that meets local guidelines prior to screening Key Exclusion Criteria: * Glycated haemoglobin (HbA1c) ≥ 6.5% (48 mmol/mol) as measured by the central laboratory at screening * History of type 1 or type 2 diabetes mellitus as declared by the participant or reported in the medical records * Any planned or previous surgery within 90 days prior to screening for sleep apnoea, including septoplasty, turbinoplasty, or other ear, nose, and throat surgeries, including tonsillectomy and adenoidectomy * Significant craniofacial abnormalities that may affect breathing at baseline, for example Treacher Collins syndrome and Pierre Robin Sequence * Treatment with glucagon-like-peptide-1 (GLP-1) receptor agonist (RA), dual GLP-1/gastric inhibitory peptide (GIP) RAs (or any other GLP-1 based treatment) or amylin analogues before screening
About the study
This study is being done to look at the efficacy and safety of NNC0487-0111 in participants with excess body weight and obstructive sleep apnoea not treated with positive airway pressure lose weight and improve sleep apnoea. There are 2 study treatments in this study taken as injections under the skin once a week. Participants will either get NNC0487-0111, (the treatment being tested) or Placebo (a treatment that has no active medicine in it) and which treatment participants get is decided by chance.
What is being tested
- NNC0487-0111 (drug)
- Placebo (matched to NNC0487-0111) (drug)
Sponsor: Novo Nordisk A/S · Participants: 300 · Started: May 5, 2026
Contact the study team
- Novo Nordisk · Phone: (+1) 866-867-7178
Official record on ClinicalTrials.gov — NCT07571005
Locations in the U.S.
| California | Artemis Insitute for Clin Res, San Diego |
| Florida | PharmaDev Clinical Research Institute LLC, Miami Essence MD Research, Naples (Not yet recruiting) Renstar Medical Research, Ocala |
| Georgia | Conquest Research, Atlanta Physicians Research Associates, Lawrenceville |
| Illinois | University Of Chicago, Chicago |
| New York | Weil Cornell Medicine, New York |
| Ohio | CTI Clinical Research Center, Cincinnati |
| Pennsylvania | Clinical Research Associates of Central PA, LLC, DuBois (Not yet recruiting) |
| Texas | Epic Medical Research, DeSoto Advanced Neurology Epilepsy and Sleep Center ANESC, El Paso Biorhythms Center for Integrative Sleep Medicine, El Paso Houston Pulm Med Res Network, Houston Sleep Therapy Research Center, San Antonio Tricoastal Sleep Center, Sugar Land |
| Washington | Rainier Clin Res Ctr Inc, Renton |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.