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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

RecruitingPhase 3

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

Sponsor: Novo Nordisk A/S · Participants: 300 · Started: May 5, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07571005

Locations in the U.S.

CaliforniaArtemis Insitute for Clin Res, San Diego
FloridaPharmaDev Clinical Research Institute LLC, Miami
Essence MD Research, Naples (Not yet recruiting)
Renstar Medical Research, Ocala
GeorgiaConquest Research, Atlanta
Physicians Research Associates, Lawrenceville
IllinoisUniversity Of Chicago, Chicago
New YorkWeil Cornell Medicine, New York
OhioCTI Clinical Research Center, Cincinnati
PennsylvaniaClinical Research Associates of Central PA, LLC, DuBois (Not yet recruiting)
TexasEpic 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
WashingtonRainier 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.