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Clinical Trials in India / NCT07571005
Recruiting Phase 3

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

NCT07571005 · tracked via the Priya Life Science India tracker
Sponsor
Novo Nordisk A/S
Phase
Phase 3
Started
2026-05-05
Last updated
2026-09-11

Condition(s) studied

ObesityOverweightObstructive Sleep Apnoea

Investigational drug(s) / intervention(s)

NNC0487-0111Placebo (matched to NNC0487-0111)

NNC0487-0111: NNC0487-0111 will be administered subcutaneously using PDS290 pre-filled pen-injectors to one of the body parts: thigh, abdomen or upper arm.

Placebo (matched to NNC0487-0111): Placebo matched to NNC0487-0111 will be administered subcutaneously using PDS290 pre-filled pen-injectors to one of the body parts: thigh, abdomen or upper arm.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (80)

FacilityCityRegionStatus
Artemis Insitute for Clin Res San Diego California Recruiting
PharmaDev Clinical Research Institute LLC Miami Florida Recruiting
Essence MD Research Naples Florida Not Yet Recruiting
Renstar Medical Research Ocala Florida Recruiting
Conquest Research Atlanta Georgia Recruiting
Physicians Research Associates Lawrenceville Georgia Recruiting
University Of Chicago Chicago Illinois Recruiting
Weil Cornell Medicine New York New York Recruiting
CTI Clinical Research Center Cincinnati Ohio Recruiting
Clinical Research Associates of Central PA, LLC DuBois Pennsylvania Not Yet Recruiting
Epic Medical Research DeSoto Texas Recruiting
Advanced Neurology Epilepsy and Sleep Center ANESC El Paso Texas Recruiting
Biorhythms Center for Integrative Sleep Medicine El Paso Texas Recruiting
Houston Pulm Med Res Network Houston Texas Recruiting
Sleep Therapy Research Center San Antonio Texas Recruiting
Tricoastal Sleep Center Sugar Land Texas Recruiting
Rainier Clin Res Ctr Inc Renton Washington Recruiting
Woolcock Institute Macquarie Park New South Wales Recruiting
University of Sunshine Coast - Vitality Village Birtinya Queensland Recruiting
Mater Research - RIO Clinical Trials Unit South Brisbane Queensland Not Yet Recruiting
Nightingale Research Adelaide Adelaide South Australia Recruiting
University of Western Australia - Centre for Sleep Science Crawley Western Australia Recruiting
Peking University People's Hospital-Endocrinology Beijing Beijing Municipality Recruiting
The Second Affiliated Hospital of Nanjing Medical University-Endocrinology Nanjing Jiangsu Recruiting
The First Affiliated Hospital of Soochow University-Endocrinology Suzhou Jiangsu Recruiting
The Affiliated Hospital of Jiangsu University-Endocrinology Zhenjiang Jiangsu Recruiting
Huzhou Central Hospital-Endocrinology Huzhou Zhejiang Recruiting
Regionshospitalet Gødstrup, Øre-næse-hals-kirurgisk Herning Denmark Recruiting
Sjællands Universitetshospital, Køge - Øre-Næse-Hals afdeling Køge Denmark Recruiting
Siteworks GmbH Bochum Bochum Germany Recruiting
Wendisch - Dahl Hamburg - DZHW Hamburg Germany Recruiting
Siteworks GmbH Hannover Hanover Germany Recruiting
Siteworks GmbH Karlsruhe Karlsruhe Germany Recruiting
Institut für Diabetesforschung GmbH Münster - Dr. med. Rose Münster Germany Recruiting
Siteworks GmbH - Prüfzentrum Schleswig | RespiRatio Schleswig Germany Recruiting
Guntur Government medical College Guntur Andhra Pradesh Completed
Government Siddhartha Medical College & Government General Hospital, Vijayawada Vijayawada Andhra Pradesh Recruiting
Rajarajeswari Medical College and Hospital Bengaluru Karnataka Recruiting
Amrita Institute Of Medical Sciences & Research Centre Kochi Kerala Recruiting
Bhaktivedanta Hospital & Research Institute Mumbai Maharashtra Recruiting

+ 40 more sites — see the full list on the official registry below.

More Novo Nordisk A/S trials in India

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07571005 on ClinicalTrials.gov ↗ ← All trials in India