Menu
Recruiting NCT07503210

AMAZE 12: A Research Study Investigating How Well the Medicine NNC0487-0111 Helps People With Excess Body Weight Maintain Their Weight Loss

Phase III Interventional Obesity

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: NNC0487-0111, Placebo (matched to NNC0487-0111).
Who it may be relevant to
Registry conditions: Obesity. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States, Argentina, Australia, Belgium, Bulgaria +7
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Efficacy and Safety of NNC0487-0111 s.c. Once Weekly in Participants With Obesity Who Have Reached Target Dose During run-in Period (AMAZE 12)

Overview

The purpose of this clinical study is to find out if NNC0487-0111 is safe and effective for treating people who have excess body weight. 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). Which treatment participants get is decided by chance.

Interventions

  • Drug NNC0487-0111
    NNC0487-0111 will be administered subcutaneously.
  • Drug Placebo (matched to NNC0487-0111)
    Placebo will be administered subcutaneously.

Primary outcome measures

  • Relative change in body weight [Time frame: From week 40 to week 92]
Secondary outcome measures (12)
  • Relative change in body weight [Time frame: From week 0 to week 92]
  • Change in waist circumference [Time frame: From week 40 to week 92]
  • Change in systolic blood pressure (SBP) [Time frame: From week 40 to week 92]
  • Change in Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) physical function score [Time frame: From week 40 to week 92]
  • Change in SF-36v2® Health Survey Acute (SF-36v2 Acute) physical functioning score [Time frame: From week 40 to week 92]
  • Change in body weight [Time frame: From week 40 to week 92]
  • Change in body mass index (BMI) [Time frame: From week 40 to week 92]
  • Change in body weight [Time frame: From week 0 to week 92]
  • Change in BMI [Time frame: From week 0 to week 92]
  • Change in glycated haemoglobin (HbA1c) [Time frame: From week 40 to week 92]
  • Change in fasting plasma glucose (FPG) [Time frame: From week 40 to week 92]
  • Change in fasting insulin [Time frame: From week 40 to week 92]

Eligibility criteria

Inclusion criteria

  • Male or female (sex at birth).
  • Age 18 years or above at the time of signing the informed consent.

Exclusion criteria

  • Glycated haemoglobin (HbA1c) greater than or equal to ≥ 6.5% \[48 millimoles per mole (mmol/mol)\] 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.
  • Treatment with glucagon-like-peptide-1 (GLP-1) receptor agonists (RA), dual GLP 1/gastric inhibitory peptide (GIP) RAs (or any other GLP-1 based treatment), or amylin analogues before screening.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

United States · 13 centers
  • Pinnacle Research Group LLC — Anniston
  • Diablo Clinical Research, Inc. — Walnut Creek
  • Florida Inst For Clin Res LLC — Orlando
  • Endeavor Health — Skokie
  • Midwest Inst For Clin Res — Indianapolis
  • Medication Mgmnt, LLC_Grnsboro — Greensboro
  • PMG Research of Wilmington LLC — Wilmington
  • UPA Ctr Weight and Eating Dis — Philadelphia
  • … and 5 more centers
Bulgaria · 8 centers
  • DCC 1 - Lom EOOD — Lom
  • MHAT Med Line Clinic — Plovdiv
  • UMHAT Kaspela EOOD, Endocrinology and Metabolic Diseases Clinic — Plovdiv
  • AIPSOMCEMD ENDO MED CONSULT 2020 - Dr. Aleksander Botushanov EOOD — Plovdiv
  • SGHAT Dr. Shterev EOOD — Sofia
  • UMHAT Aleksandrovska EAD, Clinic of Endocrinology and Metabolic Diseases — Sofia
  • Medical Center Maraya Med EOOD — Sofia
  • AIPSMC Dr. Traykovska EOOD — Sofia
Italy · 8 centers
  • Arcispedale Sant'Anna (Cona) - UO di Endocrinologia — Ferrara
  • IRCCS Ospedale Policlinico San Martino - Medicina Interna e Specialità Mediche — Genoa
  • Fondazione Salvatore Maugeri I.R.C.C.S. - Pavia - Dipartimento Medicina Interna e Generale — Pavia
  • Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone - Presidio Villa Belmonte — Palermo
  • Azienda Ospedaliera di Padova - UOSD Chirurgia Bariatrica — Padova
  • Azienda Ospedaliera Universitaria Integrata Verona - Ospedale Civile Maggiore Borgo Trento — Verona
  • A.O.Universitaria S.ORSOLA-MALPIGHI - U.O.Endocrinologia e Cura — Bologna
  • IRCCS Humanitas - U.O. Endocrinologia e Diabetologia — Rozzano (MI)
Germany · 7 centers
  • Diabetologikum - Diabetologische Schwerpunktpraxis Dr. Thomas Segiet — Speyer
  • Wendisch - Dahl Hamburg - DZHW — Hamburg
  • Prof. Dr. Schiefke Ingolf, EUGASTRO GmbH — Leipzig
  • Diabetologische Gemeinschaftspraxis Dr. Staudenmeyer und Dr. Schiwietz — Lingen
  • Institut für Diabetesforschung GmbH Münster - Dr. med. Rose — Münster
  • RED-Institut für medizinische Forschung und Fortbildung GmbH — Oldenburg in Holstein
  • Zentrum für klinische Studien Alexander Segner — Saint Ingbert-Oberwürzbach
Spain · 7 centers
  • Centro Periferico De Especialidades Bola Azul — Almería
  • Hospital Clinic i Provincial — Barcelona
  • H. de León_Endocrinología — León
  • Hospital Clínico San Carlos — Madrid
  • H. Clinico Univ. Virgen de la Victoria — Málaga
  • H.U. Quirónsalud Madrid — Pozuelo de Alarcón
  • Hospital Universitario Virgen del Rocío — Seville
France · 5 centers
  • CHU DE CLERMONT-FERRAND-HOPITAL GABRIEL MONTPIED_Service de Nutrition — Clermont-Ferrand
  • CHU GRENOBLE ALPES-SITE NORD MICHALLON_Endocrinologie,diabétologie,maladies de la nutritio — La Tronche
  • GROUPE SOS SANTE-HOPITAL LE CREUSOT-HOTEL DIEU_ Service de Diabétologie — Le Creusot
  • CHU LILLE-HOPITAL CLAUDE HURIEZ_Service de Chirurgie Générale et Endocrinienne — Lille
  • CHU DE POITIERS_Centre d'investigation Clinique — Poitiers
Netherlands · 5 centers
  • PreCare Trial & Recruitment — Born
  • Progress Clinical Research Den Bosch — 's-Hertogenbosch
  • EB Flevo Research BV — Almere Stad
  • Meander MC — Amersfoort
  • Rijnstate Ziekenhuis — Arnhem
Argentina · 4 centers
  • Conexa — Ciudad Autonoma de Buenos Aires
  • CICEMO- Consultorio (Av Directorio) — Ciudad Autónoma de Buenos Aires
  • Instituto de Investigaciones Clinicas Mar Del Plata — Mar del Plata
  • CIPREC Pueyrredon — Buenos Aires
Australia · 4 centers
  • Sydney Clinical Trials — Campbelltown
  • Sydney Cardiometabolic Centre — Liverpool
  • Hunter Diabetes Centre — Merewether
  • Nightingale Research — Adelaide
Belgium · 4 centers
  • Anima Research Center — Diepenbeek
  • AZ Groeninge - Kortrijk - Centrum Endo - Diabetologie — Kortrijk
  • Centre hospitalier universitaire de Liège (CHU de Liège) — Liège
  • AZ OOSTENDE (Campus DAMIAAN) — Ostend
United Kingdom · 4 centers
  • EMS Healthcare — Cheshire
  • Clifton Medical Centre — Rotherham
  • Staploe Medical Centre — Soham
  • Albany House Medical Centre — Wellingborough
Denmark · 3 centers
  • Sjællands Universitetshospital, Køge - Medicinsk Afdeling — Køge
  • Sydvestjysk Sygehus Esbjerg - Medicinsk Endokrinologisk Ambulatorium, Forskningsenheden — Esbjerg
  • Sanos Clinic - Vejle — Vejle

Identifiers

NCT: NCT07503210 · NN9490-8559 · U1111-1327-1477 · 2025-523804-62

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗