AMAZE 12: Investigating NNC0487-0111 for Weight Loss Maintenance

This research study, called AMAZE 12, is looking into how well the medicine NNC0487-0111 helps people with excess body weight maintain their weight loss. You would receive weekly injections under the skin of either NNC0487-0111 or a placebo (a substance with no active medicine). The study aims to see if NNC0487-0111 is safe and effective. To join, you must be 18 years or older and have a glycated hemoglobin (HbA1c) level less than 6.5%. The main way they will measure success is by looking at the change in body weight between week 40 and week 92. The current recruitment status is unclear, and the study plans to enroll about 600 participants.

Study design
This study is interventional, meaning participants will receive a specific treatment. It involves about 600 participants who will be randomly assigned to receive either NNC0487-0111 or a placebo.
What's involved
You would receive weekly injections under the skin. The primary endpoint for measuring body weight change is between week 40 and week 92.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint for measuring body weight change is between week 40 and week 92, suggesting follow-up during this period.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07503210

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

Recruiting
PHASE3Ages 18+InterventionalTreatment
Novo Nordisk A/S
~600 participants
Updated 2026-08-27 on ClinicalTrials.gov
What's tested:NNC0487-0111Placebo (matched to NNC0487-0111)

At a glance

Recruiting sites
15 of 72 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Relative change in body weight
Measured over From week 40 to week 92
Obesity
72 sites across 34 states
Bulgaria8
Spain7
Germany6
France5
Belgium4
Buenos Aires3
New South Wales3
Netherlands3
  • Clinical Transparency (dept. 2834) · STUDY_DIRECTOR · Novo Nordisk A/S

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

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

Exclusion

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.
  • Relative change in body weightFrom week 40 to week 92

    Measured as percentage (%) of body weight.