Phase 1 Obesity Trial, Recruiting NCT07527195 Sponsor: Novo Nordisk A/S Condition: Obesity
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Phase 1 Obesity Trial, Recruiting

NCT07527195
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are male or female, aged between 50 and 70 years old at the time of signing the consent form.
  • People whose Body Mass Index (BMI) — a measure based on height and weight — falls between 30.0 and 39.9 at the initial screening visit.
  • People whose excess body weight is considered by the investigating doctor to be due to excess body fat rather than another cause.
  • People who want to lose at least 25% of their body weight within 52 weeks of treatment.

Who may not be able to join:

  • People who have had any leg amputations.
  • Female participants who have not yet reached menopause at the time of screening.
  • People who have had a significant change in body weight of 5% or more (based on self-reporting), or who have made dieting attempts, within the 90 days before screening.
  • People who have been treated with a GLP-1 receptor agonist medication — a type of drug sometimes used for blood sugar control or weight management — or any medication with similar activity, within the 90 days before screening.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Clinical Transparency dept. 2834, Novo Nordisk A/S

Phone: (+1) 866-867-7178

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
10 April 2026
Est. completion
28 April 2028

Where this trial is recruiting

🇩🇰 Denmark

Primary endpoints

Change in insulin-stimulated fluorodeoxyglucose (FDG) uptake in skeletal muscle

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov