Phase 2 Obesity Trial, Recruiting NCT07639021 Sponsor: Novo Nordisk A/S Condition: Obesity
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Phase 2 Obesity Trial, Recruiting

NCT07639021
Recruiting Phase 2

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 were male or female at birth, including all gender identities
  • People who are 18 years of age or older at the time of signing the consent form
  • People with a Body Mass Index (BMI) of 30 or higher at the screening appointment (BMI is a number calculated from height and weight)
  • People who want to lose at least 25% of their body weight and are committed to that goal from the start of the trial

Who may not be able to join:

  • People with a known or suspected allergy or sensitivity to the study treatment or similar products
  • People who have taken any prescribed medication for obesity or weight management in the 90 days before screening — this includes medications known as GLP-1 receptor agonists (such as some injectable weight loss drugs), dual GLP-1/GIP receptor agonists, or amylin analogues
  • People whose blood sugar control measurement (called HbA1c, a test that reflects average blood sugar levels over time) is 6.5% or higher at the screening appointment
  • People with a history of type 1 or type 2 diabetes

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 19 July 2026
Phase 2: approximately ~30% 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 2
Registry
ClinicalTrials.gov
Start date
9 June 2026
Est. completion
12 July 2027

Where this trial is recruiting

Puerto Rico 🇺🇸 United States

Primary endpoints

Number of gastrointestinal adverse events

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: 19 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