Phase 1 Type 2 Diabetes Trial, Recruiting NCT07535307 Sponsor: Novo Nordisk A/S Condition: Type 2 Diabetes
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Phase 1 Type 2 Diabetes Trial, Recruiting

NCT07535307
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 18 to 75 years old at the time of signing the consent form
  • People who were diagnosed with type 2 diabetes at least 180 days (about 6 months) before the screening visit
  • People who have been taking a stable daily dose of metformin for at least 90 days before screening, at the dose the doctor considers effective or the highest dose the person can tolerate
  • People who may also be taking a second diabetes tablet called an SGLT2 inhibitor (a specific type of blood sugar-lowering medication), as long as that dose has also been stable for at least 90 days before screening — no other diabetes medications are permitted
  • People whose blood sugar control (measured by an HbA1c blood test) falls within a specific range: between 6.5% and 9.5% if taking metformin only, or between 6.0% and 9.0% if taking metformin together with an SGLT2 inhibitor

Who may not be able to join:

  • Women who are pregnant, breastfeeding, planning to become pregnant, or who are able to become pregnant and are not using a highly effective form of contraception
  • People who have type 1 diabetes
  • People who have had a significant change in body weight (5% or more, based on self-reporting) or who have been on a structured weight loss program within the 90 days before screening
  • People who have been taking any medication for type 2 diabetes or weight management — other than those listed above — within 90 days before screening (short-term insulin use of up to 14 days in a row, or past insulin use during pregnancy-related diabetes, may be acceptable — confirm with trial site)
  • People who have previously been treated with a GLP-1 receptor agonist (a type of injectable or oral diabetes medication)
  • People who have diabetic eye disease (retinopathy or maculopathy) that has required, or is expected to require, certain eye treatments such as laser therapy, eye surgery, or anti-VEGF injections — an eye examination is required to confirm this before joining the trial
  • People who have a current or recent history (within the past 180 days) of heart disease, including heart attack, stroke, mini-stroke, chest pain conditions, irregular heartbeat, or significant heart rhythm problems
  • People whose kidneys are not functioning well enough, based on a specific blood test result at screening (confirm with trial site)

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 9 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
11 November 2027

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Change in M-value in Hyperinsulinaemic euglycaemic clamp (HEC)

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: 9 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