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NCT06129409CompletedPhase 1

Effects of NT-0796 in Obese Participants at Risk of Cardiovascular Disease

A Randomized, Double -Blind (Sponsor-Open), Placebo-Controlled Study to Assess the Effect of NT-0796 on Inflammation in Obese Participants at Risk of Cardiovascular Disease

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

This trial is a Randomized, Double-Blind (Sponsor-Open), Placebo-Controlled Study to Assess the Effect of NT-0796 on Inflammation in Obese Participants at Risk of Cardiovascular Disease. Participants will be admitted to an in-patient Clinical Research Unit on Day -1 and will be discharged on Day 30. The trial will include a 7-day out-patient safety follow-up period following the last dose of study treatment. For the first approximately 20 participants effect of food will be evaluated on the Pharmacokinetics of NT-0796. MRI's will be conducted in a subset of participants.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
67 (actual)
First submitted
30 Oct 2023
Start date
10 Oct 2023
Primary completion date
15 Apr 2024
Lead sponsor
Rezera (formerly NodThera Limited)
Diseases
Obesity
NCT number
NCT06129409

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 67
  • From 10 Oct 2023 to the primary completion date, 15 Apr 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of stroke with residual neurological deficit within 2 years or transient ischemic attack within 6 months
  • History of acute coronary syndrome (ACS)
  • Stable angina.
  • Diagnosis of congestive heart failure
  • Evidence of past or current infection with Hepatitis B or Hepatitis C

Who the study is looking for

  • Male or female aged 18 years or older.
  • Body mass index (BMI) ≥30 and ≤40 kg/m2 at screening.
  • Presence of 1 or more of the following risk factors for atherosclerotic cardiovascular disease:
    • History of controlled hypertension
    • History of hypercholesterolemia
    • History of high-density lipoprotein levels
    • Controlled Type 1 or Type 2 Diabetes mellitus

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Investigative Site
Coordinator of this site? Confirm its status
AustinUnited StatesUnknown status
Investigative Site
Coordinator of this site? Confirm its status
MiamiUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.