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NCT07884058Not yet recruitingPhase 2

IGOB131 As A GLP-1 Modulator For Metabolic Disorders In Adults With Obesity

Randomized, Double-Blind, Placebo-controlled Trial Of IGOB131 As A GLP-1 Modulator For Metabolic Disorders In Adults With Obesity

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

This clinical trial will investigate the effect of standardized Irvingia gabonensis extract (IGOB131) on GLP-1 dynamics, DPP-4 activity, metabolic parameters, and inflammatory markers in adults with obesity. The study will compare IGOB131 to a placebo to find out if it exerts any significant metabolic benefits through GLP-1 and DPP-4 modulation, and the reduction of adiposity and systemic inflammation. Participants will: Take IGOB131 or a placebo every day for 16 weeks Visit the clinic once every 4 weeks for checkups and tests

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
First submitted
2 Oct 2026
Start date
Dec 2026
Primary completion date
Oct 2027
Lead sponsor
University of Yaounde 1
Diseases
Obesity
NCT number
NCT07884058

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 80
  • From Dec 2026 to the primary completion date, Oct 2027
  • No sites listed in no 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.

Prior treatment

  • Use of any medication or natural health product that might affect the parameters of interest in this study

Other illness

  • Diabetes mellitus requiring daily insulin management
  • Active infection
  • Systemic diseases, including HIV/AIDS, Active hepatitis, Clinical signs of active malignancy within the past 5 years

Age

  • Participants younger than 18 years or older than 65 years

Other

  • Participants not available for the study period
  • Morbid obesity (BMI \> 34.9 kg/m²)
  • Pregnancy or breastfeeding

Who the study is looking for

  • Males and females with BMI between 25 and 34 kg/m²
  • Participants aged 18 to 65 years old
  • Participants willing to comply with the study protocol

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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