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RecruitingSpinal Cord InjuriesType 2 Diabetes

Glycemic and Weight Loss Effects of GLP-1R Agonist Therapy in Subjects With Spinal Cord Injury and Type 2 Diabetes

Eligible age

18–70 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

It is not known whether a new diabetes drug, semaglutide, is an effective treatment for type 2 diabetes for persons with spinal cord injury (SCI), a population at higher risk for this condition. Therefore, this study looks at the effect of semaglutide on glucose levels in the body and other information about type 2 diabetes and obesity.

Sponsor: Marzieh Salehi

You may qualify if…

  • 1. Male and female subjects aged 18-70 years (inclusive) at screening
  • 2. More than one year after spinal cord injury
  • 3. Levels if injury C2-L2 with Asia Impairment Scale A, B, C or D.
  • 4. Provision of signed and dated written informed consent prior to any study specific procedures
  • 5. Diagnosed with T2DM with glucose control managed with diet and metformin monotherapy where no significant dose changes (increase or decrease ≥ 50%) have occurred in the three months prior to screening
  • 6. HbA1c 6.0-9.0% at screening
  • 7. BMI \> 22 kg/m2 at screening
  • 8. Female subjects of childbearing potential must have a negative pregnancy test at screening and randomization, and must not be lactating

You may not qualify if…

  • 1. History of, or any existing condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product, put the subject at risk, influence the subject's ability to participate or affect the interpretation of the results of the study and/or any subject unable or unwilling to follow study procedures.
  • 2. Any subject who has received another investigational product as part of a clinical study within the last 30 days or 5 half-lives of the drug (whichever is longer) at the time of screening
  • 3. Taking mirabegron or other glucose altering medications
  • 4. Taking steroids within the past 1 year
  • 5. Significant anemia (hemoglobin\<11g/dL)
  • 6. History of gastric outlet obstruction or chronic diarrhea
  • 7. History of a chronic neurological illness other than SCI (i.e.; MS, etc)
  • 8. Any subject who has received any of the following medications within the specified time-frame prior to the start of the study

Where it's recruiting

Texas

San Antonio

Source: ClinicalTrials.gov · NCT06706284 · last updated 2026-04-13

Glycemic and Weight Loss Effects of GLP-1R Agonist Therapy in Subjects · TrialPath