Recruiting at 1 site Early Phase 1 Type 1 Diabetes

Type 1 Diabetes study: Semaglutide

Official title GLP-1Ra Impact on Metabolic Outcomes in Stage 2 T1DM While Receiving Teplizumab

ClinicalTrials.gov ID: NCT06338553

What this study is testing

What is Semaglutide (Rybelsus®)?

This is an investigational oral medicine being studied to see if it helps manage blood sugar in people with early-stage Type 1 Diabetes. It is designed to help the body release insulin and reduce the release of glucose from the liver.

Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This study aims to find out if a specific type of diabetes medication improves blood sugar control and heart health in people with early Type 1 Diabetes.
Who it's for
The study is looking for people with early Type 1 Diabetes who are currently receiving a treatment called teplizumab.
What's involved
Participants will drink a liquid meal and have blood drawn to check sugar levels and insulin response. They will also receive the test drug or a placebo and have an ultrasound to check blood vessel health.
Time commitment
The study involves specific testing sessions that include blood draws and an ultrasound, but the total duration is not specified.
  • Phase 1: an early, usually small safety study
  • You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 12 to 50

You may be able to join if

  • Aims 1-3: Stage 2 T1DM with TZIELD® and GLP-1Ra
  • Age: 12-50 years
  • BMI: 18-31 kg/m2 (adults) or 5-95th %ile (pediatric)
  • fasting glucose ≥ 100 mg/dL and \< 126 mg/dL OR
  • 2-hr OGTT /MMTT ≥ 140 mg/dL and \< 200 mg/dL OR

You likely can't join if

  • SBP \> 140 mmHg and DBP \> 100 mmHg
  • eGFR by MDRD equation of \< 60 mL/min/1.73m2
  • AST or ALT \> 2.5 times ULN
  • Family history of medullary thyroid carcinoma
  • Diagnosis of pancreatitis or gastroparesis within the past 3 years
  • Medications: Any diabetes medication, any antioxidant vitamin supplement (\ 35 mcg ethinyl estradiol, growth hormone, any immunosuppressant...
See the full eligibility criteria
Who can join
  • Aims 1-3: Stage 2 T1DM with TZIELD® and GLP-1Ra
  • Age: 12-50 years
  • BMI: 18-31 kg/m2 (adults) or 5-95th %ile (pediatric)
  • fasting glucose ≥ 100 mg/dL and \< 126 mg/dL OR
  • 2-hr OGTT /MMTT ≥ 140 mg/dL and \< 200 mg/dL OR
  • During an OGTT having a glucose of \> 199 mg/dL at 30, 60, or 90 minutes)
What rules you out
  • SBP \> 140 mmHg and DBP \> 100 mmHg
  • eGFR by MDRD equation of \< 60 mL/min/1.73m2
  • AST or ALT \> 2.5 times ULN
  • Family history of medullary thyroid carcinoma
  • Diagnosis of pancreatitis or gastroparesis within the past 3 years
  • Medications: Any diabetes medication, any antioxidant vitamin supplement (\ 35 mcg ethinyl estradiol, growth hormone, any immunosuppressant, antihypertensive, any antihyperlipidemic
  • Other: pregnancy, peri- or post-menopausal women, active smoker Aim 4: Early Stage 3 T1DM with GLP-1Ra Monotherapy Inclusion Criteria
  • Age: 12-50 years
  • BMI: 18-31 kg/m2 (adults) or 5-95th %ile (pediatric)
  • Early stage 3 T1DM with either
  • HbA1c 6.5% to 8.0% at diagnosis OR
  • HbA1c 5.7% to 6.4% with oral glucose test meeting ADA criteria for stage 3 T1DM within the past three months prior to or during screening visit
  • Time of stage 3 diagnosis: within eight weeks of first study visit Exclusion Criteria
  • DKA history: history of diabetic ketoacidosis requiring hospital admission
  • Family history of medullary thyroid carcinoma
  • Diagnosis of pancreatitis or gastroparesis within the past 3 years
  • Medications: Any diabetes medication, any antioxidant vitamin supplement (\ 35 mcg ethinyl estradiol, growth hormone, any immunosuppressant, antihypertensive, any antihyperlipidemic
  • Other: pregnancy, peri- or post-menopausal women, active smoker

The study team makes the final eligibility decision.

Where it is enrolling

  • Nashville, Tennessee, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 12 years to 50 years. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Nashville, Tennessee, United States. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.