Clinical trial

Does the Hematopoietic Stem Cell Govern Residual Inflammatory Cardiovascular Risk in Type 2 Diabetes

Name
NL80519.018.22
Description
To study the effect of type 2 diabetes (T2D) on vascular wall inflammation and hematopoietic stem cell composition in vivo, and whether these changes can be reversed with glucagon like peptide 1 receptor (GLP1R)-agonism.
Trial arms
Trial start
2023-01-01
Estimated PCD
2024-03-01
Trial end
2024-04-01
Status
Recruiting
Phase
Early phase I
Treatment
Semaglutide, 2.0 mg/mL
Semaglutide 2.0 mg/mL, administered subcutaneously once per week for a period of 6 months.
Arms:
Treatment arm
Size
22
Primary endpoint
Difference in coronary 68Ga-Dotatate uptake after treatment.
6 months
Eligibility criteria
Inclusion Criteria: * Age \>50 years old * Diagnosed with type 2 diabetes * HbA1c \>64mmol/mol Exclusion Criteria: 1. (History of) malignant diseases or any clinically significant medical condition that could interfere with the conduct of the study in the opinion of the investigator. 2. Chronic or recent infections and/or clinical signs of infection and/or a plasma C-reactive protein above 10ng/ml 3. Auto-immune diseases (including type 1 diabetes) 4. Recent or chronic immunosuppressant or antibiotic usage 5. Use of any GLP1R-agonist at baseline or prior intolerance to use of GLP1R-agonists. 6. Inability or unwillingness to comply with the protocol requirements, or deemed by investigator to be unfit for the study. 7. Uncontrolled hypertension (systolic blood pressure \> 180mmHg, diastolic blood pressure \> 100mmHg) 8. Uncontrolled chronic inflammatory conditions, including gout. 9. Women of childbearing age who are not using effective contraceptives. 10. Heart failure New York Heart Association (NYHA) class IV at screening visit. 11. Active liver disease or hepatic dysfunction, defined as aspartate aminotransferase (ASAT) or alanine aminotransferase (ALAT) ≥ 2 times the upper limit of normal (ULN) at screening visit. 12. Pancreatitis in medical history.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 22, 'type': 'ESTIMATED'}}
Updated at
2023-05-09

1 organization

1 product

1 indication

Indication
Type 2 Diabetes