GLP-1 Analogue in Preventing Progression of Small Vessel Disease (GAPP-SVD) - A Pilot Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Cerebral small vessel disease (cSVD), a result of neurovascular cell dysfunction, is a major cause of stroke, dementia and mobility problems worldwide. Vascular risk factor control alone may not be sufficient to prevent the development of vascular cognitive impairment (VCI) in patients with cSVD according to previous clinical trials. The presence of glucagon-like peptide-1 receptor (GLP-1R) in cerebral microglia may reveal a potential therapeutic target for prevention of cSVD progression and its disabling clinical outcomes. At the cellular and animal experimentation levels, GLP-1R agonist demonstrated reversal of some pathogenic processes in cSVD. However, its application to cSVD patients remains to be elucidated. Investigator aims to investigate the safety and efficacy of GLP-1R agonist in patients with moderate-to-severe cSVD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Maximum Age: 80
Healthy Volunteers: f
View:

• Chinese ethnicity;

• Age 55 to 80 years old;

• Age-Related White Matter Change (ARWMC) Scale of 2 or early 3 in FLAIR MRI;

• Modified Functional Ambulation Classification 5 or above;

• Montreal Cognitive Assessment (MoCA) score \< 25;

• Both diabetic and non-diabetic patient are eligible;

• Patient who understands the purpose and requirements of the study, and able to provide an informed consent;

Locations
Other Locations
Hong Kong Special Administrative Region
Chinese University of Hong Kong
RECRUITING
Hong Kong
Contact Information
Primary
Pauline Kwan, Master
paulinekwan@cuhk.edu.hk
+85226352160
Backup
Hung Trista, Bachelor
tristahung@cuhk.edu.hk
+85226352152
Time Frame
Start Date: 2022-05-25
Estimated Completion Date: 2026-12
Participants
Target number of participants: 110
Treatments
Active_comparator: Exenatide extended release
Prescribe study drug: Exenatide extended release. The dosage and frequency is 2mg once weekly via subcutaneous injection for 78 weeks
No_intervention: Standard of care
Standard medical therapy
Related Therapeutic Areas
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov