Effects of Semaglutide on Intracranial Blood Flow and Brain-Barrier Permeability in Type-2 Diabetes

PHASE4RecruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

January 11, 2024

Primary Completion Date

March 31, 2026

Study Completion Date

December 31, 2026

Conditions
Diabetes Mellitus, Type 2Stroke (CVA) or Transient Ischemic Attack
Interventions
DRUG

Semaglutide Auto-Injector

"Subjects have an equal chance of receiving semaglutide or placebo. Which treatment subjects receive is decided at random by a computer (purely by chance, like the tossing of a coin). Neither subjects, Study Site personnel nor image reviewers will know which treatment subjects are assigned to. The study drug must be taken weekly. The subject's other medications may be changed by the study's un-blinded Endocrinologist.~At baseline subject will receive and take home 0.25mg injector for use 3 more times. They will be given a 0.5mg injector and a 1mg injector for use beginning 5 and 9 weeks from baseline respectively.~The target dose for subjects is 1mg per week up to the 52 week treatment duration."

OTHER

Placebo

Placebo

Trial Locations (1)

98104

RECRUITING

University of Washington - Harborview Medical Center, Seattle

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novo Nordisk A/S

INDUSTRY

lead

University of Washington

OTHER

NCT05780905 - Effects of Semaglutide on Intracranial Blood Flow and Brain-Barrier Permeability in Type-2 Diabetes | Biotech Hunter | Biotech Hunter