LivingGLP1
Study S001880

Evaluating the Effects of GLP-1 Analogue, Oral Semaglutide, in Patients With Alzheimer's Disease

Registration

Registration
NCT07200622
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
60
Start
2025-09-25
Primary completion
2027-12-31
Lead sponsor
Imperial College London
Conditions
Alzheimer Disease
Interventions
DRUG:Semaglutide (Rybelsus®); DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • To evaluate the safety and tolerability of oral semaglutide in an AD population. [Adverse events monitoring: Baseline; Weeks 4, 8, 26, 39, 52]

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