drugset / Trial / NCT07496021

Safety and Efficacy of L. Lactis CKDB001 in Subjects With Early Alzheimer's Disease

NCT07496021 ↗

Recruiting 60 enrolled CKD Bio Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

Randomized, Placebo-Controlled, Double-Blind, 24-Week Proof-of-Concept Study to Evaluate the Safety and Efficacy of L. Lactis CKDB001 in Subjects With Early Alzheimer's Disease

Timeline

Start
2026-02-23
Primary completion
2027-05-31
Completion
2027-05-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator L. lactis CKDB001 Unknown — Oral

Indications