RecruitingNot ApplicableNCT07496021

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

A 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


Sponsor

CKD Bio Corporation

Enrollment

60 participants

Start Date

Feb 23, 2026

Study Type

INTERVENTIONAL

Conditions

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


Eligibility

Min Age: 55 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called L. lactis CKDB001 and a drug called Placebo for people with early alzheimers disease. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 55 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGL. lactis CKDB001

Oral Capsule

DRUGPlacebo

Oral Capsule


Locations(2)

Yonsei University Yongin Severance Hospital

Gyeonggi-do, South Korea

Yonsei University Severance Hospital

Seoul, South Korea

View Full Details on ClinicalTrials.gov

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NCT07496021


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