Clinical Trials Directory

Trials / Completed

CompletedNCT03363269

Evaluate the Efficacy and Safety of ID1201 for Dose-finding in Mild Alzheimer's Disease

A Multi-center, Randomized, Double-blind, Placebo-controlled Phase II Clinical Trial to Evaluate the Evaluate the Efficacy and Safety of ID1201 for Dose-finding in Mild Alzheimer's Disease

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
116 (actual)
Sponsor
IlDong Pharmaceutical Co Ltd · Industry
Sex
All
Age
55 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the safety and efficacy of ID1201 in patients with mild Alzheimer's disease

Detailed description

ID1201 is a fruit extract of Melia toosendan. ID1201 alleviates Alzheimer's disease-type pathologies and cognitive deficit through the various actions of its effective components such as α-secretase activation followed to Aβ reduction, RAGE inhibition, neuro-protection, and anti-inflammatory activities.

Conditions

Interventions

TypeNameDescription
DRUGID1201

Timeline

Start date
2016-04-12
Primary completion
2018-12-31
Completion
2019-04-17
First posted
2017-12-06
Last updated
2019-06-04

Locations

20 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03363269. Inclusion in this directory is not an endorsement.