drugset / Trial / NCT01715350

Study to Explore the Optimal Dosage/Administration in Alzheimer's Disease

NCT01715350

Phase 2 Completed 151 enrolled VTBIO Co. LTD ADM Korea Inc · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The investigators intend to perform exploratory evaluation of the treatment effectiveness and safety of PM012 Tablet of PuriMED Co., Ltd. at 2 doses in Korean patients with mild to moderate dementia of Alzheimer's type. To achieve this, this study aims to compare each dose with placebo control for the efficacy and safety to explore the clinically optimal dose of PM012 Tablet for therapeutic confirmatory (phase 3) clinical studies.

Timeline

Start
2012-05
Primary completion
2014-09
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject PM012 Unknown 650 mg Oral
Subject PM012 Unknown 1300 mg Oral

Indications