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Efficacy and Safety Study of Probucol in Patients With Diabetic Nephropathy

Diabetic Nephropathy Clinical Trial

Official title:
A Phase II, Multicenter, Randomized, Double Blind, Double-dummy, 16-week, Placebo Controlled Study to Evaluate the Efficacy and Safety of Probucol in Patients With Nephropathy Due to Type 2 Diabetes.

Clinical Trial Summary

This trial is randomized, placebo-controlled, double blind, double dummy, multi-centre trial.

- Screening period (4 week)

- Double blind treatment period (16 weeks)

Clinical Trial Description

1. Usage: 16 week, BID, Prescribed Oral with the breakfast and dinner

2. Dosage:Placebo group: placebo 2 tablets, 16 weeks Probucol 250mg group: probucol 125mg 2 tablets, 16 weeks Probucol 500mg group: probucol 250 mg 2 tablets, 16 weeks ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01726816
Study type Interventional
Source Korea Otsuka Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date October 2012
Completion date September 2014
View Details
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