drugset / Trial / NCT01005069

Efficacy of DLBS-32 in Subjects With Type-II Diabetes Mellitus

NCT01005069 ↗

Phase 2 Completed 72 enrolled Dexa Medica Group
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to investigate clinical efficacy and safety of DLBS 32 in the management of subjects with type-II-diabetes mellitus and to determine the minimal effective dose of DLBS 32 for subjects with type-II-diabetes mellitus.

Timeline

Start
2009-10
Primary completion
2010-07
Completion
2010-08

Drugs

EvaluationDrugModalityDoseRoute
Subject DLBS-32 Unknown 50 mg —
Subject DLBS-32 Unknown 100 mg —
Subject DLBS-32 Unknown 200 mg —
Subject DLBS-32 Unknown 300 mg —