A Study Of BRL49653C For The Treatment Of Type 2 Diabetes

NCT00523913 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2016-10-28

No results posted yet for this study

Summary

This study is designed to evaluate the safety of BRL49653C administrated for 52 weeks

Conditions

  • Diabetes Mellitus, Type 2

Interventions

DRUG

rosiglitazone

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-11-30
Completion
2007-04-30

Countries

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00523913 on ClinicalTrials.gov