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A Study Of BRL49653C For The Treatment Of Type 2 Diabetes (Combination Therapy With Sulfonyl Urea) -With Placebo Study

GlaxoSmithKline (GSK) logo

GlaxoSmithKline (GSK)

Status and phase

Completed
Phase 3

Conditions

Diabetes Mellitus, Type 2

Treatments

Drug: Rosiglitazone (BRL49653C)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00432679
AVD105248

Details and patient eligibility

About

This study was designed to compare the efficacy and safety of BRL49653C versus placebo with concomitant use of sulfonyl urea (SU).

Enrollment

149 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with type 2 diabetes mellitus managed by SU will be candidate for this study. These candidates will be checked up on their clinical laboratory data, and must have adequate blood, liver and kidney function.

Exclusion criteria

  • Patient with serious cardiovascular disease or serious hepatic disease will not be eligible.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

149 participants in 1 patient group

arm 1
Experimental group
Description:
study drug
Treatment:
Drug: Rosiglitazone (BRL49653C)

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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