Type II Diabetes Mellitus Clinical Trial
Official title:
A 24-Week, Open Label, Phase IV Trial to Evaluate the Efficacy of Pioglitazone 30 mg in Patients With Inadequately Controlled Type 2 Diabetes Mellitus Treated With Stable Triple Oral Therapy of Metformin, Sulfonylurea, and Pioglitazone 15 Mg (ADD Trial)
The purpose of this study is to evaluate the efficacy of pioglitazone 30 mg on glycemic control when used in participants with inadequately controlled type 2 diabetes mellitus treated with stable combinations of metformin and sulfonylurea.
The drug being tested in this study is called pioglitazone. Pioglitazone is being tested to
treat glycemic control in adults with inadequately controlled type 2 diabetes mellitus. This
study will look at glycemic control in people who take triple oral therapy of metformin,
sulfonylurea, and pioglitazone 15 mg.
The study will enroll approximately 114 patients. All participants will be asked to take one
pioglitazone tablet at the same time each day throughout the study as well as continuing
their previous dose of metformin and sulfonylurea.
This multi-center trial will be conducted in Korea. The overall time to participate in this
study is up to 25 weeks. Participants will make 4 visits to the hospital or endocrinologist's
office, and will be contacted by telephone 7 days after last dose of study drug for a
follow-up assessment.
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