Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Prospective, Multi-center, Open-label, Phase IV Study to Evaluate the Safety and Efficacy of Alogliptin as Monotherapy or Add on Therapy in Indian Patients With Type 2 Diabetes Mellitus
The purpose of this study is to evaluate the safety and efficacy of alogliptin tablets when given as monotherapy or add on therapy in participants who are on standard care for management of Type 2 Diabetes Mellitus (T2DM).
The drug being tested in this study is called alogliptin. Alogliptin is being tested to treat
people who have Type 2 Diabetes Mellitus (T2DM). This study will look at side effects and
glycemic control in people who take alogliptin in addition to standard care.
The study will enroll approximately 300 patients. All participants will receive alogliptin
tablets at a dose determined based on the creatinine clearance.
The recommended dose of alogliptin is 25 mg once daily with normal or mildly impaired renal
function (creatinine clearance [CrCl] ≥60 mL/min), dose of 12.5 mg for participants with
moderate renal impairment (CrCl ≥30 to <60 mL/min), and 6.25 mg for participants severe renal
impairment (CrCl ≥15 to <30 mL/min). Participants with end-stage renal disease (ESRD) (CrCl
<15 mL/min or requiring hemodialysis) will be excluded, in addition to standard care for the
management of T2DM.
All participants will be asked to take one tablet every morning each day throughout the
study.
This multi-center trial will be conducted in India. The overall time to participate in this
study is up to 33 weeks. Participants will make multiple visits to the clinic, and will be
contacted by telephone 30 days after last dose of study drug for a follow-up assessment.
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