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Clinical Trial Summary

The purpose of this study is to assess the pioglitazone plus alogliptin plus metformin is non-inferior to dapagliflozin plus alogliptin plus metformin on glycosylated haemoglobin (HbA1c) change from baseline at Week 26.


Clinical Trial Description

The drug being tested in this study is Alogliptin Benzoate and Pioglitazone Hydrochloride FDC. This study will assess the efficacy of pioglitazone or dapagliflozin in participants with type 2 diabetes mellitus. The study will enroll approximately 156 participants. Participants will be randomly assigned (by chance, like flipping a coin) to one of the two treatment groups. - Pioglitazone 15 mg + Alogliptin 25 mg + Metformin >=500 mg - Dapagliflozin 10 mg + Alogliptin 25 mg + Metformin >=500 mg Based on investigators opinion at Week 12, if participant has HbA1c >=7.5%, dose of pioglitazone can be titrated up to 30 mg. This multi-center trial will be conducted in Republic of Korea. The overall time to participate in this study is up to 36 weeks. Participants will make multiple visits to the clinic, and will be contacted by telephone 14 days after their last dose of drug for a follow-up assessment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03499704
Study type Interventional
Source Celltrion Pharm, Inc.
Contact
Status Active, not recruiting
Phase Phase 4
Start date February 11, 2020
Completion date June 30, 2024

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