Takeda Obtains New Drug Application Approval for Inisync® Combination Tablet
Inisync combination tablets combine 25 mg Nesina and 500 mg metformin, which is orally administered once daily. Nesina is a once-daily dipeptidyl peptidase-IV (DPP-4) inhibitor, and metformin is biguanide that inhibits sugar production in the liver administered twice or three times daily. Both of them are widely used as therapeutic drugs for the treatment of diabetes. Inisync is the only combination tablets administered once daily of a DPP-4 inhibitor and metformin in Japan.
The approval is based on the results of the existing clinical studies related to Nesina and the Phase III study for Inisync in Japan. In all studies, the efficacy and safety have been investigated for the ingredients of this combination tablets, Nesina and metformin, when they are concomitantly administered. The results of the Phase III study have shown significantly higher effects in improving HbA1c in regards to the changes in HbA1c, the primary endpoint, when Nesina and metformin are concomitantly administered once daily compared to individual administration of Nesina or metformin. It has also been confirmed that the safety and the tolerance were equal in the concomitant intake compared to the individual administration of Nesina only or metformin only.
“The number of patients with type 2 diabetes is increasing every year, but for various reasons, there are many patients who discontinue their diabetes treatment.” said Emiko Koumura,?M.D., Ph.D., Senior Director of Clinical Science, Takeda Development Center Japan. “We have various therapeutic options for the treatment of type 2 diabetes, and we have been providing therapeutic options based on the needs of medical professionals as well as of individual patients. I expect that this combination will contribute to improvement in treatment adherence for patients with type 2 diabetes, and to continue their therapies by providing new options for their treatment.”
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