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Patient disposition. Patients in the P/S group received placebo during the double‐blind period and sitagliptin 50 or 100 mg in the open‐label period. Patients in the S/S group received sitagliptin in both periods. *One patient who discontinued for lack of efficacy at week 50 was included in the efficacy analyses at week 52, thus increasing the group size to 50 patients.
