A Randomized, Open-label, Crossover Phase 1 Study to Evaluate the Bioequivalence Following a Single Oral Dose Administration of SYR-472 25mg and 50mg Tablets in Healthy Adult Male Subjects

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 25 May 2016

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25 May 2016 The time frames of the primary endpoints have changed from 21 days to "Day 1: pre dose (within 3 hours prior to dosing), and at multiple time points (up to 168 hours) post dose in each period"
08 Apr 2016 Status changed from not yet recruiting to completed.
02 Mar 2015 New trial record

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