Bioequivalence Clinical Trial
Official title:
A Phase I, Open-label, Randomised, Single-centre, 2-way Crossover Bioequivalence Study Comparing 2 Formulations of Imeglimin After Single Oral Doses in Healthy Caucasian Subjects
This is an open-label assessment of the bioequivalence of two 500 mg-tablet formulations of imeglimin (Tablet A [reference product] and Tablet B [test product]), in at least 16 healthy Caucasian volunteers.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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Phase 1 | |
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Phase 1 | |
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Early Phase 1 | |
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Phase 1 | |
| Completed |
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| Completed |
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Phase 1 | |
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Phase 1 | |
| Completed |
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Phase 1 |