multiple-
Sponsors
Bio-innova and Synchron.Co.,Ltd
Conditions
Bioequivalence study
Bioequivalence study
Alfuzosin
steady-Bioequivalence study in healthy thai male volunteers
Bioequivalence
Alfuzosin
steady-
Phase 1
A Bioequivalence study of a randomized, open-labeled, multiple-dose, two-way crossover design with two-period, two-treatment, two-sequence steady-state bioequivalence study of Alfuzosin Prolonged-Release Tablet (10 mg) relative to Xatral® XL 10 mg in healthy Thai male volunteers under fed conditions and at least 9 days washout period between the doses
Active, not recruitingTCTR20180828001
Start: 2018-10-15Target: 40Updated: 2026-08-03
A Bioequivalence study of a randomized, open-labeled, multiple-dose, fully replicate crossover design with two-period, two-treatment, two-sequence with two consecutive days of profiling at steady-state bioequivalence study of Alfuzosin Prolonged-Release Tablet (10 mg) relative to Xatral (R) XL 10 mg in healthy Thai male volunteers under fed conditions and at least 8 days washout period between the doses
Active, not recruitingTCTR20190919001
Start: 2019-10-17Target: 28Updated: 2026-08-03