sequence under fasting conditions ,A randomized,
Sponsors
Bio-innova and Synchron Co., Ltd., Bio-innova and Synchron.Co.,Ltd
Conditions
Bioequivalence study in healthy volunteersBioequivalence study in healthy volunteers
Bioequivalence
LevonorgestrelBioequivalence study in healthy volunteers
Bioequivalence
RasagilineBioequivalence study in healthy volunteers
Bioequivalence
TicagrelorBioequivalence study in healthy volunteers
Bioequivalence,
Phase 1
An open-labeled, randomized, single-dose, 2-period, 2-treatment, 2-way crossover bioequivalence study of Valsartan/Amlodipine 160/10 mg in male and female subjects under fasting conditions.
Active, not recruitingTCTR20170225001
Start: 2017-02-24Target: 60Updated: 2026-08-03
Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two treatment and two-sequence of Azithromycin Powder for Oral Suspension (200mg/5ml) relative to ZITHROMAX (Original Azithromycin Powder for Oral Suspension (200mg/5ml) in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20170227004
Start: 2017-03-27Target: 44Updated: 2026-08-03
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Levocetirizine 5 mg tablets relative to Xyzal® 5 mg tablets in healthy Thai volunteers under fasting condition.
Active, not recruitingTCTR20170516001
Start: 2017-08-07Target: 24Updated: 2026-08-03
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Rasagiline Tablets (1 mg) relative to Originator Rasagiline (1 mg) in healthy Thai volunteers under fasting condition.
Active, not recruitingTCTR20170519001
Start: 2017-08-01Target: 44Updated: 2026-08-03
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Ticagrelor Tablets (90 mg) relative to Originator Ticagrelor Tablets (90 mg) in healthy Thai volunteers under fasting condition.
Active, not recruitingTCTR20170523002
Start: 2018-02-01Target: 44Updated: 2026-08-03
Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of 2 tablets of Levonorgestrel Tablets (0.75 mg) relative to 2 tables of POSTINOR® in healthy Thai female volunteers under fasting condition
Active, not recruitingTCTR20170614001
Start: 2017-06-29Target: 26Updated: 2026-08-03