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sequence under fasting conditions and at least 14 days washout period between the doses.,A randomized&#44

6 trials

Sponsors

Bio-innova and Synchron.Co.,Ltd, POND CHEMICAL CO., LTD., Thailand

Conditions

Bioequivalence study Bioequivalence EtoricoxibBioequivalence study Bioequivalence LevonorgestrelBioequivalence study Bioequivalence study EscitalopramBioequivalence study Bioequivalence study EtoricoxibBioequivalence study in healthy thai volunteers Bioequivalence QuetiapineBioequivalence study in healthy volunteers Bioequivalence Rosuvastatin

Phase 1

Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Rosuvastatin Tablets (20 mg) relative to Crestor (Original Rosuvastatin Tablets (20 mg)) in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20180802003
Bio-innova and Synchron.Co.,LtdBioequivalence study in healthy volunteers Bioequivalence Rosuvastatin
Start: 2018-09-03Target: 32Updated: 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 Quetiapine 200 mg immediate release tablets imported by Great Eastern Drug Co., Ltd., (hereinafter referred to as “Tested Preparation”) relative to Seroquel 200 mg tablets, (hereinafter referred to as “Reference Preparation”) in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20180905005
Bio-innova and Synchron.Co.,LtdBioequivalence study in healthy thai volunteers Bioequivalence Quetiapine
Start: 2018-11-04Target: 36Updated: 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 Etoricoxib 120 mg film-coated tablets relative to Arcoxia® 120 mg film-coated tablets in healthy Thai volunteers under fasting conditions
Active, not recruitingTCTR20181031003
Bio-innova and Synchron.Co.,LtdBioequivalence study Bioequivalence Etoricoxib
Start: 2019-01-31Target: 30Updated: 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 Levonorgestrel Tablets (1.5 mg) relative to POSTINOR ONE® in healthy Thai female volunteers under fasting condition
Active, not recruitingTCTR20181206001
Bio-innova and Synchron.Co.,LtdBioequivalence study Bioequivalence Levonorgestrel
Start: 2019-01-07Target: 26Updated: 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 Etoricoxib 120 mg tablets relative to Arcoxia(R) 120 mg tablets in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20190316004
Bio-innova and Synchron.Co.,LtdBioequivalence study Bioequivalence study Etoricoxib
Start: 2019-07-29Target: 24Updated: 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 Escitalopram Tablet (20 mg) relative to Lexapro(R) in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20190523001
POND CHEMICAL CO., LTD., ThailandBioequivalence study Bioequivalence study Escitalopram
Start: 2019-08-09Target: 24Updated: 2026-08-03