sequence under fasting conditions and at least 14 days washout period between the doses.,A randomized,
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
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 Preparationâ€) relative to Seroquel 200 mg tablets, (hereinafter referred to as “Reference Preparationâ€) in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20180905005
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
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
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
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
Start: 2019-08-09Target: 24Updated: 2026-08-03