treatment and two-
Sponsors
Bio-innova and Synchron.Co.,Ltd
Conditions
Bioequivalence study
Bioequivalence
EtoricoxibBioequivalence study
Bioequivalence study
AmisulprideBioequivalence study
Bioequivalence study
AtorvastatinBioequivalence study
Bioequivalence study
DesloratadineBioequivalence study
Bioequivalence study
DonepezilBioequivalence study
Bioequivalence study
EtoricoxibBioequivalence study
Bioequivalence study
GabapentinBioequivalence study
Bioequivalence study
Levetiracetam
Early Phase 1
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Amisulpride FCT (400 mg) relative to Solian(R) 400 mg in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20190712004
Start: 2019-08-05Target: 46Updated: 2026-03-30
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 1® in healthy Thai female volunteers under fasting condition, LEV-006-19
Active, not recruitingTCTR20190807003
Start: 2019-09-01Target: 26Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of NUCOXIA 120 (Etoricoxib 120 mg tablets) relative to Arcoxia® 120 mg (Etoricoxib, MSD) tablets in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20191022001
Start: 2019-12-02Target: 28Updated: 2026-03-30
Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Gabapentin Capsule (300 mg) relative to NEURONTINTM 300 mg in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200109001
Start: 2020-03-09Target: 26Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, fully replicate crossover design with four-period, two-treatment and two-sequence of Atorvastatin 80 mg tablets relative to Lipitor(R) 80 mg tablets in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200120004
Start: 2020-03-26Target: 30Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Ondansetron Tablets USP 8 mg of Cadila Healthcare Ltd., India relative to Zofran® 8 mg (Ondansetron Tablets 8 mg) of Novartis Pharmaceuticals UK Ltd, United Kingdom in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200121003
Start: 2020-03-31Target: 28Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Pregabalin Capsules 75 mg of Cadila Healthcare Ltd., India relative to LYRICATM (Pregabalin) Capsules 75 mg of Pfizer Manufacturing Deutschland GmbH, Freiburg, Germany in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200229001
Start: 2020-05-12Target: 26Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Levetiracetam Tablets USP 500 mg of Cadila Healthcare Ltd., India relative to Keppra® 500 mg (Levetiracetam Tablets USP 500 mg) of UCB Pharma SA Braine-LʽAlleud, Belgium in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200305001
Start: 2020-05-12Target: 28Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Desloratadine Tablets USP 5 mg of Cadila Healthcare Ltd., India relative to Aerius*5 mg (Desloratadine Tablets 5 mg) of SCHERING - PLOUGH LABO N.V., HEIST-OP-DEN-BERG, Belgium in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200310001
Start: 2020-06-10Target: 28Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Donepezil Hydrochloride Orodispersible Tablets USP 10 mg of Cadila Healthcare Limited, India relative to Aricept(R) Evess 10 mg (Donepezil Hydrochloride Orodispersible Tablets) of BUSHU PHARMACEUTICALS LTD. MISATO FACTORY, JAPAN in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200428004
Start: 2020-06-28Target: 26Updated: 2026-03-30
Phase 1
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Deferasirox 250 mg dispersible tablets relative to Exjade® 250 mg dispersible tablets in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20180705002
Start: 2019-01-31Target: 38Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Etoricoxib film-coated tablets, 120 mg relative to Arcoxia® 120 mg tablets in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20181002006
Start: 2019-01-07Target: 24Updated: 2026-03-30
A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Sitagliptin Tablets USP 100 mg of Cadila Healthcare Ltd., India relative to JanuviaTM 100 mg (Sitagliptin Tablets 100 mg) of MERCK SHARP & DOHME Ltd, The United Kingdom in healthy Thai volunteers under fasting condition
Active, not recruitingTCTR20200515006
Start: 2020-07-07Target: 28Updated: 2026-03-30
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 120 mg tablets in healthy Thai volunteers under fasting condition (ETO-011-20)
Active, not recruitingTCTR20200515005
Start: 2020-06-23Target: 26Updated: 2026-03-30