release tablets
Sponsors
The Government Pharmaceutical Organization, International Bio Service
Conditions
Healthy Thai VolunteersHealthy male and female volunteersHealthy male and female volunteers
Carvedilol
BioequivalenceHealthy male and female volunteers
Metformin XR
BioequivalenceHealthy male and female volunteers
Tramadol retard
Tramadol XR
Bioequivalence
Phase 1
A Single Dose, Randomized, Open-label, Two-way Crossover Bioequivalence Study of Generic Desvenlafaxine 50 mg Extended-release Tablets and Reference Product (Pristiqâ„¢ 50 mg) in Healthy Thai Volunteers under Fasting Conditions - Pilot Study
Active, not recruitingTCTR20180924002
Start: 2018-11-30Target: 10Updated: 2026-08-03
An Open Label, Randomized, Two-treatment, Two-period, Two-sequence, Multiple Oral Dose, Crossover Bioequivalence Study of Generic Desvenlafaxine 50 mg Extended-release Tablets and Reference Product (Pristiqâ„¢ 50 mg) in Healthy Thai Volunteers under Fasting Conditions
Active, not recruitingTCTR20190417006
Start: 2019-04-11Target: 32Updated: 2026-08-03
Unknown Phase
Comparative Randomized, Single Dose, Two-Way Crossover, Open-Label Study to Determine the Bioequivalence of Tramadol Hydrochloride 100 mg Extended-Release Tablets Formulations, Tramal retard 100 mg and TRAMADOL RETARD GPO (100 MG), after Oral Administration to Healthy Thai Volunteers under Fasting Conditions
Active, not recruitingTCTR20170118003
Start: 2017-05-01Target: 24Updated: 2026-08-03
Comparative Randomized, Single Dose, Two-Way Crossover, Open-Label Study to Determine the Bioequivalence of Metformin Hydrochloride 1000 mg Extended-Release Formulation, Glucophage XR 1000 mg and Metformin XR (1000 mg), After Oral Administration to Healthy Thai Volunteers Under Fasting Conditions
Active, not recruitingTCTR20170118002
Start: 2017-03-28Target: 24Updated: 2026-08-03
Comparative Randomized, Single Dose, Two-Way Crossover, Open-Label Study to Determine the Bioequivalence of Carvedilol 6.25 mg Tablets Formulations, Dilatrend and Carvolol (6.25 mg), after Oral Administration to Healthy Thai Volunteers under Fasting Conditions
Active, not recruitingTCTR20170119001
Start: 2017-05-22Target: 62Updated: 2026-08-03
An Open Label, Randomized, Two-Treatment, Two-Period, Two-Sequence, Single Oral Dose, Crossover Bioequivalence Study of Darutab (Darunavir 600 mg) Tablets of The Government Pharmaceutical Organization, Bangkok, Thailand, with Prezista (Darunavir 600 mg) Tablets of Janssen Ortho LLC, Gurabo, Puerto Rico with Co-Administration of Norvir (Ritonavir 100 mg) Tablets in Normal, Healthy, Adult, Human Subjects under Fed Conditions
Active, not recruitingTCTR20170503002
Start: 2017-07-01Target: 50Updated: 2026-08-03
AN OPEN LABEL, RANDOMIZED, TWO-TREATMENT, TWO-PERIOD, TWO-SEQUENCE, SINGLE ORAL DOSE, CROSSOVER BIOEQUIVALENCE STUDY OF QUAPINE (QUETIAPINE 100 MG) TABLETS OF THE GOVERNMENT PHARMACEUTICAL ORGANIZATION, BANGKOK, THAILAND WITH SEROQUEL (QUETIAPINE 100 MG) TABLETS OF ASTRAZENECA PHARMACEUTICALS CO., LTD., JIANGSU, PEOPLE'S REPUBLIC OF CHINA, IN NORMAL, HEALTHY, ADULT HUMAN SUBJECTS UNDER FASTING CONDITIONS
Active, not recruitingTCTR20170619005
Start: 2017-07-14Target: 54Updated: 2026-08-03
Comparative Randomized, Single Dose, Two-Way Crossover, Open-Label Study to Determine the Bioequivalence of Sofosbuvir 400 mg Tablets Formulations, Sovaldi and HEPASOF (400 mg), after Oral Administration to Healthy Thai Volunteers under Fasting Conditions
Active, not recruitingTCTR20170622001
Start: 2017-08-07Target: 82Updated: 2026-08-03