WHO ICTRP trial

A Bioequivalence study of a randomized, open-label, single dose, two-way…

TCTR20220923001 · Thai Clinical Trials Registry (TCTR) · Not Recruiting

Key facts

Trial ID TCTR20220923001
Public title A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Finasteride 1 mg tablets relative to Propecia 1 mg tablets in healthy Thai male volunteers under fasting condition
Scientific title A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Finasteride 1 mg tablets relative to Propecia 1 mg tablets in healthy Thai male volunteers under fasting condition
Primary sponsor Bio-innova Co., Ltd.
Registry Thai Clinical Trials Registry (TCTR)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 1
Countries Thailand
Conditions Healthy subjects Bioequivalence Finasteride 1 mg ;Bioequivalence Finasteride 1 mg
Interventions The new generic products which were recently developed. Volunteer will receive a single dose of 1 tablet of Finasteride Tablets 50 mg of either test or reference with 250 mL of drinking water.,The marketed original products which were…
Registration date Sep 23, 2022
Target size 26
Secondary IDs Nil Known
Registry page thaiclinicaltrials.org

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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