WHO ICTRP trial

Investigating the in vivo bioequivalence of Celecoxib 100 mg tablet

IRCT20210519051345N15 · Iranian Registry of Clinical Trials (IRCT) · Not Recruiting

Key facts

Trial ID IRCT20210519051345N15
Public title Investigating the in vivo bioequivalence of Celecoxib 100 mg tablet
Scientific title Fasted-state in vivo bioequivalence study of Celecoxib 100 mg tablet manufactured by Farnoush Daru Teb Co. compared with innovator product
Primary sponsor Tabriz University of Medical Sciences
Registry Iranian Registry of Clinical Trials (IRCT)
Recruitment status Not Recruiting
Study type interventional
Phase Bioequivalence
Countries Iran (Islamic Republic of)
Conditions In the present study, the products will be administered to healthy volunteers..
Interventions Intervention 1: Intervention group: Intervention group will receive a single test drug product. Blood samples will be collected for48 hours at the mentioned times after drug administration and the concentration of drug in blood samples will…
Registration date Aug 17, 2022
Target size 24
Registry page irct.behdasht.gov.ir

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

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