WHO ICTRP trial

Investigating the in vivo bioequivalence of Ibrutinib 140 mg capsule

IRCT20210519051345N71 · Iranian Registry of Clinical Trials (IRCT) · Not Recruiting

Key facts

Trial ID IRCT20210519051345N71
Public title Investigating the in vivo bioequivalence of Ibrutinib 140 mg capsule
Scientific title In vivo fasted-state bioequivalence study of Ibrutinib 140 mg Capsules manufactured by Sobhan oncology Pharmaceutical Co. compared to 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 oral dose of test product (Ibrutinib capsule manufactured by Sobhan Oncology Co.) in fasted state. Blood samples will be collected for 24 hours at the mentioned…
Registration date Dec 24, 2024
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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