WHO ICTRP trial
Investigating the in vivo bioequivalence of Resmetirom tablet
IRCT20210519051345N93 · Iranian Registry of Clinical Trials (IRCT) · Not Recruiting
Key facts
| Trial ID | IRCT20210519051345N93 |
|---|---|
| Public title | Investigating the in vivo bioequivalence of Resmetirom tablet |
| Scientific title | Bioequivalence study of Resmetirom 100 mg tablet manufactured by Zist Arvand Pharmed Compared to innovator product |
| Primary sponsor | Zist Arvand Pharmed Co. |
| 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 (Resmetirom 100 mg tablet manufactured by Zist Arvand Co.) in fasted state. Blood samples will be collected for 24 hours at the mentioned… |
| Registration date | Jan 28, 2026 |
| Target size | 24 |
| Registry page | irct.behdasht.gov.ir |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: