WHO ICTRP trial
Bioequivalence study of pantoprazole 40 mg preparations
IRCT20130626013776N53 · Iranian Registry of Clinical Trials (IRCT) · Not Recruiting
Key facts
| Trial ID | IRCT20130626013776N53 |
|---|---|
| Public title | Bioequivalence study of pantoprazole 40 mg preparations |
| Scientific title | A study to compare the relative bioavailability of Avicenna and Takeda formulations of pantoprazole 40 mg Capsules in 24 healthy adult volunteers under fasting conditions |
| Primary sponsor | Avicenna Pharmaceuticals |
| Registry | Iranian Registry of Clinical Trials (IRCT) |
| Recruitment status | Not Recruiting |
| Study type | interventional |
| Phase | Bioequivalence |
| Countries | Iran (Islamic Republic of) |
| Conditions | .. |
| Interventions | Intervention 1: Intervention group: Oral administration of a single 40 mg dose of pantoprazole (1 capsule) manufactured by Avicenna to healthy volunteers under fasting condition in the morning of the experiment day. Intervention 2… |
| Registration date | Jun 19, 2021 |
| 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: