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In-vivo Bioequivalence Test of Favipiravir® tablet with brand drugs (AVIGAN® 200mgTAYOMA Chemical Ind. Co).

In- Vivo Bioequivalence study of Favipiravir tablet 200mg ABIDI with brand drugs (AVIGAN 200mg, Tayoma Chemical Co. Ind. Japan) in Iranian healthy volunteers.

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200105046010N30
Enrollment
24
Registered
2021-04-26
Start date
2021-03-05
Completion date
Unknown
Last updated
2021-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention 1: Intervention group: Intervention group received one test drug table(Favipiravir tablet 200mg ABIDI Pharmaceutical Company). Blood samples were taken two period (72 hrs) with one week w

Sponsors

ABIDI Pharmaceutical Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: General health Body mass index(18-28) Informed consent Age(18-60)

Exclusion criteria

Exclusion criteria: Smoking A history of cardiovascular disease A history of liver & kidney disease Pregnancy Alcohol & Drug addiction Hypersensitivity to the drug

Design outcomes

Primary

MeasureTime frame
Determination of blood drug concentration. Timepoint: Sampling times in this study will be 0, 1, 2, 2:30, 3, 3:20, 3:40, 4, 4:20, 4: 40, 5, 6, 8, 10, 12, 24, 48, 72 hours After prescribing the tablet. Method of measurement: High Performance Liquid Chromatography with tandem mass spectroscopy detector.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Shokri

Tabriz University of Medical Sciences

Shokri.j@gmail.com+98 41 3334 8489

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026