Bioequivalence study of celecoxib 200 mg capsule

Bioequivalence study of 200 mg cobix capsules from Farnoush Darou Teb Company compared to 200 mg Celecoxib from Pfizer, Turkey, licensed in Germany, on healthy volunteers

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230222057495N22

Enrollment

Registered

2024-10-31

Start date

2024-10-27

Completion date

Unknown

Last updated

2025-01-08

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 1: Includes oral administration of 200 mg Cobix capsules from Farnoush Darou Teb Company, Iran, on 24 healthy volunteers on an empty stomach. 5 ml of blood is taken

Eligibility

Sex/Gender

All

Age

18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Healthy volunteer between 18 and 55 years old. Body mass index less than 30 kg per square meter. All candidates must be non-smokers.

Exclusion criteria

Exclusion criteria: Blood pressure less than 90 on 60 mm Hg or more than 140 on 90 mm Hg. Consumption of any drug, alcohol or tobacco within 2 weeks before receiving the drug.

Design outcomes

Primary

Measure	Time frame
Maximum plasma concentration of celecoxib. Timepoint: Before taking the drug and: 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, 24 and 48 hours after taking the drug. Method of measurement: Liquid chromatography-mass spectrometry.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMonireh Jalalipour

Nik Azma Pars Alborz Laboratory

info@naplab.ir+98 26 3731 8748

Outcome results