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Bioequivalence Study of Furosemide 40 mg Tablet in 24 Indonesian Healthy Volunteers

Drug Use Clinical Trial

Official title:
Bioequivalence Study of Furosemide in Indonesian Healthy Volunteers

Clinical Trial Summary

The purpose of this research was to investigate whether Furosemide 40 mg tablet manufactured by PT. Kimia Farma Tbk was bioequivalent to its reference drug and Lasix® 40 mg Tablet manufactured by PT. Aventis Pharma, Indonesia.

Clinical Trial Description

Twenty four healty volunteers were given a single dose of Furosemide 40 mg Tablet or Lasix® 40 mg Tablet with 240 mL of water beneath fasting condition. Then the blood samples for Furosemide were drawn and analyzed using UPLC. All subjects sample plasma were analyzed for pharmacokinetic evaluation ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04982874
Study type Interventional
Source PT. Kimia Farma (Persero) Tbk
Contact
Status Completed
Phase N/A
Start date December 13, 2019
Completion date January 29, 2020
View Details
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