Bioequivalence study of valacyclovir 1000 mg tablet (Avicenna) versus VALTREX ® 1000 mg (GlaxoSmithKline) Tablet after single oral dosing in healthy volunteers.
Conditions
Interventions
Intervention 1: Intervention group: Receives one tablet of test drug (valaciclovir 1000 mg from Oh Sina Pharmaceutical Company). Blood samples were taken from the volunteers for 24 hours at the mentio
Sponsors
Avicenna pharmaceutical Co.
Eligibility
Sex/Gender
Male
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 18 to 55 years old Weight in range of 10 % proper body weight All volunteers should be in a good health condition on the basis of medical history ,physical examination , routine blood test. and possessing negative test for hepatitis B surface antigen (HBs-Ag),antihepatitis-C antibody (anti-HCV).and anti-HIV. just man
Exclusion criteria
Exclusion criteria: Volunteers with hypersensitivity to valacyclovir were excluded. those with known history of drug abuse. alcohol consumer or cigarette smokers. Taking medications that have drug interactions with valacyclovir until one month before studying. disinclination Blood donation or blood loss of more than 200 ml in the past month
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determination of blood concentration. Timepoint: 0,0/25,0/5,0/75,1,1/25,1/5,1/75,2,2/5,3,4,6,8,10,24,30. Method of measurement: HPLC-UV. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBardia jamali
Tam Pouya Consulting & Research Company
Outcome results
None listed