Clinical Trials Directory

Trials / Completed

CompletedNCT03005210

A Study of Sofosbuvir and Ledipasvir From Magicbuvir Plus 90/400 mg Tablets (Magic Pharma, Egypt) Versus Harvoni 90/400 mg Tablets (Gilead Sciences, USA)

Open Label Randomized, Single Dose, Three Way Three Sequence Two Treatment Partial Replicate Crossover Bioequivalence Study of Sofosbuvir and Ledipasvir From Magicbuvir Plus 90/400 mg Tablets (Magic Pharma, Egypt) Versus Harvoni 90/400 mg Tablets (Gilead Sciences, USA)

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Genuine Research Center, Egypt · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

Comparative randomized, single dose, three way three sequence two treatment partial replicate crossover open-label study to determine the bioequivalence of Sofosbuvir and Ledipasvir from Magicbuvir Plus 90/400 mg Tablets (Magic Pharma, Egypt) Versus Harvoni 90/400 mg Tablets (Gilead Sciences, Canada) in Healthy Human Volunteers Under Fed Condition.

Detailed description

Primary Pharmacokinetic Parameters: Cmax, Area under cover (AUC0→t and AUC0→∞ ) Secondary Pharmacokinetic Parameters: Ke, tmax and t1/2e. ANOVA using 5% significance level for transformed (with the 90% confidence intervals) and untransformed data of Cmax, AUC0→t and AUC0→∞ and for untransformed data of Ke, tmax and t1/2e. The confidence intervals of logarithmically transformed Test/Reference ratios for Cmax, AUC0→t and AUC0→∞ to be within 80.00-125.00%. A comprehensive final report will be issued upon the completion of the study.

Conditions

Interventions

TypeNameDescription
DRUGMagicbuvir Plus1 tablet contains 400 mg Sofosbuvir and 90 mg Ledipasvir
DRUGHarvoni (fist dose)1 tablet contains 400 mg Sofosbuvir and 90 mg Ledipasvir
DRUGHarvoni (second dose)1 tablet contains 400 mg Sofosbuvir and 90 mg Ledipasvir

Timeline

Start date
2016-11-01
Primary completion
2016-11-01
Completion
2016-12-01
First posted
2016-12-29
Last updated
2016-12-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03005210. Inclusion in this directory is not an endorsement.