drugset / Trial / NCT01615393

A Study to Compare the Bioavailability of Copegus and Vilona® in Healthy Volunteers

NCT01615393

Phase 1 Completed 40 enrolled Hoffmann-La Roche
RandomizedCrossoverSingle-blind

Summary

This prospective, randomized, single-blind, cross-over study will compare the bioavailability of Copegus (ribavirin) administered as tablets and ribavirin administered as capsules in healthy volunteers. Volunteers will be randomized to receive a single dose of 400 mg of ribavirin either as a capsule or as tablets; after a washout phase volunteers will be crossed-over to the other treatment. The anticipated time on study treatment is 10 days.

Timeline

Start
2011-06
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 400 mg Oral

Indications

No indication recorded.