drugset / Trial / NCT00885365

A Study Comparing the Efficacy and Tolerability of Tobrineb®/Actitob®/Bramitob® Versus TOBI®

NCT00885365 ↗

Phase 3 Completed 324 enrolled Chiesi Farmaceutici S.p.A.
RandomizedParallel-groupOpen-labelTreatment

Summary

The objectives of the study are to demonstrate that Tobrineb®/Actitob®/Bramitob® is non-inferior to TOBI® in the primary efficacy variable, forced expiratory volume in one second (FEV1) percent of predicted normal, and to compare the safety in participants with cystic fibrosis and chronic infection of the lungs with Pseudomonas aeruginosa.

Timeline

Start
2009-04
Primary completion
2010-04
Completion
2010-05

Outcome

Met primary endpoint

paper the non-inferiority between treatments was met PMID 24464974 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tobramycin Unknown 300 mg Inhaled

Indications