drugset / Trial / NCT03715322

Tobramycin in Bronchiectasis Colonized With Pseudmonas Aeruginosa

NCT03715322 ↗

Phase 3 Unknown 350 enrolled Guangzhou Institute of Respiratory Disease
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a phase 3 study. Patients will be enrolled from 14 medical centers in mainland China. Eligible patients will be randomly allocated to treatment group (tobramycin nebulization, 300mg bid) and control group (natural saline nebulization, 5ml bid). A total of two 28-day on-and-off cycles will be scheduled. Both tobramycin solution and natural saline and the nebulizer will be solely provided by the sponsor.

Timeline

Start
2018-10-26
Primary completion
2021-04
Completion
2021-06

Outcome

Met primary endpoint

paper TIS resulted in a significantly greater reduction in P aeruginosa density (adjusted mean difference, 1.74 log10 colony-forming units/g; 95% CI, 1.12-2.35; P < .001) PMID 35863486 ↗

paper greater improvement in Quality-of-Life Bronchiectasis Respiratory Symptoms score (adjusted mean difference, 7.91; 95% CI, 5.72-10.11; P < .001) PMID 35863486 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tobramycin Unknown 300 mg Inhaled