drugset / Trial / NCT00004829

Phase III Randomized Study of the Inhalation of Tobramycin in Patients With Cystic Fibrosis

NCT00004829

Phase 3 Completed 200 enrolled FDA Office of Orphan Products Development
RandomizedDouble-blindTreatment

Summary

OBJECTIVES: I. Determine the safety and efficacy of tobramycin in patients with cystic fibrosis who are chronically colonized with Pseudomonas aeruginosa. II. Determine whether this treatment produces tobramycin-resistant bacteria at a frequency different from the placebo group and whether the emergence of resistance is associated with a lack of clinical response.

Timeline

Start
1995-06
Primary completion
Completion
1998-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Tobramycin Small molecule Inhaled