Trial name or title |
Dose‐finding Study to Assess the Efficacy, Safety and Tolerability of Tobramycin Inhalation Powder in Patients With Non‐Cystic Fibrosis Bronchiectasis and Pulmonary P. Aeruginosa Infection (iBEST‐1) |
Methods |
Parallel group randomized trial |
Participants |
Patients with non‐cystic fibrosis bronchiectasis and pulmonary P Aeruginosa infection |
Interventions |
tobramycin inhalation powder (TIP) dose and placebo, 3 dose regimens |
Outcomes |
P aeruginosa density in sputum |
Starting date |
2 February 2017 |
Contact information |
Novartis Pharmaceuticals: email: trialandresults.registries@novartis.com |
Notes |
Estimated completion date: 10 September 2018 |