Overview

Safety of Indacaterol in Patients (≥ 12 Years) With Moderate to Severe Persistent Asthma

Status:
Completed
Trial end date:
2008-08-01
Target enrollment:
Participant gender:
Summary
This study was designed to assess the safety of indacaterol (300 µg and 600 µg (2 x 300 μg capsules) once daily [od]), compared with salmeterol (50 μg twice a day [b.i.d.]), over 26 weeks, in patients with moderate to severe persistent asthma.
Phase:
Phase 3
Details
Lead Sponsor:
Novartis Pharmaceuticals
Treatments:
Salmeterol Xinafoate