Cardiac Safety of Indacaterol
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers, Chronic Obstructive Pulmonary Disease
In brief
This study compares the cardiac safety of inhaled indacaterol with that of placebo and oral moxifloxacin.
Key facts
- Study ID
- NCT01263808
- Run by
- Novartis Pharmaceuticals
- People needed
- 404
- Starts
- 2008-04-01
- Last updated by the study team
- 2010-12-21
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy, non-smoking
- Body mass index (BMI) 18.5-32 kg/m2
- Body weight at least 50 kg
You may not qualify if…
- Recent/concurrent use of concomitant medications (except acetaminophen)
- Recent participation in other clinical trials
- Recent donation or loss of blood
- History/presence of a range of medical conditions, including electrocardiographic (ECG) abnormalities, diabetes mellitus, hyperthyroidism and impaired renal function
- Other protocol-defined inclusion/exclusion criteria may apply
Where it is running
- Novartis investigative site — Miami, Florida, United States
Full record on ClinicalTrials.gov
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