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A multi-centre randomized double blind 52-week study to assess the safety of QVA149 compared to QAB149 in patients with COPD who have moderate to severe airflow limitation

Update Il y a 4 ans
Reference: EUCTR2012-001998-93

Woman and Man

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Extract

To evaluate the safety and tolerability of QVA149 27.5/12.5 μg b.i.d. and QVA149 27.5/25 μg b.i.d. in terms of adverse event reporting rate in patients with Chronic Obstructive Pulmonary Disease (COPD) with moderate to severe airflow limitation during 52 weeks of treatment.

Inclusion criteria

  • Chronic Obstructive Pulmonary Disease (COPD)

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