Dose Finding Study in COPD

Completed · Phase 2

Conditions studied: Pulmonary Disease, Chronic Obstructive

In brief

The primary objective of this study is to determine the optimum dose of BEA 2180 BR inhalation solut ion delivered by the Respimat ? inhaler once daily for four weeks in patients with COPD.

Key facts

Study ID
NCT00122434
Run by
Boehringer Ingelheim
People needed
389
Starts
2005-07-01
Last updated by the study team
2017-12-28

Who can join

Age: 40 and older, up to 83. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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