drugset / Trial / NCT00726479

Safety and Efficacy of 4-weeks Treatment of BIBW 2948 BS in Patients With Chronic Obstructive Bronchitis

NCT00726479 ↗

Phase 2 Withdrawn Boehringer Ingelheim
Parallel-groupTreatment

Summary

The primary objective of this study is to investigate the effect of 4-week treatment with 7.5 mg b.i.d, 15 mg q.d and 15 mg b.i.d. BIBW 2948 BS and placebo on cough and sputum as determined by the CASA-Q (Cough and Sputum Assessment Questionnaire

Timeline

Start
2008-08
Primary completion
2008-09
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BIBW 2948 BS Unknown 7.5 mg Inhaled
Subject BIBW 2948 BS Unknown 15 mg Inhaled

Indications