drugset / Trial / NCT02172118

BI 1744 CL in Patients With Severe Renal Impairment in Comparison to Subjects With Normal Renal Function

NCT02172118 ↗

Phase 1 Completed 22 enrolled Boehringer Ingelheim
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Study to assess the influence of severe renal impairment on the pharmacokinetics (PK), safety, and selected pharmacodynamic (PD) parameters of BI 1744 CL (30 μg administered by inhalation with the Respimat® Inhaler)

Timeline

Start
2009-08
Primary completion
2009-12
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 1774 CL Unknown 30 ug Inhaled

Indications

No indication recorded.