drugset / Trial / NCT02263976

Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of BEA 2180 BR in Healthy Male Subjects

NCT02263976

Phase 1 Completed 101 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Main study: To investigate safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of BEA 2180 BR Sub-study; To investigate whether treatment with 36 μg tiotropium bromide is able to protect of methacholine-induced bronchoconstriction compared to baseline (methacholine challenge at screening).

Timeline

Start
2003-08
Primary completion
2004-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BEA 2180 BR Unknown 2.5 ug Inhaled
Subject BEA 2180 BR Unknown 1600 ug Inhaled
Subject Tiotropium Other / unclassified 36 ug

Indications

No indication recorded.