drugset / Trial / NCT02173678

Safety and Tolerability of COMBIVENT® HFA as Compared to COMBIVENT® CFC and Placebo HFA in Healthy Male and Female Subjects

NCT02173678

Phase 1 Completed 12 enrolled Boehringer Ingelheim
RandomizedCrossoverDouble-blindTreatment

Summary

Study to assess the safety and tolerability of COMBIVENT® hydrofluoroalkane (HFA) as compared to COMBIVENT® chlorofluorocarbons (CFC) and placebo HFA after single and repetitive dosing in healthy male and female subjects

Timeline

Start
1999-10
Primary completion
1999-11
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipratropium Small molecule 288 ug Inhaled
Subject Salbutamol Unknown 1600 ug Inhaled
Subject Salbutamol Unknown 1648 ug Inhaled

Indications

No indication recorded.