drugset / Trial / NCT01349803

PT003 MDI Cardiovascular Safety Study

NCT01349803

Phase 2 Completed 237 enrolled Pearl Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is primarily a safety study. The primary and secondary endpoints are based on 24-hour Holter monitor assessments obtained on Day 14 relative to baseline.

Timeline

Start
2011-05
Primary completion
2011-11
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Formoterol Other / unclassified 9.6 ug Inhaled
Subject Formoterol Other / unclassified 12 ug Inhaled
Subject Glycopyrrolate Small molecule 36 ug Inhaled