drugset / Trial / NCT01566773

PT001 MDI Versus Spiriva® in Patients With Moderate to Severe COPD

NCT01566773

Phase 2 Completed 140 enrolled Pearl Therapeutics, Inc.
RandomizedCrossoverQuadruple-blindTreatment

Summary

The overall objective of this study is to determine an optimal dose and dosing regimen of PT001 MDI for further evaluation in later stage studies.

Timeline

Start
2012-03
Primary completion
2012-08
Completion
2012-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrrolate Small molecule 0.6 ug Inhaled
Subject Glycopyrrolate Small molecule 1.2 ug Inhaled
Subject Glycopyrrolate Small molecule 2.4 ug Inhaled
Subject Glycopyrrolate Small molecule 4.6 ug Inhaled
Subject Glycopyrrolate Small molecule 9 ug Inhaled
Subject Glycopyrrolate Small molecule 18 ug Inhaled
Comparator Tiotropium Other / unclassified 18 ug Inhaled