drugset / Trial / NCT03081247

To Assess the Efficacy and Safety of PT010 Compared to PT009 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease

NCT03081247

Phase 3 Withdrawn Pearl Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a 12-week chronic-dosing study to assess the efficacy and safety of BGF MDI compared to BFF MDI in subjects with moderate to very severe COPD.

Timeline

Start
2018-04-16
Primary completion
2018-12-07
Completion
2018-12-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrronium Unknown 14.4 ug Inhaled
Background Budesonide Small molecule 320 ug Inhaled
Background Formoterol Other / unclassified 9.6 ug Inhaled