A Study to Assess the Safety Tolerability and Efficacy of ION-827359 in Patients With Mild to Moderate Chronic Obstructive Pulmonary Disease (COPD) With Chronic Bronchitis (CB)

  • STATUS
    Recruiting
  • days left to enroll
    87
  • participants needed
    180
  • sponsor
    Ionis Pharmaceuticals, Inc.
Updated on 19 May 2021

Summary

The purpose of this study is to evaluate the effect of ION-827359 on forced expiratory volume in 1 second (FEV1) in patients with mild to moderate COPD with CB.

Description

This is a multi-center, double-blind, placebo-controlled, randomized, Phase 2a study of ION-827359 in up to 180 participants. The participants will be randomized to receive oral inhalation of either ION-827359 or placebo for up to 13 weeks. At the end of 13 weeks, participants will enter a 10-week post-treatment evaluation period.

Details
Condition Chronic Obstructive Lung Disease, Chronic bronchitis, COPD (Chronic Obstructive Pulmonary Disease), chronic obstructive pulmonary disease, COPD, chronic obstructive pulmonary disease (copd)
Treatment Placebo, ION-827359
Clinical Study IdentifierNCT04441788
SponsorIonis Pharmaceuticals, Inc.
Last Modified on19 May 2021

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