About this trial
Compare the safety and efficacy of two different oral vapendavir doses with placebo in order to determine the appropriate dose of vapendavir to reduce the severity and/or duration of respiratory symptoms associated with RV infections in patients with COPD.
Eligibility criteria
Qualifiers
Increase frequency or dose of beta agonist(s), oxygen, breathing treatments or chronic COPD medications (Mild Exacerbation)
Use of oral or systemic steroids (Moderate Exacerbation), or
Use of Antibiotics (Moderate Exacerbation), or
Emergency room visit or hospitalization (Severe Exacerbation). CAT score ≥10 at screening. Able to comply with all study requirements, including the use of a mobile application to complete daily PROs, perform nasal swabs at home, and able to assess when they have cold symptoms.
Disqualifiers
None
Trial design
Treatments tested in this trial
- VPV 1000 mg
- VPV 500 mg
- Placebo