Trial Comparing the Safety and Efficacy of Two Different Oral VPV Doses With Placebo as Treatment for RV in Participants With COPD

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age40-85
SponsorAltesa Biosciences, Inc.

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

Treatment groups

180 Participants
are divided into 3 treatment groups

Sponsors and collaborators