drugset / Trial / NCT07610395

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

NCT07610395 ↗

Phase 2 Recruiting 180 enrolled Altesa Biosciences, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2026-05-01
Primary completion
2027-11-15
Completion
2027-11-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Vapendavir Small molecule 500 mg Oral
Subject Vapendavir Small molecule 1000 mg Oral