Trial Comparing the Safety and Efficacy of Two Different Oral VPV Doses With Placebo as Treatment for RV in Participants With COPD
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Rhinovirus Infection
In brief
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.
Key facts
- Study ID
- NCT07610395
- Run by
- Altesa Biosciences, Inc.
- People needed
- 180
- Starts
- 2026-05-01
- Expected to finish
- 2027-11-15
- Last updated by the study team
- 2026-06-24
Who can join
Age: 40 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
Where it is running
- AMR Clinical - Tempe — Tempe, Arizona, United States (enrolling)
- NewportNativeMD, Inc. — Newport Beach, California, United States (enrolling)
- Apex Clinical Research — San Diego, California, United States (enrolling)
- VM Clintrials — Miami Lakes, Florida, United States (enrolling)
- Accelerated Clinical Trials, LLC — Snellville, Georgia, United States (enrolling)
- Velocity Clinical Research - Valparaiso — Valparaiso, Indiana, United States (enrolling)
- Patient First Clinical Trials (PFCTRIALS) — Lutherville, Maryland, United States (enrolling)
- Brooklyn Clinical Research — Brooklyn, New York, United States (enrolling)
- CRC Kings Mountain — Kings Mountain, North Carolina, United States (enrolling)
- Remington-Davis, Inc. — Columbus, Ohio, United States (enrolling)
- Clinical Research Associates of Central PA, LLC — DuBois, Pennsylvania, United States (enrolling)
- Preferred Primary Care Physicians - St. Clair — Pittsburgh, Pennsylvania, United States (enrolling)
- Velocity Clinical Research - Anderson — Anderson, South Carolina, United States (enrolling)
- Clinical Research of Rock Hill — Rock Hill, South Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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