● Recruiting

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

Condition: Rhinovirus Infection · Sponsor: Altesa Biosciences, Inc.

PhasePhase 2

Planned participants180

Who can joinAll sexes, 40 Years to 85 Years

Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Karen Fusaro · 610-242-0903 · kfusaro@altesa.com

Always discuss trial participation with your own doctor first.

Locations (14)

AMR Clinical - Tempe	Tempe, Arizona, United States	Recruiting
NewportNativeMD, Inc.	Newport Beach, California, United States	Recruiting
Apex Clinical Research	San Diego, California, United States	Recruiting
VM Clintrials	Miami Lakes, Florida, United States	Recruiting
Accelerated Clinical Trials, LLC	Snellville, Georgia, United States	Recruiting
Velocity Clinical Research - Valparaiso	Valparaiso, Indiana, United States	Recruiting
Patient First Clinical Trials (PFCTRIALS)	Lutherville, Maryland, United States	Recruiting
Brooklyn Clinical Research	Brooklyn, New York, United States	Recruiting
CRC Kings Mountain	Kings Mountain, North Carolina, United States	Recruiting
Remington-Davis, Inc.	Columbus, Ohio, United States	Recruiting
Clinical Research Associates of Central PA, LLC	DuBois, Pennsylvania, United States	Recruiting
Preferred Primary Care Physicians - St. Clair	Pittsburgh, Pennsylvania, United States	Recruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07610395