ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults
Start Date
1/9/2026
Completion Date
1/1/2027
Summary
This study will evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and potential efficacy of ENV-294 in adults with moderate to severe asthma who are receiving background treatment with inhaled corticosteroids (ICS) and long-acting beta₂-agonists (LABA). Participants will take oral ENV-294 or placebo once daily for 12 weeks. The study includes a screening period of up to 28 days before randomization to confirm eligibility. Study visits and assessments will be conducted to monitor safety, measure drug levels in the blood, and evaluate effects on asthma control and lung function.
Eligibility Criteria
Age Range: 18 years to 75 years
Interventions
ENV-294
Placebo
Conditions
Locations
Enveda Investigative Site
Birmingham, Alabama 35209
United States
Enveda Investigative Site
Los Angeles, California 90025
United States
Enveda Investigative Site
San Jose, California 95117
United States
Enveda Investigative Site
West Hills, California 91307
United States
Enveda Investigative Site
Colorado Springs, Colorado 80907
United States
Enveda Investigative Site
Hialeah, Florida 33012
United States
Enveda Investigative Site
Miami, Florida 33135
United States
Enveda Investigative Site
Albany, Georgia 31707
United States
Enveda Investigative Site
Maryville, Illinois 62062
United States
Enveda Investigative Site
Kansas City, Kansas 66160
United States
Enveda Investigative Site
Owensboro, Kentucky 42301
United States
Enveda Investigative Site
Southfield, Michigan 48075
United States
Enveda Investigative Site
St Louis, Missouri 63141
United States
Enveda Investigative Site
Clackamas, Oregon 97015
United States
Enveda Investigative Site
Medford, Oregon 97504
United States
Enveda Investigative Site
North Charleston, South Carolina 29406
United States
Enveda Investigative Site
McKinney, Texas 75069
United States
Enveda Investigative Site
Madison, Wisconsin 53792
United States