ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults (NCT07301255)
A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ENV-294 in Adult Participants With Moderate-to-Severe Asthma
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Enveda Investigative Site — Birmingham, Alabama
Age range: 18 Years to 75 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (18 Sites)
- Enveda Investigative Site — Birmingham, Alabama
- Enveda Investigative Site — Los Angeles, California
- Enveda Investigative Site — San Jose, California
- Enveda Investigative Site — West Hills, California
- Enveda Investigative Site — Colorado Springs, Colorado
- Enveda Investigative Site — Hialeah, Florida
- Enveda Investigative Site — Miami, Florida
- Enveda Investigative Site — Albany, Georgia
- Enveda Investigative Site — Maryville, Illinois
- Enveda Investigative Site — Kansas City, Kansas
- Enveda Investigative Site — Owensboro, Kentucky
- Enveda Investigative Site — Southfield, Michigan
- Enveda Investigative Site — St Louis, Missouri
- Enveda Investigative Site — Clackamas, Oregon
- Enveda Investigative Site — Medford, Oregon
- Enveda Investigative Site — North Charleston, South Carolina
- Enveda Investigative Site — McKinney, Texas
- Enveda Investigative Site — Madison, Wisconsin
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Asthma
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- Efficacy of Dupilumab Added to Medium Dose Inhaled Corticosteroid/Long-acting Beta-agonist (ICS/LABA) in Comparison to ICS Dose Escalation to High Dose ICS/LABA in Adolescent and Adult Patients With Uncontrolled Asthma — Bakersfield, California
- Study of Lunsekimig (SAR443765) Compared With Placebo in Adults With High-risk Asthma — Saraland, Alabama
- Reduce IDentified UNcontrolled Asthma — San Diego, California
- A Dose Finding Study With an Anti-TSLP Antibody (GSK5784283) in Adults Aged 18 to 75 Years of Age With Uncontrolled Asthma — Little Rock, Arkansas
- REIMAGINE - Real World EvaluatIon of Mepolizumab in Severe Asthma achievinG on Treatment clinIcal remissioN, a prospEctive Study — La Jolla, California
Explore by condition: All Asthma clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.