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NCT07301255PHASE2Recruiting

ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults

Enveda Therapeutics

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

Inclusion Criteria: * Able to read, understand, and sign an informed consent form before any study procedures * Male or female adults aged 18 to 75 years with a physician diagnosis of moderate to severe asthma for at least 12 months * Receiving stable treatment with an inhaled corticosteroid (ICS) plus a long-acting beta₂-agonist (LABA) for at least 2 months before screening * Pre-bronchodilator FEV₁ between 50% and 80% of predicted normal at screening and baseline * Demonstrated bronchodilator reversibility * ACQ-5 score ≥1.25 to ≤3.0 at screening and baseline * History of at least one asthma exacerbation in the past 12 months requiring systemic corticosteroids or hospitalization/emergency care Exclusion Criteria: * Recent moderate or severe asthma exacerbation (within 4 weeks before screening) * History of life-threatening asthma * Other significant pulmonary disease * Recent bronchial thermoplasty (within 2 years) * Uncontrolled current or recurrent concomitant illness * Recent use of biologic therapies for asthma (within 6 months or 5 half-lives) * Require immunosuppressive medications or frequent systemic corticosteroids * Current smokers or former smokers with significant smoking history * Uncontrolled hypertension * Significant hepatic impairment

Interventions

DRUG

ENV-294

DRUG

Placebo

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Conditions

Asthma

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