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

NCT07301255 · Enveda Therapeutics
In plain English

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Official title
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
About this study
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
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
Study design
Enrollment target: 50 participants
Allocation: randomized
Masking: quadruple
Age groups: adult, older_adult
Timeline
Starts: 2026-01-09
Estimated completion: 2027-01
Last updated: 2026-04-23
Interventions
Drug: ENV-294Drug: Placebo
Primary outcomes
  • Incidence and Severity of Adverse Events (From first dose through approximately 16 weeks)
Sponsor
Enveda Therapeutics · industry
Contacts & investigators
ContactClinical Operations · contact · env-294.clinicaltrials@enveda.com
InvestigatorGurpreet Ahluwalia, PhD · study_director, Enveda Therapeutics, Inc.
All locations (14)
Enveda Investigative SiteRecruiting
Birmingham, Alabama, United States
Enveda Investigative SiteRecruiting
Los Angeles, California, United States
Enveda Investigative SiteRecruiting
San Jose, California, United States
Enveda Investigative SiteRecruiting
Colorado Springs, Colorado, United States
Enveda Investigative SiteRecruiting
Hialeah, Florida, United States
Enveda Investigative SiteRecruiting
Albany, Georgia, United States
Enveda Investigative SiteRecruiting
Owensboro, Kentucky, United States
Enveda Investigative SiteRecruiting
Southfield, Michigan, United States
Enveda Investigative SiteRecruiting
St Louis, Missouri, United States
Enveda Investigative SiteRecruiting
Clackamas, Oregon, United States
Enveda Investigative SiteRecruiting
Medford, Oregon, United States
Enveda Investigative SiteRecruiting
North Charleston, South Carolina, United States
Enveda Investigative SiteRecruiting
McKinney, Texas, United States
Enveda Investigative SiteNot Yet Recruiting
Madison, Wisconsin, United States
ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults · TrialPath