ENV-294 for Moderate-to-Severe Asthma: A 12-Week Study in Adults
Enveda Therapeutics · NCT07301255
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 50
- US sites recruiting
- 20
- Study start
- January 9, 2026
- Record last updated
- September 24, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: ENV-294; Placebo
Conditions: Asthma
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
Enveda Investigative Site
Birmingham, AL 35209
Enveda Investigative Site
Los Angeles, CA 90025
Enveda Investigative Site
San Jose, CA 95117
Enveda Investigative Site
West Hills, CA 91307
Enveda Investigative Site
Colorado Springs, CO 80907
Enveda Investigative Site
Hialeah, FL 33012
Enveda Investigative Site
Miami, FL 33135
Enveda Investigative Site
Albany, GA 31707
Enveda Investigative Site
Maryville, IL 62062
Enveda Investigative Site
Kansas City, KS 66160
Enveda Investigative Site
Owensboro, KY 42301
Enveda Investigative Site
Boston, MA 02115
Enveda Investigative Site
Southfield, MI 48075
Enveda Investigative Site
St Louis, MO 63141
Enveda Investigative Site
The Bronx, NY 10455
Enveda Investigative Site
Clackamas, OR 97015
Enveda Investigative Site
Medford, OR 97504
Enveda Investigative Site
North Charleston, SC 29406
Enveda Investigative Site
McKinney, TX 75069
Enveda Investigative Site
Madison, WI 53792
Study contacts (from the official record)
- Clinical Operations · env-294.clinicaltrials@enveda.com