Help move asthma care forward

Participants receive up to $2000
compensation for completing
the study

Find out if you may be eligible to participate

Now enrolling participants for a
Phase 2a clinical trial

This clinical study tests whether ENV-294 is effective in
treating moderate-to-severe asthma.

ENV-294 is an Investigational New Drug (IND). Participation in this study is voluntary and may not provide direct medical Benefit.


dependent on clinical site participation

From nature.
For Asthma.

Asthma affects more than your airways. It can impact your comfort, confidence, and quality of life. ENV-294 is a new oral investigation medicine derived from a plant used for centuries to soothe inflammation. This trial is testing how it may help people living with moderate-to-severe asthma.

Find out if you may be eligible in less than 1 minute

Check if you may be eligible to participate

Some conditions may prevent people from joining; see details.

Key Inclusion/Exclusion Criteria for Asthma Protocol Phase 2a

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, defined as ≥12% and ≥200 mL improvement in FEV1 (or ≥20% increase in peak expiratory flow) after short-acting bronchodilator use.
  • ACQ-5 score ≥1.25 and ≤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

  • Had a moderate or severe asthma exacerbation within 4 weeks before screening.
  • Have a history of life-threatening asthma, including intubation or respiratory arrest.
  • Have any other significant pulmonary disease (e.g., COPD, bronchiectasis, pulmonary fibrosis, cystic fibrosis, tuberculosis, lung cancer, or eosinophilic syndromes).
  • Had bronchial thermoplasty within 2 years before screening.
  • Used biologic therapies for asthma (e.g., benralizumab, mepolizumab, reslizumab, omalizumab, dupilumab, or tezepelumab) within 6 months or 5 half-lives prior to baseline.
  • Require immunosuppressive medications or frequent systemic corticosteroids (more than 3 courses in the past 6 months).
  • Are current smokers or former smokers with >10 pack-year history or who quit within 6 months before screening.
  • Have uncontrolled hypertension (systolic ≥160 mmHg or diastolic >95 mmHg).
  • Have significant hepatic impairment or any other condition that, in the investigator's opinion, would interfere with study participation or interpretation of results.

Answer 7 questions to see if you
may be eligible to participate

Receive up to $2000 compensation for completing the study

Participants receive

Asthma care from a study
doctor—no insurance needed

Compensation for
time and travel

No-cost service to and
from the study site

Find a nearby location

      About the Company

      Enveda uses the power of nature to discover new medicines. The company combines plant science with advanced technology like artificial intelligence and chemistry tools to find and study natural components that could become new treatments for diseases.

      Our Mission

      FAQs

      What’s a clinical study?

      It’s how new medicines are discovered and proven to work. Every prescription today started with volunteer participants

      Why do people join?

      Some want to help others. Some hope new treatments might work for them. Many join to support science and to learn more about their own health.

      Who can participate?

      Men and women ages 18 to 75 with moderate-to-severe asthma may qualify if diagnosed at least 12 months prior to the screening, are using a combination inhaler and your medication plan has been stable for at least 2 months. Participants must have asthma that is not fully controlled based on your doctor’s assessment and have had at least one asthma flare-up in the past year (but not in the past 4–8 weeks) that required steroid treatment, an emergency visit, or a hospital stay. Exclusions apply.

      Will I receive the investigational drug?

      This is a double blinded study, meaning some participants will receive the investigational drug while others will receive a placebo.

      Is it safe?

      Your safety comes first. The study is reviewed by an independent review board (IRB) and conducted by doctors who will monitor your health closely.

      Will my information be private?

      Your personal information will be kept confidential and de-identified whenever possible, unless required by law. The study doctor, the sponsor or persons working on behalf of the sponsor, and under certain circumstances, the United States Food and Drug Administration (FDA) and the Institutional Review Board (IRB) will be able to inspect and copy confidential study-related records which identify a participant by name.

      What's the time commitment?

      You’ll receive all details before joining, including the number of visits, how long each visit lasts, and the study duration.

      Are participants compensated?

      Yes. Participants may be compensated for their time and travel. The exact compensation amount is based on factors such as study-visit length, number of study visits, and travel distance.

      Can I change my mind?

      Yes, you can leave the study anytime, for any reason.

      What happens after the study ends?

      Upon completion, participants will resume ongoing medical care with their regular healthcare providers.