Study of ENV-294 in Adults With Moderate-to-Severe Atopic Dermatitis
Enveda Therapeutics · NCT07298395
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
- 105
- US sites recruiting
- 32
- Study start
- December 22, 2025
- Record last updated
- September 25, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this clinical trial is to learn about the safety and effectiveness of ENV-294 in adults with moderate to severe atopic dermatitis.
The main questions it will answer are
- Is there an impact on the severity and area of atopic dermatitis when participants take ENV-294
- What medical problems do participants have when taking ENV-294
Participants will
- Take drug ENV-294 or a placebo once every day for 12 weeks
- Visit the clinic every 2 to 4 weeks for checkups and tests
- Keep a diary of their symptoms and when they took their study drug
- Return to the clinic for the final study visit at approximately week 16
Being studied: ENV-294; Placebo
Conditions: Atopic Dermatitis (AD)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Have chronic atopic dermatitis that was diagnosed at least 12 months prior to the first study visit
- Have moderate-to-severe AD at screening and baseline as defined by the following criteria:
- A vIGA score of 3 (moderate) or 4 (severe)
- EASI score of ≥16
- BSA ≥10%
- PP-NRS score of ≥4
- Have had either a poor response or intolerance to topical treatments for atopic dermatitis (such as corticosteroids) within the past 6 months
- Use a bland moisturizer at least daily
Exclusion Criteria
- Current or recurrent medical conditions that could affect the study drug or study assessments
- Any illness that could impact participant safety or active infections
- Ongoing skin condition or large tattoos that would interfere with clinical assessment
- Clinically significant skin infection requiring treatment
- Clinically significant abnormal laboratory assessments at screening
Recruiting US locations
Enveda Investigative Site
Birmingham, AL 35244
Enveda Investigative Site
Hot Springs, AR 71913
Enveda Investigative Site
Beverly Hills, CA 90212
Enveda Investigative Site
Fremont, CA 94538
Enveda Investigative Site
San Diego, CA 92121
Enveda Investigative Site
San Diego, CA 92123
Enveda Investigative Site
Santa Monica, CA 90403
Enveda Investigative Site
West Hills, CA 91307
Enveda Investigative Site
Fort Lauderdale, FL 33308
Enveda Investigative Site
Miami, FL 33175
Enveda Investigative Site
Miramar, FL 33027
Enveda Investigative Site
Atlanta, GA 30327
Enveda Investigative Site
Chicago, IL 60657
Enveda Investigative Site
Clarksville, IN 47129
Enveda Investigative Site
New Albany, IN 47150
Enveda Investigative Site
West Lafayette, IN 47906
Enveda Investigative Site
Louisville, KY 40217
Enveda Investigative Site
Louisville, KY 40241
Enveda Investigative Site
Auburn Hills, MI 48326
Enveda Investigative Site
Bay City, MI 48706
Enveda Investigative Site
Clinton Township, MI 48038
Enveda Investigative Site
Warren, MI 48088
Enveda Investigative Site
Las Vegas, NV 89145
Enveda Investigative Site
New York, NY 10029
Enveda Investigative Site
Wilmington, NC 28405
Enveda Investigative Site
Canton, OH 44718
Enveda Investigative Site
Mayfield Heights, OH 44124
Enveda Investigative Site
Camp Hill, PA 17011
Enveda Investigative Site
Arlington, TX 76011
Enveda Investigative Site
Houston, TX 77004
Enveda Investigative Site
San Antonio, TX 78218
Enveda Investigative Site
Norfolk, VA 23502
Study contacts (from the official record)
- Clinical Operations · env-294.clinicaltrials@enveda.com
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