TRIV-573 for moderate to severe atopic dermatitis in adults
Official title: A Phase 2, Randomized, Multicenter, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Multiple Subcutaneous Doses of TRIV-573 in Participants With Moderate to Severe Atopic Dermatitis
Run by Triveni Bio · NCT07782333 · Data updated 2026-11-12
This study tests whether TRIV-573 can help adults with moderate to severe atopic dermatitis and checks its safety.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 90 (estimated) |
| Sponsor | Triveni Bio Industry-sponsored |
| Locations | 17 sites (Fountain Valley, California and 16 other locations) |
| Status | Recruiting |
| Started | September 9, 2026 |
| Main results expected | August 2027 |
| Study ends | February 2028 |
| Registry record updated | October 28, 2026 |
| Trial ID | NCT07782333 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with active, moderate to severe atopic dermatitis.
✕Probably not a fit
Participants with severe uncontrolled medical conditions or those not benefiting from TRIV-573 may not experience an improvement.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This Phase 2 interventional trial will randomize adults with moderate to severe atopic dermatitis to receive five doses of TRIV-573 or placebo. The study lasts up to 40 weeks per participant, including screening up to 30 days. Researchers will monitor efficacy signals and safety outcomes to see if TRIV-573 can improve skin symptoms and overall disease burden compared with placebo.
Why it matters
Potential benefit: If successful, participants could experience improved skin symptoms and quality of life from TRIV-573.
How similar studies have gone: Previous trials of similar agents have shown signals of efficacy in atopic dermatitis, but specific results for TRIV-573 are not yet established.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Has Atopic Dermatitis. * Has moderate to severe, active and symptomatic atopic dermatitis. Exclusion Criteria: * Severe or uncontrolled medical conditions. * Use of prohibited medications within stated washout periods.
Where it's running
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Triveni Bio Site #15
Fountain Valley, California, United States Recruiting -
Triveni Bio Site #4
Los Angeles, California, United States Recruiting -
Triveni Bio Site #11
Boca Raton, Florida, United States Recruiting -
Triveni Bio Site #7
Miami, Florida, United States Recruiting -
Triveni Bio Site #3
Miami, Florida, United States Recruiting -
Triveni Bio Site #2
Indianapolis, Indiana, United States Recruiting
Show 11 more locations
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Triveni Bio Site #13
Bay City, Michigan, United States Recruiting -
Triveni Bio Site #16
Boardman, Ohio, United States Recruiting -
Triveni Bio Site #1
Camp Hill, Pennsylvania, United States Recruiting -
Triveni Bio Site #14
Myrtle Beach, South Carolina, United States Recruiting -
Triveni Bio Site #9
San Antonio, Texas, United States Recruiting -
Triveni Bio Site #6
San Antonio, Texas, United States Recruiting -
Triveni Bio Site #8
Spokane, Washington, United States Recruiting -
Triveni Bio Site #17
Calgary, Alberta, Canada Recruiting -
Triveni Bio Site #5
Barrie, Ontario, Canada Recruiting -
Triveni Bio Site #12
Ivano-Frankivsk, Ukraine Recruiting -
Triveni Bio Site #10
Kyiv, Ukraine Recruiting
Study contacts
- Study coordinator: Triveni Bio, Inc
- Email: clinicaltrials@triveni.bio
- Phone: +1 (781) 472-2230
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Roflumilast Cream 0.3% for moderate to severe atopic dermatitis in children, adolescents, and adults
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ADBest TREAT Registry for adults with atopic dermatitis
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How lebrikizumab affects the skin microbiome and mycobiome in adults with atopic dermatitis
This study looks at whether lebrikizumab changes the skin bacteria, fungi, and specifically Staphylococcus species, in adults with moderate-to-severe atopic dermatitis.
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This study tests the safety and tolerability of QX-4533, given as a pill, in healthy adults and in patients with moderate-to-severe atopic dermatitis to see how the drug behaves in the body and what side effects may occur.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.