A Study Evaluating TRIV-573 in Atopic Dermatitis
Condition(s) studied
Investigational drug(s) / intervention(s)
TRIV-573: TRIV-573 (Subcutaneous injection)
Placebo: Placebo (Matching Placebo subcutaneous injection)
Study summary
The goal of this interventional study is to learn if TRIV-573 works to treat moderate to severe atopic dermatitis in adults. It will also evaluate the safety of TRIV-573.
Participants will receive 5 doses of the study intervention that they are randomized to (TRIV-573 or placebo).
The study duration for individual participants is up to 40 weeks, including a Screening period of up to 30 days.
Eligibility
Primary outcome measure(s)
- Percentage of participants with improvement of AD — Baseline through Week 16
Trial sites (17)
| Facility | City | Region | Status |
|---|---|---|---|
| Triveni Bio Site #15 | Fountain Valley | California | Recruiting |
| Triveni Bio Site #4 | Los Angeles | California | Recruiting |
| Triveni Bio Site #11 | Boca Raton | Florida | Recruiting |
| Triveni Bio Site #7 | Miami | Florida | Recruiting |
| Triveni Bio Site #3 | Miami | Florida | Recruiting |
| Triveni Bio Site #2 | Indianapolis | Indiana | Recruiting |
| Triveni Bio Site #13 | Bay City | Michigan | Recruiting |
| Triveni Bio Site #16 | Boardman | Ohio | Recruiting |
| Triveni Bio Site #1 | Camp Hill | Pennsylvania | Recruiting |
| Triveni Bio Site #14 | Myrtle Beach | South Carolina | Recruiting |
| Triveni Bio Site #9 | San Antonio | Texas | Recruiting |
| Triveni Bio Site #6 | San Antonio | Texas | Recruiting |
| Triveni Bio Site #8 | Spokane | Washington | Recruiting |
| Triveni Bio Site #17 | Calgary | Alberta | Recruiting |
| Triveni Bio Site #5 | Barrie | Ontario | Recruiting |
| Triveni Bio Site #12 | Ivano-Frankivsk | Ukraine | Recruiting |
| Triveni Bio Site #10 | Kyiv | Ukraine | Recruiting |
More Triveni Bio trials in the USA
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07782333 on ClinicalTrials.gov ↗ ← All trials in the USA