drugset / Trial / NCT07167758

A Study Evaluating TRIV-509 in Atopic Dermatitis

NCT07167758 ↗

Phase 2 Active not recruiting 95 enrolled Triveni Bio
RandomizedCrossoverQuadruple-blindTreatment

Summary

The goal of this interventional study is to learn if TRIV-509 works to treat moderate to severe atopic dermatitis in adults. It will also evaluate the safety of TRIV-509. Participants will receive 4 doses of the study intervention that they are randomized to (TRIV-509 or placebo), and at Week 16 will cross over and receive 4 doses of the other study intervention. The study duration for individual participants is up to 57 weeks, including a Screening period of up to 30 days.

Timeline

Start
2025-08-26
Primary completion
2026-10
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject TRIV-509 Unknown — Subcutaneous

Indications