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NOT YET RECRUITING
NCT07782333
PHASE2

A Study Evaluating TRIV-573 in Atopic Dermatitis

Sponsor: Triveni Bio

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

90

Start Date

2026-08

Completion Date

2028-02

Last Updated

2026-08-24

Healthy Volunteers

No

Interventions

DRUG

TRIV-573

TRIV-573 (Subcutaneous injection)

DRUG

Placebo

Placebo (Matching Placebo subcutaneous injection)