drugset / Trial / NCT07277660

A Dose-ranging Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Galvokimig in Adult Study Participants With Atopic Dermatitis

NCT07277660 ↗

Phase 2 Recruiting 160 enrolled UCB Biopharma SRL
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the dose-response relationship of galvokimig compared with placebo in study participants with moderate-to-severe atopic dermatitis (AtD).

Timeline

Start
2025-12-29
Primary completion
2027-05-17
Completion
2028-03-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Galvokimig Monoclonal antibody — —

Indications