drugset / Trial / NCT07151937

A Study of LAD191 in Adults With Hidradenitis Suppurativa

NCT07151937

Phase 2 Recruiting 200 enrolled Almirall, S.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main purpose of this study is to assess the efficacy of multiple dosing regimens of LAD191 compared to placebo in participants with moderate-to-severe Hidradenitis Suppurativa (HS) and to access the safety, tolerability, pharmacokinetic and immunogenicity in participants with moderate-to-severe HS.

Timeline

Start
2025-11-05
Primary completion
2027-05-25
Completion
2027-11-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody Subcutaneous
Subject LAD191 Unknown Subcutaneous