drugset / Trial / NCT06046729

A Study of Eltrekibart (LY3041658) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

NCT06046729

Phase 2 Active not recruiting 352 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to find the appropriately safe and effective dose and dosing frequency for eltrekibart in adults with moderate-to-severe hidradenitis suppurativa (HS) for further clinical development. The study will last approximately 62 weeks and may include up to 31 visits.

Timeline

Start
2023-10-23
Primary completion
2025-09-30
Completion
2026-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Eltrekibart Monoclonal antibody Subcutaneous