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Active Not RecruitingNCT06046729

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

A Phase 2b, Double-Blind, Placebo-Controlled Study to Evaluate Eltrekibart in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
352 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGEltrekibartAdministered SC
DRUGPlaceboAdministered SC

Timeline

Start date
2023-10-23
Primary completion
2025-09-30
Completion
2026-08-01
First posted
2023-09-21
Last updated
2025-10-16

Locations

74 sites across 6 countries: United States, Australia, Canada, Germany, Greece, Poland

Regulatory

Source: ClinicalTrials.gov record NCT06046729. Inclusion in this directory is not an endorsement.

A Study of Eltrekibart (LY3041658) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa (NCT06046729) · Clinical Trials Directory