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Completed Phase 2 Interventional Results available

A Study of LY3041658 in Adults With Hidradenitis Suppurativa

ClinicalTrials.gov ID: NCT04493502

Public ClinicalTrials.gov record NCT04493502. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 26, 2026, 5:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of LY3041658 in Adults With Moderate-to-Severe Hidradenitis Suppurativa

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The reason for this study is to see if the study drug LY3041658 is effective in participants with moderate-to-severe hidradenitis suppurativa (HS).

Study identification

NCT ID
NCT04493502
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
72 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 25, 2020
Primary completion
Mar 14, 2022
Completion
Oct 12, 2022
Last update posted
Apr 27, 2023

2020 – 2022

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
Northwest Arkansas Clinical Trials Center Rogers Arkansas 72758 —
First OC Dermatology Fountain Valley California 92708 —
Dermatology Research Associates Los Angeles California 90045 —
Skin Care Research, Inc Hollywood Florida 33021 —
Nova Clinical Research, LLC Miami Florida 33125 —
ForCare Clinical Research Tampa Florida 33613-1244 —
Marietta Dermatology Clinical Research Marietta Georgia 30060 —
Advanced Medical Research Sandy Springs Georgia 30328 —
Allcutis Research, Inc. Beverly Massachusetts 01915 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Washington University School of Medicine St Louis Missouri 63110 —
ALLCUTIS Research Portsmouth New Hampshire 03801 —
Duke University Medical Center Durham North Carolina 27710 —
UC Physicians Office Dermatology Cincinnati Ohio 45267 —
University Hospitals Case Medical Center Cleveland Ohio 44106 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04493502, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 27, 2023 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04493502 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →