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NCT04493502 · ClinicalTrials.gov registry record · Phase 2

A Study of LY3041658 in Adults With Hidradenitis Suppurativa

A Phase 2 study of Hidradenitis Suppurativa, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
72
Enrollment target
20
Study locations

NCT04493502 is a Phase 2 study of Hidradenitis Suppurativa that has completed, run by Eli Lilly and Company. The registered enrollment target is 72 participants, below the 597-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (88% lower). The trial reports 20 study locations across 14 states.

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The verdict

NCT04493502, a Phase 2 study of Hidradenitis Suppurativa, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
72 participants
Enrollment target
20
Study locations

Study Summary

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

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG LY3041658

Study Locations (20)

Florida

  • Skin Care Research, Inc - Hollywood
  • Nova Clinical Research, LLC - Miami
  • ForCare Clinical Research - Tampa

California

  • First OC Dermatology - Fountain Valley
  • Dermatology Research Associates - Los Angeles

Georgia

  • Marietta Dermatology Clinical Research - Marietta
  • Advanced Medical Research - Sandy Springs

Massachusetts

  • Allcutis Research, Inc. - Beverly
  • Beth Israel Deaconess Medical Center - Boston

Ohio

  • UC Physicians Office Dermatology - Cincinnati
  • University Hospitals Case Medical Center - Cleveland

Arkansas

  • Northwest Arkansas Clinical Trials Center - Rogers

Missouri

  • Washington University School of Medicine - St Louis

New Hampshire

  • ALLCUTIS Research - Portsmouth

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2020-08-26
Est. Completion 2022-10-13
Phase Phase 2

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT04493502

The ClinicalTrials.gov registry entry for NCT04493502 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 597-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (88% lower). The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hidradenitis Suppurativa appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04493502 reports 20 study locations spanning 14 distinct geographic areas - top geographies include Florida, California, Georgia.

Frequently Asked Questions

What is clinical trial NCT04493502 about?

NCT04493502 is a clinical study titled "A Study of LY3041658 in Adults With Hidradenitis Suppurativa". The reason for this study is to see if the study drug LY3041658 is effective in participants with moderate-to-severe hidradenitis suppurativa (HS).

What is the current status of trial NCT04493502?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 72 participants. The study started on 2020-08-26. Estimated completion is 2022-10-13.

What conditions does trial NCT04493502 study?

This clinical trial studies the following conditions: Hidradenitis Suppurativa.

What interventions are being tested in trial NCT04493502?

The interventions under investigation include: Placebo (DRUG), LY3041658 (DRUG).

Who is sponsoring clinical trial NCT04493502?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04493502 being conducted?

This trial has 20 study locations across Arkansas, California, Florida, Georgia, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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