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Recruiting Phase 3 Interventional

A Study of Enpatoran in Participants With Cutaneous Manifestations of Lupus With or Without Systemic Disease

ClinicalTrials.gov ID: NCT07332481

Public ClinicalTrials.gov record NCT07332481. 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 1, 2026, 1:21 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 Phase 3, Randomized, Double-Blind,Placebo-Controlled Parallel Study to Evaluate the Efficacy and Safety of Enpatoran in Participants With Active Cutaneous Manifestations of Lupus Erythematosus With or Without Systemic Disease Receiving Standard of Care (ELOWEN-1)

Brief summary

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

The purpose of this global, multicenter, Phase 3 study is to evaluate the efficacy and safety of enpatoran over 24 weeks in participants with active cutaneous manifestations of lupus erythematosus with or without systemic disease. Study details include: Study Duration: Up to 35 weeks. Treatment Duration: 24 weeks. Visit Frequency: every 4 weeks, with the exception of the Week 2 televisit. Study Intervention Name: Enpatoran, Placebo. Intervention Form: Film-coated tablet.

Study identification

NCT ID
NCT07332481
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Enrollment
202 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 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
Mar 9, 2026
Primary completion
May 23, 2029
Completion
May 23, 2029
Last update posted
Aug 13, 2026

2026 – 2029

United States locations

U.S. sites
12
U.S. states
5
U.S. cities
10
Facility City State ZIP Site status
Dermatology Research Associates - 300204025 Los Angeles California 90045 Recruiting
Cohen Medical Centers Thousand Oaks California 91360 Recruiting
GNP Research at Mark Jaffe, MD Cooper City Florida 33024 Recruiting
Advance Medical Research Center Miami Florida 33135 Recruiting
Diverse Clinical Research LLC Miami Florida 33175 Recruiting
D&H National Research Centers, Inc. Tamarac Florida 33321 Recruiting
Clinical Research of West Florida, Inc. Tampa Florida 33606 Recruiting
Emory University School of Medicine Atlanta Georgia 30303 Recruiting
Revival Research Institute, LLC Troy Michigan 48084 Recruiting
Allen Arthritis Allen Texas 75013 Recruiting
Arthritis and Rheumatology Research Institute PLLC Allen Texas 75013 Recruiting
Arthritis Care of Texas Corpus Christi Texas 78415 Recruiting

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07332481, 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 Aug 13, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07332481 live on ClinicalTrials.gov.

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