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Terminated Phase 2 Interventional

Study of Daxdilimab (HZN-7734) in Participants With Moderate-to-Severe Primary Discoid Lupus Erythematosus

ClinicalTrials.gov ID: NCT05591222

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT05591222. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 2:41 PM EST

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Official title

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Trial to Investigate the Efficacy and Safety of Daxdilimab Subcutaneous Injection in Reducing Disease Activity in Adult Participants With Moderate-to-Severe Primary Discoid Lupus Erythematosus

Brief summary

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

A Phase 2, double-blind, randomized, placebo-controlled parallel-group study to evaluate the efficacy and safety of daxdilimab in participants with moderate-to-severe active primary Discoid Lupus Erythematosus (DLE) refractory to standard of care.

Study identification

NCT ID
NCT05591222
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Amgen
Industry
Enrollment
72 participants

Conditions and interventions

Interventions

Drug

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
Dec 29, 2022 (Actual)
Primary completion
May 8, 2025 (Actual)
Completion
May 8, 2025 (Actual)
Last update posted
May 14, 2026

2022 – 2025

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Arkansas Research Trials North Little Rock Arkansas 72117 —
Wallace Medical Group Beverly Hills California 90211 —
The Center for Dermatology Clinical Research Fremont California 94538 —
Clinical Science Institute Santa Monica California 90404 —
Miami Dermatology & Laser Research Miami Florida 33173 —
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46250 —
Detroit Clinical Research Center, PC Farmington Hills Michigan 48334 —
Michigan Dermatology Institute Waterford Michigan 48328 —
Minnesota Clinical Study Center New Brighton Minnesota 55112 —
MediSearch Clinical Trials Saint Joseph Missouri 64506 —
Forest Hills Dermatology Forest Hills New York 11375 —
Ohio State University Columbus Ohio 43210 —
Wright State Physicians Fairborn Ohio 45324 —
Paddington Testing Company, Inc. Philadelphia Pennsylvania 19103 —
Autoimmune Skin Diseases Unit, Dept. of Dermatology Philadelphia Pennsylvania 19104 —
Center for Clinical Studies (Cypress) Houston Texas 77065 —

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05591222, 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 May 14, 2026 · Synced Nov 12, 2026

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