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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

Subcutaneous Anifrolumab in Adult Patients With Systemic Lupus Erythematosus

ClinicalTrials.gov ID: NCT04877691

Public ClinicalTrials.gov record NCT04877691. 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 Jul 24, 2026, 5:47 AM 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 Multicentre, Randomised, Double-Blind, Placebo-controlled, Phase 3 Study Evaluating the Efficacy and Safety of Subcutaneous Anifrolumab in Adult Patients With Systemic Lupus Erythematosus

Study identification

NCT ID
NCT04877691
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
367 participants

Conditions and interventions

Interventions

  • Medi-546 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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
Jun 7, 2021
Primary completion
Aug 21, 2025
Completion
Nov 5, 2026
Last update posted
Jun 22, 2026

2021 – 2026

United States locations

U.S. sites
33
U.S. states
15
U.S. cities
30
Facility City State ZIP Site status
Research Site Birmingham Alabama 35233
Research Site Paradise Valley Arizona 85253
Research Site Phoenix Arizona 85032
Research Site El Cajon California 92020
Research Site Fullerton California 92835
Research Site Hemet California 92543
Research Site La Mesa California 91942
Research Site Los Angeles California 90095
Research Site Menifee California 92586
Research Site Upland California 91786
Research Site Aurora Colorado 80045
Research Site Brandon Florida 33511
Research Site Clearwater Florida 33759
Research Site Clearwater Florida 33765
Research Site Miami Florida 33180
Research Site Tampa Florida 33613
Research Site Tampa Florida 33614
Research Site Idaho Falls Idaho 83404
Research Site Flint Michigan 48504
Research Site Lansing Michigan 48911
Research Site Newark New Jersey 07103
Research Site Las Cruces New Mexico 88011
Research Site Brooklyn New York 11201
Research Site Manhasset New York 11030
Research Site New York New York 10032
Research Site Potsdam New York 13676
Research Site Charlotte North Carolina 28203
Research Site Charlotte North Carolina 28204
Research Site Oklahoma City Oklahoma 73104
Research Site Pittsburgh Pennsylvania 15224
Research Site Reading Pennsylvania 19610
Research Site Memphis Tennessee 38119
Research Site Grapevine Texas 76051

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 107 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04877691, 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 Jun 22, 2026 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04877691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →