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Active, not recruiting Phase 3

Subcutaneous Anifrolumab in Adult Patients With Systemic Lupus Erythematosus

NCT04877691 · tracked via the Priya Life Science Poland tracker
Phase
Phase 3
Started
2021-06-08
Last updated
2026-07-27

Condition(s) studied

Systemic Lupus Erythematosus

Investigational drug(s) / intervention(s)

Medi-546 →Placebo

Medi-546: Patients will have IP administered or will self-administer IP under supervision by site staff at Week 0 and Week 1 and, for patients participating in the OLE period, at Week 52. For weekly doses coinciding with subsequent on-site visits, patients will also have IP administered or will self-administer IP under supervision by site staff, and in addition will receive a set of kits (including back-up kits) for at-home administration.

Placebo: Solution for injection in aPFS

Study summary

The purpose of this study is evaluating the efficacy and safety of SC antifrolumab in adult patients with moderate -to-severe SLE despite receiving standard therapy

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients who have a diagnosis of pediatric or adult SLE according to the ACR 1997 revised criteria for ≥ 24 weeks prior to signing the ICF 2. To be eligible a patient must have SLEDAI-2K ≥ 6 points and "Clinical" SLEDAI-2K score ≥4 points at screening 3. BILAG2004 with at least 1 of the following: 1. BILAG2004 level A disease in ≥ 1 organ system 2. BILAG2004 level B disease in ≥ 2 organ systems 4. Physician's Global Assessment (PGA) score ≥ 1.0 on a 0 to 3 VAS at Screening 5. Antinuclear antibody, and/or Anti-dsDNA and/oranti-Smith positive at Screening, 6. Must be on stable background standard therapy with DMARD, glucocorticoids or anti-malarials alone or in combinations. Exclusion Criteria: 7. Active severe or unstable neuropsychiatric SLE 8. Active severe SLE-driven renal disease 9. History of any non-SLE disease that has required treatment with oral or parenteral corticosteroids for more than a total of 2 weeks within the last 24 weeks prior to signing the ICF. 10. History of recurrent infection requiring hospitalization and IV antibiotics (eg, 3 or more of the same type of infection over the previous 52 weeks). 11. Known history of a primary immunodeficiency, splenectomy, or any underlying condition that predisposes the patient to infection, or a positive result for human immunodeficiency virus (HIV) infection confirmed by central laboratory at Screening. 12. At Screening, confirmed positive test for hepatitis B serology and positive test for hepatitis C antibody 13. Any severe case herpes zoster infection at any time prior to Week 0 (Day 1), 14. Opportunistic infection requiring hospitalization or IV antimicrobial treatment within 3 years of randomization. 15. History of cancer, apart from: 1. Squamous or basal cell carcinoma of the skin treated with documented success of curative therapy ≥ 3 months prior to Week 0 (Day 1) 2. Cervical cancer in situ treated with apparent success with curative therapy ≥ 1 year prior to Week 0 (Day 1).

Primary outcome measure(s)

  • British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) response — At week 52
    BICLA response is a composite binary endpoint whereby responders are defined by meeting all of the following criteria: * Improvement from baseline in disease activity as measured by BILAG-2004. Improvement is defined as a reduction of all baseline BILAG-2004 A to B/C/D and baseline BILAG-2004 B to C/D and no BILAG-2004 worsening in other organ systems, where worsening is defined as ≥ 1 new BILAG-2004 A or ≥ 2 new BILAG 2004 B. * No worsening from baseline in SLEDAI-2K, where worsening is defined as an increase from baseline of \> 0 points in SLEDAI-2K. * No worsening from baseline in the patient's lupus disease activity, where worsening is defined as an increase ≥ 0.30 points on a 3-point PGA VAS.

Trial sites (140)

FacilityCityRegionStatus
Research Site Birmingham Alabama
Research Site Paradise Valley Arizona
Research Site Phoenix Arizona
Research Site El Cajon California
Research Site Fullerton California
Research Site Hemet California
Research Site La Mesa California
Research Site Los Angeles California
Research Site Menifee California
Research Site Upland California
Research Site Aurora Colorado
Research Site Brandon Florida
Research Site Clearwater Florida
Research Site Clearwater Florida
Research Site Miami Florida
Research Site Tampa Florida
Research Site Tampa Florida
Research Site Idaho Falls Idaho
Research Site Flint Michigan
Research Site Lansing Michigan
Research Site Newark New Jersey
Research Site Las Cruces New Mexico
Research Site Brooklyn New York
Research Site Manhasset New York
Research Site New York New York
Research Site Potsdam New York
Research Site Charlotte North Carolina
Research Site Charlotte North Carolina
Research Site Oklahoma City Oklahoma
Research Site Pittsburgh Pennsylvania
Research Site Reading Pennsylvania
Research Site Memphis Tennessee
Research Site Grapevine Texas
Research Site Ciudad de Buenos Aires Argentina
Research Site La Plata Argentina
Research Site Mendoza Argentina
Research Site Pergamino Argentina
Research Site Quilmes Argentina
Research Site Rosario Argentina
Research Site Salta Argentina

+ 100 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04877691 on ClinicalTrials.gov ↗ ← All trials in Poland