Last Update: Nov 19, 2024
A Randomized, Double-blind, Parallel Group, Placebo-controlled, Multicenter Phase 3 Trial to Evaluate Efficacy, Safety and Tolerability of Ianalumab on Top of Standard-of-care Therapy in Participants With Active Lupus Nephritis (SIRIUS-LN).
ClinicalTrials.gov Identifier:
Novartis Reference Number:CVAY736K12301
All compounds are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation.

Study Description

This trial will evaluate efficacy, safety, and tolerability of subcutaneous (s.c.) ianalumab given every 4 weeks (q4w) or every 12 weeks (q12w) compared to placebo, in combination with SoC, in adult participants with active LN This trial will evaluate the efficacy, safety, and tolerability of subcutaneous (s.c.) ianalumab given every 4 weeks (q4w) or ianalumab given every 12 weeks (q12w) compared to placebo, in combination with SoC, in adult participants with active LN (ISN/RPS class III, IV active glomerulonephritis with or without co-existing class V features, or pure class V membranous). using the 2003 International Society for Nephrology (ISN)/Renal Pathology Society (RPS) criteria).

Lupus Nephritis
Phase3
Recruiting
420
Jul 14, 2022
Jul 15, 2030
All
18 Years - (Adult, Older Adult)

Interventions

Drug

ianalumab s.c. q12w

ianalumab s.c. q12w in addition to SoC
Drug

ianalumab s.c. q4w

ianalumab s.c. q4w in addition to SoC
Drug

placebo s.c.

placebo s.c. q4w in addition to SoC

Eligibility Criteria

Inclusion Criteria:

Participants eligible for inclusion in this study must meet all of the following criteria:

* Adult male and female participants aged 18 years or older at the time of screening
* Weigh at least 35 kg at screening
* Have a confirmed clinical diagnosis of SLE according to European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) Systemic Lupus Erythematosus (SLE) classification criteria
* Have a positive anti-nuclear antibody (ANA) test result; ANA titer ≥ 1:80 at screening visit based on central or local laboratory result
* Active LN at screening, as defined by meeting the 3 following criteria:
* Renal biopsy within 6 months prior to screening period indicating ISN/RPS class III or IV active glomerulonephritis with or without co-existing class V features, or pure class V membranous LN. If no biopsy was performed within 6 months prior to screening period, a biopsy will need to be performed during the screening period after having met all other inclusion/exclusion criteria.
* UPCR ≥ 1.0 g/g on 24h urine collection at Screening
* eGFR ≥ 25mL/min/1.73 m2. Participants with eGFR \< 30 mL/min/1.73 m2 require renal biopsy during the screening period showing sclerosis in ≤ 50% of glomeruli
* Newly diagnosed participants as well as pre-treated LN participants (including refractory cases) can be included, as long as they are currently on, or willing to initiate SoC induction therapy for LN using MPA

* Induction therapy, as defined by treatment including both high dose corticosteroids and MPA, should be initiated prior to or on day of randomization
* Anti-malarial treatment at stable dosing prior to randomization is strongly recommended, in the absence of contraindications
* Participants on azathioprine treatment at Screening must be switched to MPA prior to randomization
* Receipt of at least one dose of pulse methylprednisolone i.v. (250 - 1000 mg per day up to 3000 mg cumulative dose) or equivalent for treatment of current episode of active LN within 60 days prior randomization. Participant who cannot take the pulse i.v. corticosteroid therapy should directly start on 0.8-1.0 mg/day (max 80mg/day) oral predniso(lo)ne.
* Able to communicate well with the Investigator to understand and comply with the requirements of the study

Exclusion Criteria:

Participants meeting any of the following criteria are not eligible for inclusion in this study:

* Severe renal impairment as defined by i.) presence of oliguria (defined as a documented urine volume \<400 mL/24 hrs) or ii.) End-Stage Renal Disease (ESRD) requiring dialysis or transplantation
* Sclerosis in \> 50% of glomeruli on renal biopsy
* Use of other investigational drugs within 5 half-lives of enrollment, or within 30 days or until the expected pharmacodynamic effect has returned to baseline. Use of certain Traditional Chinese Medicines
* Prior use of ianalumab (ever); or prior use other B cell depleting therapy within 36 weeks prior to randomization or if therapy was administered \< 36 weeks prior to randomization, B cell count less than the lower limit of normal or patient's own baseline value prior to having received an earlier B cell-depleting therapy
* Prior treatment with any of the following within 12 weeks prior to randomization

* Belimumab, telitacicept, abatacept, TNF-α mAb, immunoglobulins (i.v./s.c.) plasmapheresis
* Any other immuno-suppressants (i.v. or oral cyclophosphamide, calcineurin inhibitors, JAK inhibitors or other kinase inhibitors)
* Thalidomide treatment and/or methotrexate
* Combination of DMARDs
* Imidazole derivative (e.g., azathioprine, mizoribine) must be discontinued prior to starting treatment with MPA
* Receipt of more than 3000 mg i.v. pulse methylprednisolone (cumulative dose) within 12 weeks prior to randomization
* History of major organ transplant or hematopoietic stem cell/bone marrow transplant or are due to receive transplantation
* Any one of the following laboratory values at screening:

* Hemoglobin levels \< 8.0 g/dL (\< 5 mmol/L), or \< 7.0 g/dL (\< 4.3 mmol/L) if related to participant's SLE such as in active hemolytic anaemia
* Platelet count \< 25 x 1000/µL
* Absolute neutrophil count (ANC) \< 0.8 x 1000/µL
* Active viral, bacterial or other infections requiring intravenous or intramuscular treatment for clinically significant infection or history of recurrent clinically significant infection which in the opinion of the investigator will place the participant at risk for participation.
* History of known intolerance/hypersensitivity to MPA, oral corticosteroids, or any component of the study drug(s) or its excipients
* Receipt of live/attenuated vaccine within a 4-week period prior to randomization
* History of primary or secondary immunodeficiency, including a positive HIV test result
* History of malignancy of any organ system (other than localized basal cell carcinoma or squamous cell carcinoma of the skin or or in-situ cervical cancer), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases
* Any surgical, medical (e.g., uncontrolled hypertension, heart failure or diabetes), psychiatric or additional physical condition that the Investigator feels may jeopardize the participants in case of participation in this study
* Chronic infection with hepatitis B (HBV) or hepatitis C (HCV). Positive serology for hepatitis B surface antigen (HBsAg) excludes the participant
* Evidence of active tuberculosis (TB) infection (after anti-TB treatment, participants with history of TB may become eligible according to national local guidelines)
* Pregnant or nursing (lactating) women
* Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for 6 months after stopping of investigational medication
* Sexually active male participants, who do not agree to use barrier protection during intercourse with women of child-bearing potential while taking study treatment

Other protocol -defined Inclusion/Exclusion may apply.

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Tallinn,10138,Estonia

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Poitiers,86021,France

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Angers Cedex 9,49933,France

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Besancon Cedex,25030,France

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Bordeaux Cedex,33076,France

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Lyon,69003,France

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Quetzaltenango,9001,Guatemala

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Guatemala City,01011,Guatemala

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Guatemala,01010,Guatemala

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Kwun Tong,Kowloon,Hong Kong

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Tuen Mun,999077,Hong Kong

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Budapest,H-1032,Hungary

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Debrecen,4032,Hungary

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Lucknow,Uttar Pradesh,226014,India

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Firenze,FI,50134,Italy

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Udine,UD,33100,Italy

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Gwangju,61469,Korea, Republic of

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London,Se1 9rt,United Kingdom

NY Nephrology

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Clifton Park,New York,12065,United States

Frank Cortazar
Howard Phelan

UMC New Orleans

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New Orleans,Louisiana,70112,United States

Jasmine McGary
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Philadelphia,Pennsylvania,19104,United States

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Wayne State University

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Detroit,Michigan,48201,United States

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Orange,California,92868,United States

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Kelly Acero

Baylor Scott and White Research

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Temple,Texas,76502,United States

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Michell Trevino

Northwell Health

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New York,New York,10028,United States

Richard Furie
Justina D Costa

Emory University School of Medicine

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Atlanta,Georgia,30303,United States

Kennedy Vela
S Sam Lim

University Of Alabama

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Birmingham,Alabama,35294,United States

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Jane Vines

UC Davis School of Medicine

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Sacramento,California,95817,United States

Annie Trinh
Nasim Wiegley

Northern Assoc of Northern VA

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Fairfax,Virginia,22033,United States

Gregory Wang

Circuit Clinical

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Orchard Park,New York,14127,United States

Isha Gupta

Wallace Rheumatic Study Center

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Los Angeles,California,90048,United States

Carla Martinez
Daniel Wallace

Liberty Research Center

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Dallas,Texas,75230,United States

Irfan Agha
Laurie Jones

Univ of Nevada School of Med

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Las Vegas,Nevada,89102,United States

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Walter Winn Chatham

Univof Texas Southwestern Med Cntr

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Dallas,Texas,75235,United States

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VA NM Healthcare System

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Albuquerque,New Mexico,87108,United States

Anthony Sedillo
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Mayo Clinic Jacksonville

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Jacksonville,Florida,32224,United States

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Brookview Hills Research Assoc

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Winston-Salem,North Carolina,27103,United States

Janice Rogers
Nicholas McLean

Fides Clinical Research

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Atlanta,Georgia,30342,United States

Dillon Ha
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University of Texas Medical Branch

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Galveston,Texas,77555-0144,United States

Jana Lee
Tina Kochar

Kaiser Permanente

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San Diego,California,92111,United States

Hui Xue
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University of California LA

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Los Angeles,California,90095,United States

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Maureen McMahon

Hospital for Special Surgery

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New York,New York,10021,United States

Haley Slosberg
Kyriakos Kirou

Uni of Texas Health Science Center

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San Antonio,Texas,78284,United States

Agustin Escalante

University of Kansas Hospital

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Kansas City,Kansas,66160,United States

Kelly Liang

James J Peters VA Medical Center

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Bronx,New York,10468,United States

Kelly Steed

University Of Cincinnati

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Cincinnati,Ohio,45267,United States

Leksi Travitz
Manish Anand

Parris and Associates Rheumatology

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Lawrenceville,Georgia,30044,United States

Glenn Parris

Uni Wisconsin School Med Pub Health

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Madison,Wisconsin,53792,United States

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University Of Miami

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Miami,Florida,33136,United States

Maria Fernanda Carpintero
Priscilla Madero

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Hanoi,100000,Vietnam

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Ho Chi Minh,700000,Vietnam

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