Study of safety, efficacy and tolerability of ianalumab versus placebo, in combination with SOC therapy, in participants with active lupus nephritis
- Conditions
- upus nephritisMedDRA version: 21.1Level: PTClassification code 10025140Term: Lupus nephritisSystem Organ Class: 10038359 - Renal and urinary disordersTherapeutic area: Diseases [C] - Immune System Diseases [C20]
- Registration Number
- EUCTR2020-005830-14-EE
- Lead Sponsor
- ovartis Pharma AG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- All
- Target Recruitment
- 420
Participants eligible for inclusion in this study must meet all of the
following criteria:
1. Adult male and female patients aged 18 years or older at the time of screening
2. Signed informed consent must be obtained prior to participation in the study.
3. Have a confirmed clinical diagnosis of SLE according to EULAR/ACR SLE classification criteria
4. • Have a positive anti-nuclear antibody (ANA) test result defined as an ANA titer =1:80 (based on an indirect HEp-2 immunofluorescence assay or solid-phase ANA immunoassay with at least equivalent performance) at screening based on central laboratory results or a documented, positive historical result (ANA titer =1:80)
5. Presence of active LN at screening requiring induction therapy, as defined by meeting the 3 following criteria, requiring:
• Renal Biopsy within 6 months prior to screening period indicating ISN/RPS class III or IV active glomerulonephritis with or without coexisting class V features, or pure class V membranous LN. If no biopsy was performed within 6 months prior to screening period, a biopsy willneed to be performed during the screening period after having met all other inclusion/exclusion criteria.
• Urine protein creatinine ratio (UPCR) =1.0 g/g on 24-hour urine
collection at Screening
• Threshold renal function requirement or eGFR =25 mL/min/1.73 m2
(Patients with eGFR <30 mL/min/1.73 m2 require renal biopsy during
the screening period showing sclerosis in =50% of glomeruli)Induction
therapy, as defined by starting high dose corticosteroids and MPA, may
begin before Screening but should be initiated upon or within 60 days
prior to randomization. Participants who have been on MPA for SLE
including LN may be eligible if they have received, or will receive, the
induction therapy within 60 days prior to or on Day 0. This is comprised
of initiation of high dose corticosteroids with MPA dose increased to
reach the target dose for induction in the participant.
5. Presence of active LN at screening requiring induction therapy, as
defined by meeting the 3 following criteria, requiring:
• Renal Biopsy within 6 months prior to screening period indicating
ISN/RPS class III or IV active glomerulonephritis with or without coexisting
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.
• Urine protein creatinine ratio (UPCR) =1.0 g/g on 24-hour urine
collection at screening
• Threshold renal function requirement or eGFR =25 mL/min/1.73 m2(Patients with eGFR <30 mL/min/1.73 m2 require renal biopsy during the screening period showing sclerosis in =50% of glomeruli)Induction therapy, as defined by starting high dose corticosteroids and MPA, may begin before Screening but should be initiated upon or within 60 days prior to randomization. Participants who have been on MPA for SLE including LN may be eligible if they have received, or will receive, the
induction therapy within 60 days prior to or on Day 0. This is comprised of initiation of high dose corticosteroids with MPA dose increased to reach the target dose for induction in the participant.
6. Newly diagnosed patients, 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 includ
Participants meeting any of the following criteria are not eligible for
inclusion in this study.
1. 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.
2. Sclerosis in >50% of glomeruli on renal biopsy.
3. 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 the following Traditional Chinese Medicines:
Total glucoside of peony (TGP) or Tripterygium glycosides (TG)
administered within 30 days prior to randomization
4. Prior use of ianalumab (ever); or prior use of any other B celldepleting
therapy (e.g., rituximab or other anti-CD 20 mAb, anti-CD22
mAb, or anti-CD52 mAb): administered 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
participant's own baseline value prior to having received an earlier Bcell-depleting therapy
5. Prior treatment with any of the following:
Within 12 weeks prior to randomization:
• belimumab (anti-BAFF mAb), telitacicept, abatacept (CTLA4-Fc Ig),
anti-tumor necrosis factor-alpha (TNF-a) mAb, immunoglobulins
(i.v./s.c.) plasmapheresis
• any other immuno-suppressants, calcineurin inhibitors, JAK inhibitors
or other kinase inhibitors
• thalidomide treatment and/or methotraxate
• Use of anti-malarials permitted if stable dosing regimen prior to
randomization
Imidazole derivative must be discontinued prior to starting treatment
with MPA
6. Receipt of more than 3000 mg i.v. pulse methylprednisolone
(cumulative dose) within 12 weeks prior to randomization
7. History of major organ transplant or hematopoietic stem cell/bone
marrow transplant or are due to receive transplantation
8. Any one of the following laboratory values at screening:
• Hemoglobin levels <8.0 g/dL (one re-test is allowed during the
screening period)
• Platelet count <25 x 103/µL
• Absolute neutrophil count (ANC) <0.8 x 103/µL (one re-test is allowed
during the screening period)
9. 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.
10. History of known intolerance/hypersensitivity to MPA, or oral
corticosteroids, or any component of the study drug(s) or its excipients
or to drugs of similar chemical classes
11. Receipt of live/attenuated vaccine within a 4-week period prior to
randomization
12. History of primary or secondary immunodeficiency, including a
positive human immunodeficiency virus (Enzyme-linked immunosorbent
assay [ELISA] and Western blot) test result
13. History of malignancy of any organ system (other than localized
basal cell carcinoma or squamous cell carcinoma of the skin or in-situ
cervical cancer), treated or untreated, within the past 5 years,
regardless of whether there is evidence of local recurrence or
metastases.
14. Any surgical, medical (e.g., uncontrolled hypertension, heart failure
or diabetes), psychiatric or additional physical condition that the
Investigator feels may jeopardize the patient in case of participation in
this study.
15.Chronic infection with hepatitis B or hepatitis C. Positive serology for
HBsAg excludes the particip
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method