Last updated: 05/07/2026 15:00:13
Open-label study of Belimumab plus standard therapy in Chinese Pediatric participants with active Systemic Lupus Erythematosus (SLE)
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A Multi-Center, Open-Label Study to Evaluate Safety, Efficacy and Pharmacokinetics of Belimumab Plus Standard Therapy in Chinese Paediatric Patients with Active Systemic Lupus Erythematosus (SLE)
Trial description: This study will be conducted to evaluate the safety, efficacy and pharmacokinetics of belimumab administered in combination with background standard therapy in pediatric participants with active SLE.
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Not applicable
Primary outcomes:
Number of Participants with Adverse Events of Special Interest (AESIs) Through Week 52
Timeframe: Up to Week 52
Number of Participants With Greater than Equal to (>=) 4 Points Reduction from Baseline to Week 52 in Safety of Estrogen in Lupus National Assessment - Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) Score
Timeframe: Baseline (Day 0) and Week 52
Secondary outcomes:
Number of Participants With AEs and Serious Adverse Events (SAEs) Through Week 52
Timeframe: Up to Week 52
Percentage of Participants With >=4 Points Reduction from Baseline in SELENA-SLEDAI Score by Each Visit
Timeframe: Baseline (Day 0) and Weeks 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, and 52
Change from Baseline to Week 52 in Physician Global Assessment (PGA)
Timeframe: Baseline (Day 0) and Week 52
Change from Baseline to Week 52 in Parent Global Assessment (ParentGA)
Timeframe: Baseline (Day 0) and Week 52
Change from Baseline in Average Daily Prednisone Equivalent Dose at Week 52
Timeframe: Baseline (Day 0) and Week 52
Time to First Flare Over 52 Weeks
Timeframe: Up to Week 52
Time to First Severe Flare Over 52 Weeks
Timeframe: Up to Week 52
Median Belimumab Concentration Levels at Day 0, 7, and 14 Days Post First Dose, and Pre-infusion and Post-infusion at Day 84
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Apparent Total Clearance of Belimumab
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Volume of Distribution of Belimumab
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Terminal Half-life (t1/2) of Belimumab
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Maximum Plasma Concentration (Cmax) of Belimumab at Steady State
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Minimum Plasma Concentration Reached Prior to Administration of Next Dose (Cmin) of Belimumab at Steady State
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Average Plasma Concentration (Cavg) of Belimumab at Steady State
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Area Under the Concentration Curve (AUC) of Belimumab at Steady State
Timeframe: Days 0, 7, and 14 days post first dose, and pre-infusion and post-infusion at Day 84
Interventions:
Drug: Belimumab
Drug: Standard therapy
Enrollment:
67
Observational study model:
Not applicable
Primary completion date:
2024-23-05
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Systemic Lupus Erythematosus
Product
belimumab
Collaborators
NA
Study date(s)
October 2021 to August 2024
Type
Interventional
Phase
4
Participation criteria
Sex
Female & Male
Age
5 - 17 Years
Accepts healthy volunteers
No
- Participants have or have had in series, 4 or more of the American College of Rheumatology (ACR) 11 criteria for the classification of SLE.
- Participant’s age is 5 to 17 years at the time of informed consent.
- Have an estimated glomerular filtration rate (eGFR) as calculated by Schwartz Formula of less than 30 mL/minutes.
- Have acute severe nephritis defined as a significant worsening of renal disease (for example [e.g.], the presence of urinary sediments and other lab abnormalities) that, in the opinion of the study investigator, may lead to the participant requiring induction therapy with intravenous (IV) cyclophosphamide, Mycophenolate mofetil (MMF) or high dose corticosteroids during the first 6 months of the study.
Inclusion and exclusion criteria
Inclusion criteria:
- Participants have or have had in series, 4 or more of the American College of Rheumatology (ACR) 11 criteria for the classification of SLE.
- Participant’s age is 5 to 17 years at the time of informed consent.
- Have active SLE disease defined as a SELENA SLEDAI score >= 8 at screening (SELENA SLEDAI scoring).
- Have unequivocally positive autoantibody test results defined as an anti-nuclear antibody (ANA) titer >=1:80 and/or a positive anti-Double stranded deoxyribonucleic acid (dsDNA) serum antibody test.
- Are on a stable SLE therapy at Baseline. The stable treatment at Baseline consists of corticosteroids, anti-malarials, immunosuppressive/immunomodulatory agents and Non-steroidal anti-inflammatory drugs (NSAIDs), alone or in combination, at a fixed dose for a period of at least 30 days prior to Day 0.
- No gender restriction. Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
- The investigator, or a person designated by the investigator, will obtain written informed assent from each study participant or the participant's legally acceptable representative, parent(s), or legal guardian and the participant’s assent, when applicable, before any study-specific activity is performed. The investigator will retain the original copy of each participant's signed assent document.
Exclusion criteria:
- Have an estimated glomerular filtration rate (eGFR) as calculated by Schwartz Formula of less than 30 mL/minutes.
- Have acute severe nephritis defined as a significant worsening of renal disease (for example [e.g.], the presence of urinary sediments and other lab abnormalities) that, in the opinion of the study investigator, may lead to the participant requiring induction therapy with intravenous (IV) cyclophosphamide, Mycophenolate mofetil (MMF) or high dose corticosteroids during the first 6 months of the study.
- Have a history of a major organ transplant (e.g., heart, lung, kidney, liver) or hematopoietic stem cell/marrow transplant.
- Have clinical evidence of significant, unstable or uncontrolled, acute or chronic diseases not due to SLE (cardiovascular, pulmonary, hematologic, gastrointestinal, hepatic, renal, neurological, malignancy or infectious diseases) which, in the opinion of the investigator, could confound the results of the study or put the participant at undue risk.
- Have a planned surgical procedure or a history of any other medical disease (e.g., cardiopulmonary), laboratory abnormality, or condition (e.g., poor venous access) that, in the opinion of the investigator, makes the participant unsuitable for the study.
- Have a history of malignant neoplasm within the last 5 years.
- Have a history of a primary immunodeficiency.
- Have an Immunoglobulin A (IgA) deficiency (IgA level less than [<]10 mg/deciliters [milligrams/dL]).
- Have acute or chronic infections requiring management.
- Have recent infections that, in the opinions of the investigator, makes the participant unsuitable for the study or could put the participant at undue risk.
- Have current drug or alcohol abuse or dependence, or a history of drug or alcohol abuse or dependence within 364 days prior to Day 0.
- Have a Grade 3 or greater laboratory abnormality based on the protocol toxicity scale except for the following that are allowed: a) Stable Grade 3 prothrombin time (PT) secondary to warfarin treatment. b) Stable Grade 3 partial thromboplastin time (PTT) due to lupus anticoagulant and not related to liver disease or anti-coagulant therapy. c) Stable Grade 3 hypoalbuminemia due to lupus nephritis and not related to liver disease or malnutrition. d) Any grade proteinuria e) Stable Grade 3 gamma glutamyl transferase (GGT) elevation due to lupus hepatitis and not related to alcoholic liver disease, uncontrolled diabetes or viral hepatitis. If present, any abnormalities in the Alanine aminotransferase (ALT) and/or Aspartate aminotransferase (AST) must be Grade 2. f) Stable Grade 3 neutropenia; or stable Grade 3 lymphopenia; or stable Grade 3 leukopenia, due to SLE
- Have a history of an anaphylactic reaction to parenteral administration of contrast agents, human or murine proteins or monoclonal antibodies.
- Have evidence of serious suicide risk including any history of suicidal behavior in the last 6 months or who in the investigator's judgment, poses a significant suicide risk.
- Have received treatment with belimumab at any time.
- Have received any of the following within 364 days of Day 0: a) Treatment with any B-cell targeted b) Abatacept c) A biologic investigational agent
- Have required 3 or more courses of systemic corticosteroids for concomitant conditions (e.g., asthma, atopic dermatitis) within 90 days of Day 0.
- Have received any of the following within 90 days of Day 0: a) Anti-Tumour Necrosis Factor (TNF) or anti-interleukin (IL)-6 therapy (e.g., adalimumab, etanercept, infliximab, tocilizumab certolizumab, golimumab) b) Interleukin-1 receptor antagonist (anakinra) c) Intravenous immunoglobulin (IVIG) d) Plasmapheresis
- Have received any of the following within 30 days of Day 0: a) IV cyclophosphamide b) A non-biologic investigational agent (30 days window OR 5 half-lives, whichever is longer) c) Any new immunosuppressive/immunomodulatory agent, anti-malarial, NSAID d) High dose prednisone or equivalent (>1.5 mg/kilogram/day) or any intramuscular or intravenous steroid injection.
- Have received a live or live-attenuated vaccine within 30 days of Day 0.
- Have active central nervous system (CNS) lupus (including seizures, psychosis, organic brain syndrome, cerebrovascular accident [CVA], cerebritis or CNS vasculitis) requiring therapeutic intervention within 60 days of Day 0.
- Have required renal replacement therapy (e.g., hemodialysis, peritoneal dialysis) within 90 days of Day 0 or be currently on renal replacement therapy.
- Participation in an interventional clinical study either concurrently or within 6 months of screening. Participation in an observational study may be permitted.
- Have a historically positive test or test positive at screening for Human immunodeficiency virus (HIV) antibody.
- Evidence of active or latent tuberculosis (TB) as documented by medical history and examination, chest X-rays (posteroanterior) and a positive (not indeterminate) QuantiFERON-TB Gold Plus test.
- Hepatitis B: Serologic evidence of Hepatitis B (HB) infection defined as Hepatitis B surface antigen positive (HBsAg+) or Hepatitis B core antibody positive (HBcAb+).
- Hepatitis C: Positive test for Hepatitis C antibody at screening.
Trial location(s)
Study documents
Study report synopsis
Available language(s): English
Protocol
Available language(s): English
Statistical analysis plan
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2024-23-05
Actual study completion date
2024-13-08
Plain language summaries
Summary of results in plain language
Available language(s): English, Chinese (Simplified)
To view plain language summaries on trialsummaries.com click here.
Additional information about the trial
Additional information
Not applicable
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