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Systemic Lupus ErythematosusPhase 4NCT06411249

A Study Describing the Efficacy and Safety of Belimumab Administered in Adult Participants With Early Systemic Lupus Erythematosus (SLE)

A Phase 4 study testing Belimumab (GSK1550188) in people with Systemic Lupus Erythematosus, run by GlaxoSmithKline at 104 sites in 11 countries.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This is a prospective, open-label, single arm 3-year clinical study to describe the short-term and long-term efficacy and safety of belimumab in participants with autoantibody positive early SLE with ongoing disease activity despite stable first-line SLE therapy. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Systemic Lupus Erythematosus
What is being tested?
Belimumab (GSK1550188)
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
302 participants
Where
104 sitesin 11 countries
Study dates
6 Jun 2024to 30 Jul 2029
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Documented diagnosis of systemic lupus erythematosus (SLE) within 2 years of signing the informed consent according to the European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) SLE classification criteria 2019
  • Have unequivocally positive autoantibody test results defined as an Anti-nuclear antibody (ANA) titer greater than or equal to (>=) 1:80 and/or a positive anti-Double stranded deoxyribonucleic acid (dsDNA) serum antibody test from 2 independent time points
  • Active SLE defined as:
  • Clinical SLEDAI-2K (excluding anti-dsDNA and C3/C4) score greater than (>) 4, OR
  • Clinical SLEDAI-2K (excluding anti-dsDNA and C3/C4) score 1 to 4 and prednisone or equivalent dose >=10 milligram per day (mg/day)
  • The Systematic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI) = 0 at Screening
Show all 10Show fewer
  • Male and/or female; a female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies:
  • Not a Woman of childbearing potential (WOCBP) OR
  • Is a WOCBP and using a contraceptive method that is highly effective
  • Capable of giving signed informed consent

Who cannot join

  • Lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.
  • Have clinical evidence of significant unstable or uncontrolled acute or chronic diseases not due to SLE (i.e., cardiovascular, pulmonary, hematologic, gastrointestinal (GI), hepatic, renal, neurological, psychiatric, malignancy, or infectious diseases) and/or a planned surgical procedure, which, in the opinion of the principal investigator (PI), could confound the results of the clinical study or put the participant at undue risk.
  • Participants with history of major organ transplant or hematopoietic stem cell/marrow transplant or renal transplant.
  • Have an acute or chronic infection including requiring management as follows:
  • Currently on any suppressive therapy for a chronic infection such as pneumocystis, cytomegalovirus, herpes simplex virus, herpes zoster, or atypical mycobacteria.
  • A serious infection requiring treatment with intravenous or Intramuscular (IV/IM) antibiotics and/or hospitalization if the last dose of antibiotics or the hospital discharge date was within 60 days of the first day of dosing (Day 1). Prophylactic anti-infective treatment is allowed.
Show all 55Show fewer
  • Confirmed active or untreated latent tuberculosis (TB):
  • Diagnosis of active TB confirmed by: 1) evidence of active TB disease from chest imaging (posterior anterior and lateral x-rays or chest computed tomography [CT]), 2) medical history and physical examination, and 3) either positive microscopy smear/culture for mycobacteria or positive TB polymerase chain reaction (PCR), i.e., Xpert. A tuberculin skin test (TST) or an interferon gamma release assay (IGRA) will be done for all participants. A positive TST or a positive (not indeterminate) IGRA TB test such as QuantiFERON-TB Gold Plus test is indicative but not required for diagnosis of active TB. A positive TST is defined as a skin induration >=5 millimeter (mm) at 48 to 72 hours (regardless of Bacillus Calmette-Guerin or other vaccination history).
  • Untreated latent tuberculosis infection (LTBI) confirmed by: 1) no evidence of active TB based on chest imaging, medical history and physical examination and laboratory evaluation of sputum; and 2) a positive TST, defined as a skin induration >5 mm at 48 to 72 hours, regardless of Bacillus Calmette-Guerin or other vaccination history); or a positive (not indeterminate) IGRA TB test such as QuantiFERON-TB Gold Plus test. Those with IGRA positive tests or positive TST who can document ongoing LTBI treatment for at least 4 weeks may be enrolled. Those with IGRA positive tests with documentation of the following may also be enrolled:
  • Successful completion of treatment for active TB.
  • Completion of treatment for LTBI (with treatment as per local practice, for example: 3 months of isoniazid and rifampin or 4 months of rifampin or 3 months weekly isoniazid and rifapentine, or 9 months of isoniazid).
  • Confirmed Progressive multifocal leukoencephalopathy (PML) or unexplained new-onset or deteriorating neurologic signs and symptoms.
  • Have severe 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 Screening.
  • Active Lupus Nephritis defined as active urinary sediment and/or proteinuria >500 milligrams (mg) per 24 hours, or equivalent using spot urine protein to creatinine ratio, requiring induction therapy not permitted by protocol.
  • Participants with patient health questionnaire (PHQ)-9 score >=10 that in the opinion of a mental healthcare professional pose a serious suicide risk, or any history of suicidal behavior in the last 6 months and/or any suicidal ideation in the last 2 months, or who in the investigator's judgment, poses a significant suicide risk. NOTE: For participants with a PHQ-9 score >=10, at the Screening visit or at the day 1 visit before the first administration of the study drug, it is required that they be referred for an assessment by a mental healthcare professional (e.g., locally licensed psychiatrist, psychologist, or master's level therapist) before the investigator makes a final decision regarding suitability for enrollment.
  • Known to have titers of human anti-mouse antibody or history of hypersensitivity reactions when treated with diagnostic or therapeutic monoclonal antibodies
  • Live or live-attenuated vaccine(s) within 35 days prior to Screening or plans to receive such vaccines during the Screening period or during the clinical study
  • Chronic oral steroid use for a non-SLE disorder at the Screening study visit (e.g., for asthma). Inhaled steroid use will be allowed.
  • Treatment at or prior to Screening study visit:
  • Treatment at Screening study visit with any of the following:
  • Azathioprine (AZA) >200 mg/day
  • Methotrexate (MTX) (any formulation) >25 mg/week
  • Mycophenolate mofetil (MMF) (oral [PO])/MMF hydrochloride (IV) >2 grams (g)/day
  • Mycophenolate acid/sodium (PO) >1.44 g/day
  • Oral cyclophosphamide >2.5 mg/kilograms (kg)/day
  • Tacrolimus >0.2 mg/kg/day
  • Cyclosporine (PO) >2.5 mg/kg/day
  • Treatment within specified timeframe prior to Screening:
  • Intra-articular, IM, or IV corticosteroids within 6 weeks of Day 1
  • Daily use of >1 Nonsteroidal anti-inflammatory (NSAID) within 2 weeks prior to Day 1
  • Treatment at any time prior to Screening with any of the following:
  • Second line use of conventional immunosuppressants (ISs) or anti-malarials (AMs)
  • Commercially available Belimumab (BEL)
  • Anifrolumab
  • Rituximab or other B cell depleting therapies
  • Anti-tumor necrosis factor (TNF) therapy (e.g., adalimumab, etanercept, infliximab)
  • Other treatments with effects on the immune system (e.g., abatacept, interleukin-1 receptor antagonist [anakinra], Janus kinase (JAK) inhibitors)
  • IV cyclophosphamide
  • IV immunoglobulin
  • Plasmapheresis Any addition of a new IS or AM, or IS or AM switch, performed more than 3 months after initiating first line therapy in response to inadequate disease control is considered second-line therapy and is therefore exclusionary. Therapy changes made due to intolerance or toxicity are not considered second-line, provided that the intolerance/toxicity is clearly documented. Any therapy changes after initiating first line therapy considered to be due to intolerance/toxicity must be reviewed and confirmed by the EAC prior to determining eligibility.
  • History of primary immunodeficiency, or hypogammaglobulinemia (Immunoglobulin G [IgG] <400 mg/deciliter [dL]) or Immunoglobulin A (IgA) deficiency (IgA <10 mg/dL) at Screening
  • Have a Grade 3 or greater neutropenia, defined as absolute neutrophil count <1000/cubic millimeter (mm3) (<1.0 x10^9/liter [L]) based on the Common terminology criteria for adverse events (CTCAE) version (v) 5.0
  • Alanine aminotransferase >2 x upper limit of normal (ULN)
  • Total bilirubin >1.5 x ULN; For participants with Gilbert's syndrome can be included with total bilirubin >1.5xULN if direct bilirubin is ≤1.5xULN. Cirrhosis or current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice. NOTE: Stable non-cirrhotic chronic liver disease (including Gilbert's syndrome), asymptomatic gallstones, and chronic stable hepatitis B (in whom Hepatitis D [HDV] has been excluded) or C are acceptable if participant otherwise meets entry criteria.
  • Have any other clinically significant abnormal laboratory value, that in the opinion of the investigator, is capable of significantly altering the absorption, metabolism, or elimination of the clinical study intervention; or constitutes a risk when taking the clinical study intervention or interferes with the interpretation of the clinical study data.
  • Positive Human immunodeficiency virus (HIV) antibody test
  • Serologic evidence of Hepatitis B (HB) infection based on the results of testing for hepatitis B surface antigen (HBsAg), anti-hepatitis B core (HBc) and anti-HBs will be excluded as follows:
  • Participants positive for HBsAg.
  • Participants negative for HBsAg but positive for Anti-HBc and detectable hepatitis B virus (HBV) DNA, regardless of Anti-HBs antibody status.
  • Positive Hepatitis C antibody test result at Screening or within 3 months prior to starting study intervention. NOTE: Participants with positive Hepatitis C antibody due to prior resolved disease can be enrolled, only if a confirmatory negative Hepatitis C Ribonucleic acid (RNA) test is obtained.
  • Positive Hepatitis C RNA test result at Screening or within 3 months prior to first dose of study intervention. NOTE: Test is optional and participants with negative Hepatitis C antibody test are not required to also undergo Hepatitis C RNA testing.
  • Sensitivity to the clinical study intervention, or components thereof, or monoclonal antibodies or drug or other allergy that, in the opinion of the investigator, contraindicates participation in the clinical study
  • Current drug or alcohol dependence, or a history of drug or alcohol abuse or dependence within 364 days prior to Day 1
  • Current enrolment or past participation in any other clinical study involving an investigational study intervention (including investigational vaccines) within 3 months or 5 half-lives of the investigational drug (whichever is longer) before enrolment
  • Unable to administer clinical study intervention by subcutaneous (SC) auto-injector at home and has no other reliable resource to administer the study intervention at home.

Trial locations and contacts

104 sites in 11 countries.

104 sites in 11 countries

United States40 sites
  • GSK Investigational Site

    Anniston, Alabama, 36207

  • GSK Investigational Site

    Atlanta, Georgia, 30152

  • GSK Investigational Site

    Austin, Texas, 78745

  • GSK Investigational Site

    Aventura, Florida, 33180

  • GSK Investigational Site

    Baton Rouge, Louisiana, 70836

  • GSK Investigational Site

    Baytown, Texas, 77521

  • GSK Investigational Site

    Brooklyn, New York, 11201

  • GSK Investigational Site

    Charlotte, North Carolina, 28202

  • GSK Investigational Site

    Clearwater, Florida, 33765-2616

  • GSK Investigational Site

    Colleyville, Texas, 76034-5913

  • GSK Investigational Site

    Covina, California, 91722

  • GSK Investigational Site

    Danville, Virginia, 24541

  • GSK Investigational Site

    Detroit, Michigan, 48202

  • GSK Investigational Site

    Duncansville, Pennsylvania, 16635-8445

  • GSK Investigational Site

    Flagstaff, Arizona, 86001

  • GSK Investigational Site

    Fontana, California, 92335

  • GSK Investigational Site

    Fort Worth, Texas, 76109-3559

  • GSK Investigational Site

    Fullerton, California, 92835-3827

  • GSK Investigational Site

    Glendale, Wisconsin, 53217

  • GSK Investigational Site

    Houston, Texas, 77089

  • GSK Investigational Site

    Katy, Texas, 77494-1341

  • GSK Investigational Site

    Lansing, Michigan, 48910

  • GSK Investigational Site

    Long Beach, California, 90720

  • GSK Investigational Site

    Los Angeles, California, 90211

  • GSK Investigational Site

    Mesa, Arizona, 85210

  • GSK Investigational Site

    Mission Hills, California, 91345-1116

  • GSK Investigational Site

    Morton Grove, Illinois, 60521

  • GSK Investigational Site

    New Orleans, Louisiana, 70112

  • GSK Investigational Site

    Plano, Texas, 75024

  • GSK Investigational Site

    Rockford, Illinois, 60123

  • GSK Investigational Site

    San Diego, California, 92128

  • GSK Investigational Site

    Tamarac, Florida, 33321

  • GSK Investigational Site

    Tampa, Florida, 33606

  • GSK Investigational Site

    Temecula, California, 92592

  • GSK Investigational Site

    Tucson, Arizona, 85748

  • GSK Investigational Site

    Tujunga, California, 91042-2706

  • GSK Investigational Site

    Van Nuys, California, 92307-2333

  • GSK Investigational Site

    Van Nuys, California, 92586

  • GSK Investigational Site

    Whittier, California, 90602

  • GSK Investigational Site

    Winston-Salem, North Carolina, 27157

Other trials in United States

Brazil11 sites
  • GSK Investigational Site

    Belo Horizonte, Minas Gerais, 30150-221.

  • GSK Investigational Site

    Cuiabá, 78020-840

  • GSK Investigational Site

    Juiz de Fora, 36010-570

  • GSK Investigational Site

    Passo Fundo, 99010-080

  • GSK Investigational Site

    Porto Alegre, 90035-001

  • GSK Investigational Site

    Porto Alegre, 90430-001

  • GSK Investigational Site

    Porto Alegre, 90610-000

  • GSK Investigational Site

    Salvador, 41820-020

  • GSK Investigational Site

    São José do Rio Preto, São Paulo, 15090-000

  • GSK Investigational Site

    São Paulo, 01323-001

  • GSK Investigational Site

    São Paulo, 05403-000

Other trials in Brazil

Argentina10 sites
  • GSK Investigational Site

    Berazategui, 1884

  • GSK Investigational Site

    Buenos Aires, C1121ABE

  • GSK Investigational Site

    Buenos Aires, C1406AGA

  • GSK Investigational Site

    Ciudad Autonoma Buenos Aires, C1015ABO

  • GSK Investigational Site

    Ciudad Autonoma de Buenos Aire, 1425

  • GSK Investigational Site

    La Plata, B1900AX

  • GSK Investigational Site

    Mar del Plata, 7600

  • GSK Investigational Site

    Quilmes, B1878GEG

  • GSK Investigational Site

    San Miguel de Tucumán, CP 4000

  • GSK Investigational Site

    Santa Fe, S2000DSV

Other trials in Argentina

Mexico10 sites
  • GSK Investigational Site

    Cuauhtémoc, Mexico City, 06090

  • GSK Investigational Site

    DF, 14000

  • GSK Investigational Site

    Guadalajara Jalisco, 44950

  • GSK Investigational Site

    León, 37000

  • GSK Investigational Site

    Mérida, 97000

  • GSK Investigational Site

    Mexico City, 06700

  • GSK Investigational Site

    Mexico City, 06726

  • GSK Investigational Site

    Monterrey Nuevo LeOn, 64000

  • GSK Investigational Site

    San Luis Potosí City, 78200

  • GSK Investigational Site

    Torreón, 27000

Other trials in Mexico

Italy7 sites
  • GSK Investigational Site

    Brescia, 25123

  • GSK Investigational Site

    Ferrara, 44124

  • GSK Investigational Site

    Milan, 20132

  • GSK Investigational Site

    Pisa, 56100

  • GSK Investigational Site

    Reggio Emilia, 42123

  • GSK Investigational Site

    Rome, 00168

  • GSK Investigational Site

    Rozzano, 20089

Other trials in Italy

Spain6 sites
  • GSK Investigational Site

    Barcelona, 08003

  • GSK Investigational Site

    Castellon, 12004

  • GSK Investigational Site

    Córdoba, 14004

  • GSK Investigational Site

    Murcia, 30120

  • GSK Investigational Site

    Valladolid, 47012

  • GSK Investigational Site

    VigoPontevedra, 36213

Other trials in Spain

Germany5 sites
  • GSK Investigational Site

    Herne, 44649

  • GSK Investigational Site

    Lübeck, 23538

  • GSK Investigational Site

    Mainz, Rhineland-Palatinate, 55131

  • GSK Investigational Site

    Mainz, 55131

  • GSK Investigational Site

    Meerbusch, 40668

Other trials in Germany

Greece5 sites
  • GSK Investigational Site

    Athens, 11 527

  • GSK Investigational Site

    Athens, 12462

  • GSK Investigational Site

    Athens, 16673

  • GSK Investigational Site

    Heraklion, 71500

  • GSK Investigational Site

    Thessaloniki, 54642

Other trials in Greece

Japan4 sites
  • GSK Investigational Site

    Fukuoka, 807-8556

  • GSK Investigational Site

    Miyagi, 980-8574

  • GSK Investigational Site

    Osaka, 590-0197

  • GSK Investigational Site

    Tokyo, 104-8560

Other trials in Japan

France3 sites
  • GSK Investigational Site

    Angers, 49933

  • GSK Investigational Site

    Saint-Priest-en-Jarez, 42270

  • GSK Investigational Site

    Toulouse, 31400

Other trials in France

Portugal3 sites
  • GSK Investigational Site

    Almada, Setúbal District, 2805-267

  • GSK Investigational Site

    Lisbon, 1069-166

  • GSK Investigational Site

    Porto, 4050-342

Other trials in Portugal

About this study

Official title: A Phase 4, Multicenter, Prospective, Open-Label Study Describing the Efficacy and Safety of Belimumab Administered Subcutaneously in Adult Participants With Early Systemic Lupus Erythematosus

This is a prospective, open-label, single arm 3-year clinical study to describe the short-term and long-term efficacy and safety of belimumab in participants with autoantibody positive early SLE with ongoing disease activity despite stable first-line SLE therapy.

Being tested
Belimumab (GSK1550188)
Keywords
Belimumab, Benlysta, Efficacy, Safety, Early Use, Systemic Lupus Erythematosus, Autoimmune Diseases
Medical subject headings
Lupus Erythematosus, Systemic, Autoimmune Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Belimumab (GSK1550188)Biological

    Also called BEL (BENLYSTA)

    GSK1550188 will be administered subcutaneously.

Study groups in NCT06411249
Study groupRoleWhat they receive
Belimumab (GSK1550188)ExperimentalParticipants will receive GSK1550188.
Receives: Biological: Belimumab (GSK1550188)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Part A: Percentage of Participants Achieving Lupus Low Disease Activity State (LLDAS) at Week 52

    LLDAS is defined as Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) less than or equal to (<=) 4, with no activity in major organ systems (renal, central nervous system, cardiopulmonary, vasculitis, fever) and no new features of lupus disease activity compared with the previous assessment, Physician Global Assessment (PGA) <= 1, with a 7-day average oral prednisone equivalent dose for SLE reasons <= 7.5 milligram (mg)/day and stable treatment and without discontinuing due to lack of efficacy, dying, or taking prohibited medications.

    Measured: At Week 52

Secondary outcomes (10)
  1. Part A: Percentage of Participants Achieving SLE Responder Index 4 (SRI4) at Week 52

    SRI4 is defined as greater than or equal to (>=) 4-point reduction from baseline in SLEDAI-2K score and no worsening (increase of less than [<] 0.30 points from baseline) in PGA and no new Easy- British Isles Lupus Assessment Group (BILAG) A organ domain score or 2 new Easy-BILAG B organ domain scores compared with baseline at the time of assessment without participants discontinuing due to lack of efficacy, dying, taking prohibited medications or meeting treatment failure criteria.

    Measured: At Week 52

  2. Part A: Percentage of Participants Achieving Lupus Low Disease Activity State (LLDAS) for >= 25 percent (%) of time from Day 1 to Week 52

    LLDAS is defined as Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) less than or equal to (<=) 4, with no activity in major organ systems (renal, central nervous system, cardiopulmonary, vasculitis, fever) and no new features of lupus disease activity compared with the previous assessment, Physician Global Assessment (PGA) <= 1, with a 7-day average oral prednisone equivalent dose for SLE reasons <=7.5 milligram (mg)/day and stable treatment and without discontinuing due to lack of efficacy, dying, or taking prohibited medications.

    Measured: Day 1 and up to Week 52

  3. Part A: Percentage of Participants Achieving Average Oral Prednisone Equivalent Dose <= 5 mg/day at Week 52

    A seven-day average oral prednisone equivalent dose <= 5 mg/day at week 52, if oral prednisone equivalent dose is greater than (>) 5 mg/day at baseline without study intervention discontinuation due to lack of efficacy, serious AE, prohibited medication intake, or treatment failure by Week 52.

    Measured: At Week 52

  4. Part A: Estimate of probability of having a Severe Flare defined as modified SELENA-SLEDAI Flare Index (SFI) at Week 52

    SFI Flare was defined as a mild/moderate or severe flare according to the modified Safety of Estrogen in Lupus National Assessment Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) SLE Flare Index (modified excluded severe flares from the SELENA-SLEDAI flare assessment that were triggered only by an increase in SLEDAI-2K score to >12). Change in SELENA SLEDAI instrument score of greater than 12.

    Measured: At Week 52

  5. Part A: Percentage of Participants Achieving a >= 50% Improvement in Cutaneous Lupus Disease Area and Severity Index (CLASI) Activity Score at Week 52

    The CLASI is used to assess the cutaneous lesions of SLE and consists of 2 separate scores: the activity score and the damage score. The activity score evaluates erythema, scale/hypertrophy, mucous membrane lesions, recent hair loss, and nonscarring alopecia, measured at 13 anatomical sites on the skin. The total activity score ranges from 0 to 70. Higher scores indicate greater disease activity and severity in SLE.

    Measured: At Week 52

  6. Part A: Change from Baseline in Functional Assessment of Chronic Illness Therapy (FACIT) -Fatigue at Week 52

    The FACIT-Fatigue is a 13-item participant-completed questionnaire used to assess the impact of fatigue over the previous 7 days. Item responses range from 0 (Not at All) to 4 (Very Much). The FACIT-Fatigue is scored as the sum of item responses, with range from 0 to 52, where higher scores indicate less fatigue and a better quality of life.

    Measured: Baseline (Day 1) and at Week 52

  7. Part A: Number of Participants With Adverse Events (AEs), Serious AEs (SAEs), and AEs of Special Interest (AESIs)

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. An SAE is defined as any untoward medical occurrence that, at any dose, meets one or more of the criteria listed: results in death; is life-threatening; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent or significant disability/incapacity; is a congenital anomaly/birth defect in a participant's offspring; abnormal pregnancy outcomes; is a suspected transmission of any infectious agent via an authorized medicinal product; or other situations as per the Investigator's medical or scientific judgment. AESIs will include hypersensitivity or post-injection systemic reactions, infections of special interest, malignancy, psychiatric events, and fatal events.

    Measured: Up to Week 52

  8. Part B: Percentage of Participants Achieving Definition of Remission in SLE (DORIS) Remission at Week 104

    DORIS remission is defined as clinical SLEDAI-2K equal to (=) 0 (excluding anti- double stranded deoxyribonucleic acid [dsDNA] and complement); and PGA < 0.5; and prednisone (or equivalent dose) < 5 mg/day on stable anti-malarial (AM), immunosuppressants (ISs) and biologic therapy.

    Measured: At Week 104

  9. Part B: Percentage of Participants Maintaining Systematic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI) of 0

    The SDI measures irreversible changes occurring since the diagnosis of SLE. The questionnaire contains 39 items covering 12 different organ systems. Individual ranges for organ systems are ocular: 0-2, neuropsychiatric: 0-6; renal: 0-3; pulmonary: 0-5; cardiovascular: 0-6; peripheral vascular: 0-5; gastrointestinal: 0-5; musculoskeletal: 0-6; skin: 0-3; endocrine (diabetes): 0-1; gonadal: 0-1; and malignancies: 0-2. The SDI score is calculated by summing the individual scores for 12 organ systems and ranges from 0 (no damage) to 45 (increasing disease damage) where higher score indicates increasing disease damage severity.

    Measured: Up to Week 156

  10. Part B: Number of Participants With AEs, SAEs, and AESIs up to Week 104 and Week 156

    An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. An SAE is defined as any untoward medical occurrence that, at any dose, meets one or more of the criteria listed: results in death; is life-threatening; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent or significant disability/incapacity; is a congenital anomaly/birth defect in a participant's offspring; abnormal pregnancy outcomes; is a suspected transmission of any infectious agent via an authorized medicinal product; or other situations as per the Investigator's medical or scientific judgment. AESIs will include hypersensitivity or post-injection systemic reactions, infections of special interest, malignancy, psychiatric events, and fatal events.

    Measured: Up to Week 104 and Week 156

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 May 2024
  2. Study start6 Jun 2024
  3. Primary completion29 Jun 2027 (estimated)
  4. Study completion30 Jul 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
302 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06411249
Sponsor's protocol ID
219240
Other IDs
2023-509146-35, 2023-509146-35-00, 2023
Status last verified
Oct 2026
First submitted
8 May 2024
Last updated
27 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Qualified researchers may request access to anonymized individual patient-level data (IPD) and related study documents of the eligible studies via the Data Sharing Portal. Details on GSK's data sharing criteria can be found at: https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Belimumab (GSK1550188) in people with Systemic Lupus Erythematosus, run by GlaxoSmithKline at 104 sites in 11 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 55 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 27 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 104 sites in United States, Brazil, Argentina, Mexico, Italy and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Part A: Percentage of Participants Achieving Lupus Low Disease Activity State (LLDAS) at Week 52 (time frame: At Week 52). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Oct 2026.

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