New hope for kids with lupus: drug study shows promise
NCT ID NCT05687526
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tested a drug called telitacicept in 16 children with lupus. The goal was to see how the drug moves through the body and if it helps control the disease. While not a cure, it may offer a new way to manage lupus symptoms in young patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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16 people
The number who actually took part.
- Started
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May 2023
- Finished
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Nov 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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5 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Main Inclusion Criteria: 1. Fulfills SLICC 2012 or 2019 EULAR/ACR classification criteria for SLE. 2. 5-17 years of age when signing the informed consent. 3. Suject and/or legal guardian or parent provided written informed consent. 4. SELENA SLEDAI score ≥ 8 at screening. 5. Serum autoantibodies (ANA and/or anti ds-DNA) tested positive at screening. 6. Have been on a stable standard of care for SLE for at least 30 days prior to randomization. 7. Female patients are required to be non-pregnant, non-lactating or sterile. Main Exclusion Criteria: 1. Have received Telitacicept at any time. 2. Have received any of the following therapies within 6 months of baseline: B-cell targeted treatment, e.g., belimumab, rituximab, abatacept, other investigational biologicals. 3. Have received any of the following therapies within 90 days of baseline: anti-TNF or anti-IL-6 therapy, interleukin-1 receptor antagonist, intravenous immunoglobulin (IVIG), plasmapheresis. 4. Have received any of the following therapies within 30 days of baseline: Intravenous cyclophosphamide, non-biological investigational agents (within 30 days of baseline or 5 half-lives, whichever is longer), newly added immunosuppressive/immunomodulatory agent, anti-malarial, NSAID, high-dose prednisone or equivalent (\> 1.5 mg/kg/day) or any intramuscular or intravenous steroid. 5. Have received live vaccine within 30 days of baseline. 6. Participated in an interventional clinical trial within 6 months of screening. 7. Active CNS lupus requiring treatment within 60 days of baseline, including seizure, psychosis, organic brain syndrome, cerebrovascular accident, cerebritis or CNS vasculitis. 8. Currently on kidney replacement therapy (hemodialysis, peritoneal dialysis) or in need of such therapy within 90 days of baseline. 9. eGFR\<30 mL/min/1.73m2. 10. Acute severe nephritis. 11. History of vital organ transplant (e.g., heart, lung, kidney, liver) or hematopoietic stem cell/marrow transplant. 12. Significant unstable or uncontrolled acute or chronic diseases (cardiovascular, lung, hematology, gastrointestinal, liver, renal, neurologic, malignancy or infectious disease) that could be explained by causes other than SLE. 13 Have planned surgery, laboratory abnormalities, other diseases or conditions that, in the opinion of the investigator, makes the subject unsuitable for the study. 14\. History of malignant neoplasm in the past 5 years. 15. Primary immune deficiency. 16. Acute or chronic infections requiring treatment. 17. HIV or HCV positive. 18. Tuberculosis. 19.HBsAg/HbcAb positive. 20.HBcAb positive. 21.History of COVID-19 within 4 weeks prior to screening. 22.History of hospitalization due to severe Covid-19 within 12 months prior to screening. 23.History of allergy to parenteral administration of contrast agents, human or murine proteins or monoclonal antibodies. 24.History of drug or alcohol abuse or dependence within 364 days prior to baseline. 25.Investigators believe that there are other factors that are not suitable for participating in the experiment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Chengdu Women's & Children's Central Hospital
Chengdu, Sichuan, China
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Children's Hospital of Capital Institute of Pediatrics
Beijing, Beijing Municipality, China
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Children's Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, China
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Children's Hospital of Fudan University
Shanghai, Shanghai Municipality, China
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Children's Hospital of Zhejiang University School of Medicine
Hangzhou, Zhejiang, China
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Henan Children's Hospital
Zhengzhou, Henan, China
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Hunan Children's Hospital
Changsha, Hunan, China
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Nanjing Children's Hospital
Nanjing, Jiangsu, China
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Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
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The First Hospital of Jilin University
Changchun, Jilin, China
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The Second Affiliated Hospital of Wenzhou Medical University
Wenzhou, Zhejiang, China
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Xi'an Children's Hospital
Xi'an, Shaanxi, China
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