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New hope for kids with lupus: drug study shows promise

NCT ID NCT05687526

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

16 people

The number who actually took part.

Started

May 2023

Finished

Nov 2025

Lead sponsor

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

5 to 17 years

Sex

Anyone

Healthy volunteers

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

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

  • Chengdu Women's & Children's Central Hospital

    Chengdu, Sichuan, China

  • Children's Hospital of Capital Institute of Pediatrics

    Beijing, Beijing Municipality, China

  • Children's Hospital of Chongqing Medical University

    Chongqing, Chongqing Municipality, China

  • Children's Hospital of Fudan University

    Shanghai, Shanghai Municipality, China

  • Children's Hospital of Zhejiang University School of Medicine

    Hangzhou, Zhejiang, China

  • Henan Children's Hospital

    Zhengzhou, Henan, China

  • Hunan Children's Hospital

    Changsha, Hunan, China

  • Nanjing Children's Hospital

    Nanjing, Jiangsu, China

  • Peking Union Medical College Hospital

    Beijing, Beijing Municipality, China

  • The First Hospital of Jilin University

    Changchun, Jilin, China

  • The Second Affiliated Hospital of Wenzhou Medical University

    Wenzhou, Zhejiang, China

  • Xi'an Children's Hospital

    Xi'an, Shaanxi, China

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