Overview
This is a multi-center, open-label, phase 1 study.
Description
The purpose of this study is to evaluate the pharmacokinetics (PK) of multiple doses of Telitacicept in subjects with childhood-onset systemic lupus erythematosus (cSLE) on a background of standard of care therapy and explore the safety and efficacy of Telitacicept in patients with cSLE.
Eligibility
Main Inclusion Criteria:
- Fulfills SLICC 2012 or 2019 EULAR/ACR classification criteria for SLE.
- 12-17 years of age when signing the informed consent.
- Parent or legal guardian provided written informed consent.
- SELENA SLEDAI score ≥ 8 at screening.
- Serum autoantibodies (ANA and/or anti ds-DNA) tested positive at screening.
- Have been on a stable standard of care for SLE for at least 30 days prior to randomization.
Main Exclusion Criteria:
- Have received Telitacicept at any time.
- Have received any of the following therapies within 6 months of baseline: B-cell targeted treatment, e.g., belimumab, rituximab, abatacept, other investigational biologicals.
- 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.
- 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.
- Have received live vaccine within 30 days of baseline.
- Participated in an interventional clinical trial within 6 months of screening.
- Active CNS lupus requiring treatment within 60 days of baseline, including seizure, psychosis, organic brain syndrome, cerebrovascular accident, cerebritis or CNS vasculitis.
- Currently on kidney replacement therapy (hemodialysis, peritoneal dialysis) or in need of such therapy within 90 days of baseline.
- eGFR<30 mL/min/1.73m2.
- Acute severe nephritis.
- History of vital organ transplant (e.g., heart, lung, kidney, liver) or hematopoietic stem cell/marrow transplant.
- 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.
- History of malignant neoplasm in the past 5 years.
- Primary immune deficiency.
- Acute or chronic infections requiring treatment.
- HIV/HCV/HBsAg/HBcAb positive.
- Tuberculosis.
- Have planned surgery, laboratory abnormalities, other diseases or conditions that, in the opinion of the investigator, makes the subject unsuitable for the study.