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NCT06342960TerminatedPhase 1/2

KYSA-3: A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Refractory Lupus Nephritis

KYSA-3: A Phase 1/2, Open-Label, Multicenter Study of KYV-101, an Autologous Fully-Human Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Refractory Lupus Nephritis

Source: ClinicalTrials.gov · Last updated 31 Aug 2026

Brief summary (registry, in English)

A Study of Anti-CD19 Chimeric Antigen Receptor T Cell Therapy for Subjects With Refractory Lupus Nephritis

Status (registry)
Terminated
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
2 (actual)
First submitted
27 Mar 2024
Start date
1 Dec 2022
Primary completion date
22 Dec 2025
Lead sponsor
Kyverna Therapeutics
Diseases
Lupus (SLE)
NCT number
NCT06342960

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment with cellular therapy (CAR-T) or gene therapy product directed at any target
  • Previous or concurrent malignancy with the following exceptions:
    • Adequately treated basal cell or squamous cell carcinoma (adequate wound healing is required prior to screening)
    • In situ carcinoma of the cervix or breast, treated curatively and without evidence of recurrence for at least 3 years prior to screening
    • A primary malignancy which has been completely resected, or treated, and is in complete remission for at least 5 years prior to screening

Other illness

  • Rapidly progressive glomerulonephritis; history of or currently active severe central nervous system (CNS) lupus, including cerebritis, cerebrovascular accident, and seizures
  • History of allogeneic or autologous stem cell transplant
  • Evidence of active hepatitis B or hepatitis C infection
  • Positive serology for HIV
  • History of splenectomy
  • History of stroke, seizure, dementia, Parkinson's disease, coordination movement disorder, cerebellar diseases, psychosis, paresis, aphasia, and any other neurologic disorder investigator considers would increase the risk for the subject.
  • Impaired cardiac function or clinically significant cardiac disease

Other

  • Primary immunodeficiency

Who the study is looking for

  • Age ≥18 years
  • Clinical diagnosis of SLE according to 2019 European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) classification criteria
  • Biopsy-proven proliferative LN Class III or IV according to 2018 International Society of Nephrology/Renal Pathology Society (ISN/RPS) criteria
  • Positive anti-nuclear antibody (ANA) (titer ≥1:80 ), anti-dsDNA (≥30 IU/mL on enzyme-linked immunosorbent assay [ELISA]), or anti-Smith at screening or by documented medical history
  • Up to date on recommended vaccinations, including against coronavirus disease 2019/ severe acute respiratory syndrome coronavirus 2 (Covid-19/SARS-Cov-2), per Centers for Disease Control and Prevention (CDC) or institutional guidelines for immune compromised individuals

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Charite- Universitätsklinikum BerlinBerlinGermanyUnknown status
Universitätsklinikum Carl Gustav Carus DresdenDresdenGermanyUnknown status
Universitätsklinikum DüsseldorfDüsseldorfGermanyUnknown status
Universitätsklinikum ErlangenErlangenGermanyUnknown status
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMPFrankfurtGermanyUnknown status
Universitätsklinikum Hamburg-EppendorfHamburgGermanyUnknown status

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.