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
Sites (6)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Charite- Universitätsklinikum Berlin | Berlin | Germany | Unknown status |
| Universitätsklinikum Carl Gustav Carus Dresden | Dresden | Germany | Unknown status |
| Universitätsklinikum Düsseldorf | Düsseldorf | Germany | Unknown status |
| Universitätsklinikum Erlangen | Erlangen | Germany | Unknown status |
| Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP | Frankfurt | Germany | Unknown status |
| Universitätsklinikum Hamburg-Eppendorf | Hamburg | Germany | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.