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

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NCT06342960 · readout ≤ 803 d

Sponsored by Kyverna Therapeutics (industry) · KYTX — their whole pipeline →.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
2actual
Sites
6
Country
Germany

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-12-01actualWhen the study began enrolling
Primary completionOct 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2029estimatedThe whole study's end, after follow-up
First posted2024-04-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Lupus Nephritis
  • Lupus Nephritis - WHO Class III
  • Lupus Nephritis - WHO Class IV

Interventions

  • Biological: KYV-101 anti-CD19 CAR-T cell therapy
  • Drug: Standard lymphodepletion regimen — also filed as Cyclophosphamide, Fludarabine

Primary outcomes

what the primary-completion date above is the date OF
Incidence adverse events (AEs) and laboratory abnormalities (Phase 1 and Phase 2)
measured Up to 2 years
Frequency of dose limiting toxicities (Phase 1)
measured Up to 2 years

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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