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NCT06400303TerminatedPhase 1/2

KYSA-5: A Study of Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Systemic Sclerosis

KYSA-5: A Phase 1/2, Open-Label, Multicentre Study of KYV 101, an Autologous Fully Human Anti-CD19 Chimeric Antigen Receptor T Cell (CD19 CAR T) Therapy, in Subjects With Systemic Sclerosis

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 Systemic Sclerosis

Status (registry)
Terminated
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
3 (actual)
First submitted
29 Aug 2023
Start date
6 Aug 2024
Primary completion date
16 Jun 2026
Lead sponsor
Kyverna Therapeutics
NCT number
NCT06400303

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

  • 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

  • Clinically significant ILD
  • Primary immunodeficiency

Who the study is looking for

  • Clinical diagnosis of SSc according to 2013 ACR/EULAR classification
  • Clinical disease as follows: Classified as diffuse cutaneous SSc; ≤ 6 years since first non-Raynaud's sign or symptom; active disease
  • Up to date on all recommended vaccinations per 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 (2)

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

SiteCityCountrySite status
Northwell HealthGreat NeckUnited StatesUnknown status
Stanford University Medical CenterPalo AltoUnited StatesUnknown status

Are you the coordinator? Confirm the details

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