Condition: Refractory Lupus Nephritis · Myasthaenia Gravis · Stiff Person Syndrome · Sponsor: Kyverna Therapeutics
The purpose of this long-term follow-up (LTFU) study is to collect delayed adverse events (AEs) and understand the persistence of KYV-101 (autologous CAR T cell product; gene-modified product), in participants who have been administered KYV-101 (gene-modified product; autologous CAR T cell product). This LTFU protocol will be open to any participant who received at least one infusion of KYV-101 in a previous Kyverna sponsored clinical trial or Investigator Initiated Trial (IIT).
This description comes directly from the study's public registry record.
Kyverna Therapeutics · 510-925-2484 · clinicaltrials@kyvernatx.com
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| University of Colorado, Denver | Denver, Colorado, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07403188