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Taking people in GermanyPhase 2/3

Long-term follow-up of people previously treated with KYV-101 for autoimmune diseases

Follows adults treated with KYV-101 earlier to watch for delayed side effects.

Plain-language title generated from the registry record
Registry title: A Long-Term Follow-Up Study for Participants Previously Treated With KYV-101

Key facts

Where
Berlin, Bochum, Hamburg, and Hanover, GermanySee the 4 sites
Phase
Phase 2/3

Where in Germany

  • Charite Universitaetsmedizin Berlin KöRBerlin, GermanyTaking people
  • Katholisches Klinikum Bochum gGmbHBochum, GermanyTaking people
  • Leibniz Institute Of VirologyHamburg, GermanyTaking people
  • Medizinische Hochschule HannoverHanover, GermanyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Kyverna Therapeutics
Trial code
NCT07403188EU 2024-511198-31-00
Record updated
11 February 2026
Original description
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).Read full original descriptionShow less

A Long-Term Follow-Up Study for Participants Previously Treated With KYV-101

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).

Inclusion: Provided informed consent for the LTFU study; Received at least 1 infusion of KYV-101 as part of a previous KYV-101 parent treatment protocol.

Exclusion: Not applicable.

ClinicalTrials.gov NCT07403188 · EU CTIS 2024-511198-31-00