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

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

Recruiting
18 years and older
All
Phase N/A
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  • Simplified (AI rewritten)

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Overview

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).

Eligibility

Inclusion Criteria:

  • 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 Criteria:

  • Not applicable

Study details
    Refractory Lupus Nephritis
    Myasthaenia Gravis
    Stiff Person Syndrome
    Rheumatoid Arthritis (RA)
    Multiple Sclerosis
    Dermatomyositis
    Systemic Sclerosis (SSc)

NCT07403188

Kyverna Therapeutics

26 February 2026

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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