KYSA-8 Principal Investigators

Amanda Piquet, MD
Director, Autoimmune Neurology
University of Colorado School of Medicine Anschutz Medical Campus, CO
Marinos Dalakas, MD
Director, Neuromuscular Division
Thomas Jefferson University School of Medicine, PA 
Anastasia Zekeridou, MD, PhD
Co-Director Neuroimmunology Laboratory
Associate Professor of Neurology
Mayo Clinic, Rochester, MN

Frequently Asked Questions

Why is the KYSA-8 trial being conducted?

The KYSA-8 clinical trial aims to show efficacy and confirm safety of KYV-101, a CAR T-cell therapy, as a potential treatment for people living with SPS.

Who is conducting the KYSA-8 clinical trial?

The KYSA-8 clinical trial is sponsored by Kyverna Therapeutics, a company dedicated to developing therapies to help reset the immune system and help eliminate the need for long-term or suboptimal therapies.

What is a Phase 2 clinical trial? 

  Phase 1: Safety. In a Phase 1 clinical trial, doctors want to understand if a treatment is safe and well tolerated in humans. Phase 1 trials are the first stage of human clinical trials and usually involve only a small number of people.

Phase 2: Efficacy. In a Phase 2 clinical trials expand the study to a larger group of individuals to assess the treatment’s effectiveness and further evaluate its safety.

What safety precautions are in place for the clinical trial?

To ensure that clinical trials are conducted safely, doctors take safety precautions which include:

• Informed consent : Participation in the trials is voluntary. Participants in a clinical trial are to provide informed consent before they can participate in the study. This means that participants will be given information about the clinical trial, including the risks and benefits, before the participants indicate if they want to join the study.

• Data safety monitoring : An independent data safety monitoring board (DSMB) is a group of independent experts who review the data collected in a clinical trial on a regular basis. The DSMB is responsible for ensuring that the clinical trial is being conducted safely and that the participants are not being put at risk.

• Side effect reporting : All side effects that occur in a clinical trial must be reported to the clinical trial team. An adverse event is any unwanted or unexpected medical occurrence that happens to a participant during a clinical trial.

• Withdrawal from the clinical trial : Participants in a clinical trial have the right to withdraw at any time.

Is there a placebo in this clinical trial?

No. All participants will receive KYV-101 and will be closely monitored by a team of healthcare professionals.

Will my personal information be kept private?

Yes, to protect your privacy, steps taken by the clinical trial team will include:

• Use of codes or pseudonyms instead of your real name.

• Secure storage of your data without access by unauthorized individuals.

• Requiring clinical trial investigators to sign confidentiality agreements.

You will also have the right to withdraw from the study at any time. Data that was collected by your study doctor will still be able to be used by the sponsor.

What causes stiff-person syndrome (SPS)?

It is believed that it is an autoimmune disorder caused by a type of cell called B cells.

Has KYV-101 been studied before?

This is the first study using KYV-101 in SPS, but several patients with SPS have been treated with KYV-101. Patients with Lupus Nephritis, Myasthenia Gravis, Systemic Sclerosis (Scleroderma), and Multiple Sclerosis have also been treated with KYV-101.

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