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Kyverna's KYV-101 Gets FDA IND Clearance For Treatment Of Stiff-Person Syndrome In Phase 2 Trial

By RTTNews Staff Writer   ✉   | Published:   | Follow Us On Google News
rttnewslogo20mar2024

Thursday, Kyverna Therapeutics, Inc. (KYTX) announced that the FDA has approved its Investigational New Drug or IND application for KYV-101. This clearance allows the utilization of KYV-101 in the treatment of stiff-person syndrome in Kyverna's Phase 2, open-label KYSA-8 clinical trial.

KYV-101 is a fully human anti-CD19 CAR T-cell product designed for patients with B-cell-driven autoimmune diseases. It is currently under evaluation in sponsored, open-label Phase 1/2 and Phase 2 trials for rheumatology and neurology.

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