drugset / Trial / NCT06152172

CARTIMMUNE: Study of Patients With Autoimmune Diseases Receiving KYV-101

NCT06152172

Phase 1 Active not recruiting 24 enrolled David Porter Kyverna Therapeutics · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, tolerability, and clinical activity of KYV 101 (a fully-human anti-CD19 CAR T-cell therapy) in adult subjects with B cell-driven autoimmune diseases. The trial anticipates enrolling participants to reach a maximum of 24 participants who will receive 1 dose of KYV-101 and will be followed for 2 years.

Timeline

Start
2024-08-05
Primary completion
2027-02
Completion
2027-02

Drugs

EvaluationDrugModalityDoseRoute
Subject KYV-101 Cell therapy 1e+08 cells Intravenous
Background Cyclophosphamide Other / unclassified 300 mg/m2 Intravenous
Background Fludarabine Small molecule 30 mg/m2 Intravenous