KYSA-1: A Phase 1/2, Open-Label, Multicenter Study of KYV-101, an Autologous Fully-Human Anti-CD19 Chimeric Antigen Receptor T-Cell (CD19 CAR T) Therapy, in Subjects With Refractory Lupus Nephritis
Latest Information Update: 21 Nov 2024
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At a glance
- Drugs KYV-101 (Primary)
- Indications Lupus nephritis
- Focus Adverse reactions
- Acronyms KYSA-1
- Sponsors Kyverna Therapeutics
- 14 Nov 2024 According to Kyverna Therapeutics media release, company will present updated clinical data from LN patients treated with KYV-101 in ongoing Kyverna-sponsored KYSA-1 Phase 1/2 study at a company symposium titled, "KYV-101 Anti-CD19 CAR T-Cell Therapy: The Future of Autoimmune Disease Treatment," to be held at ACR Convergence 5:45 pm ET on November 18, 2024.
- 14 May 2024 According to Kyverna Therapeutics media release, treated 30 patients cumulatively as of May 14, 2024, including eight patients with myasthenia gravis, seven patients with lupus nephritis, and four patients with multiple sclerosis
- 16 Apr 2024 The protocol has been amended to change in phase change to Phase 1/2 with addition of primary endpoint for efficacy of drug (Phase 2) with addition of treatment Arm with respective increase in patient population.