The US Food and Drug Administration (FDA) has approved Artiva Biotherapeutics’ investigational new drug (IND) application for the combination of AlloNK (AB-101) and rituximab to treat systemic lupus erythematosus (SLE) in active lupus nephritis (LN) patients.
Designed to improve antibody-dependent cellular cytotoxicity (ADCC), AlloNK is a non-genetically modified, allogeneic, cord blood-derived, cryopreserved NK cell therapy candidate.
AlloNK is currently under assessment in two cancer trials, where it is being studied alongside antibody or NK-engager biologics.
In May 2022 the company revealed preliminary results from the dose-escalation stage of its Phase I/II clinical trial involving AB-101.
The trial, which focused on patients with relapsed/refractory B-cell non-Hodgkin’s lymphoma (B-NHL), showed AlloNK’s therapeutic potential and favourable safety profile when used in conjunction with rituximab.
Artiva CEO Fred Aslan stated: “AlloNK given in combination with rituximab, an anti-CD20 antibody that targets B-cells, is already driving complete responses in late line B-NHL patients in an ongoing Phase I study by enhancing the activity of rituximab.
“Our hypothesis is that AlloNK plus rituximab also has the potential to drive deep B-cell depletion in LN patients with an off-the-shelf therapy that could be administered and managed in an outpatient setting.”
SLE is a severe autoimmune condition characterised by faulty B-cell activity and production of autoantibodies. Its clinical symptoms include end-organ damage and increased risk of death.
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