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Arovella Therapeutics takes key manufacturing step on ALA-101’s path to clinic

Published 02/01/2024, 12:05 pm
Updated 02/01/2024, 12:30 pm
© Reuters.  Arovella Therapeutics takes key manufacturing step on ALA-101’s path to clinic

Arovella Therapeutics Ltd (ASX:ALA) has completed a key manufacturing step to progress lead product ALA-101 to clinic with its Good Manufacturing Practice (GMP)-grade lentiviral vector for ALA-101 successfully manufactured and quality release testing passed.

ALA-101 is being developed by Arovella to treat CD19+ lymphomas and leukemias.

A key requirement for the development of an iNKT cell therapy product is the establishment of the manufacturing process under GMP conditions.

Critical component

The GMP-grade lentiviral vector is a critical component for clinical manufacturing as it carries the genetic material to program iNKT cells to target and eliminate cancer cells.

ALA-101’s vector is a third-generation lentiviral vector manufactured by Lentigen Technology, Inc, a world-leading manufacturer of lentiviral vectors for cell and gene therapies.

“A tremendous step”

Arovella’s CEO and MD Dr Michael Baker said: “This is a tremendous step forward for the ALA-101 program and for Arovella.

"Producing GMP lentiviral vector is essential to developing ALA-101 and we are delighted this major step was completed on schedule.”

About Arovella and ALA-101

Arovella is a biotechnology company focused on developing its invariant natural killer T (iNKT) cell therapy platform from Imperial College London to treat blood cancers and solid tumours.

Its lead product is ALA-101, which consists of CAR19-iNKT cells that have been modified to produce a Chimeric Antigen Receptor (CAR) that targets CD19, which is an antigen found on the surface of numerous cancer types.

iNKT cells also contain an invariant T cell receptor (iTCR) that targets α-GalCer bound CD1d, another antigen found on the surface of several cancer types.

ALA-101 is being developed as an allogeneic cell therapy, which means it can be given from a healthy donor to a patient.

Arovella is also expanding into solid tumour treatment through its CLDN18.2-targeting technology licensed from Sparx Group.

Additional tumour-targeting technologies are anticipated to be used in conjunction with Arovella’s iNKT cell therapy platform.

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