TxCell completes CAR-Treg manufacturing process development

TxCell, a developer of cellular immunotherapies based on regulatory T cells (Tregs) for inflammation, autoimmunity and transplantation, has completed the development of its first-generation production process for its proprietary CAR-Treg technology.

The process will be transferred to a contract manufacturing organisation (CMO) before the start of a first-in-man clinical trial.

For its first CAR-Treg manufacturing process, TxCell has isolated a subset of Treg cells that have shown to be stable and to display a strong anti-inflammatory activity.

Despite the rarity of the selected Treg subset, TxCell has successfully produced its CAR-Treg cellular product within two weeks (before post-production quality control). TxCell will present additional details on this manufacturing process at the CAR‑TCR Summit Europe to be held on February 20-22, 2018, in London.

TxCell is currently finalising its selection of the CMO for clinical supply of its lead HLA-A2 CAR‑Treg product. Once CMO contractual agreements are executed, the transfer of TxCell’s manufacturing process will follow immediately.

A regulatory dossier to start a first-in-man study is expected to be filed in Q4 2018. The start of clinical development will be subject to regulatory approval and availability of appropriate funding.

Stephane Boissel, CEO of TxCell, said: “Our personalised cellular approach could offer an alternative therapy to prevent chronic rejection of transplanted organs. There is a significant risk of post-transplant organ rejection. In lung transplants, for example, this results in a mortality rate of 40% to 55% five years after surgery. As a result, there remains a significant medical need for a novel therapeutic approach.”

 

 

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