Allogene And Foresight Collaborate To Develop MRD Test For Large B-Cell Lymphoma
Allogene and Foresight Diagnostics extend partnership to co-develop a companion MRD assay for LBCL patients, supporting the ALPHA3 trial.


Allogene Therapeutics, Inc., a clinical-stage biotech company focused on allogeneic CAR T therapies, has further expanded its collaboration with Foresight Diagnostics, Inc. to develop a sensitive minimal residual disease (MRD) assay as a companion diagnostic. The purpose of this test is to identify all patients diagnosed with large B-cell lymphoma (LBCL). Those patients may greatly benefit from treatment with cemacabtagene ansegedleucel (cema-cel).
“The continued collaboration with Foresight Diagnostics strengthens our commitment to advancing next-generation cancer therapies by integrating MRD detection as a powerful tool in patient care. We believe that this strategic expansion will help accelerate the development and potential approval of cema-cel as we continue our mission to transform the LBCL treatment landscape for patients beyond the United States,” said David Chang, M.D., PhD, President, Chief Executive Officer and Co-Founder of Allogene. “
Under the revised agreement, Allogene and Foresight will co-develop the MRD assay in the EU, UK, Canada, and Australia to support the ALPHA3 trial, which evaluates cema-cel as a first-line treatment to improve LBCL cure rates. The assay will detect MRD-positive patients at high risk of relapse, allowing them to receive a one-time consolidation dose of cema-cel. Allogene will invest $37.3 million in the MRD assay’s development, regulatory submissions, and clinical testing. Both companies will work toward securing regulatory approvals and advancing their joint development plan.

Simantini Singh Deo works on the latest and trending news happening daily in the pharma world.
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