Amgen and Xencor have entered into a cancer-drug collaboration, that could be potenitally worth about $1.7bn.
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The companies will work together in developing and commercializing novel therapeutics in the fields of cancer immunotherapy and inflammation.
Amgen agreed to pay $45m upfront to license Xencor’s XmAb bispecific technology platform in five preclinical programs intended to treat cancer and inflammatory diseases.
The company will also make $1.7bn in clinical, regulatory and sales milestone payments.
XmAb bispecific Fc domains will be used to make half-life extended T cell engagers and dual targeting bispecific antibodies.
The deal also includes a preclinical bispecific T cell engager program directed at CD38 and CD3 for multiple myeloma.
Amgen executive vice president of research and development Sean Harper said: "We are especially excited about the T cell engaging bispecific antibody directed against CD38, which complements Amgen’s BiTE platform, while growing our hematology and oncology portfolio that includes two bispecific T cell engager antibodies, BLINCYTO (blinatumomab) and AMG 330, as well as Kyprolis (carfilzomib) for relapsed multiple myeloma."
Xencor president and CEO Bassil Dahiyat said: "Xencor will continue to focus on its internal programs including its immuno-oncology XmAb bispecifics, XmAb14045 in acute myeloid leukemia and XmAb13676 in B-cell malignancies, which are expected to enter clinical development in 2016."
Xencor developed XmAb bispecific Fc domain technology to maintain full-length antibody properties in a bispecific antibody, potentially allowing favorable in vivo half-life and simplified manufacturing.
The company’s initial bispecific programs are tumor-targeted antibodies that include a tumor antigen binding domain and a cytotoxic T-cell binding domain (CD3 binding domain).
Image: Amgen headquarters in Thousand Oaks, California. Photo: courtesy of Coolcaesar.