RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:My opinionOn a brighter note. Cancer deal.
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With a recent approval for lung cancer bispecific amivantamab, J&J is looking to build a franchise in that space with a growing crop of drugs in the pipeline. The drug giant has now tapped a familiar partner to drive that work ahead, and the pair is going after a well-known target. J&J's Janssen unit has inked a licensing deal worth $100 million in upfront cash and $25 million in equity for global licensing rights to Xencor's CD20/CD3 bispecific antibody plamotamab currently in Phase I testing against B cell malignancies, the companies said Monday.
The deal will come with up to $1.18 billion in downstream milestones as well as potential royalties in the "mid-teens to low twenties," according to a release.
Janssen will hold exclusive development and commercialization rights worldwide for plamotamab, including in monotherapy and combo regimens, with Xencor and Janssen splitting future clinical trial costs 20-80, respectively. Those plans include a subcutaneous formulation trial for the bispecific, which is expected to begin in 2022. Meanwhile, Xencor will exclusively fund a Phase II combo study of plamotamab, tafasitamab and lenalidomide in patients with B-cell lymphoma set to start in late 2021 or early 2022.
The collaboration will also fuel R&D for new CD28-targeting bispecifics out of Xencor's pipeline, with the partners collaborating on a two-year research project. Janssen will hold an exclusive worldwide license to develop any selected molecules that come out of that work as part of a combo with plamotamab or other antibodies, including those targeting CD3, where they would compete directly with Regeneron."