Sweden’s BioInvent International today said it will receive a $0.5 million milestone payment related to the acceptance by the US Food and Drug Administration of the Investigational New Drug (IND) application for TAK-169, a first-in-class CD38-targeted fusion protein.
BioInvent’s shares rose 2.17% to 1.45 Swedish kronor on the news.
The IND was filed by Japan’s Takeda Pharmaceutical under a co-development agreement with Molecular Templates. This milestone relates to BioInvent's proprietary n-CoDeR antibody library and its role in the discovery of the investigational compound.
Martin Welschof, chief executive of BioInvent, said: "This is validating that our n-CoDeR platform not only yields highly promising drug candidates for BioInvent's proprietary programs, but is also helping our partners in building their own pipelines."
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