With the upcoming patent expirations in oncology biologics, biosimilar developers must act quickly to capitalize on ADCs and BsAbs.

In this article, explore the opportunities and challenges shaping the landscape, including:
- How patent expirations, and a shift from monoclonal antibodies, is driving opportunities for biosimilar innovation in ADCs and BsAbs
- Why the structural complexities of ADCs and BsAbs require new bioanalytical tools and manufacturing processes
- The evolving regulatory landscape: EMA, FDA and WHO are developing regulatory pathways with flexibility, but challenges still remain
- The global market forecast, opportunity and key timelines - but why sponsors must act fast
- How biosimilars can deliver cost savings of $54 billion over the next decade, while broadening patient access to cancer treatments
- And more
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