October 7, 2025 | 10:00AM EST

 

In this webinar, you will learn:

  • About paratope-centered patenting as a way to build stronger, structurally defined claims that withstand enablement and design-around challenges.
  • How evolving case law, USPTO guidance, and antibody characterization tools can open new avenues for securing robust protection for therapeutic antibodies.
  • Experimental strategies for resolving epitope and paratope including efficiently permutating and screening amino acid substitutions

Paratope-Based mAb Patent Protection

While the most straightforward method of patenting monoclonal antibodies (mAbs) is to claim their exact amino acid sequences, these claims are highly vulnerable; minor sequence modifications can preserve antigen recognition and function while circumventing IP. Broad claims covering any antibody that binds the antigen or epitope are no longer permissible in the USA, creating a need for new strategies for robust patent protection.

As an alternative, Dr. Ulrich Storz, patent attorney with expertise in therapeutic mAbs, suggests a paratope-centered strategy for robust protection. By defining mAbs through shared paratope residues and permissible CDR substitutions that maintain binding, inventors can construct structurally anchored claims, meet enablement and written description requirements, and reduce opportunities for design-arounds.

This webinar will highlight how case law, USPTO guidance, and advances in antibody characterization technologies provide a stronger, more resilient framework for protecting next-generation antibody therapeutics.

Speaker Bios

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