Get in touch

Submit

Thank you

We are able to support pharmaceutical clients across the full patent lifecycle, from invention harvesting and evaluation through to patentability assessment, drafting, filing and prosecution. Our advice and support extend to patent and supplementary protection certificate (SPC) strategy, lifecycle management, freedom to operate (FTO), commercial agreements, and the defence of valuable patent rights, including providing specialist European Patent Office (EPO) Opposition and Appeal representation for companies in the pharmaceutical sector. We represent pharmaceutical clients who file patent applications in upwards of 30 separate countries/legal jurisdictions, and we have a trusted, strong network of local attorneys to support our clients in those territories, which is backed up by our own extensive experience of prosecuting patents and devising patent protection strategies simultaneously in multiple different countries.

 

A lifecycle that needs a patent strategy to match

We understand that pharmaceutical innovation and protection involve a complex lifecycle, not just a moment.

The IP strategy for a pharmaceutical asset must achieve several objectives, including establishing a strong primary patent that protects the active pharmaceutical ingredient (API); extending exclusivity through polymorphs, enantiomers, salt forms, formulations, new indications, dosage regimens and combination products, for example; and securing SPCs and patent term extensions, where they are available.

IP decisions made during early clinical development can shape the strength and duration of protection when generic competitors eventually enter the market, making a well-considered strategy from the outset essential.

Our team has the expertise to advise our pharmaceutical clients throughout that journey to ensure robust protection for their assets. From initial filing strategy through to portfolio management and enforcement, we work to ensure valuable innovations are protected in a way that supports long-term commercial objectives. We also help clients navigate contentious matters such as opposition proceedings, validity challenges and litigation when they arise.

 

How we build multidisciplinary pharmaceutical IP teams

Pharmaceutical innovation spans many fields. A pharmaceutical matter at Keltie typically draws from our chemistry and life sciences attorneys. When the science involves AI-driven drug discovery, generative chemistry, in silico target prediction or other computational approaches (as it frequently does), we are able to rely on patent specialists in our software and AI patent teams to ensure that all valuable IP is identified and appropriately protected, whether that be through a registered IP right, such as a patent (e.g. for a product), or through non-registered rights, such as trade secrets – which can be even more important than a registered right in some business strategies.

At Keltie, we have the strength and depth of expertise to provide a range of skill sets that are able to support and work with our clients, whatever the mix of science and the development stage they are at.

Our pharmaceutical patent expertise

Our patent attorneys combine strong technical backgrounds with extensive patent prosecution experience across the full breadth of the pharmaceutical sector, including oncology, immunology, inflammatory diseases, neuroscience, cardiovascular diseases, metabolic diseases, infectious diseases, and respiratory diseases, to name a few areas.

Keltie’s pharmaceutical clients benefit from our combined legal expertise and strong scientific ability. Most of our attorneys hold a PhD in a relevant discipline, and many have previous experience working as research scientists in the pharmaceutical industry and also as in-house IP attorneys. These experiences allow us to fully appreciate our clients’ interests and concerns and enable us to interact with both in-house legal teams and scientists in a manner that is as seamless and integrated as our clients desire.

We are creative and innovative in the way we work. In particular, we work in teams that have strengths that extend far beyond those of any individual, and we are determined to not only deliver the results that our clients hope for, but to exceed any expectations. We measure our success by the success that we are able to deliver to our clients, and we are motivated by the desire to always learn and improve.

Pharmaceutical IP services

We support pharmaceutical clients across the full IP lifecycle. Key areas in which we advise and provide assistance are:

  • Portfolio strategy and lifecycle management
  • Invention harvesting and evaluation
  • Patentability assessment
  • Patent drafting, filing and prosecution before the EPO, UKIPO, USPTO and other major offices
  • Supplementary protection certificates (SPCs) and patent term extensions (PTE)
  • Regulatory data protection and the interplay between SPCs and orphan, paediatric and other regulatory exclusivities
  • EPO Oppositions and Appeals, and Unified Patent Court (UPC) representation in contentious proceedings
  • Freedom to operate (FTO) analyses across crowded therapeutic landscapes
  • Fractional in-house support
  • IP due diligence for licensing, partnering, fundraising, and mergers and acquisitions (M&A)
  • Commercial agreements: licensing, collaboration, supply, manufacturing and material transfer
  • Trade marks and design rights for marketed medicines
Continue reading about Pharmaceuticals & Drug Discovery

Get in touch

Submit

Thank you