Cell Therapy

We are delighted to be working with innovative companies and academic institutions in the exciting field of cell therapy. We leverage our huge depth of experience in the fields of monoclonal antibody technology, cellular biology, immunology and regenerative medicine to build robust, investable patent portfolios for our clients in this space. While applying our wealth of existing knowledge, we are also alive to the fact that new technologies require fresh thinking and an innovative approach to patent protection.

We understand the importance of considering the practicalities of the production and administration of the therapeutic agent(s) at the earliest possible stage, and work with closely with our clients to understand that fine details of the technology and develop an appropriate supporting global patent strategy. For example, in the field of adoptive cellular therapy, strategy for protecting an autologous cell therapy, in which the therapeutic ‘product’ to be administered is a personalised product derived from a patient’s own cells requires a different approach to protecting an allogeneic cell therapy (towards which the field is increasingly moving), which in some aspects is closer to a traditional ‘off-the-shelf’ product.

We have considerable experience in drafting and prosecuting patent applications relating to innovative cell therapies, including for novel CAR/TCR molecules, new platform approaches and innovations relating to the production, expansion and medical use of cell therapies. As earlier generation products continue to mature through clinical trials, we also help our clients to protect innovation throughout the product lifecycle, for example with patent applications related to personalised medicine or new dosage regimes. We also help our clients to navigate the dynamic and increasingly complex patent landscape in the field of cell therapy, strategising with them to minimize the risk presented by patents held by third parties.

Mewburn Ellis is very proud to be working with the entities operating right at the cutting edge of innovation in this exciting field, developing the new platform technologies, designing novel recombinant molecules (CARs, TCRs, etc.) and moving into new disease frontiers (solid cancers, autoimmune disease, viral disease), that will re-shape the therapeutic landscape for the years to come.

Open Pages of Validation Strategies for Pharmaceutical Patents in Europe Report

Validation Strategies for Pharmaceutical Patents in Europe

Special Report

The decision on where to validate a pharmaceutical European patent is a big one. With costs often precluding an “everywhere” approach for small- to medium-sized companies, research institutions and universities, it is necessary to choose from the long list of available countries. The choice typically factors in costs, business interests, likely markets and market size, possible manufacturing and import locations and the regulatory framework in Europe.

This report explores these choices and factors using publicly available data, seeking to answer questions such as:

  • Which countries are most commonly picked by patent holders at the EPO?
  • Is the distribution the same for pharmaceutical patents?
  • Where does “big pharma” choose to validate?
  • What factors might affect the choice of countries?
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Read our blogs

Fast Growing Techbio: Data, Computational Research, IP and How to Leverage Those for Commercial Success

Fast Growing Techbio: Data, Computational Research, IP and How to Leverage Those for Commercial Success

by Christopher Casley

On Wednesday 6 May we were delighted to co-host a panel discussion and networking event: “Fast growing techbio: data, computational research, IP and how to leverage those for commercial success” at ...

PROTACs reach the market: what the first regulatory approval means for drug discovery and the patent landscape

PROTACs reach the market: what the first regulatory approval means for drug discovery and the patent landscape

by Andrew Pitts

Just as the attention of the pharmaceutical industry appeared to have shifted over the past few years towards biologics with blockbuster potential, a new and exciting therapeutic modality has emerged ...

Artificial Intelligence in Modern Fertility Technologies

Artificial Intelligence in Modern Fertility Technologies

by Charlotte Lynch

In vitro fertilisation (IVF) represented a major technological breakthrough when it first became available more than forty years ago. However, despite incremental improvements, overall IVF success ...

How Plurify is purifying cell pools with bespoke RNA

How Plurify is purifying cell pools with bespoke RNA

by Anja Koller

Forward speaks to Mantas Matjusaitis, Plurify co-founder and chief technical officer, tells Mewburn Ellis about the company’s method of sorting stem cells at bioreactor scale.

The quest to build heat-resistant vaccines

The quest to build heat-resistant vaccines

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Forward speaks to Asel Sartbaeva, the co-inventor of a method to make temperature sensitive medicines withstand heat, with the potential to transform the way they are stored, transported and ...

The global boom in microbial crop solutions and what it means for your IP strategy

The global boom in microbial crop solutions and what it means for your IP strategy

by Ben Tolley

Experts predict that global food production will need to more than double in the next 25 years. There is no historical precedent for achieving growth of that magnitude in a single generation.

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