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

Beyond PROTACs and molecular glues: where next for heterobifunctional drug discovery?

Beyond PROTACs and molecular glues: where next for heterobifunctional drug discovery?

by Annabel Cardno

A broader heterobifunctional tool emerges Targeted protein degradation has rapidly progressed from a conceptual curiosity to one of the most closely watched areas in drug discovery. As discussed in ...

Global considerations for innovators in microbial biostimulants and biocontrol agents

Global considerations for innovators in microbial biostimulants and biocontrol agents

by Ben Tolley

Our recent analysis found that global patent activity in microbial biostimulants and biocontrol agents is surging, with strong growth in both patent applications and granted patents. For a detailed ...

EPO decision T 0655/24: inventive step and the unpredictability of antibody mutations

EPO decision T 0655/24: inventive step and the unpredictability of antibody mutations

by Chris Denison

This is the final post in a series on decision T 0655/24 and its implications for antibody practice at the EPO. In the first post, Chris discussed the Board’s strict approach to post-filing evidence ...

EU NGT Regulation Approved: A Step Towards Innovation

EU NGT Regulation Approved: A Step Towards Innovation

by Louise Atkins

The EU’s long‑awaited regulation on New Genomic Techniques (NGTs) has now cleared its final legislative hurdle, with the European Parliament voting to approve the agreed framework, rejecting ...

Molecular Glue Degraders (MGDs): what they are, how they work and key IP Issues

Molecular Glue Degraders (MGDs): what they are, how they work and key IP Issues

by Tim Nash

Molecular glue degraders (MGDs) are small molecules that induce or stabilise protein–protein interactions, often by recruiting an E3 ligase to a target protein and triggering its ubiquitination and ...

Ageing as a disease: Groundbreaking or Ground-Shaking?

Ageing as a disease: Groundbreaking or Ground-Shaking?

by Emily Garnett

As a species, humans have long been preoccupied with living longer and healthier lives. However, prior to the advent of modern medicine, any real prospect of fulfilling these ambitions existed more ...

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