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?
DOWNLOAD THE REPORT

Read our blogs

Singapore's Synthetic Biology Moment: Building a Global Translation Hub

Singapore's Synthetic Biology Moment: Building a Global Translation Hub

by Thomas Driver

Synthetic biology has become one of the most exciting technology sectors of the past decade. Advances in gene editing, enzyme engineering, AI-guided protein design and industrial biomanufacturing are ...

Cell-free systems and the next wave of biomanufacturing IP

Cell-free systems and the next wave of biomanufacturing IP

by Kate Fitzpatrick

Biomanufacturing is undergoing a structural shift. For decades, engineered cells have been the dominant production platforms, but a new paradigm is emerging: cell free systems.

Dr Tim Lu: “We can programme computers. Why can't we do that in biology?”

Dr Tim Lu: “We can programme computers. Why can't we do that in biology?”

by Richard Clegg

Dr Tim Lu is a pioneer in synthetic biology. He and his team are editing immune cells to upgrade the way they detect disease. His method introduces computer logic gate thinking, where cells ...

The Microbiome in Metabolic Health: more than a gut feeling?

The Microbiome in Metabolic Health: more than a gut feeling?

by Annabel Cardno

Metabolic health has traditionally been viewed through the lens of the host: diet, exercise, genetics, hormones and, more recently, pharmacological intervention. However, over the last decade, it has ...

Innovative Diagnostics: Can New Testing Transform Endometriosis Care?

Innovative Diagnostics: Can New Testing Transform Endometriosis Care?

by Frances Salisbury

The BBC covered an encouraging development this week in the diagnosis of endometriosis, a condition that is still all too often characterised by delay, uncertainty, and a reliance on invasive ...

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 ...

Learn More
ME Forward Masthead White 2