Biologics & Cell Therapies

Our large team of patent attorneys means that we can offer individuals with genuine expertise across all classes of biologics, including polypeptides, monoclonal antibodies, nucleic acid therapeutics, vaccines, stem cells and cellular immunotherapy.

Mewburn Ellis has a long history of working with leaders in the field of monoclonal antibodies and continues to be a go-to IP firm in this space. We are proud to have worked with the 2018 Nobel Prize winner Professor Winter on patents for phage display for the directed evolution of antibodies. We have since developed and protected the patent portfolios for numerous blockbusters, including Herceptin®, Humira®, Avastin®, Rituxan®, Lucentis®, Xolair® and Perjeta®.

We know how to support drug development from conception to marketing and have done so for numerous biologics, including Lyxumia® and Nutropin®. We also have expertise in obtaining broad IP protection for novel and emerging classes of drugs. For instance, we obtained the first class-level patent protection for aptamers and have since prosecuted over 150 patents related to aptamer technology.

Cell therapy is highly active field at present and we are excited to be working at the forefront. We have considerable experience in drafting and prosecuting patent applications relating to innovative cell therapy products, including their generation, expansion and medical use. We always bear in mind that new technologies may require fresh thinking and a new approach to patent protection. For example, in autologous cellular immunotherapy, the product is not an off-the-shelf drug but is based on isolation of the patient’s own cells. We understand the importance of considering the practicalities of the therapeutic process at the earliest possible stage and we work with our clients to develop global patent strategies which will fit the new therapeutic landscape.

Read more about protecting your innovations

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Antibodies & ADCs

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CAR-T & Other Cell Therapies

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Nucleic Acid Therapeutics

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Protein Therapeutics

Open Pages of Validation Strategies for Pharmaceutical Patents in Europe Report

Special Report

Validation Strategies for Pharmaceutical Patents in Europe

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?

Read our blogs

Efficiency in Expansion: Meeting the Scale-Up Challenge in Cell and Gene Therapies

Efficiency in Expansion: Meeting the Scale-Up Challenge in Cell and Gene Therapies

One of the pivotal challenges in the development and commercialisation of cell and gene therapies lies in scaling-up production. This challenge is particularly pronounced as companies transition from ...

Cellular Agriculture – Innovating through the Challenges

Cellular Agriculture – Innovating through the Challenges

The last year (2023) has seen a difficult environment for Cellular Agriculture (Cell Ag) companies working to commercialise cultivated meat.

Top marks for Iovance as FDA approves first-in-class cell therapy Amtagvi for solid tumours

Top marks for Iovance as FDA approves first-in-class cell therapy Amtagvi for solid tumours

On February 16, 2024, a real milestone was reached in the cell therapy field, as the FDA approved the first cell therapy for solid tumours. The therapy is called Amtagvi (lifileucel), a ...

We work at every stage of the IP lifecycle

Protect

Drafting, Filing & Prosecution
Portfolio Management
Searching & Watching
Renewals & EP Validations

Defend

Pre-action Advice
Oppositions & Appeals
Litigation
Alternative Dispute Resolution

Exploit

Strategic Advice
Commercial Issues
Transactions
Corporate Support

Forward Magazines Overlapping 8

Mewburn Ellis

FORWARD MAGAZINE

Mewburn Ellis Forward is a biannual publication that celebrates the best of innovation and exploration. Through its pages we hope to inform and entertain, but also to encourage discussion about the most compelling developments taking place in the scientific and entrepreneurial world. Along the way, we’ll engage with the IP challenges that international organisations face every day.