Pharma and nutrition

Our team has commercial and in-house IP experience at a senior level in the pharmaceutical industry, including large, small and start-up companies. More recent graduates and post-graduates bring up-to-the-minute scientific skills to the group.

The group has a reputation for succeeding in difficult legal questions where others have failed, thus providing success in cases which are often commercially very valuable.

Our clients represent both small and large pharma areas, mostly in the USA and Europe. We are well-known for having in-depth practical skills in dealing with pharmaceutical issues and we frequently deal with ground-breaking technologies and products.

Our team

Mathew Leese

Dr Mathew Leese

Title

Technology Specialist

Details

Introduction

Mathew has a BSc (Hons) in Chemistry and a PhD in Organic Synthesis. He has spent the last 12 years leading a drug discovery team within the Pharma industry focusing on oncology and endocrinology targets. He has over 40 academic publications and several patents.


Qualifications

Mathew has a BSc in Chemistry (First Class, Nottingham) and a PhD in Organic Chemistry (Cardiff). He is a Member of the Royal Society of Chemistry (MRSC) and a Chartered Chemist (CChem).

Technical

Mathew has a broad technical background in organic chemistry obtained during graduate and post-doctoral research spells in the UK and Japan, with particular emphasis in the areas of synthesis, organometallic and supported aqueous phase catalysis, analytical techniques and polymer chemistry. Following on from his academic career, Mat spent 12 years leading a drug discovery team in a spin-out pharmaceutical company focusing on oncology and endocrinology targeted drugs.  During this period Mat developed an expertise in medicinal chemistry and drug development processes from discovery to the clinic. His research is documented in over 40 academic papers and a number of patents and he has presented at several conferences.

Click here to view Mathew's publications, patents and conferences.

Legal

Mathew is presently training as a Chartered UK and European Patent Attorney.

Commercial

Prior to joining Avidity IP, Mathew experienced the life cycle of a University spin-out biotechnology company from out licensing, through venture capital fund raising and eventual takeover. The intellectual property of his company was a key element of its corporate value and his own interest in the field arose through engagement in the patenting process from the inventor’s perspective.

Publications

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Laura Fletcher

Laura Fletcher

Title

Associate Attorney

Details

Introduction

Laura has a BSc (Hons) in Chemistry and provides technology support to the Pharma & Nutrition team. She is experienced in drafting and prosecuting cases across Europe especially in the areas of nutrition, formulation chemistry and small molecule therapeutics for cancer, diabetes, obesity, ophthalmic indications, dermatological diseases, lipid storage diseases, pain and inflammation.

Qualifications

BSc (hons) Degree in Chemistry, Durham University. Laura’s dissertation was based on antimicrobial peptides as alternatives to antibiotics and more specifically on the chemical synthesis of lantibiotics, via biomimetic synthesis or sulphur extrusion, and the effects on activity resulting from introduction of carbon mimics.

Technical

Laura provides technology support to the Pharma and Nutrition group. She has experience of drafting and prosecuting cases towards grant in Europe across all areas of the group. In particular, Laura has experience relating to nutrition, process chemistry, innovative small molecule therapeutics as well as innovative formulations for the delivery of therapeutic agents in the treatment of, for example, cancer, diabetes, obesity, ophthalmic conditions, dermatological diseases, lipid storage diseases, pain and inflammation.

Legal

Laura’s responsibilities include prosecution of UK, European and International patent applications for a variety of domestic and overseas clients.  She has also played a supporting role in various Oppositions and Appeals of commercial importance.

Laura has also undertaken legal research into topics of interest to clients. For example, she has authored a publication in our European Law & Practice series entitled “End is nigh for Swiss claim: Enlarged Board decides patentability requirements for further medical uses under the EPC”, which looks at the G2/08 decision in some detail.  Laura has also co-authored the publication “A Guide to Invoking the Specific Mechanism for Parallel Imports of Medicinal Products” which provides guidance and detail on the specific requirements needed for selected jurisdictions. 

Commercial

Laura has managed several projects requiring corporate name changes and change of ownership for UK, European and International patents and patent applications.  Laura is also assisting in the management of transfer of European patent portfolios.

Publications

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Sally Mannion

Dr Sally Mannion

Title

Senior Attorney

Details

Introduction

Sally is the Manager of our Pharma & Nutrition Professional Service Group. She has spent most of her professional career in major pharmaceutical and chemical industries before joining Avidity IP.  Sally provides an extensive experience of pharmaceutical and nutritional portfolio management from the initial drafting and prosecution stages all the way through to co-ordination of multinational patent litigation.  

Qualifications

Chartered UK Patent Attorney; European Patent Attorney; Degree in Agricultural Science (University of Leeds); PhD Agricultural Biology (University of Newcastle-upon-Tyne)

Technical

Sally has worked in the pharmaceutical industry for nearly 20 years and in the chemical industry for more than 25 years.  Prior to joining Avidity IP, she was Chief Patent Counsel of Wyeth Pharmaceuticals heading up a team of European patent attorneys. 

In addition to the pharmaceutical, nutrition and animal health industries, her experience in intellectual property includes working in the agrochemical and speciality chemical fields (such as biodegradable polymers), in ICI and Zeneca.

Her group's specialisations in the pharmaceutical area include new chemical entities, medical uses, formulation chemistry, drug delivery, process chemistry, obtaining supplementary protection certificates and advising on parallel trade matters.  With her substantial chemical and biologics experience, Sally also adds an important bridge to our Life Sciences and Chemistry and Material Science Groups.  

Legal

Sally has conducted multi-national infringement and validity litigation in Europe and other jurisdictions (including questions referred to the European Court of Justice), Oppositions and Appeals at the European Patent office and various national patent offices, restoration cases, freedom to operate opinions and has been involved with a variety of agreement matters, including licensing of pharmaceutical products.

Sally’s responsibilities include drafting and prosecution of UK, European and international patent applications, European oppositions, freedom to operate and due diligence activities for a variety of domestic and overseas clients.  

Commercial

Sally’s long term background in industry gives her an excellent understanding of commercial and corporate needs in a business environment including experience of interfacing with other disciplines such as regulatory affairs and competition law. 

Her extensive in-house interdisciplinary IP management experience across a range of chemical fields means she is able to provide cost effective advice and portfolio management to both large and small pharmaceutical businesses.   

Publications

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Elena Lasterra

Dr Elena Lasterra

Title

Senior Attorney

Details

Introduction

Elena has many years experience in the pharmaceutical industry and in the management of IP for small and start up companies. She believes in the importance of designing, implementing and managing innovative patent strategies to ensure that a company’s IP is maximised.

Qualifications

European Patent Attorney; Degree in Chemistry (Universidad Complutense de Madrid); PhD Chemistry (Imperial College)

Technical

Elena has worked in the pharmaceutical industry for more than 13 years. In addition to her intellectual property expertise her experience includes working as a research synthetic chemist and as an information specialist. Prior to joining Avidity IP Elena was the Head of IP for a start-up pharmaceutical company.

Elena’s industrial experience coupled with a strong technical and research background gives her the ability to work well with inventors as well as having a good understanding of commercial and corporate needs. She specialises in the pharmaceutical area which includes new chemical entities, medical uses, formulation chemistry, drug delivery, re-profiling of old drugs and process chemistry.

Legal

Elena’s responsibilities include the original drafting and prosecution of UK, European and international patent applications for a variety of domestic and overseas clients.

Elena also has experience in freedom to operate issues and in due diligence activities for the licensing of pharmaceutical products.

Commercial

Due to Elena’s experience in small and start-up companies she is able to understand their needs and to help them design, implement and manage innovative patent strategies to protect the company’s pipeline within defined budgets.

Elena believes strongly that it is important to meet clients and inventors regularly and to have firsthand knowledge of their business in order to provide the best advice.

Publications

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Malcolm Lawrence

Malcolm Lawrence

Title

Senior Attorney & CEO

Details

Introduction

Malcolm is a founder Director in the company and was a founder partner in the predecessor partnership of Hepworth Lawrence Bryer & Bizley. Malcolm became the Chief Executive Officer shortly after incorporation of the partnership business in early 2006. He has over 30 years IP experience including more than 20 years as a proprietor.

Qualifications

Malcolm is a UK and European Patent Attorney and a Registered Trade Mark Attorney. He has had a current Litigator’s Certificate since 2001.

Technical

Malcolm’s leadership role remains blended with primarily contentious IP practise in and outside Europe, and in particular with EPO opposition and appeal practise in the pharma and life sciences areas – in recent times particularly in the vaccinology and oncology areas.

Although outside his area of technical expertise, Malcolm has traditionally managed a number of clients in the electronic, telecoms and internet areas. This function has included critical strategic roles in a number of EPO oppositions with successful client outcomes, counselling several clients with arm’s length perspectives on US litigation issues and a past appointment in a mentoring role for the IP manager of a European telecoms company.

Legal

Malcolm has always had an intense and imaginative approach to legal practise, witnessed by a success rate of near 80% in contentious matters and a recognised talent for creative arguments.

As a European Patent Attorney, Malcolm’s practice is primarily EPC patent practice. This has become increasingly concentrated on opposition and other contentious matters over the last 10 years.

He has also built a substantial default recovery practice, and frequently has lapsed cases referred to him for attempted restoration. Malcolm’s success rate in default recovery is over 90%. This special interest in purely legal issues has led to appearances before the Legal Board of Appeal of the EPO.

Apart from patent practice expertise, Malcolm has a range of trade mark responsibilities, mostly in contentious practise areas and in supervising attorneys in our Trade Marks Group. Malcolm successfully prosecuted some of the very first EU applications for registration of 3D marks, some of which have since been enforced against infringers in Europe.

Commercial

Malcolm was Managing Partner of HLBBshaw until its incorporation and has been CEO since March 2006. He has led the development of the business through organic growth, acquisitions and reorganisation from a small practice to a company of around 100 staff.

He has been responsible for the process of transformation of the practice from the owner-managed, inward-facing culture of the predecessor business to that of a forward-looking organisation in full engagement with both its internal and external stakeholders.

Publications

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James Legg

Dr James Legg

Title

Senior Attorney

Details

Introduction

James joined the company in 2007 and qualified as a European Patent Attorney in 2011. Recently, he has focused on European opposition and appeal work, as well as providing European advice to companies involved in US litigation. This work relates to technologies including small molecule and biologic drugs, and high density DNA arrays. Prior to entering the patent profession, James gained commercial experience working on strategy and innovation projects for medical and consumer goods companies.

Qualifications

Registered Patent Attorney; European Patent Attorney; PhD, University of Cambridge, on calcium signalling in the model organism C. elegans; and MA, University of Cambridge, in Natural Sciences.

Technical

James’ specialist area is molecular biology and biological therapeutics. In this field he has experience of working on patent applications for biological therapeutics and vaccines, oligonucleotide arrays, PCR based assays, antibody based assays, RNA interference (RNAi) and phage display.

In addition, James has experience of prosecuting patent applications and defending patents directed to small molecule therapeutics and pharmaceutical formulation chemistry. He has also worked on IP matters relating to technologies that underpin nutritional supplements and food additives, medical adhesives and a range of medical devices.

Legal

Much of James’ current work involves representing clients in opposition and appeal proceedings before the European Patent Office.  James is also responsible for the filing and prosecution of UK and European patent applications.  In addition, he has provided European and UK advice in relation to IP litigation in the UK, Germany and the USA.

Commercial

Previously, James worked for Sagentia Ltd in their innovation and technology management group, working on a broad range of consulting assignments aimed at exploiting opportunities in the life science and healthcare sectors. These included IP analysis, technology scouting and assessment, market evaluations and stakeholder research. Clients ranged from venture capital-backed SMEs to international healthcare and consumer goods companies including Bayer, Celanese, Hill’s Pet Nutrition, Millipore, PepsiCo, Procter & Gamble and Unilever. James has also worked for Procter & Gamble in Brussels in their Research & Development department.

Publications

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Emma Longland

Dr Emma Longland

Title

Associate Attorney

Details

Introduction

Emma is a valuable member of our Pharma & Nutrition Group as well as our Life Sciences Group where she has made a significant contribution to the success of the Avidity IP opposition team.

Her enthusiasm and attention to detail enables her to provide a service which combines considerable technical and legal knowledge with a friendly and approachable manner.

Qualifications

Emma has a Master of Natural Sciences degree and a Bachelor of Arts degree, both from the University of Cambridge where she specialised in Biochemistry. Emma also has a PhD from the University of Cambridge which she completed in the Department of Pathology, studying the gene expression changes that occur during the progression of HPV-induced, pre-cancerous lesions of the cervix.

She is a student member of the Chartered Institute of Patent Attorneys and a student member of the European Patent Representatives Institute.

Technical

During her time at Avidity IP Emma has worked on cases in a wide-range of technology areas, with particular emphasis on the medical and biotechnology fields. This has included cases concerning nucleic acid extraction and amplification, adenovirus-based vaccines, influenza vaccines, humanised antibodies, anti-cancer pharmaceuticals and medical devices, such as arterial stents.

Her ability to readily comprehend complex subject-matter and clearly and simply explain it to others is a valuable skill which she uses to the benefit of her clients.

Legal

Emma’s work encompasses both UK and EPO patent application prosecution, and she frequently provides assistance on EPO opposition cases.  She also has experience of providing validity and infringement opinions, and she assisted in the successful re-establishment of rights in a European patent application.

Commercial

Emma works for clients ranging from individual inventors in business as sole traders to large multinational pharmaceutical companies, and therefore she understands the importance of tailoring service and advice to the needs of the client and their business.

Publications

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Gwyn Cole

Dr Gwyn Cole

Title

Senior Attorney

Details

Introduction

Gwyn has outstanding experience throughout the whole range of patent related matters. He has managed intellectual property departments for major corporations, conducted oppositions and appeals personally and managed legal teams carrying out oppositions, appeals and litigation.

Qualifications

European Patent Attorney; UK Patent Attorney; BcS. Chemistry, First Class; PhD Chemistry (Cambridge).

Technical

Gwyn has many years of experience in patent drafting, prosecution, oppositions and appeals in his specialist areas of pharmaceutical and healthcares industries. This has been broadly based and includes neurologicals, anti-inflammatories, anti-cancer agent, cardiovascular medications, vaccines, antibodies, medical implants, medical devices and polymers for medical uses.

Legal

In the pharmaceutical and medical areas, Gwyn has managed legal teams in several European Countries involved in infringement and revocation actions before the Courts and he is a former member of the Intellectual Property Committee of the UK’s Pharmaceutical Manufacturers Association.

Commercial

Gwyn has previously set up the Intellectual Property Department of Smith & Nephew plc and headed Merck & Co. Inc’s. patent department in Europe. At present he is on the Board of some smaller and start-up companies where is ensures that patent protection is obtained within defined budgets.

Publications

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Technology group areas

  • New small molecule chemical entities
  • Synthetic and semi-synthetic processes
  • Vaccinology/immunology
  • Antigen preparation and purification
  • Antigenic adjuvanticity
  • Anti-psychotic agents
  • Anti-inflammatory agents
  • Anti-alzheimers agents
  • Antibodies for treatment of cancer
  • Vaccine technology
  • Medical implants and devices
  • Drug formulation methods
  • Protein drug conjugates
  • Use of microfluidic devices
  • X-ray crystallography
  • Small molecule pharmaceutically-active ingredients
  • Biocompatible synthetic materials (eg for use in structures such as stents)