Lydia Torne advises clients in the life sciences industry on complex collaborations and licensing transactions, as well as UK regulatory compliance issues.

Lydia represents the full range of life sciences clients, including global pharmaceutical and medtech companies, leading biotechs, and academic institutions, on business-critical IP transactions involving:

  • Licensing
  • Collaborations
  • Joint ventures and consortium agreements
  • Commercialization and co-promotion agreements
  • Corporate transactions, financings, and royalty monetizations

Lydia also assists life sciences clients in material regulatory compliance issues, including product classification, interactions with healthcare professionals, clinical trials, market access, supply chain requirements, marketing, and pharmacovigilance.

A recognized thought leader, Lydia regularly writes and speaks about the complexities of licensing transactions and digital health, including in The Lancet, Pharma Focus America, and Drug Discovery Today.

Lydia’s experience includes advising:

  • GlaxoSmithKline on:
    • Its US$2 billion collaboration with ABL Biotechnology for the use of ABL’s proprietary best-in-class shuttle antibody technology, which facilitates penetration of the blood-brain barrier*
    • A multi-million dollar collaboration with Muna Therapeutics, leveraging Muna’s MiND-MAP platform to identify, validate, develop, and commercialize novel drug targets for Alzheimer’s disease*
    • A multi-million dollar collaboration with Relation Therapeutics, leveraging Relation’s Lab-in-the-Loop platform to identify, validate, develop, and commercialize novel drug targets for the treatment of osteoarthritis*
    • Its license with Adrestia Therapeutics for the use of platform software technology for the accelerated development of new drug products, as well as a related investment into, and sale of, Adrestia*
    • Its joint venture fund with Johnson & Johnson Innovation and AstraZeneca, Imperial Innovations, UCL Business, and Cambridge Enterprise to establish Apollo Therapeutics LLP to fund early-stage scientific research from Imperial College of Science, Technology and Medicine; University College London; and/or the University of Cambridge, for licensing to industry partners for further development and commercialization*
  • Genmab on various strategic licensing agreements, including:
    • Its US$1.8 billion acquisition of Profound Bio, with its Rina-S molecule*
    • Its US$3.9 billion global license and collaboration agreement with AbbVie for the development and commercialization of three assets, including epcoritamab*
    • A leading collaboration with BioNTech for the development of novel cancer drugs*
  • UCB on key foundational in-licenses with research institutes around the globe for early-stage development*
  • Eisai on:
    • The exclusive worldwide license of its product E6005 (a selective PDE4 inhibitor) to Roivant Sciences*
    • Selling the European and UK rights to Targretin, a hematology specialty product with bexarotene as an active ingredient, to HAC Pharma*
  • Cooper Consumer Healthcare on the IP, licensing, and regulatory aspects of its multi-billion dollar acquisition of Viatris’ OTC business*
  • An international cosmetics company on acquiring a probiotics-based consumer health and cosmetics business*
  • Institute of Global Health Innovation (IGHI) in connection with its strategic advice to the NHS regarding industry collaborations*
  • Venture Life Group on various consumer health acquisitions and related licensing arrangements*
  • Adherium on the long-term supply and development agreement for its smart inhaler with AstraZeneca*

*Matter handled prior to joining Latham

Bar Qualification

  • England and Wales (Solicitor)

Education

  • Postgraduate Diploma in Intellectual Property Law and Practice, University of Oxford, 2011
  • LLB, University College London, 2006
  • Diplôme Universitaire du Droit Français, Aix-Marseille University, 2005