Recent experience includes:
Advised this AIM-listed pioneering drug discovery company following its risk-share collaboration with LifeArc in relation to the company taking on the leadership of the MALT-1 programme from LifeArc to drive it towards the later stages of drug discovery and deliver a commercial deal.
Advised this previously AIM listed pharmaceutical company on various licence and collaboration agreements including:
- a drug discovery collaboration with Genentech utilising Vernalis' fragment and structure-based drug discovery platform against an undisclosed target
- the out-licensing of the worldwide rights to Vernalis' proprietary adenosine receptor antagonist programme to Corvus Pharmaceuticals Inc.
- a collaboration agreement with Servier, which focuses on complicated molecular targets, some of which, like Mcl1, were considered undruggable
- the acquisition by Juno Therapeutics, Inc. of RedoxTherapies, Inc., a licensee of Vernalis under its worldwide rights to vipadenant
- a licence agreement granting Cumulus Oncology exclusive worldwide rights to develop and commercialise VER250840, a novel, oral, selective, preclinical Chk1 Kinase Inhibitor discovered using Vernalis’ Design Platform.
Advised this cellular therapeutics company on a number of transactions including:
- its collaboration with Cell Therapy Catapult in relation to Cell Medica's Cytovir cytomegalovirus product
- a research collaboration agreement and associated option and licence agreement with University College London and UCL Business Plc in relation to modified T cell receptor products for the treatment of cancer
- its acquisition of a WT1-TCR cancer immunotherapy from Cell and Gene Therapy Catapult and a collaboration agreement to establish cell therapy manufacture. The transaction involved a suite of agreements including licence agreements, a sale and purchase agreement and a services agreement.
In addition to assisting on day-to-day queries, we advised UCB in relation to a number of business development projects over the past few years. These include a licensing deal in the digital health space, both licensing in and out of products and a collaboration with a manufacturer of a wearable injection device for use with one of UCB’s products.
Shield Therapeutics plc
Advised this specialty pharmaceutical company in relation to the exclusive out-licensing of its lead product Feraccru/Accrufer with:
- Norgine B.V. in Europe, Australia and New Zealand
- Beijing Aosaikang Pharmaceutical Co. Ltd in China, Hong Kong, Macau and Taiwan.
Oxford Biomedica plc
Advised this FTSE250 gene and cell therapy company on a number of transactions including:
- a discovery collaboration with PhoreMost Limited to develop next-generation CAR-T cell therapies. PhoreMost will deploy its in-house expertise and next-generation phenotypic screening platform, SITESEEKER®, to identify therapeutic candidates for Oxford Biomedica’s LentiVector gene therapy delivery system.
- a licence and clinical supply agreement with Juno Therapeutics, a Bristol-Myers Squibb company. The agreement granted Juno Therapeutics a non-exclusive licence to Oxford Biomedica’s LentiVector® platform for its application in CAR-T and TCR-T programmes in oncology and other indications, and additionally put in place a five year Clinical Supply Agreement, which may be extended further. Oxford Biomedica received an upfront payment of $10 million in cash and the agreement provides for the potential of up to an additional $86 million to be payable to Oxford Biomedica upon achievement of certain development and regulatory milestones related to multiple products and indications; up to $131 million in sales-based milestone payments and an undisclosed royalty on the net sales of products sold by Juno Therapeutics utilising the LentiVector® platform.
Acacia Pharma Ltd
Advised this EURONEXT-listed biopharmaceutical company focused on developing and commercialising novel products to improve the care of patients undergoing serious medical treatments in relation to a strategic in-licensing transaction with Cosmo Pharmaceuticals N.V. The transaction granted Acacia exclusive US commercialisation rights to BYFAVO (remimazolam) (an ultra-short acting and reversible intravenous sedative/anaesthetic) and was made alongside an equity investment and debt facility by Cosmo. We also advised on the subsequent assignment of such rights from Cosmo to Acacia with the consent of PAION AG, the original developer of remimazolam.
Advised this international specialist healthcare company in relation to its exclusive out-licence agreement with Carrick Therapeutics Ltd for the development and commercialisation of “BTG945” a targeted ovarian cancer drug.
International pharmaceutical company
Advised this company on a strategically important collaboration agreement with Verily LLC (the life sciences arm of Alphabet) in relation to the use of a wearable technology to measure and record patient's symptoms in the context of a Phase 2 clinical trial.
We have advised this leading company in relation to a number of research and licensing collaborations with respect to its "Kymouse" human antibody model.
The RNA Medicines Company
Advised this company on a variety of agreements in relation to the exploitation of its proprietary small molecule drug discovery platform targeting small noncoding RNA.
Footfalls & Heartbeats
Advised this Nottingham-based company in relation to a number of licensing deals to commercialise its proprietary process for manufacturing smart fabric which uses nano-scale interactions within the textile to make the fabric itself the sensor, avoiding the need for wires or miniature electronics.