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Archimedes Pharma Further Expands Team with Three Senior Appointments

READING, 14th March 2008 – Archimedes Pharma Ltd (“Archimedes”), a European specialty pharmaceutical company, today announces it has expanded the management teams of its commercial and development businesses with three senior hires.

Dr Arun Mistry has joined as Director of Medical Affairs and will further develop the medical affairs strategy for Archimedes’ existing product portfolio in Europe, working closely with the business units. Arun joins from Astellas Pharma Europe Limited where he was European Therapeutic Head for Urology within Medical Affairs. Prior to Astellas, Arun worked as a Senior Medical Science Physician at Bayer HealthCare in the UK with a role covering both UK Medical Affairs and Global Clinical Development within the areas of anti-infectives, Oncology and Haematology. He has also held posts at AstraZeneca as Medical Advisor for Gastroenterology and at Parexel International as Associate Medical Director for Medical Services. Arun joined the pharmaceutical industry following a NHS career in paediatrics and general practice. He will report to Dr Mark Watling who is Medical Director for the Archimedes group of companies.

Dr John Gilbody has joined as Medical Director, Archimedes Development, responsible for bringing additional medical input into Archimedes’ pipeline, which applies Archimedes’ proprietary drug delivery technologies to proven molecules which have yet to achieve full market potential due to their current mode of delivery. Archimedes’ lead product, NasalFent® is based on the Company’s PecSysTM technology and is currently in Phase III. John was previously at Wyeth Pharmaceuticals where he was Medical Team Leader for the Specialist Care Team, covering marketed and pipeline oncology products as well as palliative care. Prior to Wyeth, John worked at Solvay Healthcare Ltd and Procter & Gamble, and has over 14 years’ experience in the pharmaceutical industry. John will also report to Dr Mark Watling.

Jackie Mitchell joins as Director of Regulatory Affairs working primarily on NasalFent and the Archimedes Development pipeline. Previously Jackie was at Johnson & Johnson, where she was Global Regulatory Lead for Eprex and also responsible for a number of early development oncology compounds. Prior to J&J, Jackie spent six years at Abbott where she led teams that were responsible for the immunology, oncology and cardiovascular portfolios throughout Europe and North Africa.  Before Abbott, Jackie held a number of positions within the UK and global regulatory departments at Boehringer Ingelheim, culminating in setting up and running a regulatory intelligence function. Jackie joined the pharmaceutical industry in 1991 working for Pharmakopius Services Ltd. She will report to Archimedes’ Regulatory Affairs Director, Barbara Clarke.

Richard de Souza, CEO said “I am very pleased to welcome Arun, Jackie and John to Archimedes. They all have proven track records in the pharmaceutical industry and I am extremely confident that their knowledge and expertise will contribute to our continued success as we grow our commercial organisation in Europe and continue to develop our high-value pipeline from our world-class drug delivery technologies.”

Enquiries
Archimedes Pharma: Michael Clark, +44 (0)118 931 5077

Citigate Dewe Rogerson: Chris Gardner/Heather Keohane, +44 (0)207 638 9571

For more information on Archimedes, visit: www.archimedespharma.com

Notes to Editors

About Archimedes Pharma
Archimedes Pharma is a pharmaceutical company marketing an expanding portfolio of products to specialist prescribers in major European territories whilst building a platform for its future growth through the development of a high-value pipeline from its world-class drug delivery technologies.

Archimedes’ strategy is to expand its current European commercial presence through partnering and acquisition. It is also building a robust pipeline of in-house products in pain, Parkinson’s disease and critical care by applying its drug delivery technologies to proven molecules which have yet to achieve their market potential due to their current mode of delivery. Archimedes’ lead product, NasalFent®, intranasal fentanyl for rapid relief of breakthrough cancer pain, is in Phase III clinical development. This product, which has blockbuster potential, is targeted for launch in 2009.

Archimedes’ marketed products include Gliadel, a biodegradable wafer impregnated with an anti-cancer drug, carmustine, for high-grade glioma; Zomorph, an oral sustained release morphine product for pain; Nozinan, a neuroleptic used in psychiatry and as a supportive therapy for cancer patients; and Pabrinex, a high potency vitamin formulation used to treat the symptoms of malnutrition, especially in patients with acute alcohol problems.

Archimedes’ drug delivery technologies - ChiSys®, PecSys™ and TARGIT® - are also used in a number of partnered products in late-stage clinical development. Additionally, Archimedes’ innovative drug delivery technology has proven potential for vaccine delivery, with pre-clinical and clinical studies of nasally administered vaccines demonstrating enhanced immune response.

Archimedes Pharma is based in Reading, UK and has development facilities in Nottingham, UK. The Company was founded in December 2004 and is backed by Warburg Pincus, a leading private equity investor with extensive experience in the healthcare sector. In 2007 Archimedes had sales of US$40 million.

About Archimedes Development Limited
Archimedes Development Limited (ADL) is a subsidiary of Archimedes Pharma, a fast growing pharmaceutical company focused on meeting the needs of specialist prescribers in Europe. ADL is focused on partnering with companies which have compounds which could benefit from its suite of world-class drug delivery technologies. These comprise two cutting intra-nasal delivery technologies ChiSys® and PecSys™ as well TARGIT®, which is designed to deliver drugs to precise regions of the large intestine. These technologies are able to optimise the profile of a wide range of drugs by allowing targeted or controlled release.

ADL’s world-class drug delivery technologies have been validated in a series of partnerships with pharmaceutical and biotechnology companies. ADL has a flexible approach to its partnering activities and can apply its technologies to both existing and new therapeutic products.

ADL currently has development deals in place with a range of companies. Archimedes’ transmucosal enhancement technology ChiSys® is being used by Javelin Pharmaceuticals for its nasally-delivered morphine product, Rylomine™* and PecSys™, a novel pectin-based nasal drug delivery technology designed to maximise the potential of systemically absorbed drugs by enhancing drug performance and improving patient acceptance is also being used in other development deals.

ADL also has a co-development and commercialisation agreement with Pharmalink AB under which the two parties are developing a TARGIT® formulation for an anti-inflammatory product candidate. The TARGIT® technology is also licensed to Invapharm for specific drug candidates for various indications.

About NasalFent®
NasalFent® is an innovative fentanyl citrate nasal spray aimed at providing a fast, effective and convenient treatment for breakthrough cancer pain – sudden, unpredictable episodes of intense pain that occur despite background pain medication and which can affect up to 95% of cancer patients with pain.

NasalFent uses Archimedes’ proprietary PecSys™ nasal drug delivery system to ensure rapid, but controlled, delivery of fentanyl to match the time-course of the typical breakthrough pain episode experienced by these patients. An international Phase III clinical development programme is underway and the product is targeted for launch in 2009.

Fentanyl is a highly effective opiate analgesic and is seen as the drug of choice for breakthrough cancer pain. However, there remains a need for a presentation that provides fast and reliable onset of action coupled with ease of use and high patient acceptability. Archimedes believes NasalFent offers potential benefits over currently marketed oral and injectable presentations in these key parameters. Phase II results for NasalFent showed clinically meaningful pain relief within five minutes of dosing and that the product is well-tolerated.

Archimedes will market NasalFent through its own commercial organisation in Europe and is seeking licensees in North America, Japan, the Far East and Latin America.

(*Rylomine is a trade mark of Javelin)

NasalFent® is a registered trade mark of Archimedes Development Limited in the EU, USA and certain other jurisdictions.

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