Product category:
Antibodies
News Release from: Oxford BioMedica | Subject: LentiVector
Edited by the Laboratorytalk Editorial
Team on 08 January 2008
Oxford Biomedica buys RNA interference
technology
The rights granted are exclusive for RNAi gene silencing using lentiviral vector technology for human gene therapy applications, including Oxford BioMedica's proprietary LentiVector system
Oxford BioMedica has signed a license agreement with the Carnegie Institution of Washington and the University of Massachusetts Medical School that grants it rights to key RNA interference (RNAi) technology invented by Nobel Prize-winning scientists Andrew Fire, and Craig Mello Oxford BioMedica will make an upfront payment, milestone payments, and royalties on sales
This article was originally published on Laboratorytalk on 25 Jun 2003 at 8.00am (UK)
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Oxford BioMedica has signed a further licence agreement for its LentiVector technology with a large biopharmaceutical company
These rights will run concurrently with the rights of the existing licensees of the RNAi technology.
The concept of gene silencing in mammalian cells using short pieces of RNA was first published by Fire and Mello and colleagues in 1998 (see Nature volume 391, 19 February 1998).
For this ground-breaking work they were awarded the Nobel Prize in physiology or medicine in 2006.
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The discovery of RNAi has created a new paradigm of drug discovery and potential therapeutics.
Lentiviral vectors are already used extensively in drug discovery research for delivery of RNAi to a range of different cell types.
Oxford BioMedica has licensed its LentiVector patents for research use in this area to many companies together with its corporate partner Sigma Aldrich.
In a separate agreement, the Carnegie Institution of Washington and the University of Massachusetts have agreed to subscribe for a total of 2,369,818 ordinary shares of 1p each at £0.24 per share.
The shares are expected to commence trading on 10 January 2008.
Professor Alan Kingsman, chief executive of Oxford BioMedica, commented: "There is growing acceptance that to develop RNAi therapeutics, an effective delivery system is essential and increasingly lentiviral vectors are becoming the system of choice for this purpose.
"Oxford BioMedica, with its broad LentiVector patent portfolio and its expertise in developing LentiVector-based products, is therefore well positioned to develop a range of novel RNAi therapeutics either independently or in collaboration with other companies".
James McNamara, executive director of the Office of Technology Management of the University of Massachusetts Medical School, commented: "As the medical school looks toward the convergence of RNAi, gene therapy, and cellular therapy, including stem cells as medical treatments, the potential drug development opportunities presented by Oxford BioMedica's lentiviral vector delivery technology is intriguing to us.
"We have structured these license agreements to help the company pursue novel applications of RNA interference based on their established broad IP in the lentiviral vector delivery space.
"Our hope is to see the further advancement of the RNAi field toward novel therapies in the public interest.".
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