Friday, 21 September 2007

Polyplus-transfection to supply RNAi therapeutic delivery technology to Alnylam Pharmaceuticals

Collaboration targets improving delivery of RNAi-based therapies

Strasbourg, France, September 21, 2007 — Polyplus-transfection, a company specialized in the research, development and marketing of innovative reagents for RNA interference (RNAi) and transfection, announced today that it has signed a collaboration agreement with Alnylam Pharmaceuticals, the leading RNAi therapeutics company, based in Cambridge, Massachusetts.


Under the terms of the agreement, Polyplus-transfection will provide Alnylam with its RNAi therapeutic delivery solutions and share its expertise in formulation for siRNAs, the molecules that mediate RNAi, in vivo. Alnylam will evaluate Polyplus' formulations for delivery of RNAi therapeutics. Other terms were not disclosed.

The companies believe the collaboration has the potential to bring about improvements in the delivery of siRNA therapies. Although there has been significant progress in this area to date, creating delivery solutions for RNAi therapeutics remains an important component in realizing the full potential of this promising technology.

"As Alnylam is the leading RNAi therapeutics company, we at Polyplus-transfection are delighted to be collaborating with a firm at the cutting edge," said Joëlle Bloch, CEO of Polyplus-transfection. "A big advantage of this relationship is that Polyplus-transfection will benefit from having its chemical carriers tested in several disease models while working with the most advanced target sequences and mixed chemical siRNA modifications from Alnylam."

Polyplus-transfection is developing several in vivo siRNA formulation solutions based on its lead compounds in vivo-jetPEI (now GMP available) and INTERFERin, as well as on an original RNA modification, sticky siRNA (ssiRNA).


RNA interference (RNAi)

RNA interference (or RNAi) is a naturally occurring mechanism within cells for selectively silencing and regulating specific genes. The discovery of RNAi has been widely acknowledged as a major breakthrough in biology, and the technology was recognized for its potential broad impact in medicine with the award of the 2006 Nobel Prize for Physiology or Medicine. Since many diseases are caused by the inappropriate activity of specific genes, the ability to silence genes selectively through RNAi has accelerated the understanding of these genes and their related pathways. Additionally, RNAi could provide a new way to treat a wide range of human diseases. RNAi is induced by small, double-stranded RNA molecules. One method to activate RNAi is with chemically synthesized small interfering RNAs, or siRNAs, which are double-stranded RNAs that are targeted to a specific disease-associated gene. The siRNA molecules are used by the natural RNAi machinery in cells to cause targeted gene silencing.

About Polyplus-transfection

Polyplus-transfection is focused on developing innovative solutions for intracellular delivery of nucleic acids. The company has been marketing its transfection reagents worldwide since 2001 and is reinvesting most of its revenues into research and development. Transfection consists in introducing a gene or a small interfering RNA into cells. This technique makes it possible to cross the cellular barriers and deliver such biomolecules into the cell for research or therapeutic purposes.

Customers of Polyplus-transfection's products and services include biotechnology and pharmaceutical companies as well as life science academic laboratories. Polyplus-transfection offers high quality consultancy, personalized scientific support and expertise in regulatory affairs related to the use of its reagents in clinical trials. Phases I/II cancer gene therapy and AIDS trials are underway in Israel, USA, Sweden and Germany using GMP-compliant reagents from Polyplus-transfection.

Polyplus-transfection R&D has well-established partnerships with biotech companies and is also involved in several European research collaboration networks, such as GIANT (Gene Therapy, an Integrated Approach to Neoplastic Treatment) and RIGHT (RNA Interference Technology as Human Therapeutic Tool). The company also drives the OligoPlus research program for the "Therapeutic Innovations" Competitiveness Cluster, focusing on new tools for diagnostic.

The Strasbourg-based company is recognized as a leading innovator in the transfection market, with ISO 9001:2000 certification, three exclusive licenses from the CNRS and numerous patent filed.

For more information, visit: http://www.polyplus-transfection.com


Source: Polyplus-transfection
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Monday, 17 September 2007

BT PHARMA appoints Martin Koch as Vice President Finance and Administration

Professional in Biotech Finance brings top management and international experience to BT PHARMA &mdash forerunner in Therapeutic Vaccines

Toulouse, France — Monday September 17, 2007. BT PHARMA S.A., forerunner in the development of therapeutic vaccines for treatment of neoplasia and cancer caused by the Human Papillomavirus (HPV), announced today that Martin Koch, engineer and INSEAD MBA, has been elected to the position of Vice-President Finance and Administration.

Before joining BT PHARMA, Martin Koch had an international career in financial and operational management positions at Eli Lilly Company, Cap Gemini / Ernst & Young, Elan Pharmaceuticals, Zeneus Pharma and Cephalon Pharmaceuticals. In particular, Mr Koch was instrumental in the transaction whereby a large part of Elan’s continental European activities were spun off to Zeneus Pharma.

"We are very pleased to welcome Martin Koch who brings over 15 years of pharmaceutical industry experience to our management team", explained Benedikt Timmerman, Chief Executive Officer of BT PHARMA. "We are entering in an accelerated growth phase and the recruitment of Martin fits well in our objective to reinforce our management with executives of top management level. Martin’s experience will be of great value for BT PHARMA as we start identifying strategic partners to finance our clinical trials Phase I and II."


About BT PHARMA S.A.

BT PHARMA is a privately held biopharmaceutical company spun out of the Institut Pasteur in 2002 and registered in Toulouse, France (home of Airbus Industries). The company develops immuno-therapeutics for cervical neoplasia and cancer. BT PHARMA’s key technology is a protein-based delivery system (the Adenylate Cyclase vector) that allows inducing tailor-made and targeted T cell immune responses in the patient. BT PHARMA exploits this technology to develop innovative therapeutic vaccines in-house and in partnership with biotech and pharmaceutical companies.

The young company’s most advanced product, ProCervix®, will enter phase I / II clinical trials in 2008. This bivalent therapeutic vaccine targets cervical neoplasia and cancer provoked by the human Papillomavirus (HPV). ProCervix® aims to replace ablative surgery or conisation in millions of women already infected by HPV16 or HPV18 and at risk for invasive cervical cancer.

Further information: http://www.btpharma.com


Source: BT Pharma
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