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TimTec LLC, Newark, DE, USA and EnBioTec Co, Ltd, Tokyo, Japan, have entered into a collaboration agreement focusing on discovering unique and novel lead compounds.

TimTec LLC, Newark, DE, USA and EnBioTec Co, Ltd, Tokyo, Japan, have entered into a collaboration agreement focusing on discovering unique and novel lead compounds. TimTec will supply targeted compound collections for newly developed assay technology sharing its experience in synthetic organic chemistry. Enbiotech recently expended into drug discovery area having successfully introduced Receptor Cofactor Assay System (RCAS). The system allows evaluating the interaction between nuclear hormone receptors and co-factor in the presence of a compound. RCAS is cell-free and highly sensitive being able to distinguish agonist or antagonist interactions. EnBioTec and TimTec plan on a series of functional assays to co-develop nuclear receptor based lead compounds for drug discovery.

EnBioTec, Tokyo, Japan, emerged as an environmental biotechnology company specializing in R&D and product development for environmental diagnostics, contamination clean-up, and developing of environmentally-friendly materials. EnBioTec initiated Nuclear Receptor based Drug Discovery Consortium, a network of government, academic, and for-profit organizations, to combine resources to foster drug discovery.

Contact person:

EnBioTec

http://www.enbiotec.co.up

Mike Tanaka, Business Development

Phone: (408) 966-6902

Email: tanaka@enbiotec.co.jp

Timtec Corporation is a privately held company located in Newark Delaware, USA. It was founded in 1995 and began its work in the areas of acquisition and distribution of synthetic organic and natural compounds for Highthroughput screening, custom synthesis, and Cheminformatics to become a full service partner for drug discovery. Timtec has established a global network of thousands of scientists from many research centers around the world. The company has developed strong in-house expertise in assembling general, targeted, and custom library collections for variety of research applications. International customers include major pharmaceutical, biotech, agricultural and educational companies and institutions, which use Timtec products for research and development programs.

Contact person:

TimTec

http://www.timtec.net

Kay Denisova, Marketing and Business Development

Tel 302 292 8500 x 206
Fax 302 292 8520
info@timtec.net

MerLion Pharmaceuticals Pte Ltd Announces The Completion Of Merger With Combinature Biopharm AG And Athelas SA; Closure Of US $30 Million Financing Round

MerLion Pharmaceuticals Pte Ltd (MerLion) of Singapore, the world’s leading natural products based drug discovery company, announces that it has completed a merger by exchange of shares with Combinature Biopharm AG (Berlin, Germany) and Athelas SA (Geneva, Switzerland).

SINGAPORE, Singapore | Aug 21, 2006 |
MerLion Pharmaceuticals Pte Ltd (MerLion) of Singapore, the world’s leading natural products based drug discovery company, announces that it has completed a merger by exchange of shares with Combinature Biopharm AG. (Berlin, Germany) and Athelas SA (Geneva, Switzerland). Both European companies become 100% subsidiaries of MerLion whose headquarters and drug discovery research centre is based in Singapore. Drug development of its anti-infective programmes and nuclear magnetic resonance screening activities will be conducted from Berlin.

Dr Tony Buss, CEO of MerLion said “This major expansion of our capabilities, combined with proven drug discovery technologies and promising clinical candidates, position MerLion for its next exciting phase of growth. The company will continue its lead discovery activities in a range of therapeutic areas and will focus on the clinical development of anti-infective drugs.”

Dr Harald Labischinski, CEO of Combinature Biopharm and the new Chief Scientific Officer of MerLion, said “Combinature is very pleased to enter into such a strategic agreement with the leading natural compound research company and is now for the first time in the position to forward the new company’s most advanced antibiotic compounds from late stage pre-clinical development through phase I and phase II clinical. We expect to start our first clinical programmes with a novel mode of action resistance breaker antibiotic as well as with a new subclass of a broad spectrum antibiotic class within a few months from now.”

Dr Christine Deuschel, CEO of Athelas, said “MerLion offers Athelas an exceptional opportunity to progress the development of our novel anti-pathogenicity platform. The integration of Athelas’ DiVi Technology will provide MerLion with a broad and completely novel way of discovering new molecules based on a mechanism of action unexploited to date”.

The company has also completed the first closure of US$ 25M from a US$30M round of financing, which will be completed in full during the fourth quarter of 2006. This funding will propel the company towards an initial public offering within two years. The round, led by Aravis Venture of Switzerland and Bio*One Capital Pte Ltd of Singapore, represents one of the largest private rounds of funding raised for a drug discovery and development company in the region.

Ms. Swee Yeok Chu, CEO of Bio*One Capital and Mr. Jean-Philippe Tripet, Managing Partner of Aravis stated: “We believe that this cross border merger and financing is a landmark deal in Asia that confirms the ability of biotechnology companies to successfully develop from Singapore, capitalising on international alliances, funding from international investors, as well as strong local infrastructure that supports the growth of the company. With this financing and acquisitions, MerLion has now built a profile that compares with the best emerging biotechnology companies globally.”

Other participants in this round of funding include Nomura Research and Advisory, Aurelia Private Equity, Brandenburg Capital, Bioveda Capital, Novartis Venture Fund Mitsubishi Corporation and 3i Group Investment LP.

Michael Toenes of BC Venture GmbH , Juergen Leschke, Management Partner Aurelia Private Equity, Dr. Clemens Doppler of 3i Group Investment LP and Dr Dirk Honold, former CFO of Combinature stated: “The new company is now in the exciting position to further fill and advance the pipeline and to start clinical testing with very promising antibiotic drugs which have already shown exciting profiles. By the transaction the combined entity will have a strategic position to enter into the highly attractive and growing markets in the important area of novel anti-infectives.” In addition to progressing at least two anti-infective candidates into clinical proof of concept studies and developing the growing portfolio of earlier candidates towards the clinic, MerLion will retain its strong partnership alliances in natural products drug discovery and will expand in two main areas;

Novel Anti-Infectives Discovery The acquisition of the anti-infectives DiVi discovery platform of Athelas, which received an award at the 2005 Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC), provides MerLion with strong target generation capabilities and proprietary drug discovery screening systems in the area of bacterial pathogenicity.

Nuclear Magnetic Resonance (NMR) Screening The experienced NMR screening group based in Berlin will continue to utilise their expertise and technology with existing partners and in support of ongoing MerLion portfolio projects. This technology is the subject of increasing interest to the industry and is capable of advancing discovery by closely identifying how active compounds interact with drug targets and how these interactions may be optimised. MerLion would like to recognise the professional services provided during this complex transaction by Jones Day, CMS, Wong Partnership, Schellenburg-Wittmer, Vischer, PriceWaterhouseCoopers, Ernst & Young and Maidavale Consulting.

For more information, please visit http://www.merlionpharma.com Contact Chris Molloy, MerLion Pharmaceuticals Pte Ltd, The Capricorn #05-01, Singapore Science Park II, Singapore 117528 Tel: +65 6829 5606 Fax: +65 6829 5601 enquiries@merlionpharma.com

SOURCE: MerLion Pharmaceuticals Pte Ltd

MerLion Pharmaceuticals Pte Ltd Announces The Completion Of Merger With Combinature Biopharm AG And Athelas SA; Closure Of US $30 Million Financing Round

MerLion Pharmaceuticals Pte Ltd (MerLion) of Singapore, the world’s leading natural products based drug discovery company, announces that it has completed a merger by exchange of shares with Combinature Biopharm AG (Berlin, Germany) and Athelas SA (Geneva, Switzerland).

SINGAPORE, Singapore | Aug 21, 2006 |
MerLion Pharmaceuticals Pte Ltd (MerLion) of Singapore, the world’s leading natural products based drug discovery company,

announces that it has completed a merger by exchange of shares with Combinature Biopharm AG (Berlin, Germany) and Athelas SA (Geneva, Switzerland). Both European companies become 100% subsidiaries of MerLion whose headquarters and drug discovery research centre is based in Singapore. Drug development of its anti-infective programmes and nuclear magnetic resonance screening activities will be conducted from Berlin.

Dr Tony Buss, CEO of MerLion said “This major expansion of our capabilities, combined with proven drug discovery technologies and promising clinical candidates, position MerLion for its next exciting phase of growth. The company will continue its lead discovery activities in a range of therapeutic areas and will focus on the clinical development of anti-infective drugs.”

Dr Harald Labischinski, CEO of Combinature Biopharm and the new Chief Scientific Officer of MerLion, said “Combinature is very pleased to enter into such a strategic agreement with the leading natural compound research company and is now for the first time in the position to forward the new company’s most advanced antibiotic compounds from late stage pre-clinical development through phase I and phase II clinical. We expect to start our first clinical programmes with a novel mode of action resistance breaker antibiotic as well as with a new subclass of a broad spectrum antibiotic class within a few months from now.”

Dr Christine Deuschel, CEO of Athelas, said “MerLion offers Athelas an exceptional opportunity to progress the development of our novel anti-pathogenicity platform. The integration of Athelas’ DiVi Technology will provide MerLion with a broad and completely novel way of discovering new molecules based on a mechanism of action unexploited to date”.

The company has also completed the first closure of US$ 25M from a US$30M round of financing, which will be completed in full during the fourth quarter of 2006. This funding will propel the company towards an initial public offering within two years. The round, led by Aravis Venture of Switzerland and Bio*One Capital Pte Ltd of Singapore, represents one of the largest private rounds of funding raised for a drug discovery and development company in the region.

Ms. Swee Yeok Chu, CEO of Bio*One Capital and Mr. Jean-Philippe Tripet, Managing Partner of Aravis stated: “We believe that this cross border merger and financing is a landmark deal in Asia that confirms the ability of biotechnology companies to successfully develop from Singapore, capitalising on international alliances, funding from international investors, as well as strong local infrastructure that supports the growth of the company. With this financing and acquisitions, MerLion has now built a profile that compares with the best emerging biotechnology companies globally.”

Other participants in this round of funding include Nomura Research and Advisory, Aurelia Private Equity, Brandenburg Capital, Bioveda Capital, Novartis Venture Fund Mitsubishi Corporation and 3i Group Investment LP.

Michael Toenes of BC Venture GmbH , Juergen Leschke, Management Partner Aurelia Private Equity, Dr. Clemens Doppler of 3i Group Investment LP and Dr Dirk Honold, former CFO of Combinature stated: “The new company is now in the exciting position to further fill and advance the pipeline and to start clinical testing with very promising antibiotic drugs which have already shown exciting profiles. By the transaction the combined entity will have a strategic position to enter into the highly attractive and growing markets in the important area of novel anti-infectives.” In addition to progressing at least two anti-infective candidates into clinical proof of concept studies and developing the growing portfolio of earlier candidates towards the clinic, MerLion will retain its strong partnership alliances in natural products drug discovery and will expand in two main areas;

Novel Anti-Infectives Discovery The acquisition of the anti-infectives DiVi discovery platform of Athelas, which received an award at the 2005 Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC), provides MerLion with strong target generation capabilities and proprietary drug discovery screening systems in the area of bacterial pathogenicity.

Nuclear Magnetic Resonance (NMR) Screening The experienced NMR screening group based in Berlin will continue to utilise their expertise and technology with existing partners and in support of ongoing MerLion portfolio projects. This technology is the subject of increasing interest to the industry and is capable of advancing discovery by closely identifying how active compounds interact with drug targets and how these interactions may be optimised. MerLion would like to recognise the professional services provided during this complex transaction by Jones Day, CMS, Wong Partnership, Schellenburg-Wittmer, Vischer, PriceWaterhouseCoopers, Ernst & Young and Maidavale Consulting.

For more information, please visit http://www.merlionpharma.com Contact Chris Molloy, MerLion Pharmaceuticals Pte Ltd, The Capricorn #05-01, Singapore Science Park II, Singapore 117528 Tel: +65 6829 5606 Fax: +65 6829 5601 enquiries@merlionpharma.com

SOURCE: MerLion Pharmaceuticals Pte Ltd


BrainCells In-Licenses Clinical-Stage CNS Compound From Mitsubishi Pharma

SAN DIEGO, Aug. 10 /PRNewswire/ — BrainCells Inc. (BCI) today announced it has in-licensed a clinical-stage compound from Mitsubishi Pharma Corp. (MPC) that BCI will reposition and develop for the treatment of central nervous system (CNS) diseases, including mood disorders.

MPC extensively developed the compound for another CNS indication, then suspended the program when the drug met safety expectations but did not reach the defined efficacy endpoints. BCI applied its proprietary technology in the area of neurogenesis — the process by which endogenous stem cells in the adult human brain produce new brain tissue, including neurons — to identify different indications for the drug. The company expects to begin development and initiate additional Phase 2 clinical trials of the compound, BCI-540, next year.

“This is indicative of the extensive opportunity that exists for us in the CNS drug development space,” said James A. Schoeneck, BCI’s CEO. “We can screen compounds efficiently for neurogenic properties and pursue the development of these compounds for indications that weren’t part of a licensor’s original plans. The license from MPC provides us with the ability to capitalize on the predictive power of our screening platform, enabling us to develop a novel product for CNS disorders that affect millions of patients.”

“BCI has a unique approach to the identification and development of drugs that can be repositioned for a variety of CNS diseases,” said Akihiro Tobe, managing executive officer of MPC. “We believe that BCI has the right mix of cutting-edge science and development expertise to maximize the opportunity for the compound.”

About Mitsubishi Pharma Corp.

Mitsubishi Pharma Corporation (MPC), a research-driven pharmaceutical company, is the core member in the Mitsubishi Chemical Holdings group, under which Mitsubishi Chemical, a leading chemical company in Japan, and MPC exist as wholly-owned subsidiaries. Formed in 2001 by the merger of Mitsubishi-Tokyo Pharmaceuticals & Welfide Corporation (formerly Yoshitomi), MPC is committed to scientific progress, pharmaceutical advancement and the creation of products that benefit worldwide people’s welfare. Its core therapeutic areas are psychiatric and central nervous system diseases, cardiovascular and metabolic diseases, immunological and respiratory diseases and hepatic diseases. More information about the company can be found by visiting http://www.m-pharma.co.jp/.

About BrainCells Inc.

BrainCells Inc. (BCI) is a San Diego-based drug discovery and development company that is applying proprietary neurogenesis-based technology to identify and reposition compounds for the treatment of central nervous system (CNS) diseases. With its predictive screening platform, BCI can direct the selection and development of neurogenic compounds, increasing the opportunity for successful clinical trials in a variety of CNS indications. For more information, visit http://www.braincellsinc.com.

Chinese chemists synthesize compounds for BASF’s crop protection discovery research

10 Aug 2006 : Cooperation with partners throughout the world is an important aspect of the research strategy of BASF. The company spends nearly €100 million a year on a current total of 1,300 cooperations. One of them, a cooperative arrangement that has been in place for more than a year with Chinese company WuXi Pharmatech in Shanghai, has proven so fruitful that the number of chemists working there for BASF has now been increased to more than 20. The Agricultural Products division of BASF engages its Chinese partner to synthesize chemical compounds that are needed in the wide-ranging search for new active ingredients. The subsequent modification of the new substances and their screening for biological effectiveness are then conducted in the central research units at Ludwigshafen and Limburgerhof.

”Purchasing new substances for primary screening and building blocks for synthesis from external partners on the one hand and focusing our internal efforts on developing promising compounds for crop protection active ingredients on the other hand is successful and has stood the test of time,“ says Dr. Peter Eckes, Senior Vice President Agricultural Products Research and Development. “We work with 10 external partners – some of them for several years already – who synthesize new compounds for us.“ Global crop-protection research is the first unit of BASF to work together with a Chinese company in an extensive synthesis cooperation.

The development of innovative products and processes – including new crop protection active ingredients – is indispensable for the profitable growth of BASF. Before identifying an agent that promises to be successful, many thousands of chemical compounds must be run through the numerous optimization cycles each year in the Agricultural Products division. If a new class of substances shows an interesting effect against harmful fungi, insects or weeds, its chemical structure is systematically modified. Then it is run once again through the cycle of chemical synthesis, screening and evaluation of results. An optimized lead structure emerges at the end of this process.

“Cooperation with external partners makes a valuable contribution to the efficient organization of our research processes,“ said Dr. Alfred Hackenberger, President Specialty Chemicals Research. “We enhance flexibility and can thus achieve even more with our research budget, for example by screening more substances in a shorter period of time. That is an important success factor because only a few of those substances turn out to be successful crop-protection active ingredients.”

All external partners are extensively assessed to make sure that no know-how leaks out and that no potentially new active ingredients are jeopardized. Success factors in cooperation are unconditional reliability and open communication. In addition, product quality and synthetic competence are evaluated because BASF must be able to depend on its partners to do as much as it itself would when trying to solve tricky problems.

UNICEF, MOH hold workshop on bird flue

Amman, 03 July (Petra)–Specialists, participating in a one day workshop on bird flue disease, on Monday affirmed the importance of communication strategies between health sector and mass media in the field of confronting bird flue. The workshop, organized by the Ministry of Health (MOH) in cooperation with UN ICEF and WHO, is meant to further strengthen communication and information exchange between governmental and non-governmental institutions and the concerned international organizations concerning bird flue.

MOH Director of Disease Control Adel Belbeissi told the workshop that the Ministry, along with other official departments, is going on in surveillance and observation, because of possible return of the disease in Jordan.

Officer in Charge of UNICEF Jordan Nassr Moeini said that mass media play a pivotal role in spreading awareness and conveying proper messages to all people of all walks of life.

WHO Acting Coordinator Muhammad Khan highlighted the importance of media’s role in combating fear and distress through adopting scientific means and depicting accuracy in delivering information, in order to bridge the gap between decision makers and people.

UNICEF communication and media Bureau Hend Mango pointed out that since the the disease appeared on the world level, the number of cases reached 228 which lead to 130 deaths.

Protected: BIT’s 4th Annual Congress of International Drug Discovery Science & Technology 2006 (IDDST-2006)

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Scottish Biomedical Announces Korean Drug Discovery Collaboration

Scottish Biomedical has announced that it has entered into a research collaboration focused on the development of a new drug for diabetes with South Korean pharmaceutical company Chong Kun Dang (CKD).

Under the terms of the agreement, Scottish Biomedical will provide biology and medicinal chemistry expertise to optimize small molecule compounds that have been identified by Scottish Biomedical as active against a validated diabetes drug target.

The Scottish Biomedical/CKD collaboration was one of 7 international projects submitted to KHIDI, the Korean Health Industry Development Institute under the International collaborative Research Programme for Drug Development.

“We are delighted to have won through against extremely strong international competition and we are looking forward to joining with CKD in exploiting a discovery made in Scotland to develop a drug offering hope to diabetes sufferers everywhere,” said Dr Stephen Hammond, CEO of Scottish Biomedical.

Scottish Biomedical’s drug discovery business integrates ethical tissue acquisition, molecular biology, protein technology, high-throughput screening, cell biology, medicinal chemistry and pharmacology, to identify & validate drug targets and discover & optimise lead compounds.

Further Information: http://www.scottish-biomedical.com

OncoTherapy Science (OTS) announced on February 1 that it has signed a joint research agreement with Carna Biosciences (CARNA) and CrystalGenomics (CG).

Tokyo, Feb 1, 2006 (JCN) – OncoTherapy Science (OTS) announced on February 1 that it has signed a joint research agreement with Carna Biosciences (CARNA) and CrystalGenomics (CG).

The three companies will collaborate in searching low-molecular compounds that inhibit the activities of two different cancer-specific protein kinases possessed by OTS. Specifically, CARNA will be in charge of protein expression, assay formulation and screening while CG will handle virtual screening of compounds, compound library creation and X-ray crystallographic analysis.

Further, using the newly-identified low-molecular compounds, the three companies will strive to develop compound candidates for cancer treatment. The partners will co-own rights to the new compounds, but OTS will be in charge of commercializing them.

Source: JCNnetwork

WuXi PharmaTech Appoints Angela Wong as Service Biology VP

SHANGHAI, China, Jan. 23 /Xinhua-PRNewswire/ — WuXi PharmaTech Recently announced the key appointment of Dr. Angela Wong as Vice President of Service Biology.

Dr. Wong has board experiences in pharmacology, high throughput screening and preclinical pharmacokinetics. Prior to joining WuXi PharmaTech, she spent 20 years in pharmaceutical research at SmithKline, Pharmacopeia and Vitae Pharmaceuticals. She made significant contributions in multiple therapeutic areas including inflammation, cancer, hypertension, and osteoporosis. One of her compounds is currently in clinical trial for the treatment of asthma.

At her new post, Dr. Wong will be responsible for creating and managing Biology Service Group that provides services in the areas of drug metabolism, pharmacokinetics, toxicokinetics, immunoassay/biomarker, biological assay development and screening.

”I am very pleased to announce the appointment of such a highly accomplished professional to our management team. The addition of Dr. Wong to our scientific leadership broadens our service spectrum and enhances our capability. With her research experience and knowledge WuXi PharmaTech is one step closer to becoming an integrated R&D service provider,” WuXi PharmaTech’s Chairman & CEO Dr. Ge Li said.

Dr. Wong received her Bachelor of Science Degree in Biochemistry in 1977 and Master of Philosophy Degree in Biochemistry in 1980 from Chinese University of Hong Kong, and Ph.D. in Pharmacology from Baylor College of Medicine in Texas, United States.

Founded in 2001 and located in WaiGaoQiao Free Trade Zone, Shanghai, WuXi PharmaTech is a research service company that provides services to support new drug discovery and the chemical development of new drug candidates from discovery through to market. It engages in chemistry research, from lead discovery, optimization, bioanalytical services, and development to commercial manufacturing.

Wuxi PharmaTech assists its partners to shorten the cycle and lower the cost of drug development by providing complete, cost-effective and rapid chemistry solutions. The competent management team consists of many experienced ”returnees” and is well-versed in the latest drug R&D methodologies and Western style business practices. With over 650 scientists, the company has a 300,000 sq. ft. state-of-the-art research center and a 250,000 sq. ft. GMP plant. The company’s current customers include 18 of the top 20 pharmaceutical companies and 8 of the top 10 biopharmaceutical companies in the world.

For more information, please contact:

David Yin, PR Department,
WuXi PharmaTech Co., Ltd.
Tel: +86-21-5046-4003
Fax: +86-21-5046-1000
Email: Yin_Xiaojun@pharmatechs.com

PharmaDesign and Euroscreen Form Strategic Alliance for GPCR Deorphanization

PharmaDesign, Inc. and Euroscreen s.a. today announced a partnership to identify novel natural peptide ligands for orphan human G protein coupled receptors. PharmaDesign’s proprietary peptide library offers novel opportunities for identification of novel natural ligands while Euroscreen’s expertise in GPCR target discovery, functional screening of orphan receptors and pharmacological characterization will provide rapid screening of PharmaDesign’s Library and subsequent target validation. The partnership will provide novel Targets for partnering with shared income for the companies.

PharmaDesign, Tokyo, Japan; and Euroscreen, Brussels, Belgium (PRWEB) January 5, 2006 — PharmaDesign, Inc. and Euroscreen s.a. today announced a partnership to identify novel natural peptide ligands for orphan human G protein coupled receptors. PharmaDesign’s proprietary peptide library offers novel opportunities for identification of novel natural ligands while Euroscreen’s expertise in GPCR target discovery, functional screening of orphan receptors and pharmacological characterization will provide rapid screening of PharmaDesign’s Library and subsequent target validation. The partnership will provide novel Targets for partnering with shared income for the companies.

“We really wish this collaborative research will be so productive that it shows a novel way in drug discovery.” said Dr. Toshio Furuya, President &CEO of PharmaDesign Inc.

“This should provide our companies with a rapid opportunity to identify novel targets for original drug discovery programs,” said Dr. François Roman, the Head of Drug Development R&D at Euroscreen.

For further information, please contact:

Euroscreen s.a. Tel: +32 71 348 500
Pierre Nokin, Ph.D.
President and CEO

PharmaDesign, Inc. Tel: +81 3 3523 9630
Sam Noda
General Manager, Business Development Division

About PharmaDesign Inc.

PharmaDesign was established in 1999 as a genome-based drug discovery company specialized in structure bioinformatics and drug design. The Company conduct consulting research business in genome-based drug discovery as well as its own research to search novel drug targets by predicting proteins’ functions based on 3-D structures, and find lead compounds.

The Company has also developed PharmaGPEP, a library of peptides designed as intrinsic ligand candidates from human genome sequence using bioinformatics.

About Euroscreen s.a.

Euroscreen is a world leader in G-protein coupled receptors (GPCRs). The Company integrates its research expertise in this area with its patented high-throughput AequoScreenâ„¢ cellular assay platform to patent new GPCR targets and drug candidates.

The Company is building its own patent portfolio of GPCR targets and novel drug leads for licensing to biopharmaceutical companies, and to date has agreements with Amersham/GE Healthcare, Cephalon, ChemDiv, Evotec, ICOS, Merck & Co, Pfizer Inc, Solvay, Syngenta and UCB. Euroscreen has also established collaborations with numerous academic centers for access to licenses to help in making available its broad menu of GPCR-based products (recombinant cell lines and membrane preparations) and services (custom screening and cloning).

Euroscreen has grown significant and strong patent positions to protect many key drug targets for licensing. Such patents include CCR5, ChemR23, GPR43, GPR7/8, purinergic receptors (P2Y4, P2Y11 and P2Y13) and SHIP2 for type II diabetes. Euroscreen is able to offer intellectual property rights to companies for the development of therapeutic drugs that act through the above-mentioned targets. For more information regarding the Euroscreen’s portfolio, please contact Dr. Vincent Lannoy.

Euroscreen is a privately held company based in Brussels, Belgium with 80 employees of which 50 are in R&D.

Pharma companies increase efforts to release new med

Source: Manila Times – Philippines

By Ayn Veronica L. de Jesus

SUPERIOR health-care accessibility is one indicator of an economy’s vigor. But such a service can’t be merely left for the government to provide. The private sector has a hefty stake in ensuring that medicines and services are available to the consumers.

The plateauing of existing diseases
and the emergence of new ones is
driving companies to develop
stronger treatments.

In the Philippines, the health-care sector has been nothing more than an afterthought in the government’s budget. Even with that, pharmaceutical companies are trying to do their fair share to improve the system by launching related programs, providing significant discounts on medicines and reaching out to the population via medical missions.

Painstaking effort

For its part, the pharmaceutical company, Pfizer, is stepping up research and development efforts that could launch 20 new medicines by the end of 2009.

In the pipeline are medicines for nervous system disorders, cardiovascular diseases, oncology, metabolic diseases, infectious diseases, ophthalmology, inflammation and respiratory diseases.

In 2005 the company released treatments for macular degeneration (leading cause of blindness in the elderly) and for renal cancer. This year, the company is gearing up to unveil medicines to cure candidiasis and insomnia, and an antibiotic for skin and soft tissue infection; and smoking addiction. It will also introduce an inhaled form of insulin.

The company time table includes HIV/AIDS treatment (2007); osteoporosis prevention medicine, bipolar disorder treatment, medicine that will raise HDL while lowering LDL (2008); and stroke, cancer, obesity, macular degeneration, pain treatments (2009).

Villanueva explained that, “It takes about 11 to 15 years and $800 million before a compound can reach patients based on the company’s stringent rules in discovery, screening and clinical trials.” She added that out of nearly 7 million compounds tested, only one on average will reach the market after more than a decade of research and development.

Over that period, a compound must undergo phases of clinical pharmacology, preclinical safety, exploratory development and full development before it reaches the market. Factors that could delay or halt a compound’s development include complexity or lack of information about a disease, adverse reactions among tested patients, poor absorption by the body, side effects, safety, instability and its impracticality to produce.

Business and social institution

Noel Isberto, vice president for corporate affairs of GlaxoSmithKline, said that his company is developing medicines to treat cervical cancer for women, as well as those for asthma, diabetes and hypertension.

These medicines will be tied to the company’s Value Health program, which was launched in 2004. After the pilot year, GSK is ready this year to fully forge ahead with the program with the addition of more medicines.

The program offers significant price reductions of up to 30 percent on some original branded medicines that guarantee superior quality, efficacy, safety and affordability. To avail of these discounts, all patient has to do is to voluntarily register upon receiving doctor’s prescriptions of medicines included in the program. Upon the doctor’s recommendation, the patient can officially join the program.

Besides the much-reduced prices, enrollment in the program entitles the patient to information through newsletters and other printed materials and regular checkups.

The medicines include those for the treatment of asthma, diabetes and cardiovascular diseases.

“Pharmaceutics is a business and social institution because medicine is a right, and pharmaceutics is a responsibility,” said Isberto.

Dr. Cesar Recto, medical director of Merck Sharp and Dohme (MSD) said that, “cancer is about to overtake cardiovascular disease as the number one killer” worldwide. Although not able to cite actual figures, he said this was the conclusion of studies conducted in the United States, showing that “the rate of cardiovascular diseases is plateauing.”

As such, MSD is shifting its focus toward oncology treatments.

As well, the company is in the thick of developing treatments for cholesterol normalization, osteoporosis, arthritis, antibiotics and diabetes, and is researching treatments for diseases of the central nervous system such as Parkinson’s and depression.

At the moment, MSD has not set up any long-term programs, such as the GSK’s Value Health, but Recto said some of the company’s short-term programs are up for review this year.

Facing the challenges

Even as the companies increase investments and accelerate R&D efforts, many obstacles need to be hurdled in 2006 and the years ahead.

One is the continued local manufacture and distribution or importation of counterfeit medicines.

While the companies are knowledgeable in the telltale signs of a fake drug—such as poor printing quality on the packaging, differences in the company logo, spelling errors—consumers still need to be educated. “We are looking for new technology” that will thwart the efforts of counterfeiters, said Isberto of GSK.

One sure sign of a counterfeit drug is its bargain basement price. “Don’t look for bargains when it comes to medicines,” Isberto said. He added that consumers should only buy from leading and reliable drug stores, and not from friends or individual peddlers.

Of the P80-billion value of pharmaceutical market, 8 to 10 percent succumb to fake drugs, the biggest manufacturers of which are China and India.

Pfizer’s Villanueva said another difficulty the industry faces is the level of patient compliance in following doctors’ prescriptions.

“Patients are directed to take the medicine for 30 days, but they only take it for 22 days,” she said, referring to a company studies. “We are discovering the rate of compliance through our company programs,” she said.

Low patient compliance is also true for patients with chronic diseases, meaning diseases that require a lifetime of medication.

MSD’s Recto said that another challenge is that of herbal and organic medicines.

“Filipinos have no hesitation to buy herbal medicines that have not been studied, but think twice before buying well-researched medicine from the pharmaceutical companies,” he lamented. He ironically noted that herbal medicines promise to alleviate or eliminate diseases, yet a warning on their packaging states, “No approved therapeutic effects.”

“Many patients stop taking their medicines and shift to herbal treatments. But herbal medicines are not also cheap.” He warned that consumers should “be wary of herbal products that promise to be cure-alls.”

Evotec Reaches First Milestone and Receives Success Payment in Alzheimer’s Disease Collaboration With Takeda

HAMBURG, Germany, December 06, 2005 /PRNewswire-FirstCall/ — Evotec AG announced today that the first milestone has been achieved in its four-year drug discovery collaboration with Takeda Pharmaceutical Company Limited (Osaka, Japan, “Takeda”).

Evotec has granted Takeda exclusive rights in a novel target in Alzheimer’s disease based on successful target identification and validation work triggering a milestone payment of a few million Euro. Importantly, Evotec is eligible for further substantial milestone payments on the successful clinical development of compounds acting on the selected target. Further work within the collaboration is rapidly and productively progressing. Evotec is entitled to additional milestone payments should Takeda select additional targets from Evotec.

Dr John Kemp, Executive Vice President R&D Evotec Pharmaceuticals Division, commented: “We are extremely proud that we have reached our first project milestone with Takeda. Over the past two years we have made excellent progress in building substantial expertise and IP around novel Alzheimer’s disease targets. The relationship with Takeda is very productive and we are looking forward to jointly leverage our innovative Alzheimer’s disease toolbox during the years to come.”

The four-year collaboration between Evotec and Takeda (see press release of 1 August 2003) is aimed at jointly identifying and validating novel targets relating to different aspects of the causes and progression of Alzheimer’s disease, with the goal of developing innovative small molecule therapeutics. Total payments to Evotec will reach up to EUR 20 million covering access fees to Evotec’s proprietary database of Alzheimer’s disease-related targets, research funding and success based milestone payments relating to the selection of targets for further drug discovery. Additional substantial milestones would also be payable on the successful clinical development of compounds acting on selected targets. Further financial details of the collaboration are not disclosed.

About Evotec AG

Evotec is a leader in the discovery and development of novel small molecule drugs. Both through its own discovery programmes and through contract research partnerships, the Company is providing highest quality research results to its partners in the pharmaceutical and biotechnology industries.

In proprietary projects, Evotec specialises in finding new treatments for diseases of the central nervous system (CNS). Evotec has two Phase I clinical programmes: EVT 201, a GABAA modulator for the treatment of insomnia, and EVT 101, a subtype selective NMDA receptor antagonist for the treatment of Alzheimer’s disease, Parkinson’s disease and neuropathic pain.

In contract research, Evotec has established itself as the partner of choice for pharmaceutical and biotechnology companies worldwide. The Company provides innovative and often integrated solutions from drug target to clinic through an unmatched range of capabilities, including early stage assay development and screening through to medicinal chemistry and drug manufacturing.

In 2004, Evotec has generated sales of EUR 73 million with over 600 people located in Hamburg, Germany and near Oxford and in Glasgow, UK.

www.evotec.com

About Takeda Pharmaceutical Company, Ltd.

Takeda is a research-based global company with its main focus on pharmaceuticals. More than 1,000 researchers at Takeda carry out world-class research using advanced technology in such fields as human genetics, receptors, and enzymes, while the company is putting its R&D focus into several therapeutic areas including CSN. As the largest pharmaceutical company in Japan and one of the leaders in the world, Takeda is committed to striving toward better health for individuals and progress in medicine by developing superior pharmaceutical products.

www.takeda.co.jp/index-e.html

Contact:

Evotec AG
Anne Hennecke, Director Investor Relations & Corporate Communications
Phone: +49-40-56081-286
E-mail:

anne.hennecke@evotec.com

XIXth International Symposium on Medicinal Chemistry

Istanbul, Turkey – August 29 – September 2, 2006

The ISMC-2006 Symposium will be organized by the Turkish Association of Pharmaceutical and Medicinal Chemistry under the auspices of the European Federation for Medicinal Chemistry (EFMC).

This symposium is recognized worldwide as one of the leading Medicinal Chemistry meetings, as proven by its large international attendance, which varies between 1200 and 1500 participants from all over Europe, but also from the United States and Asia.

The Symposium will focus on important new scientific and technological developments in the drug discovery process; particularly those relevant to medicinal chemistry. The meeting will create an environment for in-depth, informed discussions highlighting the importance of medicinal chemistry in the pharmaceutical industry, academia and drug research. It will also provide opportunities to re-emphasise the crucial position of medicinal chemistry in the drug discovery process and its pivotal role in linking and exploiting the associated biological sciences. Therefore, the ISMC-2006 intends to create a forum for all scientists interested in medicinal chemistry and related fields.

More details regarding the participation and the scientific program are available via the symposium website: www.ismc2006.org

Trans Genic Receives Japanese Patents on Knockout Mice for Drug Development

By Bruce Porter, JCN Staff Writer

Tokyo (JCN) – Trans Genic has announced that its patents on genetically modified (“knockout”) mice are now registered by the Japan Patent Office (Japanese Patent No. 371167 and 3713513). In collaboration with Kumamoto University, the Japan Science and Technology Agency and EU GENE, which was absorbed by Trans Genic as of July 1, the company filed application for patents for the mice.

Trans Genic expects that the knockout mice will play a role in the process of screening and assessing candidate compounds for neovascularization with the aim of contributing to drug development.

Trans Genic has announced that its patents on genetically modified (“knockout”) mice are now registered by the Japan Patent Office (Japanese Patent No. 371167 and 3713513). In collaboration with Kumamoto University, the Japan Science and Technology Agency and EU GENE, which was absorbed by Trans Genic as of July 1, the company filed application for patents for the mice.

Trans Genic expects that the knockout mice will play a role in the process of screening and assessing candidate compounds for neovascularization with the aim of contributing to drug development.

MerLion teams up with UK firm in anti-cancer drugs research

SINGAPORE : A Singapore-based drug discovery company, MerLion Pharmaceuticals, and UK’s Cancer Research Technology (CRT) are teaming up to identify new anti-cancer drugs from natural product chemistry.

Under the collaboration, MerLion will screen their natural compound collection against high throughput screens developed by scientists at CRT.

The aim is to isolate new therapeutic compounds against validated cancer targets.

Targets will be selected from research carried out by Cancer Research in the UK and CRT’s other partners.

MerLion and CRT will work closely throughout the target selection and screening process.

The results of the collaboration will be jointly owned.

The tie-up is the first since the Joint Statement on Science, Engineering and Technology signed by Prime Ministers Lee Hsien Loong and Tony Blair two months ago.

- CNA /ls

Cerenis Therapeutics Announces License Agreement with Nippon Chemiphar to Develop New Therapies Based on PPAR Delta Agonists

ANN ARBOR, Mich. & TOKYO–(BUSINESS WIRE)–Aug. 30, 2005–Cerenis Therapeutics, a privately held biotechnology company working to develop novel HDL therapies, has entered into a license agreement with Nippon Chemiphar Co., Ltd. (TOKYO:4539), to develop new small molecule therapies based on PPAR (peroxisome proliferator activated receptor) delta agonists.

PPAR delta agonists have been shown to play a role in elevating levels of HDL, also known as the body’s “good cholesterol.” Under the terms of the agreement, Cerenis will have access to a broad range of PPAR delta agonists for use in research and development of HDL therapies with the potential to help reduce cholesterol buildup through a natural process known as reverse lipid transport.

“PPAR delta agonists represent a very promising area of research that could lead to novel oral HDL therapies in the years ahead. This agreement positions Cerenis to move forward in this area of research, which represents an important complement to our other HDL-focused research and product development initiatives,” said Dr. Jean-Louis Dasseux, president and chief executive officer, Cerenis Therapeutics.

“We anticipate close collaboration between the companies and are looking forward to the prospect of identifying and developing first in class small molecule HDL therapies from our patented compounds,” said Mr. Kazushiro Yamaguchi, president and chief executive officer, Nippon Chemiphar.

Nippon Chemiphar will retain development and marketing rights in Asia for any new product candidates developed through this licensing agreement. Cerenis will be granted exclusive development and commercialization rights in the United States, Europe and other markets outside Asia. Cerenis will make milestone payments of up to US$30 million to Chemiphar during the research and development stage and will make royalty payments based on sales, after marketing.

About Cerenis Therapeutics

Cerenis Therapeutics is a pharmaceutical company focused on the discovery, development and commercialization of breakthrough HDL-related therapies for the treatment of cardiovascular and metabolic diseases. Cerenis is pursuing a range of HDL product candidates that reflect breakthrough research in HDL therapy and significant commercial opportunities in the treatment of atherosclerosis. The Cerenis management team includes world leaders in HDL therapy research and development. The company has operations in Ann Arbor, Michigan and Toulouse, France. For further information please visit the company website at: www.cerenis.com.

About Nippon Chemiphar Co., Ltd.

Nippon Chemiphar is a Japanese pharmaceutical company listed on the First Section of the Tokyo Stock Exchange. The company develops and markets new chemical entities (NCEs) as NSAID and antihypertensives. The company focuses on drug discovery in a number of the fields, including orthopedics and urology, and is interested in working with other pharmaceutical companies to accelerate development and commercialization. With its depth of expertise in drug discovery, Chemiphar strategically focuses on identifying drug leads for further development. Chemiphar’s current R&D is focused on analgesics, therapies for life-style diseases, and hyperuricemia, which is recognized as an increasingly important clinical condition in Japan. With a view to accelerating commercialization, Chemiphar is speeding up development and candidate screening of its compounds, and their licensing overseas. Given its venture-based drug research, Chemiphar is seeks licensing opportunities so that it might more quickly bring its pharmaceuticals to the global market. For further information, please visit: http://www.chemiphar.co.jp/.

SA, India, Brazil in resource deal

Cape Biotech is investigating a possible bio-prospecting partnership which would enable South Africa, Brazil and India to share each other’s resources in order to capitalize on their rich biodiversity.

Bio-prospecting is the search for valuable compounds in nature – plants, animals or micro-organisms – that can assist in the development of new drugs or industrial products.

Dr Mark Fyvie, Managing Director of Cape Biotech recently attended an India-Brazil-South Africa (IBSA) trade delegation where he met with his counterparts in New Delhi, and where a bio-prospecting memorandum of understanding was signed. Fyvie believes the three countries have “huge tracts of biodiversity” that can benefit each other, particularly sharing and collaborating on information platforms.

Biotechnology is one of the core focus areas of the IBSA agreement and representatives from government and industry met to discuss, among other issues, setting up tangible collaborations in the areas of functional genomics and high throughput biology.

“We are starting off very pragmatically and see this as a process that will gradually align the biodiversity objectives of the three countries,” he said.

Fyvie adds that they would like to create the ability for a powerful screening presence for the three countries, thereby enabling access to samples that are being poorly managed.

“This partnership is an agreement to work together going forward and is one of a number of areas of co-operation, where we could optimally exploit value from biodiversity and potentially embark on a joint bio-diversity project,” he says.

“The rollout is envisaged in three stages: sharing and learning, exchanging technologies and technology transfer, and eventually shared facilities among the three countries, but this will only be potentially possible once the alignment of national policies has begun.”

Fyvie was very impressed with India’s investment in skills development.

“There are many highly skilled people in India, which has contributed enormously to the country’s success in the biotech industry. The message is that you cannot over-invest in skills. This coupled with the strong IT industry, as biotech is becoming more information rich, will sustain the future expansion of the biotech sector of the Indian economy.”

Where South Africa is at an “advantage” says Fyvie, is that our infrastructure is better developed, our business culture is more westernised and the language barrier is less of an issue for foreign investors.

“What we don’t have is as big a local market to justify working on and developing expensive products like India, and this is probably why they are the 12th largest biotechnology entity in the world.” he said.

Fyvie hopes that this cooperative effort will allow all three countries to maximize their biodiversity by capitalising on each country’s areas of strength and experience.

Cape Biotech is the Western Cape-based Biotechnology Regional Innovation Centre (Bric) an initiative of the Department of Science and Technology.

I-Net Bridge

3rd Annual Congress of International Drug Discovery

WHTS’ Annual Congress of International Drug Discovery Science and Technology (IDDST) Organizing Committee is proud to present:

3rd Annual Congress of International Drug Discovery
Science and Technology
Oct. 28-30, Shanghai, China, 2005;
Oct. 31-Nov. 1, Dalian, China, 2005
Website

PRESENT YOUR EXPERTISE IN FRONT OF THIS ELITE AUDIENCE
WITH A 20-MINUTE WORKSHOP

Corporate and Institution Sponsors:
Shanghai Municipal People’s Government
World High Technology Society
Shanghai Personnel Information Center
China International Talent Exchange Foundation
Dalian BIT Co., Ltd., Links, Diversa, Qiagen,
Invitrogen, Angilent
Waters, GE, Amersham (GE)
Novartis Pharmaceuticals Corporation
Eli Lilly & Company(China)
China Foreign Expert Bureau
Journal of China Biotechnology
Medical World Magazine
Biotech World
More are joining us.

Present in front of 2000+ prospects with titles of:
Executives or Directors of pharmaceutical Industries, Research Scientists in Drug Discovery, Regulatory Personnel and Intellectual Property Officers, Pharma and Biotech Research Managers, Research Chemists and Biologist, computational Researchers, Policy Makers at Drug Administration Organization. Directors, Senior Scientists, Entrepreneur, Professors, Graduate Students, and Senior Researchers in System Biology and Functional Genomics, Biomarkers, Bio-Chips, New tools for target validations, New Mechanism, Business Aspect of Drug Discovery, Structure Based Drug Designs, New Finding in Drug Search, Nature Products and Drug Discovery, Predictive Toxicology/ADMET, New Delivery systems, Nanotech in Drug Discovery, Clinical studies and regulation issues etc and more…

*Workshops produce results… don’t miss out!*
The Highlights of the congress:
- Scientific and Technological Presentation
- Networking with 1000+ attendees
- 35 Product / Technology Exhibition
- Meet the leading Scientists at Special Topics
- New Deal Making and News Release
- Workshop for Business Development and Round Table Negotiation

View 2004 Attendee Profiles
View Conference Agenda

For more information about sponsorship and exhibit opportunities
Contacts:
Ms. Annie Sun
Attendee and Exhibition Coordinator
26 Gaoneng St. R405
Dalian Hightech Zone
Dalian, LN 116025, China
Tel: 0086-411-84799609
Fax: 0086-411-84799606
Email: annie@whts.org

Ms. Emily Liu
Media and Advertisement Coordinator
26 Gaoneng St. R402
Dalian Hightech Zone
Dalian, LN 116025, China
Tel: 0086-411-84799616
Fax: 0086-411-84799629
Email: emily@whts.org

The BioSciences Group of Fujitsu Introduces CELLINJECTOR(TM) Automated Microinjection System

WESTWOOD, Mass., Aug. 10 /PRNewswire/ — The BioSciences Group of Fujitsu
Computer Systems today announced that it has developed an automated
microinjection system called CELLINJECTOR, to enable very large-scale direct
injection of agents through cell membranes for biochemical research.
The CELLINJECTOR system is a high-throughput, efficient, automated method
for directly injecting a large number of cells. CELLINJECTOR is computer-
controlled, so operators do not need months or years of injection training to
perform accurate cellular injections.
According to Dr. Michael J. McManus, vice president for business
development of the BioSciences Group, “CELLINJECTOR was developed to overcome
the challenges scientists face using cell-based screening techniques to learn
more about the intracellular activity of chemical compounds, therapeutic
proteins, siRNA agents and other structures of interest. Understanding exactly
how a structure behaves in situ is often far more useful than in silico or in
vitro experiments. By placing an agent directly in a cell, the researcher can
observe the activity of the agent at the sub-cellular level to determine what
cellular structures are affected, and how.”
He added, “To date, the main obstacle for drug researchers has been the
difficulty, labor-intensiveness and expense of performing cellular-level
screening on a large scale, which is increasingly becoming necessary to
biochemical research. The precision and automation of CELLINJECTOR vastly
improves the precision and volume of cell injections, easily performing
thousands of successful injections per day compared to hundreds done
manually.”
CELLINJECTOR is comprised of several components, including a glass
capillary, a moving X-Y platform, a perforated silicon chip, a digital camera,
a microscope and a computer controller. The computer instructs the X-Y
platform how to position the capillary at each cell membrane on the perforated
silicon chip and then to inject the cell. This process is repeated for each
cell on the chip.
The automatic nature of CELLINJECTOR makes it ideal to integrate cellular
injection into pre-existing robotic workflows. Robots used to handle, incubate
and analyze cell assays can easily be used with CELLINJECTOR, once they are
configured to incorporate the CELLINJECTOR process into the workflow.

About The BioSciences Group of Fujitsu Computer Systems
The BioSciences Group of Fujitsu Computer Systems Corporation is an
established leader in creating innovative and reliable solutions for
experimental scientists. BioSciences Group solutions enable researchers to
make in silico predictions about leads, targets, and interactions, and to
validate these hypotheses experimentally. BioSciences Group offerings include
the CELLINJECTOR(TM) system for high-throughput, automated cellular injection,
the isS(TM) (in silico Screening) platform for large-scale docking and free
energy of binding simulations, and the CAChe(TM) suite of life sciences
predictive modeling and automated docking tools, for drug discovery lead-
generation. For more information, please see: us.fujitsu.com/biosciences

About Fujitsu Computer Systems
Headquartered in Sunnyvale, Calif., Fujitsu Computer Systems is a wholly
owned subsidiary of Fujitsu Limited (TSE:6702) committed to the design,
development and delivery of advanced computer systems and managed services for
the business enterprise. The company offers a complete line of high-
performance mobile computers, scalable and reliable servers, storage, and
middleware as well as managed and professional services.
Fujitsu Computer Systems emphasizes leading-edge technology, exceptional
product quality and user comfort and productivity, as well as outstanding
customer service. More information on Fujitsu Computer Systems is available
at: us.fujitsu.com/computers

About Fujitsu
Fujitsu is a leading provider of customer-focused IT and communications
solutions for the global marketplace. Pace-setting device technologies, highly
reliable computing and communications products, and a worldwide corps of
systems and services experts uniquely position Fujitsu to deliver
comprehensive solutions that open up infinite possibilities for its customers’
success. Headquartered in Tokyo, Fujitsu Limited (TSE:6702) reported
consolidated revenues of 4.7 trillion yen (US$44.5 billion) for the fiscal
year ended March 31, 2005. For more information, please see: http://www.fujitsu.com

NOTE: Fujitsu, the Fujitsu logo, CELLINJECTOR, isS, and CAChe are
trademarks or registered trademarks of Fujitsu Limited in the United States
and other countries. All other trademarks and product names are the property
of their respective owners.

The statements provided herein are for informational purposes only and may
be amended or altered by Fujitsu Computer Systems Corporation without notice
or liability. Product description data represents Fujitsu design objectives
and is provided for comparative purposes; actual results may vary based on a
variety of factors. Specifications are subject to change without notice.

SOURCE Fujitsu Computer Systems Corporation
Web Site: http://www.fujitsu.com