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Archive for November, 2005

New Generation Drug Discovery Software Enters Market

Quantum 3.1 is a suite of drug discovery software for Linux and Windows designed to enhance stages of drug discovery workflows, such as target identification, drug hit identification, lead identification and lead optimization.

The Quantum software was developed using a new paradigm in molecular modeling – applying quantum and molecular physics instead of statistical scoring-function-like and QSAR-like methods.

The key benefit of Quantum is the outstanding precision of molecular modeling and calculations. Using Quantum 3.1, researchers can calculate the IC50 of protein-ligand and protein-protein complexes, perform ligand docking, perform virtual screening of small-molecule libraries, analyze large-scale protein movements, perform de novo drug design and calculate the solvation energy and solubility.

Quantum 3.1 also helps detect potential moderate-to-serious adverse activity, additional unexpected activity and broad relative selectivity for a library of compounds by screening them against several hundred ADME/TOX-associated proteins.

The Mutagenesis module of Quantum 3.1 provides an interface for changing the protein sequence at specific sites through alterations to its amino acids and predicts changes in the bioactivity after mutations.

The Quantum software was successfully applied in different in-house and collaborative drug discovery projects of Quantum Pharmaceuticals. As a result of applying Quantum software, the range of the novel chemical inhibitor classes were discovered for disease targets, including HIV-I integrase (AIDS), Beta-Secretase (Alzheimer’s disease), Human Neutrophil Elastase (CF, COPD), FtsZ (TB) and some others. Quantum technology has demonstrated itself to be very effective in creating revolutionary new medicine, and it has demonstrated its ability to discover new classes of inhibitors.

The free demo version of Quantum 3.1 can be downloaded from Quantum’s web site.

About Quantum Pharmaceuticals

Quantum Pharmaceuticals, the leader in drug discovery technology, serves the life sciences industry and research community by providing top-of-the-line drug discovery products and services.

Since 2002 Quantum Pharmaceuticals has been developing its superior proprietary computer-based molecular modeling technology. The Quantum technology includes the latest achievements in the fields of physics, mathematics and chemistry. It demonstrates outstanding speed and accuracy of affinity calculations using fast quantum calculations which take into account the full flexibility of molecules, solvation effects and entropy contribution. This provides unprecedented possibilities for drug discovery.

The headquarters of Quantum Pharmaceuticals is in Moscow, and its worldwide distribution network is expanding.

www.q-pharm.com

Welichem reports positive results with its lead anticancer agent

VANCOUVER, Sept. 23 /CNW/ – Welichem Biotech Inc. (the “Company”) (TSX-V:
WBI), a biotechnology company developing therapeutic drugs in the fields of
autoimmune diseases and cancer, today announces positive results on the
anticancer activity of its WBI-2000 series of compounds. These results, from
work done by Dr. M. Alaoui-Jamali at the Centre of Translational Research in
Cancer of the Jewish General Hospital in Montreal, showed a potent delay of
tumor growth following administration of the Company’s drug lead, WBI-2100, in
a human melanoma cancer model grown in mice. The results are consistent with
those from in vitro and in vivo studies on WBI-2100 conducted by the US
National Cancer Institute (“NCI”). The Company’s WBI-2100, a fully
synthesized, small molecule compound, delayed the growth of common cancers
such as breast, ovary and colon.
“These positive results of WBI-2100, in studies from different research
laboratories are very encouraging, and the nature of the data open-up
potential for use of this novel agent alone or in conjunction with existing
therapies” said President and CEO Dr. John M. Webster.
Activity against major types of cancer was demonstrated by NCI for
several members of the WBI-2000 series in vitro, and ten of them were selected
by the NCI for further in vivo testing, including in human xenograft models.
This group of compounds can be readily developed and formulated and have no
structural similarity to current therapeutic agents.
Welichem’s compounds in the WBI-2000 series are tested, under a November,
1996 screening agreement, with the Cancer Treatment and Diagnosis Division of
NCI, the principal agency for cancer research of the United States government.

About Welichem Biotech Inc.

Welichem Biotech Inc. is a pioneering Canadian biopharmaceutical company
that is developing proprietary small molecule drugs with large potential and
significant competitive advantages in areas of auto-immune/ inflammatory
diseases and cancer. The first lead compound is in formal preclinical
development for therapeutic application against psoriasis.

ON BEHALF OF THE BOARD

John M. Webster

President and CEO

The TSX Venture Exchange has not reviewed and does not accept
responsibility for the adequacy or accuracy of the content of this news
release. This press release contains forward-looking statements that include
our belief as to the potential of our WBI-2000 series compounds. Certain risks
and uncertainties such as results of pre-clinical tests of our products, the
availability of funds and resources to pursue research and development
projects, outcomes of our patent applications, and our ability to successfully
commercialize the products could cause the Company’s actual results to differ
materially from those in the forward-looking statements.
%SEDAR: 00021386E

For further information: Dr. John Webster, President & CEO,
(604) 432-1703, email: jwebster@welichem.com or Allan McGirr, Investor
Relations, (604) 317-2981, email: amcgirr@welichem.com

MARCUS EVANS LIFE SCIENCES SUMMITS: UPCOMING EVENTS FOR 2006

The Leading Events for the European Pharmaceutical Industry

NICOSIA, Cyprus. – 25 Nov. 2005 – marcus evans announces that the Life Sciences Summits 2006 will include the following areas: Drug Discovery, Clinical Trials, Manufacturing and Marketing.

World-renowned experts and senior executives from leading pharmaceutical companies will address the most relevant and impacting issues faced by corporations at this time.

A select group of innovative solution providers will meet with senior pharmaceutical executives to discuss vital industry issues in a variety of fields.

“The marcus evans Life Sciences Summits focus on providing the latest information in Drug Discovery, Clinical Trials, Manufacturing and Marketing. Our programmes are renowned for their quality and the real, tangible benefits they provide to all participants. Our goal is always to create the foremost event for Europe‘s leading pharmaceutical executives.” John Farry, General Manager Europe

About marcus evans Life Sciences Summits

marcus evans Life Sciences Summits deliver the highest quality events tailored to meet the demands of an evolving industry, responding to the industry players’ most pressing needs. Designed to meet the requirements of senior market representatives, our Life Sciences Summits are a unique opportunity to gain knowledge from undisputed experts while having the opportunity to network in a very interactive and stimulating environment.

Upcoming Summits:

ManuPharma – 3rd Annual Pharmaceutical Manufacturing Summit
27 – 29 March 2006
Raffles Le Montreux Palace, Montreux, Switzerland
www.manupharmaeurope.com

Discovery – 6th Annual Drug Discovery Summit
10 – 12 April 2006
The Monte-Carlo Bay Hotel and Resorts, Monaco
www.discovery-summit.com

PharmaBrand – 3rd Annual Pharmaceutical Marketing Summit
30 May – 1 June 2006
Hotel Hermitage, Monaco
www.pharmabrandeurope.com

Evolution – 5th Annual Clinical Trials Summit
23 – 25 October 2006
The Monte-Carlo Bay Hotel and Resorts, Monaco
www.evolution-summit.com

About marcus evans

marcus evans, one of the worlds leading business information companies is dedicated to the provision of global business intelligence and information to assist in strategic and effective decision making. marcus evans products include business and economic summits, high-level conferences, industry congresses, professional training and sports hospitality. The company employs over 3,000 staff in 54 global offices. marcus evans provides clients with business information and knowledge which enables them to sustain a valuable competitive advantage and makes a positive contribution to their success.

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For more information, please contact:
Sabah Khennouf – Georgiou
marcusevans
PO Box 24797
CY-1304 Nicosia
tel: +357 22 849314
fax: +357 22 849307
SabahK@marcusevanscy.com
www.marcusevans.com

Screening Europe Provisional Agenda Released

Select Biosciences have again assembled a world class mixture of the best minds in this dynamic field. Over 400 attendees are expected and 50 exhibition booths will be presenting the latest technologies available. To be held 20-22 Feb 2006 in the beautiful city of Prague, this conference will provide a major networking opportunity and an un-missable event for those wishing to keep abreast of new developments in the field of biomolecular screening.

The second MedChem Europe conference will be held in parallel to this event to allow interfacing with colleagues from the closely aligned field of medicinal chemistry.

Agenda sessions include:

- ADME-Toxicology

- Kinases

- Compound Libraries

- Cell Based Assays

- Biomarkers

- High Content Screening

For the full downloadable agenda (pdf) please visit www.ScreeningEurope.com

Selected media partnerships are available for this event.

About Select Biosciences

www.SelectBiosciences.com

Select Biosciences Ltd. is focused on organizing specialist biomedical meetings. Experts from both academia and commerce present timely information from current research through to commercial implementation of new technologies. These events also provide a unique networking facility and the opportunity to reach a highly targeted scientific audience.

For further information on this conference, contact: Karen Saunders ksaunders@selectbiosciences.com

MedChem Europe Provisional Agenda Released

MedChem Europe Provisional Agenda Released

Select Biosciences have again assembled a world class mixture of the best minds in this dynamic field. Over 400 attendees are expected and 50 exhibition booths will be presenting the latest technologies available. To be held 21-22 Feb 2006 in the beautiful city of Prague, this conference will provide a major networking opportunity and an un-missable event for those wishing to keep abreast of new developments in the field of medicinal chemistry.

The third Screening Europe conference will be held in parallel to this event to allow interfacing with colleagues from the closely aligned field of biomolecular screening.

Agenda sessions include:

- Drug Discovery and Optimization

Chaired by Dr. Mark Bradley

Professor of High Throughput Chemical Biology University of Edinburgh

- Information, Analysis and Data Management Chaired by Dr. Miles Congreve Associate Director Astex Therapeutics

- Enhanced Synthesis Tools in Medicinal Chemistry Chaired by Dr. C. Oliver Kappe Associate Professor of Chemistry Karl-Franzens-University Graz

For the full downloadable agenda (pdf) please visit www.MedChemEurope.com

Selected media partnerships are available for this event.

About Select Biosciences

www.SelectBiosciences.com

Select Biosciences Ltd. is focused on organizing specialist biomedical meetings. Experts from both academia and commerce present timely information from current research through to commercial implementation of new technologies. These events also provide a unique networking facility and the opportunity to reach a highly targeted scientific audience.

For further information on this conference, contact: Karen Saunders ksaunders@selectbiosciences.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

Reluctant Businessman Helps Lead First Wisconsin Stem Cell Business

Craig January, who comfortably wears the hats of both scientist and heart doctor at UW-Madison, has had numerous chances to go into business.

But January, who developed a novel method to test drugs for heart toxicity in the late 1990s, resisted them – until recently.

“I’ve had offers from drug companies over the years, and I’d toyed with creating a company on my own,” said the 54-year-old January in a recent interview. His specialty is cardiac electrophysiology, the study of the heart’s electrical activity and pathways.

“But frankly, commercializing what we were doing was not high on my list of priorities,” said January, whose technology is licensed by the Wisconsin Alumni Research Foundation and is widely used around the globe.

His ambivalence about the business world began to change last year during talks with fellow scientist Tim Kamp, a noted cardiologist with whom January shares lab space at the university. The pair worked together at the University of Chicago and it was January who convinced Kamp to move to Madison.

The third faculty member in the discussions and their nascent enterprise is Jamie Thomson, who first isolated and reproduced human embryonic stem cells and is perhaps UW-Madison’s most famous scientist.

Though perhaps many years off, scientists believe stem cells — undifferentiated master cells — could eventually lead to cures of diabetes and Parkinson’s disease, as well as other medical breakthroughs.

Working with venture capitalists Bob and Tom Palay, founders of Madison-based companies NimbleGen and Genetics Assemblies, the trio of researchers launched Cellular Dynamics International (CDI) earlier this year to screen drugs for the pharmaceutical and biotechnology industries.

January is CDI’s medical officer. Kamp is the chief technical officer. And Thomson has the title of chief science officer. With their heavy schedules at the university, it is unclear how much time they will spend at the company as it ramps up. The fledgling firm is the first Wisconsin-based business with plans to use groundbreaking stem cell research from UW-Madison.

Initially, CDI will test altered or “transfected” kidney cells that are not derived from stem cells, but have been modified to have some of the electrical conductivity properties of human heart cells.

Within a few years, though, the company hopes to test human heart muscle cells – cardiomyocytes – created from stem cells. This technique, if broadened to include other organ tissues, could revolutionize drug screening, the scientists said.

CDI did not come to be overnight, said Nick Seay, the company’s chief operating officer.

“It was actually in the works for a long time,” added Seay, a veteran patent attorney with the Quarles & Brady law firm.

“There was a certain synergy to this,” he said. “Jamie had worked with Tim and Tim had worked with Craig. And the Palays had been talking to Jamie about stem cell opportunities for a while.”

Palay’s track record with NimbleGen and Genetic Assemblies – both biotechnology firms – helped convince the scientists to make the leap, he said. Also, over months of discussions, all the parties became comfortable about starting the enterprise.

“It wasn’t one thing made it happen,” said Seay, who signed on in June. “Let’s say there was a long get-acquainted period.

“But it is absolutely a coup,” he said. “This is not just a one shot deal. It’s a hybrid and there is a great amount of potential here for a lot of business in the future. The combined package is better than any one of these scientists alone.”

CDI is based at University Research Park on Madison’s west side – home to many other cutting-edge biotech firms. Gov. Jim Doyle recently awarded CDI $2 million in state grants and loans to help get its first products on the market. Doyle said the money would help leverage $4 million in other investments in CDI.

Though other companies offer the same service that CDI will unveil next year — and large pharmaceutical companies do similar testing internally — the Palays hope the drawing power of the names of Drs. January, Craig and Kamp will lure clients.

“This company will have Craig January’s imprimatur on it,” Seay said. “If you were a drug company, wouldn’t you want to hire the originator of this test?”

Kamp said initial tests on the human heart cells derived from embryonic stem cells he developed with Thomson in 2003 have been positive. But they are not ready for commercialization. Thomson’s initial stem cell discovery was published in 1998.

“When Jamie first started this, he saw cardiomyocytes early on because they spontaneously beat in culture,” Kamp said.

“We have proof of principal, but we are still in the development stage – which I hope won’t take more than a couple of years,” he said.

At this point, not a single product derived from human embryonic stem cells has been tested on people.

Kamp said the promise of using human heart cells and other cells derived from human embryonic stem cells is great.

“The idea is that if you want to understand how drugs work on the human heart, it’s best to test them on human hearts,” he said.

But adult heart cells don’t survive well or reproduce outside the body, so it isn’t practical to use them for screening drugs before testing on live animals or humans.

“Likewise, (living) people don’t want to part with their hearts and surgical specimens aren’t dependable,” he said.

And while using modified kidney cells is currently a state-of-the-art method, using human heart cells that are derived from stem cells in a tissue culture dish could create a new “gold standard,” Kamp said.

January concurred:

“A lot of testing – at least in principle – could be done on tissues derived from human embryonic stem cells,” he said.

Kamp chuckled at the idea of the stars being aligned for him, January and Thomson to start a company.

“I’m not good at astrology,” he said. “But I’ve worked with those guys a lot. And I can say we are fortunate to have good colleagues here at the university.”

Blake Anson, a scientist who works in January’s lab and at CDI, said he has been fortunate to have January as a mentor.

“Craig is one of the best I’ve ever worked with and he does what he can to help those beneath him,” Anson said, noting that UW-Madison is lucky that January, Thomson and Kamp have not left to work in private industry or another university.

January, for his part, said the academic world and patient care have suited him and his interests well. He spends about 60 percent of his time in his lab, with some days running well over 12 hours.

“But there is a certain beauty to CDI, what with two very similar technologies going on at one university in lab space that Tim and I share,” he mused.

“It was pretty simple to say they are both technologies that can be brought into a start-up company and that since my work is more mature, the company could have a product within a year of its inception to get off the ground,” he said.

January earned both his medical and doctoral degrees at the University of Iowa. But a brother had attended UW-Madison, a place he considered “pretty nice” from his first visits more than 30 years ago.

In 1976, January went to the University of Chicago to work with that school’s “world-renowned” electrophysiologists, including Harry Fozzard. January stayed for nearly two decades, starting as an intern and rising to cardiology fellow and ultimately an associate professor on the faculty.

“At one point, I figured I would stay there forever,” said January. He moved to UW-Madison to be the university’s chief of cardiology in 1995, a post he held for three-and-one-half years.

January called the heart a remarkable machine that in most people ticks correctly more than 3 billion times over the course of a lifetime.

But in some cases, the electrical signal that causes the heart to beat does not work properly. These irregularities in the heartbeat, called arrhythmias, have symptoms ranging in severity from mildly bothersome to deadly, he said.

To counter this in the late 1980s, anti-arrhythmic drugs were developed that prolonged the “QT interval,” the time between activation time and repolarization in each heart cycle. But if the QT interval was prolonged too much, he said, that could also cause sometimes-lethal problems.

“That was what I studied, the cellular mechanisms underlying these arrhythmias,” he said.

Then, in the 1990s, January’s work led to the removal from the market of several antihistamine drugs that had the catastrophic side effect of sudden death. He said thousands of lives have been saved because of this and other research.

“These were drugs that were developed to treat the sniffles,” said January, who began studying their compounds soon after arriving in Madison.

“We saw this happen in patients,” he said.

They included a woman admitted to the UW Hospital who’d taken an antihistamine and then collapsed from an arrhythmia in one of the lower chambers of her heart.

“Fortunately, paramedics were close by and resuscitated her,” he said. “We had the ability, which many places don’t have, to go straight from the bedside to the basic science lab because of our electrophysiology group here.”

January and other researchers’ work showed that the drug’s metabolites, or breakdown products, caused this potentially lethal arrhythmia.

At the same time in another UW-Madison lab, other scientists who were studying twitchy fruit flies identified a gene with a channel that is a key to passing electrical signals to heart muscles.

Back then, researchers trying to express, or make, these genes usually put them in frog eggs, January said. Because he worked with human patients, he didn’t want to use frog eggs. Besides, they often gave unreliable results.

So January and colleagues put the gene – called HERG – in a stable human-origin cell line that was easier to study and gave drug sensitivity similar to human heart cells.

Ultimately, they created a cell line that is used widely to screen drugs to see if they disturb the electrical conductivity of specific channels in heart muscles.

Many regulators – both here and in other countries – now require the screening before drugs can go on the market.

Ironically, January said WARF was not interested in licensing the cell line when he first approached them in the late 1990s.

“I think they didn’t understand it,” January said wryly.

Because pharmaceutical companies can spend hundreds of millions of dollars to develop a drug, January said they are keenly interested in learning early on about potential side effects – especially ones that could be fatal.

“To have a drug fail shortly after it gets to market or even shortly before is hugely expensive undertaking,” he said.

“Companies want to start screening earlier, when they are in basic development,” he said. “They will screen one, 10 or more than 100 compounds to weed out those that have high potential to cause problems.”

And while the financial interests of CDI and drug companies concern January, he said he and his colleagues hope their work will greatly reduce the need to for drug companies to kills tens of thousands of animals annually as part of their tests.

“Going to a drug company is in some ways a humbling experience,” he said. “What you see is a lot of animal research on mice, rats, rabbits, dogs, chimps…”

In some cases, animal organs – including hearts – are taken and used in toxicity tests. In others, the entire animal is given a drug.

“By creating human cell lines, we have the potential to reduce, perhaps dramatically, the use of animals by the pharmacy world,” he said. “Instead of using animals, you could use the cells.”

The difficulty with the heart, he said, is that cells from an adult animal cannot live in culture for more than a day or two, he said.

“So it is not so simple as to say I am going to take animal cells or even human cells and put them in the culture,” he said. “It won’t work.”

January called drug development a “complicated process.” And while the use of animals is a “necessary component,” he said it is something drug companies do not want publicized.

“You will never completely replace the need for animals to be tested,” he said. “But a lot of screening, we think, could be done on tissues derived from human embryonic stem cells.

January said he surprised by the extensive facilities these companies have for housing these animals for drug development.

“I was never aware of the extent of animal research until my work took me to pharmaceutical companies,” he said soberly.

“At CDI, one of our goals is to use non-animal biotechnology, including tissues derived from stem cells, for testing.

“We are creating technologies the have the potential to greatly diminish animal use in drug development. I feel good about that, though you will never get rid of it.”

Wisbusiness

Select Biosciences are delighted to announce that the provisional agendas for MedChem Europe and Screening Europe are now available.

Select Biosciences are delighted to announce that the provisional agendas for MedChem Europe and Screening Europe are now available.

Both conferences will be held concurrently in the Prague Congress Center over the period 20-22 Feb 2006. A major exhibition showcasing the latest drug discovery technologies and services will be held in parallel.

Exceptionally Affordable
To ensure the widest possible participation of laboratory and industry personnel we have paid close attention to driving down registration fees (e.g. compare the Euro 495 early bird price for our 3 day Screening meeting with similar conferences!). Academic rates are even lower. We have also negotiated an exceptionally low room rate (€110) at the 5 star Corinthia Towers Hotel adjacent to the Congress Center. Combine this with the low cost airfares now available to Prague (e.g. see here) makes this event irresistibly affordable for the whole lab.

So come and network with your peers at possibly the largest European drug discovery event in 2006.

Register for Screening Europe

Register for MedChem Europe

Altana Pharma invests in new High Throughput Screening system from Thermo Electron

11/18/2005 – Thermo Electron Corporation announced that it had secured a major contract with Altana Pharma to install a fully integrated Ultra High Throughput Screening system. Named last year as one of the most profitable pharmaceutical operations in Europe, Altana focuses on identifying new therapeutic approaches in the fields of respiratory inflammation, oncology and gastroenterology. The new system promises to significantly accelerate this complex process, shortening both compound discovery and development times.

Compound screening and profiling in early drug discovery is currently the responsibility of Altana’s HTS laboratories in Konstanz, Germany. Using cell and biochemical based assays, the laboratories focus on small volume 384 and 1536-well plates. According to Christopher McNary, Vice President & General Manager Laboratory Automation Solutions Thermo Electron, Thermo will be installing its CRS Dimension4 System, which consists of advanced robotics developed to maximize throughput in the laboratory. Thermo’s CRS Dimension4 will integrate other Thermo equipment such as Multidrop® liquid dispensers and VAL’s (vertical array loaders) with Thermo’s Cytomat incubators to maximize storage capacity.

Dr. Stuermer, Head of High Throughput Screening, Altana Pharma commented, “We have very tough criteria for the production of high quality data and the need of an ultra high throughput system that can deliver a large number of test points per day. We felt that Thermo is the company that can fulfill our specific requirements with a robust, highly automated system.” At present, up to 80,000 compounds are screened per day, but following the integration of the CRS Dimension4 System, they anticipate being able to significantly improve these capabilities to more than 180,000 compound tests per day. Dr. Stuermer also believes that the integration of such a system will boost compound profiling capabilities from currently 10,000 IC50s per day to a whole new level.

Beyond the Blockbuster Drug: Strategies for nichebuster drugs, targeted therapies and personalized medicine

The blockbuster model now delivers just 5% return on investment and only one in six new drug prospects will deliver returns above their cost of capital. As a result competitive pressures and falling R&D productivity will instigate a new pharmaceutical model that replaces the unsustainable blockbuster model; personalized medicine and the “nichebuster”.

This report, Beyond the Blockbuster Drug: Strategies for nichebuster drugs, targeted therapies and personalized medicine, examines targeted therapies and targeted drug delivery strategies as alternative investment options for pharmaceutical companies, in the face of declining returns and slow growth in the blockbuster market. This report’s strategic insight is also supported by in-depth interviews with thought leaders from the pharmaceutical industry, providing you with their insight into how tomorrow’s pharmaceutical business model will develop.

This report analyzes the niche pharmaceutical sectors with the greatest potential for profit and future growth. Harness the technological advances in personalized medicine and be part of the “nichebuster” revolution set to drive market growth and produce the market leading drugs of tomorrow.

THE ANSWERS TO YOUR QUESTIONS

In 2006, which blockbuster drugs will be exposed to patent expiration to the value of US$17bn?
What are the key factors slowing blockbuster market growth?
What is the ‘nichebuster’ model and how will it fit into the future landscape of the industry?
How is personalized medicine set to transform the future of the pharmaceutical industry?
Which sectors are currently driving growth for targeted therapies?
Which technologies will produce an explosion of poorly validated targets that may actually increase the rate of compound attrition and the costs of R&D?
What roles will alliances and partnering play in the development of the pharmaceutical sector beyond the blockbuster model?
KEY FINDINGS

From 2005 to 2008, total blockbuster sales are forecast to demonstrate a CAGR of only 1.6% compared with the 9% forecast for the period 2002 to 2005.
In order to grow by 10%, today’s big pharmaceutical companies would need to launch two or three new blockbusters per year.
Alliances and licensing will be increasingly critical to ‘BigPharma´s’ ability to access innovation in novel areas of science, new products in different therapeutic areas, and replacement compounds for late life-cycle drugs.
Technologies such as genomics and proteomics have produced an explosion of new poorly validated targets that may actually increase the rate of compound attrition and the costs of R&D.
Total pharmaceutical R&D outsourcing is expected to grow at a compound annual growth rate (CAGR) of 11-12% from its 2003 level of $7.9 billion, compared to anticipated growth in global R&D spending of only 9.6%.
REASONS TO PURCHASE

Understand how the new ‘nichebuster’ model will revolutionize the pharmaceutical sector and which new growth opportunities this model will promote.
Harness the new era of personalized medicine guided by advances in biotechnology and genetic engineering, and take advantage of the larger opportunities multiple specialist disease areas offer.
Analyze how leading players, such as Novartis and Roche, are using targeted therapies and R&D partnerships for faster growth and benchmark your portfolio growth strategy accordingly.
Evaluate new drug delivery technologies, advances in proteomics and pharmacogenomics set to transform the pharmaceutical sector and identify which technological developments your company can exploit to gain a competitive edge in the market.
Secure your frontline position in the future of the pharmaceutical industry by adapting your product portfolio to meet the healthcare needs of tomorrow.

View Table of Contents

CHEMAXON SUPPORTS OPEN SOURCE CHEMICAL INVENTORY APPLICATION FOR UNIVERSITIES

November 14th, 2005, Budapest, Hungary: ChemAxon, a software solutions provider for life sciences, announced the free provision of licenses for university users of an open source chemical inventory web application provided by Chemicalinventory.org.

Chemicalinventory.org is an open source project initiated by Dann Vestergaard and Claus Stie Kallesoe as a thesis project at their Post Graduate IT Diploma studies. Dann Vestergaard has experience as a LIMS supporter in a Danish Pharmaceutical Company but is now a full time programmer. Claus Stie Kallesoe is trained as a Medicinal Chemist and has been working with Discovery Informatics in a Danish Pharmaceutical company since 2000.

Chemicalinventory is a web application that manages the chemical stock in a laboratory-, production- or other facilities, where chemicals must be safely stored, easily found and tracked. This inventory solution is relevant to any facility which stores chemicals and is currently (since 2003) productive at The Danish University of Pharmaceutical Sciences with 70 users.

The structure input, search and visualization components of Chemicalinventory are provided by ChemAxon’s Marvin editor and viewer and JChem Base chemical search and database management tools. As a developer toolkit, with a full application programming interface (API), these tools are optimal for integrating into larger solution applications where ongoing development is a key to the application utility.

ChemAxon’s support for the chemical inventory application allows university users to receive free licenses to enable the application in their laboratories. The free provision to universities is a part of ChemAxon’s ‘Powered by Academic Package’ program where any educational establishment can receive licenses and support for all ChemAxon products at no charge. Launched last year the program has so far attracted over 270 participants. For more information or for applying to license ChemAxon’s toolkits for Chemicalinventory or your academic teaching or research please visit http://www.chemaxon.com/forum/ftopic193.html

About Chemicalinventory.org
To find out more, download or join the development of Chemicalinventory please visit http://www.chemicalinventory.org or visit the SourceForge.net location at http://sourceforge.net/projects/chi

About ChemAxon
ChemAxon is a leader in providing Java based chemical software development platforms for the biotechnology and pharmaceutical industries. With core capabilities including structure visualization and management, property prediction, virtual synthesis, screening and drug design, ChemAxon focuses upon active interaction with users and core portability to create powerful, cost effective cross platform solutions and programming interfaces to power modern cheminformatics and chemical communication. For more information please visit http://www.chemaxon.com

Galapagos Announces Third Quarter 2005 Results

— Acquisition of BioFocus completed, integration progresses as
planned

— Galapagos year to date revenues 8% below last year’s revenues,
but cash burn in line with forecast

— Revenue guidance for 4Q ’05 of 7.7 million, full year cash burn
of 7 million

— Strong cash position of 25 million on Sept. 30, 2005

— Management further strengthened with appointment of David Smith
as CFO

— New partnerships underscore competitive position in services
business

— Promising in vivo data on proprietary drug discovery programs
reported

— Galapagos rheumatoid arthritis target validated

— Optimistic outlook for partnering deals and library sales in 4Q

MECHELEN, Belgium, Nov. 10, 2005 (PRIMEZONE) — Galapagos NV (Euronext:GLPG) (LSE:GLPG) today announced its financial results for the first nine months of 2005.

Total revenue for the first nine months of 2005 amounted to 3.3 million, compared to 3.6 million in the first nine months of 2004, due to a decrease in custom adenovirus orders delivered in this period. The net loss for the first half of 2005 increased to 5.7 million from 4.3 million in the same period last year, reflecting stepped up R&D program investment. Cash and cash equivalents amounted to 25.1 million on September 30, 2005. “We have had an exciting quarter with the acquisition of BioFocus. We also have seen good service revenues but a slower custom adenovirus business. With our order portfolio, we expect to recoup some of these sales in the fourth quarter. We are optimistic on closing further deals this quarter, especially as we now have a joint sales offering with BioFocus. Consolidating their activities, we can give revenue guidance of 7.7 million for the last quarter of 2005. We have taken adequate cost control measures in order to offset the slower-than-expected third quarter sales; consequently, we remain on track to meet our full year 2005 cash burn guidance of 7 million,” said Onno van de Stolpe, Galapagos’ CEO. “Having seen the first very promising in vivo data from our rheumatoid arthritis program, we are excited about the progress in our drug discovery programs and expect to move forward rapidly toward demonstrating our first in vivo proof of concept.”

Key figures for first nine months 2005

(thousand, except net loss per share)

Sept 30, 2005 Sept 30, 2004 % change

Revenue 3,292 3,586 -8%
Loss from operations -5,812 -4,356 33%
Finance income 106 9
Loss before taxes -5,706 -4,347 31%
Taxes 32 5
Net loss for the period -5,674 -4,341 30%
Basic loss per share (Eur) -0.75 -0.73
Cash and cash equivalents 25,113 9,522

Details of financial results for first nine months 2005

Note: Consolidation of BioFocus results will start on October 12, 2005, to be published in Galapagos’ Full Year 2005 Results on March 3, 2006.

Revenue

Galapagos’ revenues for the first nine months of 2005 amounted to 3.3 million, a decrease of 8% on the 3.6 million recorded in the same period of 2004. Galadeno service division revenues amounted to 1.7 million for the first nine months compared to 1.9 million for the same period in 2004. Government grants in the period were 1.6 million compared to 1.7 million in the same period last year.

The decrease in service division revenues compared to last year is the result of fewer deliveries in the custom adenovirus business. Deliveries are expected to increase in the fourth quarter, allowing us to recoup some of these revenues. Following the BioFocus acquisition, we have decided to review the merits of pursuing medicinal chemistry work on the Alzheimer program in-house, thereby increasing the value of these targets. We have therefore decided to delay the out-licensing of the Alzheimer program, which is likely to decrease our fourth quarter 2005 contract revenues compared to the same period last year. Guidance for consolidated revenues for fourth quarter 2005 is 7.7 million.

Results

The net loss for the first nine months of 2005 was 5.7 million, or 0.75 per share, an increase of 1.4 million from the 4.3 million, or 0.73 per share for the first nine months of 2004.

Total research and development expenses in the first nine months of 2005 were 4.8 million, compared to 3.9 million in the same period 2004. The additional investment in R&D programs includes additional chemistry on our product development, including stepped up outsourcing.

Selling, general and administrative expenses increased slightly to 3.2 million in the first nine months of 2005 when compared to the 3.0 million in the same period of 2004.

Cash flow and cash position

A net increase of 14.8 million in cash and cash equivalents was recorded during the first nine months of 2005 (25.1 million compared to 10.3 million at the end of 2004). Cash used in operations was 5.1 million, on track for this year’s projected cash burn of 7.0 million. Furthermore, total lease payments made and investments in equipment amounted to 0.8 million. Galapagos raised 22.4 million in a public offering priced at 7 per share, amounting to a net cash contribution of 20.7 million. Galapagos’ cash and cash equivalents amounted to 25.1 million on September 30, 2005.

Corporate highlights

— Acquisition of BioFocus plc completed

— Listing on the AiM London

— Management further strengthened

— U.S. patent protecting target discovery platform

— Boston sales office opened

In September 2005, Galapagos announced an all share offer for BioFocus plc in the U.K. The strategic rationale for the offer was that BioFocus’ expertise in chemistry, lead discovery and lead optimization will greatly accelerate the progress of Galapagos’ programs and assist in Galapagos’ transition to a fully integrated drug development biopharmaceutical company. Additionally, the Enlarged Group would be well positioned to provide a suite of complementary biology and chemistry services to a broad base of customers, offering turnkey projects from target discovery to lead delivery.

Galapagos’ offer for BioFocus became wholly unconditional on October 17, 2005. Galapagos shares were admitted to trading on the London Stock Exchange’s Alternative Investment Market (AiM) on October 20, 2005. On October 27, 2005, Galapagos announced that acceptances had been received for over 92% of the BioFocus shares, and the offer for BioFocus was closed.

Following the completion of the acquisition of BioFocus, a number of appointments were made. Chris Newton, previous Chief Operating Officer of BioFocus, and David Phillips, previous Chief Business Officer of BioFocus, have joined the Executive Committee of Galapagos as Senior VP BioFocus and Senior VP Sales and Marketing, respectively. Also as a result of the acquisition, Galapagos’ Board of Directors will be strengthened by Geoff McMillan, previous CEO of BioFocus and David Stone, previous Chairman of BioFocus, as non-executive Directors.

David Smith was appointed as Chief Financial Officer of Galapagos and will fulfill his role starting February 1, 2006. David joins from AstraZeneca Netherlands, where he was Chief Financial Officer.

Galapagos announced that its IP position was strengthened further by receiving its third U.S. patent for its target discovery platform. This patent protects the Company’s adenoviral gene knock-down (SilenceSelect(r)) and gene knock-in (FLeXSelect(r)) collections, the core of multiple target discovery deals with pharmaceutical and biotech companies as well as patient organizations.

Additionally, Galapagos has opened a sales office in Boston, U.S., as of November 1, to support its sales and marketing activities. This office is headed by Nathalie Joly, BioFocus’ Director Business Development, North America.

Operational highlights Partnering activities

— Chemical library supply and medicinal chemistry services deal
with Serono (Switzerland) (signed in fourth quarter)

— Target discovery alliance with High Q Foundation (U.S.) for
Huntington disease

— Research collaboration with Novartis Pharmaceuticals (U.K.)

— Research collaboration with Amsterdam Molecular Therapeutics,
Netherlands Institute for Brain Research and Vrije Universiteit
Amsterdam

— BioFocus product offering broadened with two new compound
libraries and increased ion channel screening capabilities.

Galapagos is optimistic regarding the opportunities to close further partnering deals and library sales in the remaining period of the year.

Integration

With the acquisition of BioFocus, the integration with Galapagos’ partnering unit Galadeno is underway, and the integrated services unit now operates under the BioFocus brand name. BioFocus provides reagents and gene-to-preclinical drug discovery services to a broad base of customers throughout the global pharmaceutical and biotechnology industries. Several deal synergies and cross selling opportunities to our complementary client bases were identified and are being pursued actively. Galapagos drug discovery

— First in vivo results in proprietary rheumatoid arthritis
program — proprietary target validated

— Drug discovery collaboration with ZoBio, Pyxis and Leiden
University, supported by Dutch government grant of 1.2
million

— Alzheimer targets move into proof of principle studies

Galapagos focuses on bone and joint diseases to build a pipeline of new chemical entities to treat these diseases. The company’s most advanced drug discovery program is in the area of rheumatoid arthritis and focuses on proprietary targets whose modulation significantly diminishes joint destruction and where the medicine has a clear benefit over existing therapies. The market for autoimmune diseases, including rheumatoid arthritis, currently exceeds 7 billion and is expected to grow to 14 billion in the next few years. Galapagos started its drug discovery program 14 months ago. The in vivo proof of concept study currently underway investigates how a compound developed against one of Galapagos’ proprietary targets reduces paw swelling in a well-established mouse arthritis model. Our results today show a significant a nd important reduction in disease causing cytokines such as TNF-alpha, providing the first in vivo validation of a Galapagos target for rheumatoid arthritis.

The collaboration with ZoBio, Pyxis Discovery and Leiden University, which was announced in August 2005 has enabled Galapagos to take advantage of cutting-edge drug discovery technology in the progression of one of its proprietary targets in arthritis. As part of the 1.2 million government grant for the collaboration, Galapagos receives 550k in support of this program.

As further support to out-licensing efforts, we will combine the required expertise of BioFocus in medicinal chemistry with our proprietary Alzheimer targets, thereby creating additional value for these targets.

Conference call and webcast presentation

Galapagos will conduct a conference call open to the public today at 09.30 Central European Time (CET), which will also be webcast. To participate in the conference call, please call +32 2290 1608 ten minutes prior to commencement. A question and answer session will follow the presentation of the results. The live audio webcast can be accessed via Galapagos’ website at www.glpg.com, and will be available for replay a few minutes after the live version airs.

About Galapagos

Galapagos is a publicly traded, genomics-based drug discovery company (Euronext Brussels: GLPG; Euronext Amsterdam: GLPGA, London AiM: GLPG) that has drug discovery programs based on proprietary, novel targets in the bone and joint diseases — osteoarthritis, osteoporosis and rheumatoid arthritis. Galapagos offers a full suite of target-to-drug discovery products and services to pharmaceutical and biotech companies through its division BioFocus, encompassing target discovery and validation, and drug discovery services through to delivery of pre-clinical candidates. In addition, BioFocus provides adenoviral reagents for rapid identification and validation of novel drug targets and compound libraries for screening. Galapagos currently employs 193 people, including 74 PhDs, and occupies facilities in Mechelen, Belgium, Saffron Walden, U.K. and Leiden, The Netherlands. The partners of Galapagos include Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Celgene, GlaxoSmithKline, Novartis, Organon, Serono, Vertex, and Wyeth. More information about Galapagos and BioFocus can be found at www.glpg.com.

CONTACT: Galapagos NV
Onno van de Stolpe, CEO
Tel: +31 6 2909 8028
ir@galapagos.be

Source: Galapagos Genomics

Pharmacopoeial test facility expanded

Following interest from its clients, Melbourn Scientific is extending the range of pharmacopoeial testing that it offers. Managing director Steve Westcott says that it is easy to calculate the benefits of outsourcing pharmacopoeial testing: ‘Pharmacopoeial testing requires specialist skills, it is the old school chemistry that is taught at few universities because it requires expensive reagents and an investment in specialist glassware and other equipment. ‘It is rarely economical for companies to retain people with these skills for the few occasions when the tests are needed.

‘We have found that our analysts enjoy the challenge of pharmacopoeial, which puts their skills to the test.

‘The methods are very exact and the reagents specific to a particular test makes it the equivalent of Delia Smith for the pharma world.

‘The skills required to make it work are not easy to pick up and our analysts have decades of accumulated experience to call upon and it gives them an opportunity to use them’.

Melbourn Scientific provides contract analytical services to the pharmaceutical industry, it is expanding its pharmacopoeial test facility and investing in the equipment and reagents required to run the full range of tests such as organic volatile impurities (OVIs), Kjeldahl nitrogen determination, sulphated ash, optical rotation and refractive index determinations.

Steve Westcott made the decision to expand the facilities in response to market demand.

‘A number of clients had requested pharmacopoeial testing and we made an investment to support this.

‘The natural progression was to build on this and offer a complete range of tests.

‘Response from clients has been enthusiastic and the staff are keen to take on the challenge’.

Melbourn Scientific says it has invested continually in the latest equipment.

The company employs about 40 analysts at its laboratories and has grown organically to provide a range of contract analytical services to the pharmaceutical industry.

Source: Melbourn Scientific

New Research Study Provides Further Evidence of Strong Correlation of TriPath Imaging’s ProEx C Biomarkers with Biopsy Evidence of High Grade Cervical Intraepithelial Neoplasia (CIN2+)

In-house and External Retrospective Research Studies Incorporating ProEx C
Biomarkers Presented at 53rd Annual Scientific Meeting of the American Society
of Cytopathology

BURLINGTON, N.C., Nov. 7 /PRNewswire-FirstCall/ — TriPath Imaging, Inc.
(Nasdaq: TPTH) today announced that the results of a new in-house
retrospective research study demonstrated that testing of cervical cytology
specimens with Research Use Only (RUO) reagents incorporating the Company’s
proprietary ProEx C biomarkers yielded a 93% (p<0.0001) improvement in
sensitivity for detection of biopsy evidence of high grade cervical
intraepithelial neoplasia (CIN2+) when compared to a high grade abnormal
cytology classification of HSIL+. The results of this retrospective research
study also demonstrated a 65% improvement in calculated Positive Predictive
Value for detection of CIN2+ when compared to all atypical and abnormal
cytology classifications combined, defined as ASCUS and higher (ASCUS+).
These and other data relating to the performance of the ProEx C biomarkers
as well as an array of clinical and research studies incorporating the
SurePath liquid based Pap test were presented at the 53rd Annual Scientific
Meeting of the American Society of Cytopathology (ASC) in San Diego,
California. In conjunction with the meeting, the Company is also sponsoring
two symposia entitled “A New Era in Cervical Cytology: Revealing Clues from
the Cell-Cycle” and “Molecular Technology for the Cytology Lab: Initial
Impressions of In-House Use of ProEx C”.

Data from In-House Research Is Consistent with Previously Reported
External Research Studies
In a platform presentation made to the plenary session of the ASC meeting,
Adriann Taylor, Director of Product Development at TriPath Oncology, discussed
the results of a new in-house research study that was designed to evaluate the
performance of RUO reagents incorporating ProEx C biomarkers in a
retrospective study of 1,600 cervical cytology specimens collected using the
SurePath test pack. This retrospective cohort included 939 specimens that had
been classified as atypical or abnormal (ASCUS+) by standard microscopic
examination. For the purpose of this retrospective research study, the ProEx
C biomarkers were incorporated into RUO reagents designed to cytochemically
distinguish the presence of the over-expression of proteins associated with
aberrant S-phase induction in cervical smears that have been classified as
atypical or abnormal according to the generally accepted Bethesda 2001 System
for classification of cytologic morphology.
In this pre-clinical research study, the sensitivity of testing with RUO
reagents incorporating the ProEx C biomarkers for detection of biopsy evidence
of CIN2+ was 96.2%, a 93% improvement (p<0.0001) when compared to
classification of HSIL+ by microscopic examination. The calculated Positive
Predictive Value (PPV) for biopsy-confirmed CIN2+ reflected a 65% improvement
in the PPV when compared to microscopic examination.
These data are consistent with the results of external retrospective
research studies that were presented in September at the European Congress of
Cytology in Paris. In these retrospective studies from the Johns Hopkins
Medical Institutions and the Massachusetts General Hospital, the results
demonstrated an improvement of 70.6% and 95%, (p=0.0015, p=0.0002),
respectively, in sensitivity for detection of biopsy evidence of CIN2+ and an
improvement of calculated Positive Predictive Value of 113% and 136%,
respectively, when compared to microscopic examination.
“The results of our relatively large retrospective study with RUO reagents
incorporating the ProEx C biomarkers are wholly consistent with previously
reported results,” said Johnny Powers, PhD., Senior Vice President, TriPath
Oncology. “These research studies further demonstrate the correlation between
detection of aberrant S-phase induction with our ProEx C biomarkers and biopsy
evidence of high grade cervical disease.”

External and In-House Research Studies Address Analytical Performance,
Workflow, Impact on Microscopic Examination, and Specific Biomarker
Performance
In addition to the large retrospective in-house study, six additional
studies were presented at the ASC meeting. Investigators from the Johns
Hopkins Medical Institutions and the University of Colorado reported virtually
no variability with regard to scoring and staining reproducibility when using
a “home brew” version of the ProEx C Analyte Specific Reagent (ASR). These
researchers further concluded that their “home brew” assays were unaffected by
routine laboratory environment factors in these studies. In a separate study,
investigators from Johns Hopkins Medical Institutions observed that testing
with the ProEx C biomarkers may assist with the detection of cytologic
abnormalities on microscopic examination. Studies from the Company’s in-house
research staff addressed assay automation and the performance of specific
constituent biomarkers.
“We are very pleased with the results of these very practical studies,”
said Timothy Fischer, TriPath Imaging’s Vice President of Product Development.
“These studies provide early validation of our efforts to develop a product
that will be robust, easy to use and can be readily introduced into the
routine laboratory setting. Analytical performance and adaptability to routine
laboratory workflow will be critical determinants of the commercial success of
our products.”

About the ProEx C Biomarkers
The ProEx C biomarkers are monoclonal antibodies that detect over-
expression of proteins that is associated with aberrant S-phase induction, an
abnormal growth state that has been associated with cancer of the cervix,
esophagus, skin, prostate, ovary and colon. These biomarkers were identified
as the result of an outcome driven gene discovery analysis of cervical
neoplasia that was completed in 2003.

Analyst Day
Immediately following its third quarter earnings conference call on
November 10th, the Company will host an Analyst Day conference in New York
City. Management will review the results of research studies employing the
Company’s ProEx C molecular markers that were presented in conjunction with
the October meeting of the European Congress of Cytology in Paris and the
November meeting of the American Society of Cytopathology in San Diego. This
review will include the results of studies performed by investigators from
three major academic centers as well as the results of new in-house research
studies. The Company will also review the potential clinical and commercial
value of its developing pipeline in the area of molecular diagnostic products
and imaging systems.

TriPath Imaging, Inc., headquartered in Burlington, North Carolina,
develops, manufactures, markets and sells innovative solutions to improve the
clinical management of cancer, including detection, diagnosis, staging and
treatment. TriPath Oncology, a wholly owned subsidiary of TriPath Imaging,
develops molecular diagnostic products for malignant melanoma and cancers of
the cervix, breast, ovary and prostate. For more information on TriPath
Imaging please visit our web site at http://www.tripathimaging.com.

Investors are cautioned that statements in this press release that are not
strictly historical statements constitute forward-looking statements which
involve risks and uncertainties that could cause actual results and outcomes
to differ materially from what is expressed in those forward-looking
statements. Such forward-looking statements include, without limitation, those
related to the development of the ProEx C biomarker and the analyte specific
reagent for detection of aberrant S phase induction. Important factors that
may affect such forward-looking statements include, without limitation:
TriPath Oncology may be unable to successfully develop and commercialize
products and services when anticipated, if at all; clinical trials may yield
results for product candidates incorporating the ProEx C biomarkers that
differ from the results of our in-house and external research studies; TriPath
Imaging’s products may not achieve or maintain market acceptance to the degree
anticipated; TriPath Imaging and TriPath Oncology’s products may not receive
FDA or other required regulatory approval when expected, if at all; and other
risks detailed in TriPath Imaging’s filings with the Securities and Exchange
Commission, including those described in TriPath Imaging’s Annual Report on
Form 10-K for the year ended December 31, 2004.

Contact
Stephen P. Hall, Chief Financial Officer
TriPath Imaging
336-290-8721

Nanion receives Bavarian Innovation Award 2005

Munich, Germany – Octobre 2005 – The German nanobiotech company Nanion Technologies GmbH was recently awarded the Bavarian Innovation Award 2005 and is Bavarias company of the year (small/medium enterprise (SME)).
Nanion received the award for its chip-based patch clamp technique, which allows to perform sophisticated electrophysiological measurements from cells in an automated and parallel manner. Nanions entry level device, the Port-a-Patch©, supersedes the common pipette based patch clamp technique in ease of use and throughput and doesn’t require a microscope, vibration isolation or a micromanipulator. The Port-a-Patch© uses an all electrical read-out for automatically positioning and electrically contacting cells on the chip. With the Port-a-Patch©, Nanion offers the world’s smallest patch-clamp workstation. This innovative drug discovery technology makes patch clamp available also to non-electrophysiologists.
This innovation and its successful market introduction has been award the prestigious prize, which clearly is an important step and great commendation for Nanion.

Nanion
Nanion Technologies GmbH is a spin-off from the Center for Nanoscience (CeNS) of the University of Munich (LMU). Nanion combines bio- and nanotechnology in a company serving the life sciences industry by offering instrumentation for increasing the speed and efficiency of the drug discovery process in ion channel drug discovery. Nanion develops, produces and markets instrumentation and chip consumables for automated patch clamping. For more information, please contact us at info@nanion.de or visit our website at www.nanion.de.

The Port-a-Patch©
The Port-a-Patch© is a complete patch clamp setup with minimum foot print and low maintenance requirements. The system uses Nanion’s planar patch clamp chips and provides high quality data. Great ease-of-use is accomplished by automated cell positioning and sealing. The Port-a-Patch© enables fast fluid exchange on the chip, suitable not only for voltage gated, but also for ligand gated ion channels. Even the exchange of intracellular solution is possible, enabling perfusion on both sides of the cell membrane. The Port-a-Patch© offered by Nanion is a valuable tool for target validation and safety pharmacology (hERG screening).

Links:
Nanion

http://www.nanion.de

Port-a-Patch

http://www.nanion.de/pdf/Porto1004.pdf´

NPC-16s

http://www.nanion.de/pdf/npc16s.pdf

Newsletter:

http://www.nanion.de/pdf/NanionNotes3.pdf

http://www.nanion.de/pdf/NanionNotes2.pdf

http://www.nanion.de/pdf/NanionNotes1.pdf

ChemDiv, Inc. and ProQinase GmbH to Partner in Lead Discovery and

FREIBURG, Germany and SAN DIEGO, Nov. 7 /PRNewswire-FirstCall/ –

ChemDiv, Inc. of San Diego, CA, and ProQinase GmbH of Freiburg, Germany, announced that they have signed an agreement to establish a partnership in the discovery and preclinical development of new kinase inhibitors.

Under the agreement ChemDiv will support design and synthesis of

target-focused small molecule libraries, undertake medicinal chemistry for hit to lead and lead optimization, as well as DMPK and certain in vivo experiments. ProQinase will be responsible for in vitro kinase inhibitor screening and profiling on a panel of jointly selected oncology-relevant kinase targets, cellular assays and in vivo experiments. Both parties will share development costs and revenues from the planned out-licensing of optimized leads.

“Many protein kinases, when deregulated, are linked causally to the formation of human tumors. Inhibitors of protein kinases, such as Gleevec, IRESSA and Tarceva, are recently approved anti-cancer drugs. The development of protein kinase inhibitors for the treatment of cancer is still at its beginning stage. Due to the diversity of molecular alterations found in human cancers, the lack of efficient and safe drugs for treating different types of cancers is substantial,” states Dr. Michael Kubbutat, Head of Research & Development at ProQinase. “ProQinase has experience in the development of compounds that simultaneously block different mechanisms involved in tumor growth.”

Christoph Schaechtele, CEO of ProQinase, comments: “We are very optimistic about our new project with ChemDiv and are certain that this substantial investment will pay off. The selection of the panel of kinases takes into account market trends and latest scientific findings. The combination of our iProKiTe(R) platform covering powerful preclinical in vitro and in vivo methods with the medicinal chemistry expertise of our partner ChemDiv, will be successful in generating new drug candidates.”

Alex Kiselyov, VP of Chemistry at ChemDiv added: “ChemDiv has found a synergistic partner in the development of novel specific- and dual-kinase inhibitors. ProQinase offers state-of-the art molecular biology and screening capabilities, as well as an extensive set of in vivo models complementary to ChemDiv discovery biology platform. These are to strengthen our internal oncology programs. We are certain this collaboration will yield high quality pre-IND candidates for further development as anti-cancer therapies.”

About ChemDiv:

ChemDiv, Inc. (ChemDiv) is a global chemistry-driven contract research organization focused on the delivery of new scientific innovation, products and services that meet the drug discovery needs of its partners. ChemDiv provides partners with access to Discovery outSource(TM), a full service drug discovery capabilities encompassing: medicinal chemistry; pre-clinical development; synthetic chemistry; diverse and focused screening libraries, as well as global logistics. For additional information, please visit http://www.chemdiv.com.

About ProQinase:

ProQinase GmbH is a division of the KTB Tumorforschungs GmbH at the Tumor Biology Center Freiburg, Germany. Based on its Integrated Protein Kinase Technology Platform (iProKiTe(R)) ProQinase offers services to the pharmaceutical industry worldwide. At the same time this platform is used for internal drug development in collaboration with academic and industrial partners. iProKiTe(R) covers a large part of preclinical drug development in oncology, ranging from high throughput screening and kinase inhibitor profiling to cellular assays, in vivo models and soluble biomarker assays. Further information can be obtained from http://www.proqinase.com.

SOURCE ChemDiv, Inc.

-0- 11/07/2005

CONTACT: Henrik Konarkowski, Sr. Director of Business Development of ChemDiv, Inc., +1-858-794-4860, hk@chemdiv.com; or Dr. Michael Szardenings, Head Business Development of ProQinase GmbH, +49-761-206-1780, info@proqinase.com

Web site: http://www.chemdiv.com

http://www.proqinase.com/

4th Annual Cytokines and Inflammation – Call for Abstracts

The 4th annual conference on Cytokines and Inflammation will cover many important fundamental aspects of the role of cytokine and inflammation as related to drug discovery and development, including current drugs, progress of potential drugs in pre-clinical and clinical trials, and new research and developments in this field. We hope to achieve these goals by bringing together conceptual innovators from all active parties who certainly include scientists, industry leaders, entrepreneurs, and regulators.

In addition to the Keynote presentation by Dr. Joost Oppenheim from the NIH, there are 23 excellent speakers and more confirming everyday. Presenters from organizations such as NCI, Amgen, Regeneron, Aventis, FDA, Novartis, Xoma, Roche, Isis, Genentech, Genzyme Corp, Johnson & Johnson, Neopharm, Celgene, Serono, ZymoGenetics, Biogen Idec, and The Scripps Research Institute.

The 4th annual conference on Cytokines and Inflammation will take place at the San Diego Marriott in La Jolla, California on Monday and Tuesday, January 30 and 31, 2006. Come enjoy San Diego and all the delights it has to offer.

Please bring this conference to the attention of your colleagues who may benefit from attending. Please register early and submit an abstract.

ABSTRACT SUBMISSION DEADLINE: December 30, 2005
A few abstracts will be selected for oral presentation.
Early Registration Deadline: November 30, 2005

Confirmed Speakers:
Simon Blake
Centacor, (J&J)

Lawrence Blatt
Vice President
InterMune

Hal Blumberg
Inflammation
Amgen, Inc.

Chris Clegg
Associate Director
ZymoGenetics

Rosanne Crooke
Program Leader, Cardiovascular Group
Isis Pharmaceuticals

David Croteau
Dir, Clinical & Medical Affairs
NeoPharm

Raymond Donnelly
Div of Therapeutic Proteins
CBER, FDA

Scott Durum
Principal Investigator
NCI, FCRF, NIH

Alan Jackson
Novartis Research Institute
Andy Chan
Genentech, Inc.

William Farrar
Deputy, Lab of Molecular Immunoregulation
NCI, FCRF, NIH

Robert Gundel
VP, Preclinical Research
XOMA

Sam Hwang
NCI, NIH

Margaret Karow
Vice President
Regeneron

Steven Ledbetter
VP, Renal Diseases
Genzyme Corporation

Alan Lewis
President
Celgene San Diego

Joost Oppeheim
Chief, Lab of Molecular Immunoregulation
NCI, FCRF, NIH
John Carulli
Principal Scientist
Biogen Idec
Garth Ringheim
Principal Scientist, Immunology
Aventis Pharmaceuticals

Michael Pollard
The Scripps Research Institute

Nora Sarvetnick
Scripps Research Inst

Thomas Schall
President & CEO
ChemoCentryx

Robert Strieter
Prof and Chief, Div of Pulmonary & Critical Care Medicine
UCLA

Julian Symons
Head, HCV Biology
Roche Palo Alto

Ji Ming Wang
Head, Chemoattractant Receptor & Signal Group
NCI, FCRF, NIH
Tamas Oravecz
Senior Director, Immunology and Hematology
Lexicon Genetics, Inc

http://www.gtcbio.com/

SMi’s 4th Annual Conference on High Throughput Screening

23rd to 24th January 2006, Millennium Gloucester Hotel, London Sponsored by: Caliper Life Sciences & Genedata Supported by: HTScreening.net, Combichem.net, Pharmafocus, Pharmafile, Inpharm.com & DrugResearcher.com

Dear Head of High-Throughput Screening,

In recent years pharmaceutical R&D productivity has been experiencing decline despite increased research and development spending. Ten years ago high throughput screening was regarded as the potential saviour of drug discovery, but in reality HTS and uHTS have not lived up to their hype – why is this and what can still be achieved with the use of these assays?

SMi’s 4th Annual Conference, High Throughput Screening – The Application of HTS in current and Future Drug Discovery, will provide attendees with the latest insight into this important application, covering market dynamics, improved technologies and thoughts for the future. Further, the conference will address how HTS-based lead generation can be made to deliver, the benefits of this application and where the industry will be in the next 5 years. Additional key issues to be addressed by leading experts in the industry include, opportunities for in silico screening, the screening of protein-protein interactions and data analysis and mining.

Learn how to deal with critical bottlenecks and other issues reducing the efficiency of the drug discovery process through the use and application of better high throughput screening methods and tools.

A must attend event for those wishing to improve their drug discovery productivity!

**********************************************************************
EARLY BIRD BOOKING OFFER
**********************************************************************
The early bird registration deadline is 31st October 2005. Please register before this date to receive a reduced rate.

To register simply go to: http://www.smi-online.co.uk/goto/htscreening.asp?emref=T14EP31063506

Offers are also available for group bookings, contact James Holland on
tel: +44 (0)20 7827 6180 or mailto:jholland@smi-online.co.uk
**********************************************************************

A unique opportunity to learn from leading industry experts including:

- Dr Jefferson Paslay, Vice President, Screening Science, Wyeth
- Dr Jonathan Mason, Executive Director, Medicinal Informatics, Structure & Design, Pfizer
- Dr Lorenz Mayr, Executive Director, BioChemical Assay Development & Screening, Novartis
- Dr Gregory Kaczorowski, Senior Director, Ion Channel Department, Merck
- Dr David Keeling, Director, Lead Generation Biology, AstraZeneca
- Dr Mary Jo Wildey, Senior Research Fellow; Screening & Compound Logistics Centre Team Lead, Johnson & Johnson
- Dr Alexander Hillisch, Director, Medicinal Chemistry & Head, Computational Chemistry, Bayer Healthcare
- Dr Stephen Clulow, Director, Lead Discovery, Cambridge Antibody Technology
- Dr Dominique Besson, HTS Services Group Leader, Serono

=======================================================================

Benefits of Attending:

- THE APPLICATION OF HTS IN DRUG DISCOVERY TODAY AND TOMORROW: Learn how HTS-based lead generation can be made to deliver and its benefits in lead optimisation and CD delivery. What are the benefits of HTS-based drug discovery? How will HTS progress in the next 5 years?
- OPPORTUNITIES FOR IN SILICO SCREENING: Review the latest techniques taking a close look at ligand and target-based in silico screening
- SCREENING OF PROTEIN-PROTEIN INTERACTIONS: Learn how to interfere with protein-protein interactions, uncover the current challenges and limitations and hear success stories from the Lead Discovery Centre at Novartis
- HOW DOES HTS DELIVER VALUE IN DRUG DISCOVERY? Understand the link between HTS, chemoinformatics and lead generation
- DATA ANALYSIS AND MINING: Hear case examples from top pharmaceutical companies as they discuss preferred methodologies to deliver better leads in the drug discovery process
- INDUSTRY EXPERTS: Network with influential experts from leading pharmaceutical companies and learn from their experiences and expertise

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PLUS A HALF-DAY POST-CONFERENCE EXECUTIVE BRIEFING
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Cell-Based Screening
25th January 2006 (AM), Millennium Gloucester Hotel, London
In association with DiscoverX

Executive Briefing details follow the full conference programme
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For the full conference programme please scroll down

DAY ONE – 23rd January 2006

8.30 Registration & Coffee

9.00 Chairman’s Opening Remarks
Dr Lorenz Mayr, Executive Director, BioChemical Assay Development & Screening, Novartis

THE HIGH THROUGHPUT MARKET
9.10 What has been happening?
- Overview of High Throughput Screening (HTS) and
Its impact on the pharmaceutical industry
- The importance of HTS
- The current opportunities and limitations
- The future of HTS – how will HTS progress over the next 5 years? Dr Mary Jo Wildey, Senior Research Fellow; Screening & Compound Logistics Centre Team Lead, Johnson & Johnson

APPLYING HTS TO DRUG DISCOVERY

THE APPLICATION OF HTS IN DRUG DISCOVERY
9.50 Making HTS deliver
- Keeping HTS efficient
- Tracking success downstream
- The benefits of HTS-based drug discovery
- Future challenges
Dr David Keeling, Director, Lead Generation Biology, AstraZeneca

10.30 Morning Coffee

HTS AS AN INTEGRAL PART OF THE EARLY DRUG DISCOVERY PROCESS
11.00 The business of HTS
- Scaling HTS operations to meet organisational requirements
- Successful partnerships across the organisation for HTS success
- Alignment of HTS priorities with discovery goals
- HTS data deliverables that enable rapid progression of projects
- Investing in HTS related technologies that add value
Dr Jefferson Paslay, Vice President, Screening Science, Wyeth

LEAD GENERATION STRATEGIES

HOW DOES HTS DELIVER VALUE IN LEAD GENERATION?
11.40 The link between HTS, chemoinformatics and lead generation
- Optimising the use of HTS
- Ensuring quality and reproducibility in HTS
- Realising the value and investment of each section
- Developing a high quality hit list
- Setting the proper goals and metrics for HTS
Dr Frank Brown, Senior Research Fellow, Johnson & Johnson

12.20 Networking Lunch

LEARNING FROM OUR MISTAKES
1.50 Delivering starting points for successful lead development
- Corporate compound collections, an historic view
- Leadlike, druglike? Enriching corporate compound files
- Success through compound selection
- HTS and ADME
- How our processes drive physico-chemical properties
Dr Dominique Besson, HTS Services Group Leader, Serono

HIGH THROUGHPUT SCREENING STRATEGIES FOR DISCOVERING ION CHANNEL DRUGS
2.30 Ion channel HTS
- Types of ion channel high throughput screens
- Configuring fluorescence-based assays
- Methods for triggering ion channel activity in HTS
- Automated electrophysiology
Dr Gregory Kaczorowski, Senior Director, Ion Channel Department, Merck

EMERGING SCREENING METHODOLOGIES

3.10 Afternoon Tea

IN SILICO SCREENING
3.40 The emergence of screening methodologies
- Reviewing the techniques – ligand and target-based in silico screening
- Protein structure information as a prerequisite for high throughput docking
- Hit-list processing – combining potency and ADMET aspects
- Problems and success stories
Dr Alexander Hillisch, Director, Medicinal Chemistry & Head, Computational Chemistry, Bayer Healthcare

MICROFLUIDICS
4.20 Global adoption in pharmaceutical screening
- The screening dilemma: more spending, more screening, more technologies have delivered relatively low success
- High throughput or high output? The landscape is changing
- Faster, high fidelity data is the new goal for screeners = less failures in the clinic
- 75% of top pharmaceutical companies have adopted microfluidics to assist the change in screening paradigm – why? Jerome LeClercq, European Marketing Manager, Caliper Life Sciences

5.00 Chairman’s Closing Remarks and Close of Day One

5.10 Networking Drinks Reception Sponsored by DiscoverX

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DAY TWO – 24th January 2006

8.30 Re-registration & Coffee

9.00 Chairman’s Opening Remarks
Dr Stephen Clulow, Director, Lead Discovery, Cambridge Antibody Technology

PROTEIN-PROTEIN INTERACTIONS

9.10 SCREENING OF PROTEIN-PROTEIN INTERACTIONS VIA HIGH CONTENT
BIOCHEMICAL ASSAY TECHNOLOGIES
- Interfering with protein-protein interactions – current challenges/limitations
- Generating new target-specific compound collections: The key requirements
- Impact of novel assay technologies on modern drug discovery with difficult targets
- Ultra-sensitive, multi-mode assay technologies for studying protein-protein interactions
- Success stories on protein-protein interactions from the Novartis Lead Discovery Center (LDC)
- Future directions of miniaturised multi-mode high content biochemical screening Dr Lorenz Mayr, Executive Director, BioChemical Assay Development & Screening, Novartis

9.50 HOMOGENOUS ASSAYS FOR PROTEIN-PROTEIN INTERACTION
- Homogeneous protein-protein assays in lead isolation and optimisation
- Case studies for receptor-ligand and antibody-antigen interactions
- Comparison of different assay technologies
- Optimising assays to get the best hits
- How protein-protein assays influence hit to lead attrition
Dr Stephen Clulow, Director, Lead Discovery, Cambridge Antibody Technology

10.30 Morning Coffee

KINASE INHIBITORS
11.00 From hits to leads
- Kinase focussed library – design and value
- Screening and support of the drug discovery approach
- ADME screening
- The selectivity issue
Dr Doris Hafenbradl, Director, Biochemical Screening, GPC Biotech

A MINIATURISED KINASE PLATFORM
11.40 Schering’s approach
- Challenges and benefits
- Impacts on assay development, HTS processes, data quality and compound profiling Dr Christian Bergsdorf, Research Fellow, Schering

12.20 Networking Lunch

DATA MANAGEMENT

DATA ANALYSIS AND MINING TO FIND THE BEST LEADS
2.00 Experiences from big pharma
- Analysing the data to get more from the assay results
- Using the activity models to drive further library design and synthesis
- Differentiating the compounds and attrition management using biological fingerprints to select candidates to proceed to preclinical and clinical testing
Dr Jonathan Mason, Executive Director, Medicinal Informatics, Structure & Design, Pfizer

EXTRACTING INFORMATION FROM HIGH THROUGHPUT SCREENING DATA
2.40 Considerations for the setup of data management and analysis
processes
- Scientific data as a product: what makes them “good”?
- Converting complex data into useful information: data management and analysis strategies
- Maximising quality: designs, parameters, controls
- Maximising efficiency: automated processing and manual review of large-scale data sets
- Maximising information content: global analysis of potency and high
content HTS data
Stephan Heyse, Project Head, Genedata

NEW TECHNOLOGIES
3.20 A poisoned chalice?
- Possible goals of introducing new technologies in the HTS and early discovery environment
- Quantitative and qualitative benefits
- Identifying the risks and uncertainties
- How can we justify their costs?
- Some practical challenges to prepare for
Dr Andrew Chadwick, Global Analytics & Life Sciences Consulting, PA Consulting Group

4.00 Chairman’s Closing Remarks and Close of Conference

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PLUS A POST-CONFERENCE HALF-DAY EXECUTIVE BRIEFING ======================================================================
Cell-Based Screening
25th January 2006, Millennium Gloucester Hotel, London

In association with: DiscoverX

About the Executive Briefing:
This executive briefing will cover the benefits of new and emerging cell-based screening assays as critical tools in the pharmaceutical and biotechnology industries. In particular, the session will focus upon the use of high content assays in both drug discovery and development, including their application in target identification and validation, lead selection and optimisation, and preclinical studies. Since high content cell-based assays provide richer biological information at the sub-cellular level, they offer significant advantages over traditional HTS. High Content Screening (HCS) promotes efficient discovery of drugs more efficiently, while allowing substandard candidates to ‘fail fast’, saving both time and money.

8.30 Registration & Coffee

9.00 Cell-based screening – advantages and disadvantages
- Understanding the advantages of cell-based screening
- Understanding the disadvantages of the approach
- User experiences – how effective is cell-based screening in generating validated compound leads?
- Is it more useful in primary or in secondary screens?

9.45 Infrastructures needed for cell-based screening
- Automated cell culture
- Information handling
- Data analysis

10.30 Morning Coffee

10.50 High content vs high throughput screening
- High content, low throughput, cell-based assays?
- Emerging techniques for higher throughput imaging systems
- High throughput, low content, cell-based assays?
- Emerging techniques for lower throughput cell-based systems

11.30 Cell pathway screening for key target classes
- GPCRs
- Kinases
- Transcription factors, including nuclear hormone receptors

12.10 Discussion and questions – review of the session

12.30 Close of Executive Briefing

About the briefing leaders:
Richard M. Eglen (Ph.D. Molecular Pharmacology) is the Chief Scientific Officer at DiscoveRx Corp., a venture-backed private company in Fremont, CA. Dr Eglen was Vice President and Director of the Institute of Pharmacology at Syntex and subsequently Vice President of the Centre for Biological Research at Roche Bioscience until 1999. He then joined LJL Biosystems as Senior Vice President for assay development and later joined DiscoveRx Corp in 2000, and is responsible for all R&D activities. He is the author of over 300 publications, several book chapters, and patents, and serves on several journal editorial boards. He is also a member of the Board of Directors for the Society for Biomolecular Screening.

Dr Sanj Kumar joined DiscoveRx in 2001, as Vice President and General Manager of the Europe Region. During this time, his main responsibility has been the introduction of DiscoveRx’s high throughput screening technologies to the European pharmaceutical and biotech market place.

Before DiscoveRx, he worked for Biacore where he was responsible for the European sales and marketing organisation. Prior to joining industry, his academic career has included studying mitochondrial proteins as a post doctoral fellow in Nagoya, Japan; Studying for a PhD in the Institute of Neurology, London; and working as a Protein Chemist in the Institute of Cancer Research, London.

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EARLY BIRD BOOKING OFFER
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The early bird registration deadline is 31st October 2005. Please register before this date to receive a reduced rate.

To register simply go to: http://www.smi-online.co.uk/goto/htscreening.asp?emref=T14EP31063506

Offers are also available for group bookings, contact James Holland on
tel: +44 (0)20 7827 6180 or mailto:jholland@smi-online.co.uk
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Sponsorship and Exhibition opportunities:

SMi Group offers excellent opportunities to profile your company through tailored sponsorship opportunities. For details contact Adrian Johnston on tel: +44 (0)20 7827 6074 or mailto:ajohnston@smi-online.co.uk