January 6, 2009
| PharmaWeek


Top Headlines: Week of January 4, 2009
  • This Week's Feature

PharmaWeek |Dec 3| A Q&A with Dana-Farber pediatric oncologist Alan d'Andrea on his business venture, The DNA Repair Company (DNAR).

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  • Breaking R&D News and Business Insights

The Economist |Nov 27| A study published this week in PLoS Medicine, an online journal, confirms what many have suspected and what previous studies have hinted at: drug companies try to spin the results of clinical trials.

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Time |Nov 28| The pharmaceutical industry is one of the few sectors around that appears to be weathering these difficult times with relative ease. Last Friday, the European Commission suggested why that might be: it claims Big Pharma systematically rigged the market to squeeze out copycat medicines.

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PharmaTimes |Dec 1| European Commission investigators will carry out more dawn raids on pharmaceutical manufacturers, and both originator and generics companies will need to review the way they do business to ensure they do not become the subject of antitrust litigation, leading experts have warned.

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Forbes |Nov 24| Genentech’s key revenue driver, the blockbuster drug Avastin, improved the survival time for breast cancer patients in a late-stage study, putting the drug closer to full regulatory approval to treat the condition.

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Bloomberg |Nov 26| A gene-based test can predict how patients will respond to treatment for non-Hodgkin’s lymphoma.

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BusinessWeek |Dec 1| S&P equity analysts examine the ramifications for the industry of potential policy moves by the new administration.

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Straits Times |Nov 24| Foreign drug companies can quit Indonesia if they do not like new rules requiring them to have local production facilities, according to Health Minister Siti Fadilah Supari. The rules, which have drawn protests from the US Chamber of Commerce, affect 13 international pharma companies, including Lilly, Roche, and AstraZeneca.

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MarketWatch |Nov 24| The National Comprehensive Cancer Network has received funding from BMS and ImClone for a multi-institutional investigation into the use of cetuximab for bladder cancer, the fifth most common type in the US.

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New York Times |Nov 24| A group of advocates, including medical researchers, medical societies and insurers, is lobbying Congress to pay for an Institute for Comparative Effectiveness Research that would assess treatments and identify gaps in evidence. When there are gaps, the institute would initiate what are being called “real world,” or “pragmatic,” clinical research trials to gather the evidence.

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Associated Press  |Nov 26| Dozens of ALS patients are testing treatments on their own without waiting on the slow pace of medical research. They are part of an emerging group of patients willing to share intimate health details on the Web in hopes of making their own medical discoveries.

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Bloomberg |Dec 1| Israel’s largest drug company turned itself into the world’s biggest maker of generic medicines through a high-risk strategy of flouting drug patents. Its next target may be Lilly’s Evista, for osteoporosis.

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CNN Money |Dec 1| The healthcare giant faces a steep patent cliff - but it has the cash to bridge it.

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Bloomberg |Dec 1| Chris Viehbacher is now top man at Sanofi-Aventis, taking over from Gerard le Fur, who was ousted in September after the company faced issues with both Acomplia and Plavix.

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Bio-IT World |Dec 2| Just a few weeks after closing its Seattle facility, Merck announced on Tuesday that Rupert Vessey, the former Seattle site head, will become the head of basic research at Merck Research Laboratories in Boston, replacing Lex Van der Ploeg, who is retiring.

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  • Last Week's Top Stories

|November 19| A Q&A with the president and CEO of BIO, James Greenwood, on some of his hopes for pharma/industry under Obama's administration.

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White Papers & Special Reports

HP white paper image
Extreme Storage Knowledge Center
Sponsored by HP

Visit HP’s Extreme Storage Knowledge Center to find informative, complimentary white papers, case studies, videos, product information and more.  Brief overview of topics:

  • The challenges of unstructured storage and how to manage both cost-effectively and efficiently
  • Company case studies of data storage challenges that translate across pharmaceutical and biotech companies today
  • Systems that manage vast amounts of data with simple deployment, unified management, and extreme scalability at an exceptionally low price per terabyte
  • Life sciences data management; viable solutions for small and large companies to manage growing storage demands
  • Take our virtual product tour and see our storage unit from inside out
Coupa white paper 92
10 Secrets to Recession-Proof Your Business
Sponsored by Coupa


Read this white paper to discover 10 strategies smart companies deploy to recession-proof their business.
Leaders generally face hard choices on how to mange a company during an economic downturn and
behave in one of three ways:
1) “The ostrich” - Preserve the status quo/hope for the best
2) “The bull in the china shop” - Blindly cut expenses across the board
3) “The fox” - Use the downturn to make your business more effective and position it for future growth

Learn how to behave “like a fox” and use a recession as a means to pounce on emerging trends.

SGI BriefingON image
High-Performance Computing in Life Science & Education
Sponsored by SGI and Intel
The varied collection of Bio-IT World articles and insights assembled in this BriefingON examine key trends in HPC infrastructure and how researchers are putting their best computational resources to use. Provided here are stories and lessons around the effective use of high performance computing in life science. Download the BriefingON.


Life Science Webcasts & Podcasts

Medidata Solutions

Rising Clinical Trial Delays and Costs - Addressing the Cause, Not the Symptoms 

medidata podcastProtocol complexity is taking a toll on clinical study speed and efficiency: increasingly complicated and ambitious protocols are not only burdening sites and study volunteers but are also prolonging trials and increasing expenses. In response, sponsors have turned to global study placement, restructured site relationships and new site management practices, but the problem remains.

This podcast will discuss:

  • Why these responses address only the symptoms, not the underlying cause, of rising clinical trial delays and costs.
  • Results of a recent joint Tufts University / Medidata Solutions study.
  • New metrics benchmarking protocol design trends.
  • Systematic protocol design improvements and why they are essential to clinical trial performance excellence.

Speakers: Ken Getz, Senior Research Fellow at the Tufts Center for the Study of Drug Development, and Ed Seguine, General Manager, Trial Planning Solutions at Medidata.

Download Now 



More Podcasts
Related Web Sites

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technologies driving
discovery,
development, and
clinical trials 

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on technology
for healthcare

Barnett Educational Services
Leaders in
quality training
resources


PharmaMatters

The Patent Board |Dec 2| The Patent Board recently published their Pharmaceutical Patent Scorecard, a quarterly snap-shot that ranks pharmaceutical companies’ patent activity over the last 13 weeks. Each company’s portfolio was measured on technical strength, quantity, science and research strength, as well as the speed at which patents became assets. In this most recent scorecard, Wyeth holds its position as top dog, with BMS on its heels, and J&J pushing Pfizer out of third place. Celgene also managed to move into the top 10 for the first time.

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Insight Pharma Reports

FSD_IPR_immun_vacc_cancer_11_2008Immunotherapies and Vaccines for Cancer and Infectious Diseases
Reviews immunotherapies and vaccines currently available and in development for cancer and infectious diseases; the market opportunity; R&D challenges; business considerations. More Information

Industry Trends

U.S. Generic Drug Market Outlook to 2012

By Mark P. Mathieu
Since drugs with $50 billion on 2007 U.S. sales are scheduled to lose patent/exclusivity protection in 2008 – 2010, the three-year period presents formidable obstacles for the pharmaceutical industry. Marketing exclusivity… Read more


Job Openings

Sequencing Instrument Software Team Leader – Oxford Nanopore Technologies, UK
We are seeking a highly motivated and dynamic individual to join our rapidly growing informatics team, to lead the development of the software and computing subsystem of our revolutionary DNA sequencing system.   The candidate will be required to work to aggressive timelines within an agile development process.   Visit www.nanoporetech.com/vacancies



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