Industry Trends

Clinical Research
Off-shoring: A Country Attractiveness Index for Clinical Trials

By Mark P. Mathieu
For many years, pharmaceutical companies have been off-shoring manufacturing operations to lower-cost countries. Healthy margins and strong risk aversion have afforded pharmaceutical companies the luxury of staying close to home, for all but manufacturing activities. As financial pressures increase, pharmaceutical executives are finding that going offshore is not only less risky than it once was, but also too attractive to ignore.  Read More




Sponsors Developing ‘Companion Diagnostics’ for Personalized Medicines



By Deb Borfitz

March 15, 2010 | Pharmaceutical companies are beginning to embrace meaningful development of “companion diagnostics” in response to both the realities of applied genomics and the market disruption posed by personalized medicine. Companion diagnostics are tests done to determine if patients’ genetics indicate they’ll respond to a particular treatment or dosing level before the drug script is fulfilled.

So says Patrick Terry, CEO of strategic business consultancy Technic Solutions. For the pharmaceutical industry, personalized medicine represents both risk and opportunity. If a diagnostics company comes up with a test to identify probable non-responders to a blockbuster compound, sales of the drug could take an enormous hit. Developing those diagnostics internally or in partnership with test developers, on the other hand, could help offset the inevitable losses.

Perhaps no one knows better than Terry how to succeed in the business of personalized medicine diagnostics. He’s co-founder of the wildly successful and now publicly traded Genomic Health, which was the first to molecularly dissect archival tissue of patients in cancer trials seeking reasons for differential response to treatment and improved outcomes. Formerly in the facilities building side of the life sciences, Terry catapulted into the genetics arena about 15 years ago when his two children were newly diagnosed with an advanced aging disease known as PXE. Working in a Harvard lab by night, he discovered and then patented the causative gene.

This eureka became his segue into “precision medicine” that re-classifies disease on the molecular level. In 2000, after creating a genetic test for PXE, Terry teamed up with biotech entrepreneur Randy Scott to form Genomic Health. In the space of four years, the company developed the test for genetically stratifying breast cancer that is now standard-of-care. More recently, Genomic Health released a diagnostic for colon cancer.

Designing robust clinical trials for disease representing potentially dozens of molecular subtypes is no small task, says Terry. From a purely sales perspective, industry sponsors are also in a quandary about how personalized they really want their medicines to be. “But there’s no avoiding science…and a lot of capital is flowing into this type of research.” Cancer, rheumatoid arthritis, and a host of other diseases are now widely recognized as heterogeneous conditions of the genome.
 
Narrow targets can in fact make a lot of financial sense for conditions like neovascularization (blood vessel development), which has a key chemical signal (VGEF) for which dozens of therapeutics are in development. “If you’re the fifth or even the third one out of the gate with a VGEF compound, you’re probably not going to displace the first movers or be commercially successful,” Terry says. Thus the more practical option may be to look for new markers that could be used as a companion diagnostic. Genentech is already working on diagnostic tests specific to its drug development program, Terry notes, trying to stay ahead of external diagnostic and biotechnology companies working to molecularly stratify Avastin and Lucentis.

On-label use of drugs like Avastin could well expand to new molecular signatures of disease rather than affected organ. The National Institutes of Health will spend “billions of dollars” over the next few years to molecularly characterize each of the 20 or so major cancers, Terry says. In clinical trials, high priority will be put on any genes implicated in multiple cancers.

For sponsors, the question of the moment is not if but how and when to embrace personalized medicine, says Terry. “I will be one of those who push the envelope on this…in collaboration with pharma or in competition with them.” Technic Solutions has expertise in the “disruptive paradigms” that Terry predicts will collapse clinical trial timelines for personalized, stratified medicine to under five years and “put adaptive clinical trial design concepts on its head.”

Quintiles and Parexel are among the “early movers” in this arena, says Terry, and diagnostics companies will be increasingly turning to them for help. Eli Lilly, GlaxoSmithKline, and Novartis have also “completely embraced” personalized medicine. “The large multi-nationals all have risk venture divisions and they’re all investing in diagnostics companies or developing companion diagnostics through partnerships.”

Click here to log in.

0 Comments

Add Comment

Text Only 2000 character limit

Page 1 of 1

White Papers & Special Reports

Life Science Webcasts & Podcasts

medidata podcast #8 Meeting Today’s Challenges in Clinical Trial Supply Management
Sponsored by: Medidata Solutions Worldwide  

Setting up and managing the clinical trial involves many complex procedures. Among the most challenging are planning and executing the logistics of the trial’s clinical supplies. This podcast focuses in depth on the following topics which trace current practices and future evolution of this crucial aspect of clinical trials:

  • Current practices in clinical trial logistics
  • Comparing advances in clinical supply practices to  other aspects of clinical trials 
  • Where current practices fall short of meeting the challenges
  • Trends and evolving improvements that may change the way logistics are conducted

Listen Now  


More Podcasts

Job Openings

tessella logo 
Scientific Software Engineer
Boston MA
$70,000 to $95,000
 

Tessella delivers software engineering and consulting services to leading pharmaceutical and biotech companies. We are recruiting Software Engineersto work with skilled bioinformaticians and scientists to identify business needs and recommend and develop technical solutions. Applicants require BS, MS or PhD in bioinformatics, biology or chemistry and 2+ years of software development in either: Java, C#, C++, C or VB.NET. 

Apply at http://jobs.tessella.com   

 

oxford nanopore logo 


 Early Access Collaborations Managers
Oxford Nanopore Technologies is developing a novel technology, GridIONTM for the direct, electronic analysis of DNA/RNA and other analytes.  As the system approaches the market, we are building a team of technically knowledgeable, highly motivated candidates with excellent customer service and facilitation skills to join our company as Collaboration Managers.  This is a unique opportunity to work with world-leading genomics customers throughout the early adoption phase of a new generation of DNA sequencing technology.. This is a facilitative, enabling role with responsibility for managing technology development collaborations with key customers at leading genomics institutions.  It will include long term management of the collaboration plan and milestones and associated meetings and documentation. Click here to find out more and apply   

Oxford Nanopore's GridION technology, VP, Sales and Marketing Oxford Nanopore Technologies is a fast-moving technology company that is developing a novel electronic molecular analysis technology. The technology is adaptable for the analysis of DNA/RNA, proteins, chemicals and other molecules.  It is therefore suitable for use in a variety of markets including scientific research and clinical applications.  As the technology approaches the market, Oxford Nanopore is seeking a visionary VP of sales and marketing to join the senior team.  The candidate will embrace the opportunities afforded by entering the market with a truly disruptive technology that has the potential to expand the number of users and the variety of applications in each target market.  This is a rare opportunity to influence the commercial strategy at an early phase of its commercial lifetime, in a well funded company.  Oxford Nanopore welcomes applications from candidates with a track record of high-level strategic commercial  leadership, who wish to apply a fresh approach to existing markets.  Experience in Life Sciences/DNA sequencing is central to this role, however we will consider your application if you have experience of disruptive technologies in other related industries.  We are particularly interested in candidates with strong expertise in the use of digital technologies for sales and marketing of scientific/technical products.  Click to  Apply  


 





Sponsored Links

For reprints and/or copyright permission, please contact  Tim McLucas, (781) 972-1342, tmclucas@healthtech.com .