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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



Microsoft in Life Science Arena



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By Deb Borfitz

October 5, 2009 | A few short months after naming Merck & Co. as a customer and development partner, Microsoft has attracted a sizable following to its life sciences platform intent on helping scientists design better drugs, sponsors better interpret clinical trial results, and physicians better match treatments to patients.

Jim_Karkanias
Jim Karkanias
Aiding the successful launch of Amalga Life Sciences are a dozen other early adopters, including major pharmaceutical and biotechnology companies as well as two of the nation’s top cancer research centers (Fred Hutchinson and Moffitt), reports Jim Karkanias, senior director of applied research and technology for Microsoft Health Solutions Group. The first-of-its-kind product acts like a global positioning system, helping scientists and their staff navigate through all forms of data at the conceptual level—be it what a dollar means or what a molecule is doing—using a comfortable and familiar Microsoft Office interface.

Amalga Life Sciences is an extension of the Microsoft Amalga family of health enterprise products introduced in February 2008. The idea is to “add value” to existing clinical and operational information systems, including electronic data capture, electronic medical records, and patient recruitment databases, Karkanias says. “A wealth of data exists in databases and IT systems. But without a way to…access [and] make sense of the information, it adds little to no value to an organization. Amalga Life Sciences is designed to easily show contexts and relationships, so that data becomes knowledge that can actually be used.”

With minimal training, even relatively computer illiterate users can discover relationships between different pieces of data that would otherwise not be readily apparent, says Karkanias. The technology also gives organizations the wherewithal to manage and redesign processes to increase productivity, improve decision-making, and reduce errors.

Components of Rosetta Biosoftware, acquired from Merck in June, will be incorporated into the service-oriented, standards-based software over the next two years, adds Karkanias. This will give Amalga Life Sciences the ability to interface with the machinery of genomic science and further understanding of how various drugs impact DNA and proteins in the body and, ultimately, direct researchers to “biomarker needles in the haystack.” Thereafter, the software could be used to create what-if scenarios using the identified biomarkers in different population groups.

H. Lee Moffitt Cancer Center & Research Institute is using Microsoft’s Amalga Unified Intelligence System as part of its Total Cancer Care Survivorship Initiative, which follows patients post-treatment to reduce recurrence of cancer and quickly respond if it does. Test recommendations will become more personalized as researchers identify new best treatment practices gleaned from queries of an Oracle-based data warehouse, says Karkanias. The initiative, in conjunction with a growing cancer registry, is also projected to significantly shorten the process of identifying and recruiting patients for clinical trials based on their molecular traits.

In addition, the collaboration between the Fred Hutchinson Cancer Research Center and Microsoft “will drive the progress and development of an innovative software platform for life science researchers, addressing the challenges faced today in collecting, analyzing, interpreting, and sharing complex data from a wide range of diseases and experiments,” says Karkanias. The collaboration will bring together the world-class domain expertise of the cancer center’s scientists and the power of Microsoft technologies to “integrate, visualize, and generate novel hypotheses from cancer research data.”

Direct-to-Consumer Appeal
Connectivity with HealthVault, Microsoft’s two-year-old personal health application platform for consumers to store and maintain health and fitness information online, gives Amalga Life Sciences several potentially game-changing capabilities, says Karkanias. For starters, it could further the cause of personalized medicine by providing physicians with easy access to their patient’s molecular makeup. Through a patient’s HealthVault account, for example, a physician might discover the patient has the BRCA1 gene, combined with a family history of breast cancer. “This information alone, which is normally very difficult for a physician to identify, can change the course of treatment to one that’s more effective for the patient.”

Microsoft is partnering with Scripps Research, Affymetrix, and direct-to-consumer genetic testing company Navigenics in a research study that will assess the behavioral impact of personal genetic testing on consumers, says Karkanias. Those who opt into the study can learn about their genetic predisposition to more than 20 medical conditions that may be changed by lifestyle choices, and import the data into their personal HealthVault account.

A trial-sponsoring company need only write an application specific to HealthVault to initiate a patient recruitment campaign targeting those that meet a study’s inclusion and exclusion criteria—and promote compliance with the protocol once they’re enrolled, says Karkanias. Through TrialX (from Applied Informatics), HealthVault users can already opt to be matched to relevant clinical trials based on their personal health information. But the potency of HealthVault as a recruitment resource will be highly dependent not only on the platform’s popularity, but on consumer reception to its varied connectivity options.

Microsoft declined to say how many consumers have thus far established HealthVault accounts. But Karkanias notes the company has “designed HealthVault with privacy in mind, putting consumers in control of their health information. Consumers and health care providers will only share data if they trust their privacy will be protected.” Clinical trial sponsors, for now, seem to be taking a wait-and-see attitude.

Microsoft sees the potential for HealthVault to effectively reduce the cost of conducting clinical trials, making “new and different trials possible,” says Karkanias. “Companies can have trials with small measurements across large groups of patients since they’ll have a large population from which to draw. That’s a complete paradigm shift.”

Next-generation clinical research techniques, such as adaptive clinical trials, could also get a much-needed boost. “If researchers have lots of knowledge about what’s going on in a trial at the molecular level of detail for each patient, they can more accurately adjust the trial to reduce risk and cost in a statistically valid way as it goes along,” says Karkanias.

Microsoft is currently talking with all the top pharmaceutical companies about “deep partnering” opportunities with HealthVault, says Karkanias, and the feedback to date has been “extremely positive.” It remains to be seen how far Amalga Life Sciences will reach its hand into the actual administration of clinical trials. Microsoft will most likely opt to complement rather than compete against clinical trial management systems, he says.

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White Papers & Special Reports

oracle20723
The Role of Analytics in Transforming Healthcare
Sponsored by Oracle

Sharing many of the data challenges and opportunities faced by Healthcare, the Life Sciences industry remains focused on delivering new, innovative therapies and solutions to patients in a cost effective, timely and safe way. With spiraling R&D costs, new methods such as adaptive trials, and never ending need for deep pharmacovigilance, the Life Sciences companies that effectively use analytics to explore, monitor and optimize their business will rapidly become the new leaders.

Oracle’s strategy—built upon Enterprise Health Analytics and Health Data Warehouse Foundation—provides a powerful, practical, and extensible approach to delivering the IT analytics infrastructure required to confront the worldwide healthcare challenge.



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BPM-Based Case Management Approach to Optimizing Clinical Trial Efficiency
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Business Process Management (BPM) software offers liberation in the planning and management of clinical trials today. SmartBPM provides the components for automating critical clinical trial processes ranging from protocol development and patient enrollment to site management and investigator payments. Advantages are:

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Discovered is opportunity to enhance relationships with investigators, subjects, and regulators while bringing momentum to a technology-impaired study startup phase. Learn more about SmartBPM in this complimentary white paper.



Cmed paper
Next-gen Cloud-based eClinical
Sponsored by Cmed Technology

New technologies are available to leverage Cloud Computing in  managing clinical trial data. This paper discusses a next generation eClinical
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It is offered with either software-as-a-service (SaaS), or turnkey infrastructure options in which the user organization operates their own cloud using their IT teams, within their data centers. Read this paper to learn and decide how best to leverage cloud computing’s many strengths for your organization’s  particular needs.



Life Science Webcasts & Podcasts

Medidata Solutions

Evaluating a Risk-based Approach to Good Clinical Practice 

medidata5_podcastThe verification of source documents by study monitors at investigational sites is considered a good clinical practice by regulatory authorities overseeing clinical research, and is extremely important to ensuring data quality in clinical trials. Today’s challenging environment is prompting study teams to explore the use of risk-based approaches to monitoring that do not compromise data quality, but allow limited resources to be directed more effectively to where they’re most needed and to the most critical review activities.

In this podcast, industry experts and executives from Medidata will address questions such as:

  • Why are regulatory agencies and industry open to evaluating the new approaches in site monitoring and source document verification (SDV), and what attitudes and reactions towards less than 100% SDV?
  • What factors do research sponsors need to consider in adopting risk-based site monitoring?


Download Now 



More Podcasts

Job Openings

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Software Engineer – Computational Biology Center

Memorial Sloan-Kettering Cancer Center seeks an Engineer to design and develop complex data analysis systems in support of cancer genomics research projects at the Computational Biology Center. Qualified candidate will have a BA, 5+ years of software development experience and expert knowledge of Java, SQL, and HTML.

Apply: www.mskcciscareers.org.  Equal opportunity and affirmative action employer.

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