Covance Launches Xcellerate to Increase Clinical Trial Optimization
Proprietary Methodology Designed and Tested to Speed Patient Enrollment, Cut Costs
PRINCETON, NJ, June 14, 2011 – Increasing the speed of bringing important medicines from the research phase to patients who need them is a driving objective for today’s global biopharmaceutical companies. Covance Inc. (NYSE: CVD), one of the world’s largest and most comprehensive drug development companies, is launching Xcellerate™, a unique, proprietary methodology designed to help optimize clinical trial performance in order to assist biopharmaceutical companies in improving quality, reducing waste, and decreasing trial timelines – ultimately increasing their return on clinical trial investment.
Specifically, the Xcellerate methodology enables Covance to make custom recommendations on site, investigator and geographic selections for every program it manages, and to help enhance clinical trial design and execution. Xcellerate is not a stand-alone service offering, but is embedded in Covance’s approach to clinical trial management.
“Biopharmaceutical companies have come under increasing pressure in recent years to reduce their R&D spending and re-invigorate their drug development pipelines,” said Rick Cimino, Group President, Clinical Development Services, Covance. “We believe that Covance, through Xcellerate, can deliver high value to our clients by improving time-to-market speeds that ultimately should help them bring new medicines to patients faster.”
Xcellerate Clinical Trial Optimization™
“Similar to the research and development process we manage for our clients, we have developed, tested and refined the Xcellerate methodology over the years and are launching and branding it now as Xcellerate,” said Brett Bishop, Vice President, Clinical Trial Design and Strategy, Covance. “As a result, our clients can receive higher quality and more cost-effective results, even in the most competitive and challenging enrollment situations. We intend to continue to add new functionalities to the Xcellerate methodology that further enhance the clinical trial management service we provide our clients.”
Xcellerate Success in Practice
Additionally, a long Phase III respiratory clinical study with a number of pharmaceutical companies vying for the same patients presented a unique set of challenges to Covance’s client: recruiting patients and retaining investigator and patient interest in the study. Through Xcellerate, Covance was able to help the client finish patient enrollment ahead of target and minimize disruption to investigator sites and their regular activities. This gave the trial a competitive edge in investigator uptake and site enrollment. As a single provider, Covance created synergy across multiple data streams from multiple vendors, helping keep this complex trial on track.
For more information about Xcellerate, please visit www.covance.com/Xcellerate
Statements contained in this press release, which are not historical facts, such as statements about prospective earnings, savings, revenue, operations, revenue and earnings growth and other financial results are forward-looking statements pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. All such forward-looking statements including the statements contained herein regarding anticipated trends in the Company's business are based largely on management's expectations and are subject to and qualified by risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.
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