PPD Acquires RCT Logic’s Exclusive License to Patented Clinical Trial Design Technology
Expands PPD’s clinical development capabilities, particularly in neuroscience
WILMINGTON, N.C.--(BUSINESS WIRE)--Pharmaceutical Product Development, LLC (PPD) announced today that it has acquired RCT Logic’s exclusive license from Massachusetts General Hospital (MGH) for the portfolio of patents related to its sequential parallel comparison design (SPCD). SPCD is an alternative method for conducting well-controlled clinical trials that substantially decreases the impact on trial outcomes of any placebo effect and will enable PPD’s clients to significantly reduce the time and cost of conducting their clinical trials. This methodology, which PPD is branding as Trimentum™, has been particularly effective in studying major depressive disorder (MDD), but is applicable to clinical trials in many disease areas where outcomes can be impacted by placebo effects.
“Having one of the world’s leading contract research organizations continue to build on the success of SPCD is a great achievement for RCT Logic”
“Through Trimentum, PPD can offer our clients a clinical trial method that derives more information from fewer patients. As a result, our clients will be able to conduct smaller, more efficient trials in all stages of drug development, enabling more informed investment decisions and accelerating the delivery of much-needed new medicines,” said Daniel Burch, M.D., PPD vice president of global product development and therapeutic area head for neuroscience. “The pharmaceutical industry and regulatory agencies have long recognized the need for a more robust and efficient option for conducting clinical trials. We anticipate these and other stakeholders will be receptive to the design and apply it to appropriate clinical settings.”
A total of 22 SPCD trials are completed, ongoing or planned. These include Phase II and Phase III trials by corporate sponsors that are licensees of RCT Logic, as well as trials with the National Institutes of Health (NIH) and charitable funding.
The SPCD method, which was invented by Maurizio Fava, M.D., director of clinical research and executive vice chair of psychiatry at MGH, and David Schoenfeld, Ph.D., of the MGH Biostatistics Center, dramatically lessens the impact of the placebo effect in clinical trials by incorporating two sequential placebo-controlled stages into the process, the second of which includes a re-randomization of placebo non-responders from the first. Trials in psychiatric indications are particularly vulnerable to placebo effects due to the subjective nature of the assessments because some of the responses may relate to actual improvement in the patient’s condition while others may relate to expectancy, trial design or implementation flaws. Due to its basic structure, SPCD reduces the number of patients required for a given trial by 20 to 40 percent. This not only decreases the cost and time it takes to conduct a trial, but also eliminates some of the factors that make results more difficult to interpret.
“Having one of the world’s leading contract research organizations continue to build on the success of SPCD is a great achievement for RCT Logic,” said Matthias Bowman, who founded the company in 2008. “We are excited that PPD will be able to help its clients accelerate the pace and reduce the cost of developing new medical therapies through the use of MGH’s patented SPCD technology. We are particularly enthusiastic about the implications for patients who are waiting for important new treatments.”
As a result of this acquisition, PPD owns an exclusive license from MGH and can offer its clients this unique approach for conducting depression, pain and other psychiatry trials. PPD intends to continue RCT Logic’s practice of offering licenses to any qualified trial sponsor.
PPD also is associated with the MGH Clinical Trials Network & Institute (CTNI). The affiliation with CTNI will enrich PPD’s already broad neuroscience expertise and capabilities by providing PPD’s clients with access to researchers in clinical indications that include depression and schizophrenia in approximately 250 global clinical research sites, as well as patient quality services.
“The leadership of CTNI has more than 25 years of experience in industry-sponsored multicenter clinical trials,” said Fava. “CTNI already has successfully conducted or is currently overseeing the implementation of the SPCD methodology in more than 10 trials with corporate, NIH and charitable funding. By building on that experience and collaborating with PPD, we hope to further enhance our ability to help our clients meet their clinical research goals more efficiently and more effectively.”
An industry leader in neuroscience drug development, PPD has conducted more than 270 studies during the past five years in a wide range of neurology, psychiatry and pain management indications across all phases of development. CTNI has managed numerous trials in the United States, Europe, Chile, Japan and South Africa. In addition to CTNI staff in the United States, the organization has clinical trials service agreements with institutions and clinicians throughout the world.
PPD is a leading global contract research organization providing drug discovery, development, lifecycle management and laboratory services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 13,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments. For more information, visit www.ppdi.com.
Except for historical information, all of the statements, expectations and assumptions, including statements, expectations and assumptions about the acquisition of the exclusive MGH license and its contribution to PPD, contained in this news release are forward-looking statements that involve a number of risks and uncertainties. Although PPD attempts to be accurate in making these forward-looking statements, it is possible that future circumstances might differ from the assumptions on which such statements are based and could cause actual results to differ materially from the forward-looking statements. Other important factors that could cause future results to differ materially include the following: rapid technological advances that make our services less competitive; risks associated with acquisitions and investments; risks associated with and dependence on strategic relationships; PPD’s ability to win new business; the ability to attract, integrate and retain key personnel; competition in the outsourcing industry; loss, delay or modification of large contracts; higher-than-expected cancellation rates; the rate of conversion of backlog into revenue; actual operating performance; economic conditions, research and development spending, and outsourcing trends in the pharmaceutical, biotechnology and government-sponsored research sectors; overall global economic conditions; compliance with drug development regulations; changes in the regulation of the drug development process; consolidation in the pharmaceutical and biotechnology industries; and the ability to control SG&A spending. PPD assumes no obligation and expressly disclaims any duty to update these forward-looking statements in the future, except as required by applicable law. These forward-looking statements should not be relied upon as representing PPD’s estimates or views as of any date subsequent to the date hereof.