CHICAGO, IL--(Marketwired - January 24, 2017) - The Muscular Dystrophy Association announces the award of a clinical research network grant totaling $918,000 over three years to spur advances in myotonic dystrophy (DM) research. This large, multi-center grant, which provides continued funding for the Myotonic Dystrophy Clinical Research Network, reflects MDA's commitment to refocus resources in order to double research spending on drug development and clinical trials for the diseases in its program by the year 2020.
Established in 2013, and supported by funding from MDA and other patient advocacy groups, the National Institutes of Health (NIH) and pharmaceutical company Biogen, the Network's goals are to gain a more detailed understanding of the DM disease process and to collect data needed for clinical trials in order to inform what outcome measures, biomarkers and endpoints will be most appropriate.
"MDA is pleased to continue to enable this critical infrastructure for myotonic dystrophy research," said MDA Scientific Program Officer Lianna Orlando, Ph.D. "Current and upcoming clinical trials in DM would not have been possible without MDA's role in establishing the Network and supporting the creation of the tools necessary to carry out successful and informative studies."
The Network currently is comprised of six medical centers with significant expertise in DM research and clinical care. Centers include:
- California: Stanford University School of Medicine, Stanford
- Florida: University of Florida College of Medicine, Gainesville
- Kansas: University of Kansas Medical Center, Kansas City
- New York: University of Rochester Medical Center, Rochester
- Ohio: Ohio State University Medical Center, Columbus
- Washington, D.C.: National Institutes of Health
MDA funds helped establish the Network's original five university sites, and the new grant award continues to fund these programs. MDA funds do not support the NIH center. Additional sites may be added in 2017.
The Network is led by Charles Thornton, professor of neurology at the University of Rochester, who serves as its overall director.
"Now, for the first time, scientists and drug developers are coming up with good ideas about how to attack myotonic dystrophy at its root cause," Thornton said. "The hope is that one of these new treatments will have a powerful effect, or that several can be used together."
The Network was started, Thornton noted, to pave the way for testing new treatments in people.
"Experience has taught us that finding out whether a new drug is working or not is not a slam dunk. If we want to have clear answers, then we must work out many details and methods in advance," Thornton continued. "And, we have to work closely with patients and families every step of the way. If it's not a team effort, we probably won't succeed.
"We are extremely grateful for support from MDA in getting the Network launched and keeping it going. When we started we hoped that we could encourage more companies and scientists to work on developing treatment for myotonic dystrophy, because they would see that all the tools are in place to conduct good clinical trials. Our work is still at an early stage but already we can see that this is happening."
All of the researchers in the network have free and unrestricted access to data generated at all of the sites. In addition, and to further support advances in DM research, the Network is committed to making access to study results broadly available to both academic and industry researchers in the United States and around the world.
Among the Network's accomplishments:
- Network researchers have already been responsible for much critical clinical research in DM in the U.S., and through combined efforts they have standardized equipment and procedures (for measuring myotonic and muscle strength, and for obtaining blood and biopsy samples) across all sites.
- The Network investigators published a DM biomarker study in December 2013 that looked at RNA splicing in muscle biopsy tissue and identified a group of gene splicing events that are affected even before there is evidence of muscle weakness. This collection of early changes in DM1 represent a tremendous opportunity for early/pre-symptomatic therapy intervention, and is being used as a potential biomarker to determine whether a treatment was effective at targeting the root cause of the disease process.
- The five original Network centers are currently completing a multicenter observational study of type 1 DM in 100 individuals with the disease, while a companion study, conducted by the NIH site, is following 25 additional participants. The goals of both trials are to prospectively assess walking speed, muscle strength, muscle size, myotonia, heart rhythm, mental efficiency (attention, memory and cognitive tests), and overall health over a one-year period to determine how the condition changes over time.
MDA has funded more than $46 million in myotonic dystrophy research since 1950, and including this most recent award, is currently is funding nine active DM grants with a total funding commitment of more than $3 million.
The new grant was approved by MDA's Board of Directors after careful deliberations and analysis by MDA advisors and research staff. This year, MDA is funding 150 different research projects in 11 countries.
About the Muscular Dystrophy Association
MDA is leading the fight to free individuals -- and the families who love them -- from the harm of muscular dystrophy, ALS and related muscle-debilitating diseases that take away physical strength, independence and life. We use our collective strength to help kids and adults live longer and grow stronger by finding research breakthroughs across diseases; caring for individuals from day one; and empowering families with services and support in hometowns across America. Learn how you can fund cures, find care and champion the cause at mda.org.
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