JUN 26, 2014 12:00 AM PDT

DIA Patient Fellows Illustrate the Power of the Patient in Drug Development

WRITTEN BY: Jen Ellis
A Parkinson's disease patient is the driving force in the success of clinical trials, recruiting patients and transporting them to research sites while saving researchers thousands of dollars. A patient with a rare ailment that went undiagnosed for 40 years works hand in hand with researchers to develop a treatment. A widow whose husband was not diagnosed until after his death founded an organization that raises funds to pioneer research into his disease.

The Drug Information Association (DIA) 2014 50th Annual Meeting, held June 15 to 19 at the San Diego Convention Center, gave 18 patient fellows the chance of a lifetime to share the obstacles they faced in seeking diagnoses and treatments and to interact with those working in all arenas of drug development. Patient fellows gained a better understanding of the drug development process and the ways they can work with clinical trial researchers, pharmaceutical companies and regulators. They also learned what their peers at other advocacy organizations are doing to advance treatments.

"DIA's work to strengthen collaboration between patient advocates and with global industry professionals, decision-makers and researchers is unparalleled. The annual meeting will bring these patient advocates to the head of the table where open dialogue can be exchanged," said DIA Global Chief Executive Barbara L. Kunz.

Diagnosed with early-onset Parkinson's at age 48 in 2005, Steven DeWitte, from New Preston, Connecticut, began renting a van to transport Parkinson's patients to participate in clinical trials in New York City and Boston. About 80 percent of proposed clinical trials for Parkinson's are delayed or canceled because patients are reluctant to participate. DeWitte promises trial participants a ride, fellowship and lunch, prescreening them to make sure they are appropriate candidates. Columbia University researchers are amazed that such a simple solution is saving them time, as well as the thousands of dollars they typically spend recruiting patients.

"Parkinson's disease makes it difficult for patients to enroll in clinical trials," DeWitte said. "We are nervous about what's going to happen when we get to a trial, we don't want to go alone and we wake up every day with challenges. Participating in a trial with a group of your peers makes the experience less threatening. I tell them, ‘Come with me to this trial. You'll help me through it, and I'll help you through it. We are in this together."

He added, "I'm a big believer that common thoughts build ideas. The DIA Annual Meeting will connect me with those who share my issues as a patient and those who are in a position to help us."

Playing "stump the docs" with medical students during his visits to the National Institutes of Health (NIH) and the University of Maryland may make light of John Coakley Sr.'s search for what caused his muscles to weaken, but he uses his experience - and a sense of humor - to support patients and drive research. After more than 50 years of symptoms, Coakley, 71, was diagnosed with Kennedy's disease. The Taneytown, Maryland, resident became president of the Kennedy's Disease Association and provided the sole patient perspective to secure a clinical trial at NIH for a new drug developed by Novartis. The trial may result in the first treatment for the inherited neuromuscular disorder, and he muses about his experiences with a rare disease on his blog, "Coakley's Corner."

"DIA is giving us the ability to ‘put a face on' the rarity, and has made listening to patients' voices a core priority," Coakley said. "These new connections are beyond priceless."

As her husband's years-long undiagnosed condition grew more serious, Kathy Brewer of DeRidder, Louisiana, asked doctors around the U.S. for an explanation. Most had never heard of the ultra-rare disease that would take his life. His autopsy finally provided a name: Erdheim-Chester disease (ECD). Now, as founder and president of the ECD Global Alliance, Brewer leads the organization in securing hundreds of thousands of dollars in grants for the study of ECD.

"I know what it is like to helplessly watch someone you love die without a diagnosis, and I'm committed to making a difference in the lives of those who are suffering," Brewer said. "By attending the DIA Annual Meeting, I was able to better explain to ECD patients why clinical trials are important, more effectively influence research collaborations and enhance my ability to communicate and advocate for those affected by rare disease."
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