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Trojan, thriving despite rare muscle disease, inspires scientists’ research

Once a shy kid held back by physical disability, Hawken Miller has flourished since becoming an active student at USC

Hawken Miller
Journalism student Hawken Miller didn’t let having muscular dystrophy prevent him from having the full USC experience. (Photo/Peijean Tsai)

Growing up with a rare muscle disease, Hawken Miller often felt isolated. He couldn’t run around at recess, play sports or join friends on backpacking trips.

But when Miller arrived at USC over two years ago, his physical limitations didn’t prevent him from being an active student on campus. He became a reporter at the Daily Trojan. He joined the USC Photography Club and Christian Challenge, a campus ministry. Last summer, he did an internship at The Sacramento Bee newspaper. Once a shy kid held back due to physical disability, he has flourished at USC.

“It’s different now than it was before. It’s been a transformation,” said Miller, noting how physical activity is emphasized less in college. “I was really shy, but now I’m not as afraid to approach and talk to people.”

Duchenne muscular dystrophy: What we know

Miller lives with Duchenne muscular dystrophy, a progressive and fatal disease for which there is no cure. It is caused by a mutation on the X chromosome and strikes 1 of 5,000 male births, affecting 300,000 boys worldwide. It causes muscles to degenerate, and the leading cause of death is heart failure. Those with the disease typically don’t live past the age of 25. Although there are medications to help with the symptoms, there is currently no cure.

Hawken Miller in Sacramento

Hawken Miller visits the Capitol in Sacramento. (Photo/Courtesy of Hawken Miller)

Researchers at the USC School of Pharmacy have developed a new treatment for the rare muscle disease. The compound, known as RASRx1902, is an oral therapy that has shown positive effects on muscle function in animal models of Duchenne.

In these models, the compound has improved muscle strength and regeneration while decreasing muscle inflammation, degeneration and necrosis. Last year, the therapy was granted an Orphan Drug Designation by the U.S. Food and Drug Administration to treat Duchenne muscular dystrophy. The researchers formed a startup, RASRx, to continue to work on advancing this treatment invented at USC. Partnering with the foundation CureDuchenne, an organization founded by Miller’s parents, the team is now transitioning to toxicology studies to advance the new oral therapy toward human clinical trials.

By choosing to work on Duchenne, the research team has the opportunity to make a great impact by delivering a potentially life-changing therapeutic, said USC School of Pharmacy Associate Professor Stan Louie, one of the USC researchers working closely the RASRx team. Putting a face to Duchenne also motivates him to help move this therapy forward, he added.

“The inspiration is Hawken. He is part of the Trojan Family, and we look after our own,” Louie said. “The founders of RASRx all believe we are doing this for the patients, and when one of the patients is a member of the Trojan Family, then it becomes more urgent for us.”

Parents take action

When Miller was diagnosed at age 6, his doctor told his parents Debra and Paul Miller there was little to do. Instead, in 2003, the Millers started CureDuchenne, a nonprofit foundation dedicated to saving the lives of those with Duchenne, including funding new medical research.

When we were told nothing could be done, it sparked something in my husband and me.

Debra Miller

“When we were told nothing could be done, it sparked something in my husband and me,” said Debra Miller, co-founder and CEO of CureDuchenne. “We felt there had to be something we could do. We just had to give it everything we had.”

In November 2015, RASRx, the startup company initially formed by USC and University of Arizona researchers, announced a partnership with CureDuchenne to streamline the development of their new compound to treat patients with Duchenne. Funding by CureDuchenne Ventures and a collaborative U.S. Department of Defense research grant with USC accelerated the potential drug’s preclinical development.

By coincidence, Debra Miller learned about the research at the USC School of Pharmacy after her son had already been admitted to USC.

“Knowing he was going to USC and that we would be funding a project [at USC] that would be helping him and the other boys with Duchenne was really special,” she said.

Independence from Duchenne muscular dystrophy

Like many USC students, college was the first time Hawken Miller lived away from home, and life with Duchenne brings extra challenges. He takes up to 30 medications a day, including steroids to reduce inflammation. He arranges regular visits from physical therapists to stretch and care for his muscles.

Hawken Miller and mom Debra

Hawken Miller with his mother, Debra Miller (Photo/Courtesy of Hawken Miller)

He has adapted well to living independently, he said, but being on his own makes him realize how hard his parents had worked before college to make sure he had enough support.

“The goal is to be completely independent from my parents, but I also want to spend as much time as possible with them,” said the third-year journalism student at the USC Annenberg School for Communication and Journalism.

One of the reasons he chose USC was because campus was close to home. His interest in journalism came from a desire to learn something new every day and overcome shyness. Last summer his internship gave him experience reporting from the California state capital, and this spring he is interning for KTLA.

Although physical limitations impact daily tasks, Miller said he is blessed. Many with Duchenne have severe cognitive impairment. He often gets tired and uses a motored wheelchair, but mentally he hasn’t had to hold back.

“The main thing I’ve gotten from Duchenne is: I focus on what I can do and don’t think about the stuff I can’t do,” he said. “That’s how you should handle any obstacle you might face. Focus on what you can do and not what you can’t do.”

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Trojan, thriving despite rare muscle disease, inspires scientists’ research

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