Times Colonist

Trial gives ALS patients hope

Canada-wide study uses anti-psychotic drug to try to slow down the disease

- BILL GRAVELAND

Cliff Barr has no illusions about how his life is going to end, but he still has hope. The 70-year-old from Okotoks, Alta., is one of 100 patients taking part in new Canada-wide clinical trial to treat ALS — a debilitati­ng and ultimately deadly neural disease that has few treatments and no cure.

“It is a difficult and an awkward disease,” Barr said Thursday at the University of Calgary, which is running the trial.

“I found the idea of the clinical trial promising. It gives you a little more hope.”

Barr was diagnosed with amyotrophi­c lateral sclerosis, also known as Lou Gehrig’s disease, in October. It causes paralysis because the brain is no longer able to communicat­e with the body’s muscles.

Over time, as the muscles break down, an ALS patient loses the ability to walk, talk, eat, swallow and, eventually, breathe. Experts say one in 400 Canadians will die of ALS.

Even on good days, Barr said, the disease is always there.

“The disease kind of reared its head and I’m a little weaker than normal,” said Barr, who retired 10 years ago. “This morning, I couldn’t do my pants up. I couldn’t brush my hair. I needed help doing the zipper up on this sweater.”

Dr. Lawrence Korngut from the University of Calgary’s Cumming School of Medicine is running the clinical trial over the next 1 12 ⁄ years at nine different Canadian universiti­es.

He said an anti-psychotic drug called pimozide slowed down the disease in zebra fish, worms and mice, as well as in humans with ALS in a limited six-week trial a couple of years ago.

Korngut said the drug doesn’t address the primary cause of the disease, which destroys nerves. But he adds that it’s now believed that there’s an electrical failure that accompanie­s the breakdown.

“This treats that electrical failure. We’re hoping by preserving that electrical function, even if the cable keeps breaking down, that will buy people time. “It will prolong life.” Korngut said people shouldn’t jump to any conclusion­s about how well the trial will turn out and he’s only “cautiously optimistic.”

“We’ve been through this before. We know that sometimes animals behave very differentl­y from humans and we just have to do things properly and find out these answers.”

Barr said he has been told he likely has between three and five years to live. The research is a double-blind study, so only half the participan­ts will receive the drug. The rest get a placebo.

“I am a fighter. You pay your money. You take your chances,” Barr said. “It can’t make it better. It can’t repair the muscle damage … but it can slow down the progressio­n, which would, in effect, help me maintain the quality of life for longer than I would have.”

Korngut said it could be years before all the results are known and he is grateful for those willing to volunteer. “ALS is a disease of weakness, but these are the strongest people I know. These people fight this disease so courageous­ly.”

 ?? PHOTOS BY JEFF MCINTOSH, CP ?? ALS patient Cliff Barr is taking part in a new Canada-wide clinical trial to treat the disease. “It can’t repair the muscle damage … but it can slow down the progressio­n, which would help me maintain the quality of life for longer than I would have.”
PHOTOS BY JEFF MCINTOSH, CP ALS patient Cliff Barr is taking part in a new Canada-wide clinical trial to treat the disease. “It can’t repair the muscle damage … but it can slow down the progressio­n, which would help me maintain the quality of life for longer than I would have.”
 ??  ?? Dr. Lawrence Korngut is leading the clinical trial: “ALS is a disease of weakness but these are the strongest people I know.”
Dr. Lawrence Korngut is leading the clinical trial: “ALS is a disease of weakness but these are the strongest people I know.”

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