Arkansas Democrat-Gazette

Colorado reviewers OK drug’s expense

- MEG WINGERTER

Colorado’s new prescripti­on drug review board decided in a first-in-the-nation vote that a medication costing more than $200,000 a year doesn’t qualify as “unaffordab­le,” based on the drug’s benefits to patients and the availabili­ty of coupons to cover out-ofpocket costs.

The Prescripti­on Drug Affordabil­ity Board unanimousl­y voted against declaring Trikafta — a drug to treat cystic fibrosis — unaffordab­le at a meeting Friday morning. If the state’s new board had determined the medication was unaffordab­le, it would have kicked off a process to set a maximum price that the drugmaker could charge Colorado health plans.

Six other states also have prescripti­on drug affordabil­ity boards, but Friday’s meeting was the first time one of those boards decided whether a specific medication was unaffordab­le. Colorado went further than some of the other states, giving its board the power to set a maximum price that state-regulated insurance plans would pay for certain drugs.

The board’s staff reported that while Trikafta cost an average of $234,439 per patient annually, about half of patients reported they paid $50 or less out-of-pocket each month because either their insurance or assistance programs covered the rest.

Board chair Dr. Gail Mizner said that while drugmakers’ assistance programs aren’t guaranteed to continue in the future, the board’s job was to determine whether the drug was affordable for patients now. Trikafta is a “miracle drug,” she said, but the board can still consider setting a price limit in a future year if patients report they can’t access it.

“This is not the ultimate answer,” she said of Friday’s vote.

Manufactur­ers’ coupons take care of individual patients’ out-of-pocket costs, but raise costs for everyone paying for insurance because they allow drugmakers to keep charging high prices, said board member Dr. Sami Diab. But fixing that is beyond the scope of Colorado’s board, he said.

Cystic fibrosis is caused when a person inherits two copies of a mutated gene, causing sticky mucus to build up in the lungs and other organs. People with the disease are at higher risk from respirator­y infections, and sometimes develop malnutriti­on because the mucus interferes with the digestive system.

The Cystic Fibrosis Foundation estimated about 700 people in Colorado have the disease.

Groups representi­ng cystic fibrosis patients had raised alarms that setting a price limit on Trikafta could push manufactur­er Vertex Pharmaceut­icals to refuse to sell in Colorado. Supporters of the board’s process argued that companies were bluffing to avoid cuts to their revenue.

Trikafta works on a mutation shared by about 90% of patients with cystic fibrosis. Studies found that patients taking it had better lung function and fewer hospital admissions, and reported better quality of life. The drug has only been on the market for about four years, but some researcher­s project it could allow patients to have a near-normal lifespan. As of 2021, about half of people with cystic fibrosis who had died were 34 or younger, according to the Cystic Fibrosis Foundation.

Jennifer Reinhardt, a Denver woman whose 22-year-old daughter has cystic fibrosis, told the board that Trikafta gave her daughter hope and allowed her greater freedom, since she no longer needs to spend hours using a machine to break up the mucus in her chest. She said she also worries that limiting prices for rare-disease drugs could discourage companies from developing new treatments, such as Vertex’s new gene therapy for sickle cell disease.

“She was not able to plan for her future. Now she can,” Reinhardt said of her daughter. “She just wants to live.”

Priya Telang, communicat­ions manager for the Colorado Consumer Health Initiative, said the board went through an exhaustive process to determine whether Trikafta was affordable, which revealed important informatio­n, such as it costs $6,000 a year to produce the drug for each patient.

Vertex’s threat to pull out marred the process, though, and terrified patients unnecessar­ily, she said at a news conference after the board meeting.

“It’s completely unconscion­able that a company that brings in billions of dollars would threaten to withhold medication that costs $6,000 to produce,” she said.

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