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Senators call for investigation into possible abuses of Orphan Drug Act
Building on weeks of mounting pressure to address high prescription drug prices, three influential U.S. senators have asked the government’s accountability arm to probe the orphan drug program for potential misuse.
Building on weeks of mounting pressure to address high prescription drug prices, three influential U.S. senators have asked the government’s accountability arm to investigate potential abuses of the Orphan Drug Act.
In a 3 March letter to the U.S. Government Accountability Office (GAO), senators Orrin Hatch (R-Utah), Chuck Grassley (R-Iowa) and Tom Cotton (R-Arkansas) raised the possibility that regulatory or legislative changes might be needed “to preserve the intent of this vital law” that gives drugmakers lucrative incentives to develop drugs for rare diseases.
“While few will argue against the importance of the development of these drugs, several recent press reports suggest that some pharmaceutical manufacturers might be taking advantage of the multiple designation allowance in the orphan drug approval process,” the letter states.
In January, Kaiser Health News published an investigation that found the orphan drug program is being manipulated by drugmakers to maximize profits and to protect niche markets for medicines being taken by millions.
Congress overwhelmingly passed the 1983 Orphan Drug Act to motivate pharmaceutical companies to develop drugs for people whose rare diseases had been ignored. Drugs approved as orphans are granted tax incentives and seven years of exclusive rights to a market that affects fewer than 200,000 people in the United States.
In recent months, reports of five- and six-figure annual price tags for orphan drugs have amplified long-simmering concerns — and the letter reflects that sentiment.
The senators’ letter asks for a list of drugs approved and denied orphan status by the U.S. Food and Drug Administration (FDA). It also asks whether resources at the FDA, which oversees the law, have “kept up with the number of requests” from drugmakers and whether there is consistency in the department’s reviews.
Kaiser Health News’ investigation, which was also published and aired by NPR, found that many drugs that now have orphan status aren’t entirely new. More than 70 are drugs first approved by the FDA for mass-market use. Those include cholesterol blockbuster Crestor, Abilify for psychiatric disorders and rheumatoid arthritis drug Humira, the world’s best-selling drug.
Others are drugs that have received multiple exclusivity periods for two or more rare conditions. About 80 drugs fall into this latter category, including cancer drug Gleevec and wrinkle-fighting drug Botox.
Monopoly rights:
Few senators are better positioned to alter the law, if they want to. Hatch, a longtime advocate of the rare-disease community, said 6 March in a statement that there was little evidence to suggest the Orphan Drug Act needs to change.
Hatch is chairman of the Senate Finance Committee, which oversees 50 percent of the federal budget, including Medicaid and Medicare spending. He said the letter is requesting “the first GAO study exclusively reviewing the Orphan Drug Act, and such oversight will ensure those critical innovations are continued into the future.”
Grassley, the senior senator from Iowa, chairs the Senate Judiciary Committee and has jurisdiction over anti-competitive and patent-related issues. Grassley last month announced an inquiry into the Orphan Drug Act in response to Kaiser Health News‘ investigation.
Cotton, a strong conservative voice, chairs the subcommittee on economic policy under the committee on banking, housing and urban affairs. In a floor speech last month, he announced that he would find a legislative solution to price hikes associated with the orphan drug program.
Cotton focused on an orphan drug that has been a flashpoint in the recent national dialogue about drug prices, arguing that the seven-year marketing exclusivity offered by the law should not have been given to Emflaza, a corticosteroid approved to treat Duchenne muscular dystrophy. Emflaza was not mentioned in the letter to the GAO.
“Monopoly rights are not merit badges,” Cotton said in his speech. “They’re not a reward for business smarts. They’re supposed to serve the interests of patients.”
Drugmaker Marathon Pharmaceuticals triggered an uproar when it announced an $89,000 annual list price for the drug, which many individuals in the U.S. have purchased overseas for $1,000 to $1,600 a year.
Marathon responded in February by delaying the rollout of the drug, saying it will talk with stakeholders, including patients, about the price.
On 3 March, seven Democratic senators — including Senator Elizabeth Warren of Massachusetts — and one independent sent a letter to Jeff Aronin, chief executive officer of Marathon, demanding information on the private drugmaker’s pricing strategy.
Marathon spokeswoman Wanda Moebius released a statement saying the company is committed to ensuring that all individuals who need this drug have access to it and that the company will continue to work with the Duchenne community.
The three top senators asking the GAO to investigate the orphan drug program also expressed concern about patients, saying in their letter that “we feel it is important to include the patient voice in your review.”
Kaiser Health News’ coverage of prescription drug development, costs and pricing is supported in part by the Laura and John Arnold Foundation.
This story originally appeared on Kaiser Health News. It has been slightly modified to reflect Spectrum’s style.
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