The 21st Century Cures Act, which just passed a House vote yesterday in the U.S. Congress, is one of the most-lobbied healthcare bills in recent history, with nearly three lobbyists working for its passage or defeat for every member on Capitol Hill.
More than 1,455 lobbyists representing 400 companies, universities and other organizations pushed for or against an earlier House version of a Cures bill this congressional cycle, according to federal disclosure forms compiled by the Center for Responsive Politics (CRP). A compromise version was released over the Thanksgiving weekend.
The latest version of the bill would boost funding for the National Institutes of Health (NIH) by $4.8 billion over 10 years, including funding for enhanced brain, cancer and precision medicine research. The NIH’s 2017 discretionary budget is $30.3 billion. The bill would grant an additional $1 billion to address the opioid crisis. It would also speed up the drug and device approval process at the U.S. Food and Drug Administration (FDA) by pushing different evidence standards.
Other than major appropriations bills, a transportation spending bill and an energy infrastructure funding bill, the Cures Act garnered more lobbying activity than any of the more than 11,000 bills proposed in the 114th Congress, according to an analysis of the CRP data. It’s also the second-most lobbied healthcare bill since 2011, following only the Medicare Access and CHIP Reauthorization Act of 2015, which, among other things, overhauled Medicare payments to health providers.
Putting a price tag on the lobbying is difficult because spending reports don’t break down spending by specific measures. The reports show that interested groups spent as much as half a billion dollars from 2015 through the second quarter of 2016 on all lobbying disclosures that included the 21st Century Cures Act.
“In a bill of this importance and consequence, a lot of groups have a lot of interest in every line in that bill, and they’re going to put as much pressure as they can on legislators — and maybe some executive branch people as well — to get favorable language in that bill to support their interests,” says former Rep. Lee Hamilton, who founded the Indiana University Center on Representative Government after spending more than three decades in the House of Representatives. “The more intense the lobbying, the more money is at stake.”
Senate Majority Leader Mitch McConnell identified the legislation as a priority after a 2016 election that has cast doubt on the future of the Affordable Care Act. Republican President-elect Donald Trump has vowed to eliminate “red tape” at the FDA but hasn’t specifically commented on the Cures Act.
“Absolutely this has gained a lot of attention on K Street,” says Tim LaPira, associate professor of political science at James Madison University in Harrisonburg, Virginia. Every Congress, he says, a few dozen bills spark a “feeding frenzy.”
Even so, the bill hasn’t spurred as much lobbying as the Affordable Care Act in 2009, which brought out more than 1,200 organizations, according to CRP data.
The Pharmaceutical Researchers and Manufacturers of America, or PhRMA, the main trade group for brand-name drugmakers, applauded the House bill’s passage. The group’s lobbying reports naming the bill accounted for $24.7 million in spending by the group, which spent $30.3 million overall.
Its spokeswoman, Allyson Funk, said in a statement that the trade group “appreciate[s] Congress’ continued interest in improving biomedical innovation and accelerating new treatments for patients.”
Several nonprofit patient advocacy and research groups have opposed the bill, citing concerns about endangering patients with simplified drug and device approvals.
David and Goliath:
Beyond the pharmaceutical industry, the bill’s supporters include universities, medical schools and groups representing them, as well as patient groups funded by drug and device companies, says Diana Zuckerman of the nonprofit National Center for Health Research, which has not lobbied the bill but has launched a campaign to convince Congress to “fix” it.
“It really is a David and Goliath issue of where the money is,” Zuckerman says.
AbbVie, the maker of Humira, a drug used to treat arthritis, ulcerative colitis and Crohn’s disease, reported $7.7 million in lobbying expenditures in disclosures listing the bill as an issue. The company’s total lobbying was $9.5 million this cycle.
Hospitals and medical schools, which oppose rising drug costs, supported the bill because the NIH funding could propel grants to medical and research institutions, Zuckerman says.
Johns Hopkins Medicine called enhanced biomedical research funding “long overdue.” Spokeswoman Jania Matthews said in an email that the bill would also “provide new tools at the FDA to accelerate the approval of new therapies and medical devices.”
The U.S. Chamber of Commerce generally supports the bill and reported $87.1 million in expenditures in disclosure reports that cited the Cures Act, with overall spending of $136.5 million through the second quarter of 2016.
The U.S. Oil and Gas Association, with lobbying expenditures of $293,000, lists the Cures Act as a legislative issue. Funding for the bill would partly come from selling crude oil from the U.S. government’s Strategic Petroleum Reserve.
According to the House Committee on Energy and Commerce, money from selling oil would go toward NIH funding “because just as energy reserves are a national resource designed to protect and serve our citizens, so too is an investment in health innovation and research.”
The U.S. Oil and Gas Association declined to comment.
Additional lobbyists may be working on the bill under the radar. LaPira explained that lax lobbying disclosure requirements mean that some lobbyists may not disclose work on the bill, H.R. 6. That’s what he saw when the Affordable Care Act was passed, too.
“The clerk’s office is supposed to list the bill number if they know it, but nobody ever checks,” he says. “That’s another sort of trick of the trade: to hide in plain sight.”
The bill is considered a swan song for sponsor Rep. Fred Upton, whose tenure as chair of the Energy and Commerce Committee is nearing an end, says Paul Heldman, an analyst at Heldman Simpson Partners LLC, a research firm that provides health policy analysis to investors. The Michigan Republican garnered broad support from devicemakers, drug manufacturers, researchers and patient advocacy groups. He’s received more than half a million campaign dollars from pharmaceutical and health product groups in the past two election cycles.
The committee has received at least 36 letters of support. But in October, 13 groups, including the Center for American Progress, AFL-CIO and Public Citizen, urged members in a letter not to rush passage of the bill without first amending it to include drug price controls.
Before the election, it was unclear whether opposition from think tanks close to the Obama administration and Hillary Clinton would impede passage.
“It may still be an important issue, but I think less likely given the outcome of the election,” Heldman says.
This article was originally published on Lobbyists swarm around major mental health bill