Friday, December 02, 2016

Big Pharma's Lobbyists

Once again the nefarious activities of the pharmaceutical corporations have come to SOYMB’s attention.

39 of 42 patient advocacy groups who participated in discussions with the FDA over agency review processes for prescription drugs received funding from pharmaceutical companies. And at least 15 have representatives of drug or biotechnology companies on their governing boards.

The study is particularly notable now because Congress is poised to pass the 21st Century Cures Act, which trades temporary additional funding for the National Institutes of Health and the FDA for permanent weakening of the FDA’s approval process. Over 1,400 lobbyists have been working on this bill, which would be a major financial boon to the drug and medical device industries. Patient advocacy groups have factored heavily into the lobbying effort. According to an analysis from research group Avalere in December 2014, 43 percent of public comments on the House version of the bill were from patient advocacy groups.

The National Health Council, a group that calls itself “The United Patient Voice” and has advocated before the FDA for faster drug approvals, includes on its board of directors leaders of the two main trade groups for the drug industry — Pharmaceutical Research and Manufacturers of America (PhRMA), and Biotechnology Innovation Organization (BIO) – along with executives from drug companies Sanofi, Johnson & Johnson, and Alkermes. PhRMA gave the National Health Council $1.2 million in 2014; in all, 77 percent of its funding came from the pharmaceutical and biotech industries. Its “Policy Action Team” also has a PhMRA representative on it, along with an employee of Johnson & Johnson. Pfizer, the drug company giant, listed the National Health Council as a “Trade Association Membership” on its lobbying forms.

The Leukemia and Lymphoma Society, received at least $1 million in funding from Bristol-Myers Squibb, Celgene, Genentech, Gilead, Novartis, Pharmacyclics/Janssen, and Takeda Oncology. Joseph Kelley, a vice president of government affairs (which typically means lead lobbyist) for Eli Lilly, sits on the Leukemia and Lymphoma Society board, along with Bristol-Myers Squibb executive Renzo Canetta, and Dana Callow of PAREXEL, a liaison to drug companies on clinical trials.

The president of the EveryLife Foundation for Rare Diseases is also the CEO of drugmaker Ultragenyx.
Cancer Support Community’s board has eight current or former drug company executives, from such firms as Eli Lilly, Vertex Pharmaceuticals, Bristol-Myers Squibb, and Hoffman-LaRoche.
Sarcoma Foundation of America’s co-founder and president, Mark Thornton, works for a consulting firm for pharmaceuticals, medical devices, and biologic drugs.
A representative of the National Organization for Rare Disorders previously worked for Catalyst Healthcare Consultants, a “boutique regulatory advisory firm,” a euphemism for a lobbyist for the health care industry, including biopharma companies.
FasterCures, a division of the Milken Institute, hosted a recent conference about finding cures that received funding from nearly a dozen drug companies.
The Juvenile Diabetes Research Foundation enjoys tens of millions of dollars in drug industry support, and had its 2016 gala sponsored by PhRMA. A top executive of the patient advocacy group, David Wheadon, recently left to become the chief lobbyist for pharmaceutical giant AstraZeneca.
An FDA public meeting in 2015 judging a drug known colloquially as “pink Viagra” had at least six patient advocates speak who were paid by the drug’s manufacturer to attend.

The National Health Council, the EveryLife Foundation, Sarcoma Foundation of America, the National Organization for Rare Diseases, and FasterCures were among 217 patient advocacy groups that sent a letter in mid-November to House and Senate leaders supporting the 21st Century Cures Act, which passed the House on Wednesday. Bernie Sanders has called this bill a collection of “corporate giveaways that will make drug companies even richer.” It would streamline FDA reviews, secure automatic approval for certain devices and drug therapies without rigorous screening, and allow the use of “real world” evidence of drug effectiveness rather than more credible randomized clinical trials. Elizabeth Warren said that “I will fight it because I know the difference between compromise and extortion.”


Drug companies don’t only fund patient advocacy groups, but doctors, medical journals, university research, hospitals, and politicians. The industry even helps fund the FDA through “user fees.” 

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