C4i Presidential Advisory Memo: Recent Evidence in Health Care Policy

Date: February 2020*

To: 2020 Presidential Campaigns

From: Robin Feldman, Arthur J. Goldberg Distinguished Professor of Law and Director, Center for Innovation (C4i)

Health care policy is one of the most pressing issues facing Americans today. According to a January 2020 Gallup poll, 81% of Americans cited health care as extremely or very important to them in the upcoming presidential election, outranking every other issue.^[1]

The non-partisan Law & Medicine Initiative at the UC Law SF Center for Innovation (C4i) aims to:

Improve affordability, access, and quality in health care systems while protecting innovation and ensuring that markets are fair, efficient, and transparent;
Generate the data and information that policymakers need to improve health care systems;
Increase understanding of complex topics in law and medicine; and
Develop a stable of solutions.

This advisory memo highlights recent evidence on four main challenges in health care systems, policy recommendations, and resources from the Law & Medicine Initiative that may be pertinent to the new administration.

Please let us know if we can provide additional information.

*This policy memo was originally published in February 2020 and issued to all presidential candidates at the time. It has been updated subsequently through November 2020 in advance of President-elect Biden’s administration.

DRUG COMPANY EVERGREENING

Rather than creating new medicines, pharmaceutical companies largely recycle and repurpose old ones. From 2005-2015, for example, 78% of drugs with new patents were not new drugs but ones already on the market.

With evergreening, companies refresh their market monopoly by slightly modifying a drug’s dosage, delivery, or other characteristics to obtain additional exclusivities, blocking low-cost generics and driving up drug prices.

The statistics are from the peer-reviewed article, “,” Oxford Journal of Law and the Biosciences, in which our researchers studied drugs on the market between 2005 and 2015 and tracked every time a company extended its protection cliff.

THE ROLE OF HEALTH INSURANCE FORMULARIES

Health plan tiering should reflect the cost of a drug, as well as reward patients who choose generics over brands. However,

From 2010-2017, the percentage of generics on the most-preferred tier dropped from 73% to 28%.

During the same period, the percentage of drugs placed on inappropriate tiers in relation to drugs with the same active ingredient increased from 47% to 74%.
Considering nothing but patient out-of-pocket costs and payments from the federal low-income-subsidy program, these formulary abuses wasted $13.25 billion dollars over the eight-year period, with the waste rising significantly across time.

The full study can be accessed at “

PBMs AND REBATE SCHEMES

By offering lucrative payments to pharmacy benefit manager middle players (PBMs), as well as to doctors and hospitals, drug companies ensure that inexpensive drugs never gain traction.

In her book, C4i Director Professor Feldman analyzes the complex and secretive pharmaceutical industry and shows how higher-priced drugs receive favorable treatment and patients are channeled toward the most expensive medicines. The well-received book provides a strong foundation for understanding the PBM and rebate systems, along with the challenges to improving the health care system and potential policy solutions.

The book provides insights into the type and extent of these problems, which lawsuits have helped illuminate, including:

After patent protection expired on Remicade, Johnson & Johnson’s rheumatoid arthritis drug, the company created a scheme that induced hospitals and health plans to exclude the lower-priced biosimilar.
Walgreens and CVS pharmacies charged patients with health insurance more than the uninsured when purchasing certain generic drugs as part of a scheme to ensure higher payments to the middle players and enhance the brand drugs’ market position.
In the vaccine market, Sanofi charged prices up to 34.5% higher unless buyers agreed to purchase Sanofi’s vaccines exclusively, blocking out cheaper competitors.
The majority of patient advocacy groups receive significant support from drug and device companies, which may influence the groups to advocate for policies favorable to the companies. When companies donate their drugs, they are particularly tax advantaged, receiving a deduction above the cost of the drug. Today, patient assistance programs are 10 of the largest 15 charitable foundations in the US.

The scholarly paper on which the book is based can be found online: “” (Harvard Journal on Legislation.)

THE MISUSE OF TRADE SECRET LAW TO HIDE DRUG PRICING

In the pharmaceutical industry, drug companies and PBM middle players shield prices from the public and regulators by misusing trade secret law. This drives up drug prices and distorts the drug market.

Our work, “ from Yale Journal of Law and Technology, provides a legal road map showing how drug pricing does not constitute a protectable trade secret. This road map is essential so that policymakers can make bold changes in the health care system without shying away due to threats of potential trade secret rights.

POLICY SOLUTIONS AND RECOMMENDATIONS

The Law & Medicine Initiative’s resources section below, as well as other works from C4i, provide rich solutions to the distortions driving health care pricing. Our primary recommendations include:

Implement a “one-and-done” approach to pharmaceutical patent law in which each drug receives one—and only one—period of market protection.
Make list price determine each drug’s placement on formulary tiers. List price—that badly maligned, roundly dismissed figure—should become the holy grail for health insurer drug pricing. Using list price would decrease the incentive-distorting rebate schemes while recognizing that many people already pay full list price.
Use value-based pricing only when the value of a drug is measured in relation to the nation’s overall health needs, considers all diseases, and weighs the long-term, evidence-based outcomes. Value-based pricing cannot mean “the sky’s the limit.”
Ruthlessly simplify. In the case of the Hatch-Waxman and Biologics Act systems for approval of cheaper drugs, with their complicated patent challenge systems, they have spawned too many opportunities for manipulation. In contrast, a simplified, slimmed-down system would provide fewer opportunities for clever gamesmanship and require fewer resources as a whole.
Improve transparency of drug pricing information across industry and governmental health care agencies. From peeling back the veil on rebate deals and actual drug prices to expanding the Federal Drug Administration’s (FDA) disclosure of drug application information and data, there is much to be improved. Greater clarity will thwart abuses and support public accountability of the health care system.

^[1] Gallup Poll. (2020).

ADDITIONAL RESOURCES

Selected Recent Works

(Cambridge)
(Cambridge)
(Oxford Journal of Law and the Biosciences)
(Yale Journal of Law and Technology)
(Harvard Journal on Legislation)
(Green Bag)
(Columbia Science & Technology Law Review)
(New England Journal of Medicine)

Op Eds

(STAT)
(Washington Post)
(The Conversation)
(STAT)
(Washington Post)
(Washington Post)
(Washington Post)

Data

Revised 11/23/2020

More about C4i: Website |

Thumbnail photo credit: frankieleon

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