Federal
Pharmacy Benefit Manager Accountability Study Act of 2019
Source: Congress.gov ·
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II
116TH CONGRESS
1ST SESSION
S. 1532
To require the Government Accountability Office to study the role pharma-
ceutical benefit managers play in the pharmaceutical supply chain and
provide Congress with appropriate policy recommendations, and for other
purposes.
IN THE SENATE OF THE UNITED STATES
MAY 16, 2019
Mrs. BLACKBURN (for herself and Mr. BRAUN) introduced the following bill;
which was read twice and referred to the Committee on Health, Edu-
cation, Labor, and Pensions
A BILL
To require the Government Accountability Office to study
the role pharmaceutical benefit managers play in the
pharmaceutical supply chain and provide Congress with
appropriate policy recommendations, and for other pur-
poses.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Pharmacy Benefit
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Manager Accountability Study Act of 2019’’.
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SEC. 2. GAO STUDY.
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Not later than 1 year after the date of enactment
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of this Act the Comptroller General of the United States
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shall submit to the Committee on Finance and the Com-
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mittee on Health, Education, Labor, and Pensions of the
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Senate and to the Committee on Ways and Means and
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the Committee on Energy and Commerce of the House
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of Representatives a report that—
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(1) addresses, at minimum—
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(A) the role that pharmacy benefit man-
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agers play in the pharmaceutical supply chain;
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(B) the state of competition among phar-
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macy benefit managers, including the market
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share for the Nation’s 10 largest pharmacy
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benefit managers;
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(C) the use of rebates and fees by phar-
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macy benefit managers, including data for each
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of the 10 largest pharmacy benefit managers
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that reflects, for each drug in the formulary of
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each such pharmacy benefit manager—
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(i) the amount of the rebate passed on
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to patients;
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(ii) the amount of the rebate passed
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on to payors;
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(iii) the amount of the rebate kept by
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the pharmacy benefit manager; and
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(iv) the role of fees charged by the
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pharmacy benefit manager;
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(D) whether pharmacy benefit managers
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structure their formularies in favor of high-re-
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bate prescription drugs over lower-cost, lower-
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rebate alternatives;
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(E) the average prior authorization ap-
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proval time for each of the 10 largest pharmacy
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benefit managers;
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(F) factors affecting the use of step ther-
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apy in each of the 10 largest pharmacy benefit
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managers; and
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(G) the extent to which the price that
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pharmacy benefit managers charge payors, such
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as the Medicare program under title XXVIII of
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the Social Security Act (42 U.S.C. 1395 et
16
seq.), State Medicaid programs under title XIX
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of the Social Security Act (42 U.S.C. 1396 et
18
seq.), the Federal Employees Health Benefits
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Program under chapter 89 of title 5, United
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States Code, or private payors, for a drug is
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more than such pharmacy benefit managers pay
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the pharmacy for the drug; and
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(2) provides recommendations for legislative ac-
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tion to lower the cost of prescription drugs for con-
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sumers and payors, improve the efficiency of the
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pharmaceutical supply chain by lowering inter-
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mediary costs, improve competition in pharmacy
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benefit management, and provide transparency in
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pharmacy benefit management.
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Æ
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