Council on Radionuclides and Radiopharmaceuticals, Inc. v. Azar

CourtDistrict Court, District of Columbia
DecidedNovember 13, 2019
DocketCivil Action No. 2018-0633
StatusPublished

This text of Council on Radionuclides and Radiopharmaceuticals, Inc. v. Azar (Council on Radionuclides and Radiopharmaceuticals, Inc. v. Azar) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Council on Radionuclides and Radiopharmaceuticals, Inc. v. Azar, (D.D.C. 2019).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA ____________________________________ ) COUNCIL ON RADIONUCLIDES AND ) RADIOPHARMACEUTICALS, INC., ) ) Plaintiff, ) ) v. ) Civil Action No. 18-633 (RBW) ) ALEX M. AZAR II, in his official ) Capacity as Secretary of the United States ) Department of Health and Human ) Services, and ) ) UNITED STATES DEPARTMENT OF ) HEALTH AND HUMAN SERVICES, ) ) Defendants. ) ____________________________________)

MEMORANDUM OPINION

The plaintiff, the Council on Radionuclides and Radiopharmaceuticals, Inc. (the

“Council”), brings this civil action pursuant to the Administrative Procedure Act (“APA”), 5

U.S.C. §§ 701–706 (2018), against the defendants, the United States Department of Health and

Human Services (the “Department”) and Alex Azar, in his official capacity as the Secretary of

the Department (the “Secretary”), challenging the defendants’ interpretation of certain provisions

of the Social Security Act, 42 U.S.C. §§ 1396–1396w-5 (2018). See generally Complaint

(“Compl.”). Currently pending before the Court are the Plaintiff’s Motion for Summary

Judgment (“Pl.’s Mot.”) and the Defendants’ Cross-Motion for Summary Judgment and

Opposition to Plaintiff’s Motion for Summary Judgment (“Defs.’ Mot.”). Upon careful consideration of the parties’ submissions, 1 the Court concludes for the following reasons that it

must deny the plaintiff’s motion for summary judgment and grant the defendants’ cross-motion

for summary judgment.

I. BACKGROUND

Established in 1965 under Title XIX of the Social Security Act, the Medicaid program

provides states with funding to provide medical assistance to individuals “whose income and

resources are insufficient to meet the costs of necessary medical services.” 42 U.S.C. § 1396-1.

“In order to participate in the Medicaid program, a [s]tate must have a plan for medical

assistance approved by the Secretary.” Pharm. Research & Mfrs. of Am. v. Walsh, 538 U.S.

644, 650 (2003) (citing 42 U.S.C. § 1396a(b)). A state’s plan must, among other things,

“define[] the categories of individuals eligible for benefits and the specific kinds of medical

services that are covered” by the plan. Id. (citing 42 U.S.C. § 1396a(a)(10), (17)). And, a state

may choose to provide, as part of its plan, payment under the Medicaid program for “covered

outpatient drugs,” see 42 U.S.C. § 1396a(a)(54), which are defined to include drugs that (1)

“may be dispensed only upon prescription,” 42 U.S.C. § 1396r-8(k)(2)(A); (2) are “approved for

safety and effectiveness as a prescription drug,” id. § 1396r-8(k)(2)(A)(i); and (3) are not

“provided as part of, or as incident to and in the same setting as” certain specified services “and

for which payment may be made . . . as part of payment for th[ose] [services] and not as direct

reimbursement for the drug” (the “limiting definition”), id. § 1396r-8(k)(3).

1 In addition to the filings already identified, the Court considered the following submissions in rendering its decision: (1) the Defendants’ Answer (“Defs.’ Answer”); (2) the Memorandum of Points and Authorities in Support of Plaintiff’s Motion for Summary Judgment (“Pl.’s Mem.”); (3) the Memorandum in Support of Defendants’ Cross- Motion for Summary Judgment and in Opposition to Plaintiff’s Motion for Summary Judgment (“Defs.’ Mem.”); (4) the Plaintiff’s Reply in Support of Motion for Summary Judgment and Opposition to Defendants’ Cross-Motion for Summary Judgment (“Pl.’s Opp’n”); and (5) the Defendants’ Reply to Plaintiff’s Opposition to Defendants’ Cross- Motion for Summary Judgment (“Defs.’ Reply”).

2 In 1990, Congress created the Medicaid drug rebate program (the “Medicaid Drug Rebate

Program”) to offset Medicaid costs incurred by the federal government and the states for

outpatient drugs provided to Medicaid recipients. See Walsh, 538 U.S. at 652. Pursuant to the

Medicaid Drug Rebate Program, a drug manufacturer, in order to receive state Medicaid

payments for its covered outpatient drugs, must enter into a rebate agreement with the Secretary.

See Pharm. Research & Mfrs. of Am. v. Thompson, 251 F.3d 219, 221 (D.C. Cir. 2001). The

rebate agreement requires drug manufacturers to pay the state “a portion of the price of [its]

drugs” for which payment is covered by a state under the Medicaid program. Id.; see 42 U.S.C.

§ 1396r-8(a), (b). The Medicaid Drug Rebate Program also requires that drug manufacturers, on

a quarterly basis, submit, inter alia, drug pricing information, see id. § 1396r-8(b)(3)(A), and

noncompliance with these reporting obligations subjects the drug manufacturer to monetary

penalties, see id. § 1396r-8(b)(3)(C).

On February 1, 2016, the Centers for Medicare & Medicaid Services (the “CMS”), the

division of the Department that administers the Medicaid program on behalf of the Secretary,

issued a final rule revising the requirements “pertaining to [the] Medicaid reimbursement for

covered outpatient drugs . . . [and] also revis[ing] other requirements related to [covered

outpatient drugs], including key aspects of [their] Medicaid coverage and payment, and the

[Medicaid] [D]rug [R]ebate [P]rogram” (the “Final Rule”). Joint Appendix (“JA”) at 2. In its

final rule, the CMS noted, in response to comments, that radiopharmaceuticals 2 “meet the

definition of a [covered outpatient drug],” if they are approved by the United States Food and

Drug Administration (the “FDA”) as a “prescription drug,” so long as the limiting provision does

2 According to the Council, “[r]adiopharmaceuticals are used primarily as part of a variety of diagnostic imaging, and in some cases, therapeutic procedures,” Compl. ¶ 30, and “are either themselves radioactive and/or used to produce radioactive ‘patient ready’ doses,” id. ¶ 29.

3 not apply to the drug, id. at 7. CMS further stated that “radiopharmaceuticals[, including those

used in compounding patient-ready doses,] qualify as a [covered outpatient drug] because of the

approval process undergone with [the] FDA . . . [and] [t]herefore, radiopharmaceuticals are to be

reported to the [Medicaid Drug Rebate] [P]rogram in the same manner as other [covered

outpatient drugs] for the purposes of the administration of the [Medicaid Drug Rebate]

[P]rogram.” Id.

On March 19, 2018, the Council filed its complaint in this case, challenging the CMS’s

interpretation of the definition of “covered outpatient drugs” to include radiopharmaceuticals.

See Compl. at 1. Thereafter, the parties filed their cross-motions for summary judgment, which

are the subjects of this Memorandum Opinion.

II. STANDARD OF REVIEW

A moving party is entitled to summary judgment “if the movant shows that there is no

genuine dispute as to any material fact and the movant is entitled to judgment as a matter of

law.” Fed. R. Civ. P. 56(a).

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Council on Radionuclides and Radiopharmaceuticals, Inc. v. Azar, Counsel Stack Legal Research, https://law.counselstack.com/opinion/council-on-radionuclides-and-radiopharmaceuticals-inc-v-azar-dcd-2019.