Pharmaceutical Care Management Association v. District of Columbia

CourtDistrict Court, District of Columbia
DecidedMarch 19, 2009
DocketCivil Action No. 2004-1082
StatusPublished

This text of Pharmaceutical Care Management Association v. District of Columbia (Pharmaceutical Care Management Association v. District of Columbia) 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.

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Pharmaceutical Care Management Association v. District of Columbia, (D.D.C. 2009).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

PHARMACEUTICAL CARE : MANAGEMENT ASSOCIATION, : : Plaintiff, : Civil Action No.: 04-1082 (RMU) : v. : Document Nos.: 76, 77 : DISTRICT OF COLUMBIA et al., : : Defendants. :

MEMORANDUM OPINION

GRANTING IN PART THE PLAINTIFF’S MOTION FOR PARTIAL SUMMARY JUDGMENT AND DENYING IN PART THE DEFENDANTS’ MOTION FOR PARTIAL SUMMARY JUDGMENT

I. INTRODUCTION

This case comes before the court on the parties’ motions for summary judgment. The

plaintiff, Pharmaceutical Care Management Association (“PCMA”), is a national trade

association representing pharmaceutical benefit management companies (“PBMs”). The plaintiff

argues that the Employee Retirement Income Security Act (“ERISA”), 29 U.S.C. §§ 1001 et

seq., preempts Title II of the District of Columbia’s Access Rx Act of 2004 (“Access Rx Act” or

“the Act”), D.C. Code §§ 48-831 et seq. The defendants, on the other hand, contend that ERISA

does not preempt the Access Rx Act because the Act does not regulate ERISA plans and has no

connection with ERISA. As discussed in more detail below, by regulating the relationship

between PBMs and ERISA plans, the Act impermissibly intrudes upon a field exclusively

reserved for federal regulation. II. BACKGROUND

A. Factual History

At issue in this case is the District of Columbia’s attempt to regulate the relationship

between PBMs and “covered entities” such as ERISA health plans, government agencies and

insurance companies. Compl. ¶ 14. PBMs process claims for pharmaceutical drug benefits for

over 200 million Americans. Id. As time passed, PBMs began to expand their services to

include, inter alia, (1) establishing networks of pharmacies that provide discounted drugs to plan

members; (2) negotiating rebate arrangements with drug manufacturers; (3) reviewing drug

utilization to decrease prices and enhance safety; (4) creating therapeutic drug interchange

programs; and (5) establishing generic drug substitution programs. Id. ¶ 15.

In response to rising prescription drug prices, the D.C. Council unanimously passed the

Access Rx Act, which, in the Council’s estimation, would lower the cost of prescription drugs.

Mem. Op. (Dec. 21, 2004) at 2. On May 18, 2004, the Access Rx Act took effect. Compl. ¶ 1.

Title II of the Act, the only portion that the plaintiff challenges, regulates PBMs by imposing

fiduciary duties on them, as well as by requiring disclosure of certain financial information. Id. ¶

3; Mem. Op. (Dec. 21, 2004) at 2. Specifically, Title II dictates that PBMs owe a fiduciary duty

to “covered entities,” which they must discharge in accordance with all applicable laws. D.C.

CODE § 48-832.01(a). Title II also imposes several disclosure requirements on PBMs. For

instance, PBMs must disclose to their customers “information showing the quantity of drugs

purchased by the covered entity and the net cost to the covered entity for the drugs. This

information shall include all rebates, discounts and other similar payments.” Id. § 48-

832.01(c)(1)(A). Furthermore, upon request PBMs must disclose to covered entities “all

financial terms and arrangements for remuneration of any kind that apply between the [PBM]

2 and prescription drug manufacturer or labeler, including, without limitation, formulary

management and drug substitution programs, educational support, claims processing and data

sales fees.” Id. § 48-832.01(c)(1)(B).

The Act also provides that when dispensing prescription drugs, a PBM may substitute a

lower-priced therapeutically equivalent drug for a higher-priced drug. Id. § 48-832.01(d). But,

“[i]f the substitute drug costs more than the prescribed drug, the [PBM] shall disclose to the

covered entity the cost of both drugs and any benefit or payment directly or indirectly accruing to

the [PBM] as a result of the substitution.” Id. § 48-832.01(d)(2). The PBM must then “transfer

in full to the covered entity any benefit or payment received . . . as a result of a prescription drug

substitution.” Id. § 48-832.01(d)(3). Finally, the statute only applies to contracts between PBMs

and covered entities “entered into in the District of Columbia or by a covered entity in the

District of Columbia.” Id. § 48-832.02.

B. Procedural History

Because Title II imposes fiduciary duties and disclosure requirements on PBMs, as

described supra, the plaintiff moved this court to enjoin the defendants from enforcing the

Access Rx Act. Pl.’s Mot. for Prelim. Inj. The court granted preliminary injunctive relief to the

plaintiff on December 21, 2004. See generally Mem. Op. (Dec. 21, 2004). The defendants

appealed the court’s decision to the D.C. Circuit, which remanded the case for this court to

determine in the first instance whether the First Circuit’s ruling in PCMA v. Rowe, 429 F.3d 294

(1st Cir. 2005) precluded the plaintiff from further challenging the validity of the Act under

principles of collateral estoppel. PCMA v. District of Columbia, 522 F.3d 443 (D.C. Cir. 2008).

Accordingly, the court examines the Rowe decision and its effect on this case.

3 1. The First Circuit’s Decision in Rowe

The First Circuit in Rowe addressed the propriety of a statute in Maine that required

PBMs to act as fiduciaries for certain covered entities 1 by “disclos[ing] conflicts of interest,

disgorg[ing] profits from self-dealing, and disclos[ing] to the covered entities certain of their

financial arrangements with third parties.” Rowe, 429 F.3d at 299. To determine whether

ERISA preempted the state statute, the court first analyzed the “high stakes” issue of whether

PBMs are fiduciaries under ERISA. Id. at 300. The court explained that the state statute’s

“provisions requiring disclosure of conflicts of interest and payments from drug manufacturers

are administrative provisions involving no discretion on the part of the PBMs, . . . are purely

ministerial and simply not sufficient . . . to find that the PBMs are acting as fiduciaries under

ERISA.” Id. at 301. With that hurdle behind it, the court applied a two-part test in examining

whether ERISA preempts the state statute. The test first probes whether the statute has a

“connection with” an employment benefit plan and then asks whether the statute “references”

such a plan. Id. at 302 (quoting Cal. Div. of Labor Standards Enforcement v. Dillingham

Constr., N.A., Inc., 519 U.S. 316, 324 (1997)).

Turning to the first prong, the court acknowledged that a principal concern under the

“connection with” prong is “to avoid a multiplicity of regulation in order to permit the nationally

uniform administration of employee benefit plans.” Id. (quoting N.Y. State Conf. of Blue Cross

& Blue Shield Plans v. Travelers Ins. Co., 514 U.S. 645, 657 (1995)). With that in mind, the

court observed that the state statute left plan administrators with a “free hand” to “administer or

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