Vertex Pharmaceuticals Incorporated v. HHS

Court of Appeals for the D.C. Circuit·Decided September 4, 2026·No. 25-5133·Published

Opinion

United States Court of Appeals FOR THE DISTRICT OF COLUMBIA CIRCUIT

Argued February 23, 2026 Decided September 4, 2026

No. 25-5133

VERTEX PHARMACEUTICALS INCORPORATED, APPELLANT

v.

UNITED STATES DEPARTMENT OF HEALTH AND HUMAN SERVICES, ET AL.,

APPELLEES

Appeal from the United States District Court for the District of Columbia (No. 1:24-cv-02046)

Douglas H. Hallward-Driemeier argued the cause for appellant. With him on the briefs was Andrew J. O’Connor.

Daniel Winik, Attorney, U.S. Department of Justice, argued the cause for appellee. With him on the brief were Brett A. Shumate, Assistant Attorney General, and Michael S. Raab and Charles W. Scarborough, Attorneys.

Michael S. Labson and Deborah Malamud were on the brief for amicus curiae Sickle Cell Reproductive Health Education Directive in support of appellant.

John S. MacGregor was on the brief for amicus curiae Dravet Syndrome Foundation in support of appellant.

James C. Stansel, John T. Delacourt, and Kwaku A.

Akowuah were on the brief for amici curiae Pharmaceutical Research and Manufacturers of America & Biotechnology Innovation Organization.

Before: RAO and WALKER, Circuit Judges, and RANDOLPH, Senior Circuit Judge.

Opinion for the Court filed by Circuit Judge RAO.

RAO, Circuit Judge: Vertex Pharmaceuticals developed a gene therapy that treats two hereditary blood disorders but may have adverse effects on fertility. To address the risk that fertility concerns might deter individuals from taking the therapy, Vertex designed a program that would offer patients up to $70,000 to support fertility services. Vertex requested an advisory opinion from the Department of Health and Human Services to ensure its program complied with federal law. After a long delay, HHS issued an unfavorable advisory opinion, concluding that Vertex’s program would violate both the Anti- Kickback Statute and the Beneficiary Inducement Statute. Vertex sued, claiming the advisory opinion was unlawful and unreasonable. Vertex also challenged HHS’s regulations regarding the timing for issuing advisory opinions. The district court granted summary judgment for HHS across the board.

HHS correctly determined that Vertex’s program would run afoul of the Anti-Kickback Statute. We affirm summary judgment as to that part of the advisory opinion, but otherwise reverse. HHS failed to adequately explain why the program would violate the Beneficiary Inducement Statute, and the timing regulations unlawfully evade a statutory deadline for issuing advisory opinions.

I.

A.

This case turns on two statutes that protect the integrity of federal healthcare programs: the Anti-Kickback Statute (“AKS”) and the Beneficiary Inducement Statute (“BIS”).

Medicare and Medicaid provide federal funds to cover healthcare costs for certain eligible groups. Concerned about the possibility that individuals would offer payments to influence medical decisionmaking and inflate federal reimbursements, Congress enacted the AKS. See Social Security Amendments of 1972, Pub. L. No. 92-603, Title II, § 242(b), 86 Stat. 1329, 1419. Congress has amended the AKS multiple times, for instance to broaden the scope of illicit payments and to add a scienter requirement to ensure the statute penalizes only conduct that is both knowing and willful. As revised and relevant here, the AKS criminalizes “knowingly and willfully offer[ing] or pay[ing] any remuneration (including any kickback, bribe, or rebate) … to any person to induce such person … to purchase” a federally reimbursable medical product or service. 42 U.S.C. § 1320a-7b(b)(2)(B).

AKS violations are felonies punishable by up to a $100,000 fine and 10 years of imprisonment. Id. § 1320a- 7b(b)(2). The AKS contains safe harbors that except certain activities from criminal liability, and the HHS Secretary has authority to create additional safe harbors. Id. §§ 1320- 7b(b)(3), 1320a-7d(a)(1)(B).

The BIS imposes civil penalties for influencing a beneficiary’s choice of provider for services or goods paid for by Medicare or Medicaid. Specifically, the BIS prohibits “offer[ing]” or “transfer[ring]” to a beneficiary “remuneration” that a person “knows or should know is likely to influence” a

beneficiary’s choice of “provider, practitioner, or supplier.” Id. § 1320a-7a(a)(5). The BIS contains several unique exceptions, in addition to the AKS’s safe harbors, which generally extend to violations of the BIS. Id. § 1320a-7a(i)(6). Relevant here is an exception for remuneration that “promotes access to care and poses a low risk of harm to patients and Federal health care programs.” Id. § 1320a-7a(i)(6)(F) (“Promotes Access to Care Exception”).

Parties may seek an advisory opinion from the HHS Secretary regarding whether a proposed activity would violate either the AKS or the BIS. Id. § 1320a-7d(b)(1)–(2). The advisory opinion may determine whether a proposed action violates the AKS or the BIS, whether a statutory exception applies, and whether HHS will exercise discretion to not pursue violations because there is a low risk of fraud or abuse. An advisory opinion is “binding as to the Secretary and the party … requesting the opinion.” Id. § 1320a-7d(b)(4)(A).

The statutory provisions governing advisory opinions instruct the Secretary to promulgate regulations establishing procedures for the issuance of advisory opinions. Importantly, one subsection outlines the “Specific contents” for those regulations, which include that “the Secretary shall be required to issue to a party requesting an advisory opinion by not later than 60 days after the request is received.” Id. § 1320a- 7d(b)(5)(B)(i). HHS’s regulations provide that it will issue an advisory opinion “within 60 days after the request for an advisory opinion has been formally accepted.” 42 C.F.R. § 1008.43(c)(1). Furthermore, the regulations toll the 60-day period under certain circumstances, including from when HHS requests additional information until the time the requested information is submitted. Id. § 1008.43(c)(3)(ii).

B.

Vertex Pharmaceuticals is a biotechnology company that developed Casgevy, a novel treatment for sickle cell disease and transfusion-dependent beta-thalassemia, two hereditary blood disorders that afflict thousands of Americans. As part of Casgevy’s treatment course, patients must undergo intensive chemotherapy, which can have significant negative effects on fertility. Because older patients are often unable to tolerate the chemotherapy regimen, patients ideally take Casgevy when they are young, with their childbearing years ahead of them. And because of the side effects of chemotherapy, patients may require fertility treatments that can cost tens of thousands of dollars.

Recognizing that fertility concerns and the costs of associated treatment might deter some patients from choosing Casgevy, Vertex created the Fertility Support Program. The Program provides up to $70,000 to Casgevy patients for fertility services. Vertex opened the Program to privately insured patients, but did not include patients with federally provided healthcare, fearing the Program might violate the AKS and the BIS by offering a valuable service to incentivize patients to take Casgevy and choose certain healthcare providers.

On June 13, 2023, Vertex requested an advisory opinion from HHS about the lawfulness of extending the Program to federally insured patients. Vertex argued the Program did not violate the AKS and the BIS. In the alternative, Vertex argued that under the AKS, the Program posed a low risk of fraud or abuse and so HHS should exercise its discretion to withhold enforcement. And under the BIS, Vertex maintained the Program would satisfy the Promotes Access to Care Exception

because fertility concerns are a barrier to treatment that the Program would address.

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