Ass'n of Am. Physicians & Surgeons v. FDA

13 F.4th 531
CourtCourt of Appeals for the Sixth Circuit
DecidedSeptember 9, 2021
Docket20-1784
StatusPublished
Cited by88 cases

This text of 13 F.4th 531 (Ass'n of Am. Physicians & Surgeons v. FDA) is published on Counsel Stack Legal Research, covering Court of Appeals for the Sixth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ass'n of Am. Physicians & Surgeons v. FDA, 13 F.4th 531 (6th Cir. 2021).

Opinion

RECOMMENDED FOR PUBLICATION Pursuant to Sixth Circuit I.O.P. 32.1(b) File Name: 21a0212p.06

UNITED STATES COURT OF APPEALS FOR THE SIXTH CIRCUIT

┐ ASSOCIATION OF AMERICAN PHYSICIANS & SURGEONS, │ Plaintiff-Appellant, │ │ v. │ > No. 20-1784 │ UNITED STATES FOOD AND DRUG ADMINISTRATION; │ JANET WOODCOCK, M.D., Acting Commissioner of │ Food & Drugs, in her official capacity; BIOMEDICAL │ ADVANCED RESEARCH & DEVELOPMENT AUTHORITY; │ GARY L. DISBROW, PH.D., Director, Biomedical │ Advanced Research & Development Authority, in his │ official capacity; U.S. DEPARTMENT OF HEALTH AND │ HUMAN SERVICES; XAVIER BECERRA, Secretary of │ Health & Human Services, in his official capacity, │ Defendants-Appellees. │ ┘

Appeal from the United States District Court for the Western District of Michigan at Grand Rapids. No. 1:20-cv-00493—Robert J. Jonker, District Judge.

Decided and Filed: September 9, 2021

Before: SILER, THAPAR, and MURPHY, Circuit Judges. _________________

COUNSEL

ON BRIEF: Andrew L. Schlafly, Far Hills, New Jersey, for Appellant. Scott R. McIntosh, Lewis S. Yelin, UNITED STATES DEPARTMENT OF JUSTICE, Washington, D.C., for Appellees.

MURPHY, J., delivered the opinion of the court in which SILER and THAPAR, JJ., joined. SILER, J. (pg. 22), delivered a separate opinion concurring in all but Part III.A.1 of the majority opinion. No. 20-1784 Ass’n of Am. Physcians & Surgeons v. FDA, et al. Page 2

_________________

OPINION _________________

MURPHY, Circuit Judge. In Flast v. Cohen, 392 U.S. 83 (1968), the Supreme Court suggested that plaintiffs broadly have “standing” to sue over actions taken by the political branches whenever the litigants are sufficiently “adverse.” See id. at 100–01. The standing at issue in this case—associational standing—grew out of the same “judicial thinking” as Flast. Nat’l Automatic Laundry & Cleaning Council v. Shultz, 443 F.2d 689, 693 (D.C. Cir. 1971). It permits an association that has suffered no injury to sue on behalf of members who have. Yet the Court has since criticized Flast for overlooking that standing (and, in particular, its requirement that a plaintiff identify a personal injury) represents a key part of the Constitution’s separation of powers. Lewis v. Casey, 518 U.S. 343, 353 n.3 (1996). It is not clear how associational standing comports with this more recent guidance. At the least, the guidance should lead us to vigilantly ensure that an association’s members have incurred a personal injury. And here, the plaintiff (an association of physicians) failed to plausibly plead that any member has been injured by the actions of the Food and Drug Administration (FDA) that it criticizes. We thus affirm the dismissal of its complaint.

I

Under the Federal Food, Drug, and Cosmetic Act, a drug manufacturer cannot distribute a drug in interstate commerce without obtaining the FDA’s approval for the uses listed on the drug’s official label. See 21 U.S.C. § 355(a). To obtain FDA approval, a manufacturer generally must conduct clinical trials establishing that the drug is safe and effective for those intended uses. See id. § 355(d). In emergency situations, however, the FDA may allow the distribution of an unapproved drug or of an approved drug for an unapproved use. See id. § 360bbb-3(a)(1)–(2).

Although the Act regulates a manufacturer’s distribution of drugs, it does not go further by regulating a doctor’s practice of medicine. See Buckman Co. v. Plaintiffs’ Legal Comm., 531 U.S. 341, 350–51 (2001). The Act thus does not prohibit doctors from prescribing an No. 20-1784 Ass’n of Am. Physcians & Surgeons v. FDA, et al. Page 3

FDA-approved drug (say, a chemotherapy drug approved to treat leukemia) for an “off-label” use (say, treatment of other cancers). See United States v. Caronia, 703 F.3d 149, 153 (2d Cir. 2012). It instead leaves the regulation of doctors to the states. Cf. Dent v. West Virginia, 129 U.S. 114, 121–24 (1889).

This case involves “hydroxychloroquine.” The FDA approved this drug for distribution in 1955. It has now approved the drug to treat malaria, lupus, and arthritis. A CDC fact sheet describes the drug as “relatively well tolerated” and lists its most common side effects as “stomach pain, nausea, vomiting, and headache.” Fact Sheet, R.8-14, PageID 286. Still, a patient may not use hydroxychloroquine unless a doctor prescribes it.

The FDA has not approved hydroxychloroquine to treat COVID-19. Early in the pandemic, the FDA relied on the then-available data to conclude that the drug might help treat the disease. In March 2020, the agency issued an Emergency Use Authorization (“Authorization”) under § 360bbb-3(a). The Authorization permitted the hydroxychloroquine in the federal government’s strategic national stockpile to be distributed for treatment of COVID-19 patients. Yet it granted access to this large stockpile only in limited circumstances. The Authorization stated that the drug “may only be used to treat adult and adolescent patients who weigh 50 kg or more hospitalized with COVID-19 for whom a clinical trial is not available, or participation is not feasible.” Auth., R.8-8, PageID 262.

The Association of American Physicians & Surgeons, a nonprofit organization with physician members, believed that the Authorization did not offer broad enough access to the federal stockpile. It sued the FDA and its Commissioner, the Biomedical Advanced Research and Development Authority and its Director, and the Department of Health and Human Services and its Secretary. (For simplicity, we will refer to all defendants as the FDA.) The Association alleged that hydroxychloroquine can help patients if taken as a prophylaxis before they get COVID-19 or as an initial treatment after such a diagnosis. It thus sought declaratory and injunctive relief against the Authorization’s restrictions barring use of hydroxychloroquine to treat COVID-19 except for hospitalized patients. No. 20-1784 Ass’n of Am. Physcians & Surgeons v. FDA, et al. Page 4

The Association pleaded three claims. It alleged that these restrictions violated the implied equal-protection guarantee in the Fifth Amendment’s Due Process Clause. Compl., R.1, PageID 17, 20–22. It alleged that the restrictions violated the First Amendment right to associate by limiting access to medication useful for meeting in groups during a pandemic. Id., PageID 22–23. And it alleged that the restrictions violated the Administrative Procedure Act. Id., PageID 22.

The Association also pleaded three injuries. It alleged an injury to itself: The Association was considering canceling a conference purportedly due to the Authorization’s restrictions. Id., PageID 23. It next invoked associational standing on behalf of its physician members: It claimed that the members could not prescribe hydroxychloroquine for COVID-19 because of the restrictions. Id., PageID 19. The Association lastly invoked third-party standing: It alleged that its members’ patients could not obtain the drug for the treatment of COVID-19. Id.

The district court held that none of these injuries plausibly pleaded the Association’s standing to challenge the Authorization. The court dismissed the complaint for lack of subject- matter jurisdiction under Federal Rule of Civil Procedure 12(b)(1). See Ass’n of Am. Physicians & Surgeons v. FDA, 479 F. Supp. 3d 570, 579–85 (W.D. Mich. 2020). We review this decision de novo. See CHKRS, LLC v. City of Dublin, 984 F.3d 483, 488 (6th Cir. 2021).

Before doing so, we flag a mootness issue.

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13 F.4th 531, Counsel Stack Legal Research, https://law.counselstack.com/opinion/assn-of-am-physicians-surgeons-v-fda-ca6-2021.