Harkonen v. United States Department of Justice

800 F.3d 1143, 2015 U.S. App. LEXIS 15926, 2015 WL 5202141
CourtCourt of Appeals for the Ninth Circuit
DecidedSeptember 8, 2015
Docket13-15197
StatusPublished
Cited by10 cases

This text of 800 F.3d 1143 (Harkonen v. United States Department of Justice) is published on Counsel Stack Legal Research, covering Court of Appeals for the Ninth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Harkonen v. United States Department of Justice, 800 F.3d 1143, 2015 U.S. App. LEXIS 15926, 2015 WL 5202141 (9th Cir. 2015).

Opinion

*1145 OPINION

NOONAN, Circuit Judge:

In this case we must decide whether the Administrative Procedure Act and the Information Quality Act confer the right to judicial review of a federal agency’s refusal to correct allegedly false or misleading information published by the agency in a press release. Dr. W. Scott Harkonen argues that he has the right to obtain, and that the Department of Justice (“DOJ”) has an obligation to provide, the correction of statements DOJ made about him in a 2009 press release. Not so, the government counters: Individuals have no such right, even if the information DOJ published was misleading, false, or even defamatory. We conclude that in the circumstances of this case .the government is correct, and therefore we AFFIRM. 1

I.

A.

The Information Quality Act (“IQA”) was included as a brief note to the Consolidated Appropriations Act of 2001, Pub.L. No. 106-554, 114 Stat, 2763 (2000). The I.QA required the Office of Management and Budget (“OMB”) to draft guidelines “that provide policy and procedural guidance to Federal agencies for ensuring and maximizing the quality, objectivity, utility, and integrity of information ... disseminated by Federal agencies in fulfillment of the purposes and provisions” of the Paperwork Reduction Act. Id. § 515(a). The IQA further required each agency to which the guidelines applied to issue its own agency-specific guidelines and to “establish administrative mechanisms allowing affected persons to seek and obtain correction of information maintained and disseminated by the agency that does not comply with the guidelines____” Id. § 515(b)(2). OMB published its proposed guidelines with a request for public comment on June 28, 2001, an interim set of guidelines on September 28, 2001, and its final guidelines on 'February 22, 2002.

In formulating its guidelines, OMB attempted to balance several often-competing concerns. OMB recognized that “the fact that the Internet enables agencies to communicate information quickly and easily to a wide audience ... increases the potential harm that can result from the dissemination of information that does not meet basic information quality guidelines.” Guidelines for Ensuring and Maximizing the Quality, Objectivity, Utility, and Integrity of Information Disseminated by Federal Agencies; Republication (“Final OMB Guidelines”), 67 Fed.Reg. 8452 (Feb. 22, 2002). OMB also recognized that “information quality comes at a cost.” Id. at 8453. Based on this concern, OMB instructed that “agencies should weigh the costs ... and the benefits of higher information quality” during the formulation of their guidelines. Id. After receiving commentary from, among other sources, several federal agencies, OMB revised its definition of “dissemination” to exclude information distributed through press releases from coverage by the guidelines. Guidelines for Ensuring and Maximizing the Quality, Objectivity, Utility, and Integrity of Information Disseminated by Federal Agencies (“Interim Final OMB Guidelines”), 66 Fed.Reg. 49,718, 49,723, 49,725. (Sept. 28, 2001). OMB’s final guidelines maintained the exclusion of press releases from the definition of “dissemination.” Final OMB Guidelines, 67 Fed.Reg. at 8460.

*1146 DOJ subsequently issued its own agency-specific guidelines on October 4, 2002. See Information Quality: DOJ Information Quality Guidelines, available at http://www. justice.gov/iqpr/information-quality (updated Dec. 31, 2014). These closely mirrored the OMB final guidelines. Id. Relevant here, the scope of the guidelines “does not apply to information disseminated in ... press releases fact sheets, press conferences or similar communications (in any medium) that announce, support or give public notice of information in DOJ.” Id. DOJ also expressly stated that the

guidelines are not a regulation. They are not legally enforceable and do not create any legal rights or impose any legally binding requirements or obligations on the agency or the public. Nothing in these guidelines affects any otherwise available judicial review of agency action.
Id.

B.

W. Scott Harkonen is a medical doctor who served as Chief Executive Officer and member of the Board of Directors for InterMune, Inc. InterMune developed, marketed, and sold drugs, including a drug called Actimmune. Actimmune was approved by the FDA for the treatment of two rare disorders, chronic granulomatous disease and severe, malignant osteopetrosis. In October 2000, InterMune began a Phase III clinical trial (GIPF-001) to determine whether Actimmune would be effective in treating patients suffering from a different, more common disorder, idiopathic pulmonary fibrosis (“IPF”). Enrollment of 330 patients in the clinical trial was completed in October 2001. On August 27, 2002, Harkonen and other InterMune employees met with staff of the FDA to review the results of an interim analysis of the GIPF-001 study data. The FDA staff told Harkonen that because the study did not meet its primary endpoint— Actimmune had failed to reduce death or disease progression in the entire group of treated subjects — the data were insufficient for the FDA to grant approval for the use of Actimmune in the treatment of IPF.

Nonetheless, on August 28, 2002, Harkonen distributed a press release titled “InterMune Announces Phase III Data Demonstrating Survival Benefit of Actimmune in IPF.” The first paragraph of the press release stated that the GIPF-001 study “demónstratele!] a significant survival benefit in patients with mild to moderate disease randomly assigned to Actimmune versus control treatment.” The first paragraph concluded that “[t]here was also approximately a 10% relative reduction in the rate of progression-free survival associated with Actimmune versus placebo, the trial’s primary endpoint, but this was not a statistically significant difference.” The third paragraph of the press release quoted Harkonen as stating, “Actimmune may extend the lives of patients suffering from [IPF].” The fourth paragraph quoted a study investigator as stating, “Actimmune should be used early in the course of [IPF] in order to realize the most favorable long-term survival benefit.” Not until the sixth paragraph did the press release again address the failure of the study to reach its primary endpoint. Even there, the press release described the failure as demonstrating “a strong positive trend in increased survival in the overall patient population.” The tenth paragraph quoted an InterMune officer as stating “we believe [there] is compelling rationale for consideration of Actimmune for the treatment of patients with [IPF].”

On March 18, 2008, the government indicted Harkonen on one count of wire fraud for making allegedly false statements in the press release, and one count of felony misbranding related to Inter *1147 Mune’s alleged off-label marketing and sale of Actimmune for IPF. Following a jury trial, Harkonen was convicted on September 29, 2009, of wire fraud but was acquitted on the misbranding count. Harkonen’s appeal of his criminal conviction and sentence was affirmed by this court on March 4, 2013.

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Bluebook (online)
800 F.3d 1143, 2015 U.S. App. LEXIS 15926, 2015 WL 5202141, Counsel Stack Legal Research, https://law.counselstack.com/opinion/harkonen-v-united-states-department-of-justice-ca9-2015.