Genus Lifesciences, Inc. v. Azar

CourtDistrict Court, District of Columbia
DecidedSeptember 15, 2020
DocketCivil Action No. 2020-0211
StatusPublished

This text of Genus Lifesciences, Inc. v. Azar (Genus Lifesciences, 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
Genus Lifesciences, Inc. v. Azar, (D.D.C. 2020).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

GENUS LIFESCIENCES, INC.,

Plaintiff,

v.

ALEX M. AZAR II, et al., Case No. 1:20-cv-00211 (TNM)

Defendants,

LANNETT CO., INC.,

Intervenor-Defendant.

MEMORANDUM OPINION

In the pharmaceutical development arena, Congress created a “winner-take-all” prize.

Under the Federal Food, Drug, and Cosmetic Act (“FDCA”), the first developer of a “new

chemical entity” (“NCE”)—a drug approved for the first time in the United States—receives a

coveted period of exclusivity (“NCE exclusivity”). During that time, competing drugs generally

cannot can enter the market.

Three years ago, Genus Lifesciences, Inc., won five-year NCE exclusivity for its new

drug, Goprelto. But earlier this year, a competing drug sponsored by Lannett Co., Numbrino,

entered the market.

Genus now cries foul. It claims that the U.S. Food and Drug Administration (“FDA”)

infringed on its exclusivity period when it approved Numbrino. It believes that under the FDCA,

it is entitled to a five-year period of complete market exclusivity, barring all approval and

submission of applications for competing drugs. FDA and Lannett, on the other hand, claim that

everything is aboveboard. FDA explains that while Genus’s exclusivity period prohibits FDA from accepting any new competing drug applications, it does not bar it from approving

applications, like Lannett’s, that were already in the approval process.

The Court agrees with FDA that Genus’s NCE exclusivity does not cover approvals. But

it disagrees with the agency’s reasoning. The FDCA prescribes timelines for approval of

applications like Lannett’s based on the type of patent certification in the application. FDA

admits that disregarded these timelines. Since the Court finds that FDA misinterpreted the

FDCA, the Court’s inquiry stops here for now.

I.

A.

Pharmaceutical companies may market new drugs only with FDA approval. See 21

U.S.C. § 355(a). Developing and seeking approval of a pioneer drug often involves much time

and money. A company’s new drug application (“NDA”) to FDA must contain “full reports of

investigations which have been made to show whether or not such drug is safe for use and

whether such drug is effective in use.” Id. § 355(b)(1). Most of those reports “rely in large

measure on clinical trials with human subjects” and “several phases of clinical testing,” often

spanning years. See Abigail All. for Better Access to Dev. Drugs v. Von Eschenbach, 495 F.3d

695, 697–98 (D.C. Cir. 2007).

To streamline the approval process for some drugs, Congress enacted the Hatch-Waxman

Amendments to the FDCA. See Pub. L. No. 98-417, 98 Stat. 1585 (1984). These amendments

created two abbreviated pathways to new drug approval.

First, a company seeking to market a generic drug can submit an abbreviated new drug

application (“ANDA”), which “piggy-back[s] on the brand’s NDA.” See Caraco Pharm. Labs.,

Ltd. v. Novo Nordisk A/S, 566 U.S. 399, 405 (2012) (citing 21 U.S.C. § 355(j)). “Rather than

2 providing independent evidence of safety and efficacy, the typical ANDA shows that the generic

drug has the same active ingredients as, and is biologically equivalent to, the brand-name drug.”

Id.

A second streamlined application option, relevant here, is a 505(b)(2) application. See 21

U.S.C. § 355(b)(2) (codifying Section 505(b)(2) of the FDCA). A 505(b)(2) applicant must

show that its drug meets the “same safety and effectiveness standard[s] as a stand-alone NDA”

(i.e., a 505(b)(1) application). Defs.’ Mem. at 13, ECF No. 30-1. 1 Yet “unlike a stand-alone

NDA, which relies entirely on studies conducted by its applicant, a ‘505(b)(2) application’ may

rely on a combination of the applicant’s own studies and other sources, such as published reports

of studies and the Agency’s findings of safety and/or effectiveness for one or more previously

approved drugs, to meet the approval requirements.” Id. (citing 21 U.S.C. § 355(b)(2)).

FDA regulations outline the 505(b)(2) application process. Within 60 days of an

applicant submitting an NDA, FDA conducts a filing review to make “a threshold determination

that the NDA is sufficiently complete to permit a substantive review.” 21 C.F.R.

§ 314.101(a)(1). This review determines whether the application on its face includes all the

required information, is in the correct form, and whether some other drug’s exclusivity period

blocks approval or submission. Id. § 314.101(a)(1), (d)–(e). If FDA files the application, it

notifies the applicant and a 180-day review period begins to run. Id. § 314.101(a)(2). If,

however, it determines that the application is deficient, the applicant must amend and resubmit

the NDA before FDA will substantively review it. Id. § 314.101(a)(3).

1 All page citations refer to the pagination generated by the Court’s CM/ECF system. Citations to the Joint Appendix, though, use the J.A. pagination assigned by the parties. The Court has cited only the redacted, public versions of the parties’ filings. Nothing in this opinion is taken from redacted portions of the filings, although the Court fully reviewed them in reaching its conclusions.

3 Once FDA files an NDA, it conducts a substantive review of the application to determine

whether it can approve the drug. If, during this review, it “determines that [it] will not approve

the application or abbreviated application in its present form,” it issues a “Complete Response

Letter” (“CRL”). Id. § 314.110(a). This letter describes the NDA’s deficiencies and

“recommend[s] actions that the applicant might take to place the application or abbreviated

application in condition for approval.” Id. An applicant receiving a CRL has three options: it

may (1) “[r]esubmit the application or abbreviated application, addressing all deficiencies

identified in the complete response letter” (which begins a new review cycle period); (2)

“[w]ithdraw the application”; or (3) “[r]equest opportunity for hearing.” Id. § 314.110(b)(1)–(3).

Once FDA determines that an application meets all statutory requirements, it will

approve the NDA and send the applicant an approval letter. Id. § 314.105. Approval of a 505(b)

application—whether an abbreviated or stand-alone NDA—gives the “first-in-time innovator” a

“period of exclusivity.” Otsuka Pharm. Co. v. Price, 869 F.3d 987, 990 (D.C. Cir. 2017) (citing

21 U.S.C. § 355(c)(3)(E)(ii)–(iv)).

The main issue here is the breadth of that exclusivity period.

B.

Doctors have used cocaine hydrochloride (“HCI”) topical solutions in nasal and sinus

surgeries for decades, but FDA had never approved a drug that used it as an active ingredient.

J.A. at 245, ECF No. 52. Beginning in 2008, Lannett began to market an unapproved cocaine

HCI topical solution. Id. at 1075. The next year, Lannett discussed a proposal with FDA to

submit a 505(b)(2) application for its drug. Id. at 607. Meanwhile, in 2013, Genus met with

FDA to discuss developing a similar drug. Id. at 7–8.

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