Jubilant Draximage Inc. v. United States International Trade Commission

CourtDistrict Court, District of Columbia
DecidedJuly 10, 2019
DocketCivil Action No. 2019-1494
StatusPublished

This text of Jubilant Draximage Inc. v. United States International Trade Commission (Jubilant Draximage Inc. v. United States International Trade Commission) 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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Jubilant Draximage Inc. v. United States International Trade Commission, (D.D.C. 2019).

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

JUBILANT DRAXIMAGE INC.,

Plaintiff,

v. Civil Action No. 19-1494 (RDM) UNITED STATES INTERNATIONAL TRADE COMMISSION,

Defendant.

MEMORANDUM OPINION AND ORDER

Plaintiff Jubilant DraxImage Inc. (“JDI”) manufactures a Rubidium Elution System

(“RUBY”), one of only two medical devices used for Cardiac Positron Emission Tomography, a

non-invasive imaging procedure designed to evaluate patients for coronary artery disease. JDI’s

principal—indeed only—competitor in this specialized field is Bracco Diagnostics Inc.

(“Bracco”), a company manufacturing a similar device. JDI is currently in proceedings before

the United States International Trade Commission (“the Commission”) addressing whether JDI’s

RUBY technology infringes on a series of Bracco’s patents. In the course of those proceedings,

the Commission ordered JDI publicly to disclose portions of its briefs, all of which were filed

under seal. JDI objects to making public those portions of its briefs that cite or reference

Bracco’s patent claims. The reason? Revealing the specific Bracco claim elements at issue

would, according to JDI, allow Bracco to modify or remove the very claim elements that make

JDI’s products non-infringing. In other words, Bracco could use JDI’s references to particular

portions of Bracco’s lengthy patent claims, which are public, to infer the manner in which JDI

has attempted to engineer around Bracco’s patents, which is not public. JDI seeks a preliminary

1 injunction to prohibit the Commission from enforcing its disclosure order. As explained below,

JDI has demonstrated that it is entitled to preliminary relief. The Court will therefore GRANT

the motion for a preliminary injunction.

I. BACKGROUND

JDI is a radiopharmaceutical company based in Kirkland, Canada. Dkt. 1 at 3 (Compl.

¶ 7). Among other things, JDI markets a medical device named RUBY, an elution system that

generates Rubidium-82 Chloride, a chemical used for Cardiac Positron Emission Tomography, a

non-invasive imaging procedure used to evaluate regional myocardial perfusion in adult patients

with suspected or existing coronary artery disease. Id. at 4 (Compl. ¶ 11). The Food and Drug

Administration (“FDA”) first approved RUBY in 2016. Id. (Compl. ¶ 12). As soon as the FDA

approved JDI’s device, Bracco submitted a FOIA request to the FDA and obtained a RUBY

product manual from the agency. Id. (Compl. ¶ 13). Bracco was able to claim priority to earlier-

filed patent applications and, between September and November 2017, Bracco used information

in the product manual to seek and to obtain three continuation patents crafted to claim the

technology found in the RUBY product. Id. at 4–5 (Compl. ¶ 13). As soon as those patents

issued, Bracco filed a complaint with the Commission, alleging violations of Section 337 of the

Tariff Act of 1930, 19 U.S.C. § 1337. Id. at 5 (Compl. ¶ 14). The Commission instituted the

current investigation in May 2018. Id.

In response to Bracco’s complaint with the Commission, JDI created two new versions of

RUBY “specifically designed to avoid infringement of Bracco’s three patents”—Versions 3.1

and 4. Id. (Compl. ¶ 17). In proceedings before the Commission, JDI attempted to show that

these new versions did not infringe Bracco’s existing patents. JDI filed a motion for summary

determination (“MSD”)—the equivalent of a summary judgment motion—which compared the

2 technology behind Versions 3.1 and 4 against Bracco’s patent claims. Id. at 6 (Compl. ¶ 21); see

also Dkt. 4-5 at 15–56 (Ex. 1 to Confidential Ex. E). To show that the new versions did not

infringe Bracco’s patents, JDI quoted specific portions of—and highlighted key terms in—

Bracco’s lengthy patent claims. Dkt. 4-5 at 24–27. “Because the emphasized claim limitations

identif[ied] the specific features of the RUBY product that were redesigned,” JDI feared that, if

made aware of the precise claim elements that JDI had designed around, Bracco would file yet

another set of continuation patents in an effort to exclude the new designs utilized in Versions

3.1 and 4. Dkt. 1 at 6–7 (Compl. ¶¶ 23–24). JDI, accordingly, treated all references to Bracco’s

claim elements as “confidential business information” pursuant to Commission regulations and

“redacted the portions of its [briefs] discussing, quoting, and emphasizing these limitations of

Bracco’s patent claims in the public version of its brief.” Dkt. 1 at 6 (Compl. ¶ 23). JDI did this

in four portions of its brief: the background sections for Versions 3.1 and 4, which list the

particular claim elements at issue, and in the merits sections for Versions 3.1 and 4, which argue

that the new designs do not infringe the identified claim elements.

Commission staff attorneys objected to a number of JDI’s redactions and filed a motion

to declassify portions of JDI’s brief. See Dkt. 4-1 (Confidential Ex. A). Specifically, the

Commission staff argued that “passages quoting from [Bracco’s] patents or descriptions of the

scope of patents and claims do not fall within the Commission’s definition of confidential

business information” and that, “unless the sentence explicitly describes the specific aspects of

the RUBY Version 3.1 and Version 4 systems, any quotation from or discussion of the asserted

[Bracco] patents should not be redacted.” Id. at 4–5. JDI opposed the motion, arguing that

“[a]ny patent attorney reading a brief seeking a determination of noninfringement that provides a

background overview of specific claim limitations would readily recognize that those claim

3 limitations form the basis for why the confidential products do not infringe” and that, “for

example,” one of Bracco’s limitations “concerns a binary design option.” Dkt. 4-2 at 11

(Confidential Ex. B). Reviewing a proposed, redacted brief provided by Commission staff,

moreover, JDI compared redactions approved by the Commission staff to those rejected and

argued that “there is no real difference between the redacted passages reproduced below that the

Staff seeks to reclassify. . . and those it has approved.” Id. at 12–13.

On March 21, 2019, a Commission Administrative Law Judge (“ALJ”) issued Order No.

31, “Initial Determination Granting-in-Part Commission Investigative Staff’s Motion to

Declassify Portions of Respondents’ Motion for Summary Determination.” Dkt. 4-3

(Confidential Ex. C). The Order explained that “confidentiality determinations . . . are governed

by the definition given in 19 C.F.R. § 201.6(a).” Id. at 4. That definition, according to the ALJ,

mandates a “two-part test.” Id. First, the ALJ “asks whether the contested information ‘concerns

or relates to the trade secrets, processes, operations, style of works, or apparatus, or to the

production, sales, shipments, purchases, transfers, identification of customers, inventories, or

amount or source of any income, profits, losses or expenditures of any person, firm, partnership,

corporation, or other organization, or other information of commercial value.’” Id. at 3 (citation

omitted) (quoting 19 C.F.R. § 201.6(a)).

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