Theravectys SA v. Immune Design Corp.

CourtCourt of Chancery of Delaware
DecidedOctober 31, 2014
DocketCA 9950-VCN
StatusPublished

This text of Theravectys SA v. Immune Design Corp. (Theravectys SA v. Immune Design Corp.) is published on Counsel Stack Legal Research, covering Court of Chancery of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Theravectys SA v. Immune Design Corp., (Del. Ct. App. 2014).

Opinion

COURT OF CHANCERY OF THE STATE OF DELAWARE

417 SOUTH STATE STREET JOHN W. NOBLE DOVER, DELAWARE 19901 VICE CHANCELLOR TELEPHONE: (302) 739-4397 FACSIMILE: (302) 739-6179

October 31, 2014

P. Clarkson Collins Jr., Esquire Todd Charles Schiltz, Esquire Morris James LLP Drinker Biddle & Reath LLP 500 Delaware Avenue, Suite 1500 222 Delaware Avenue, Suite 1410 Wilmington, DE 19801 Wilmington, DE 19801

John D. Hendershot, Esquire Richards, Layton & Finger, P.A. 920 North King Street Wilmington, DE 19801

Re: Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN Date Submitted: October 28, 2014

Dear Counsel:

Non-Party Novasep Inc. (“Novasep US”) has moved for a protective order

pursuant to Court of Chancery Rule 26(c). Its motion arises in the context of

litigation between Plaintiff Theravectys SA (“TVS”)1 and Defendant Immune

Design Corporation (“IDC”). TVS’s claims against IDC derive from Henogen 1 TVS has filed a Cross-Motion to Compel that deals with the same issues as Novasep US’s Motion for a Protective Order. This letter opinion addresses arguments raised in both motions and is dispositive as to both. Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN October 31, 2014 Page 2

SA’s (“Henogen”) manufacture of antiviral vectors for IDC, in violation of a

services contract between Henogen and TVS.2 TVS alleges tortious interference,

unfair competition, misappropriation of trade secrets, and unjust enrichment, and

seeks to establish that IDC knowingly induced Henogen to breach its contract with

TVS and/or that IDC intentionally used TVS’s confidential and proprietary

information.

In its efforts to establish its case, TVS served Novasep US, a corporate

affiliate of Henogen, with discovery requests. Novasep US and Henogen, neither

of which is a party to this litigation, share a corporate parent, Novasep Holdings

S.A.S. (“Novasep S.A.S.”), which is headquartered in France. Novasep US is

based in Pennsylvania and serves as the American sales and marketing force for its

foreign affiliates, including Henogen. Based in Belgium, Henogen is a contract

manufacturing organization specializing in the development and production of

2 “Lentiviral vectors are gene transfer vectors derived from HIV, able to integrate the genome of dividing and non-dividing cells, allowing a stable expression of transgene in host cells and serve as biological instruments to treat or prevent all pathologies. In prophylactic and therapeutic vaccination settings, lentiviral vectors are used to induce an antigen-specific immune response to fight infectious diseases and cancers.” Compl. ¶ 5. Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN October 31, 2014 Page 3

biomolecules for third parties. Novasep US markets Henogen’s services to

American clients, but generally ceases its interaction with a client after the client

signs an initial contract with Henogen.

Novasep US’s involvement in the events underlying the TVS-IDC litigation

was limited to marketing communications with IDC before IDC and Henogen

entered into the Master Agreement for Development & Manufacturing Services on

April 27, 2012 (the “Manufacturing Agreement”). After the Manufacturing

Agreement was signed, all products created for IDC were manufactured, tested,

and shipped to IDC by Henogen.

I. TVS’S DISCOVERY REQUESTS

Novasep US objects to TVS’s requests for documents related to (i) the

manufacture and testing of the lentiviral vectors for IDC, (ii) the shipment of those

vectors to IDC, (iii) the negotiation and formation of the Manufacturing

Agreement, (iv) the litigation between TVS and IDC, and (v) Novasep US’s

corporate structure and relationships with its affiliates.

Novasep US argues that documents related to the manufacture, testing, and

shipment of the lentiviral vectors (the “Foreign Affiliate Documents”) are outside Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN October 31, 2014 Page 4

of its possession, custody, or control. It was not involved in these processes and

the Foreign Affiliate Documents are possessed and controlled by Henogen and

Novasep US’s other European affiliates.

Novasep US contends that even if it controlled the Foreign Affiliate

Documents, French and Belgian laws prevent their production. Further, Novasep

US argues that none of the categories of documents that it resists producing is

relevant to TVS’s claims, and their production would be unduly burdensome.

As explained below, TVS has not established Novasep US’s control over the

Foreign Affiliate Documents or any documents related to agreements between

Henogen and IDC to cooperate with respect to litigating against TVS.

Accordingly, Novasep US need not produce those documents. However, to the

extent that Novasep US controls documents responsive to TVS’s remaining

requests, Novasep US will produce them.

A. There is Insufficient Evidence That Novasep US Controls the Foreign Affiliate Documents

Court of Chancery Rule 34(a) provides that a party may only request

documents “which are in the possession, custody or control of the party upon Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN October 31, 2014 Page 5

whom the request is served.”3 The Foreign Affiliate Documents are not in

Novasep US’s possession or custody. However, TVS argues that Novasep US has

“control” over those documents.

“In the Rule 34 context, [c]ontrol has been defined to include the legal right

to obtain the documents requested upon demand. Thus, the key inquiry is whether

the company has the power, unaided by the court, to force production of the

documents.”4 Both state and federal courts in Delaware “decline[] to apply a

broader definition of ‘control’ that would also include an inquiry into the practical

ability of the subpoenaed party to obtain documents.”5 Separate corporate

identities are generally respected “except in rare circumstances justifying the

application of the alter ego doctrine to pierce the corporate veil of the subsidiary.” 6

3 Ct. Ch. R. 34(a). 4 Deephaven Risk Arb Trading Ltd. v. UnitedGlobalCom, Inc., 2005 WL 1713067, at *11 (Del. Ch. July 13, 2005) (alteration in original) (internal quotation marks omitted). 5 Cradle IP LLC v. Tex. Instruments, Inc., 2013 WL 1794992, at *1 (D. Del. Apr. 29, 2013). 6 Id. Theravectys SA v. Immune Design Corp. C.A. No. 9950-VCN October 31, 2014 Page 6

The alter ego doctrine typically only applies when the use of “the corporate form in

and of itself operates to serve some fraud or injustice.”7

The strongest pieces of evidence supporting an application of the alter ego

doctrine are (i) the Mutual Confidential Disclosure Agreement between IDC and

Novasep US, signed January 9, 2012 (the “CDA”), and (ii) the Cooperation

Agreement between Henogen (and its group companies) and IDC, dated

February 13, 2014 (the “Cooperation Agreement”).

Novasep US entered into the CDA “acting on its own name and behalf and

on the name and behalf of its ‘Affiliates.’”8 The CDA defines Affiliates to include

Henogen, as well as Novasep US’s French parent, Novasep S.A.S. TVS argues

that Novasep US’s ability to bind its affiliates shows that the entities are

intertwined and that Novasep US exercises control.

The CDA was entered into in contemplation of a potential business

relationship between Henogen and IDC. As Henogen’s marketing agent in the

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