Courter v. CytoDyn Inc

CourtDistrict Court, W.D. Washington
DecidedMarch 3, 2022
Docket3:21-cv-05190
StatusUnknown

This text of Courter v. CytoDyn Inc (Courter v. CytoDyn Inc) is published on Counsel Stack Legal Research, covering District Court, W.D. Washington primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Courter v. CytoDyn Inc, (W.D. Wash. 2022).

Opinion

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5 UNITED STATES DISTRICT COURT 6 WESTERN DISTRICT OF WASHINGTON AT TACOMA 7 BRIAN JOE COURTER, et al., CASE NO. C21-5190 BHS 8 Individually and on Behalf of All Others Similarly Situated, ORDER GRANTING PLAINTIFFS’ 9 MOTION TO PARTIALLY Plaintiffs, MODIFY THE PSLRA 10 v. DISCOVERY STAY 11 CYTODYN, INC., et al., 12 Defendants. 13

This matter comes before the Court on Lead Plaintiff Brian Joe Courter and 14 Courter and Sons LLC and Named Plaintiffs Diane Hooper, Thomas McGee, and Candra 15 Evans’s motion to partially modify the discovery stay imposed by the Private Securities 16 Litigation Reform Act of 1995 (“PSLRA”). Dkt. 90. The Court has considered the 17 briefing filed in support of and in opposition to the motion and the remainder of the file 18 and hereby grants the motion for the reasons stated herein. 19 I. FACTUAL & PROCEDURAL BACKGROUND 20 Plaintiffs filed their amended class action complaint in December 2021, alleging 21 violations of federal securities laws against Defendants CytoDyn, Inc., a publicly-traded 22 1 biotechnology company, and its officers and directors, Nader Pourhassan, Michael 2 Mulholland, and Scott Kelly. Dkt. 83. Specifically they allege that Defendants violated 3 Sections 10(b), 20(a), and 20A of the Securities Exchange Act of 1934 by: (1) making

4 materially false and misleading statements in CytoDyn’s submission to the United States 5 Food and Drug Administration of a Biologics License Application for the use of 6 leronlimab to treat HIV and the use of leronlimab to treat COVID-19; (2) engaging in a 7 scheme to promote leronlimab and the likelihood of FDA approval of its use to treat 8 COVID-19; and (3) selling 7.8 million shares of CytoDyn stock at inflated prices while in

9 possession of material, non-public information. See id. ¶ 1. 10 Plaintiffs allege that Defendants constructed a materially false narrative that 11 leronlimab, CytoDyn’s only drug prospect, was safe and effective for the treatment of 12 COVID-19 and that regulatory approval for treating COVID-19 was imminent. Id. ¶¶ 43, 13 137–38. They assert that Defendants engaged in a stock promotion scheme with these

14 materially false and misleading statements and sold millions of shares of CytoDyn stock. 15 See id. ¶¶ 407–35. Plaintiffs allege that the fraud scheme began to unravel in March 2021 16 when CytoDyn announced disappointing trial results, id. ¶¶ 268–70, 272, and when the 17 FDA issued a public statement on leronlimab, exposing Defendants’ fraud, id. ¶¶ 287–91. 18 On July 30, 2021, CytoDyn disclosed that the Securities and Exchange

19 Commission and Department of Justice were investigating it and its executives. Id. ¶ 295. 20 Specifically, the SEC issued subpoenas “requesting documents and information,” and the 21 DOJ issued subpoenas seeking “testimony and/or records” regarding CytoDyn’s “public 22 statements regarding the use of leronlimab as a potential treatment for COVID-19 and 1 related communications with the FDA, investors, and others and trading in the securities 2 of CytoDyn.” Id. Plaintiffs additionally assert that on January 10, 2022, CytoDyn 3 disclosed that the SEC and DOJ investigations had expanded to include CytoDyn’s

4 statements about the use of leronlimab to treat HIV, litigation involving former 5 employees, and CytoDyn’s retention of investor relations consultants. Dkt. 90 at 8 (citing 6 Dkt. 90-1 at 7). 7 Plaintiffs assert that the SEC and DOJ investigations are related to the fraud they 8 have alleged in their amended complaint. Discovery has been automatically stayed during

9 the pendency of Defendants’ motion to dismiss, Dkt. 95, which will not be ripe for 10 consideration until May 26, 2022, see Dkt. 93. Plaintiffs now move for a partial 11 modification of the discovery stay “to obtain a copy of productions that Defendants have 12 provided or will provide to the SEC and DOJ” in response to the subpoenas described 13 herein. Dkt. 90 at 8. Defendants oppose the motion, arguing in part that there are not

14 exceptional circumstances to warrant partially lifting the stay. Dkt. 91. 15 II. DISCUSSION 16 The PSLRA provides for an automatic stay of discovery “during the pendency of 17 any motion to dismiss” in a private securities fraud action. 15 U.S.C. § 78u-4(b)(3)(B). 18 Congress enacted the discovery stay “to minimize the incentives for plaintiffs to file

19 frivolous securities class actions in the hope either that corporate defendants will settle 20 those actions rather than bear the high cost of discovery . . . or that the plaintiff will find 21 during discovery some sustainable claim not alleged in the complaint.” In re WorldCom, 22 Inc. Sec. Litig., 234 F. Supp. 2d 301, 305 (S.D.N.Y. 2002) (internal citations omitted). 1 However, the statute expressly provides courts with discretion to allow limited discovery 2 during the stay “upon the motion of any party that particularized discovery is necessary to 3 preserve evidence or to prevent undue prejudice to that party.” 15 U.S.C. § 78u-

4 4(b)(3)(B). 5 A. Particularized Discovery 6 Under 15 U.S.C. § 78u-4(b)(3)(B), a discovery request is particularized if “the 7 party seeking discovery under the exception adequately specifies the target of the 8 requested discovery.” In re FirstEnergy Corp. Sec. Litig., No. 2:20-cv-03785, 2021 WL

9 2414763, at *3 (S.D. Ohio June 14, 2021) (internal alteration omitted). Plaintiffs seek the 10 discovery Defendants have provided or will provide to the SEC and DOJ in response to 11 the subpoenas described in CytoDyn’s July 30, 2022 and January 10, 2022 SEC filings. 12 Dkt. 90 at 11–12. They argue that this discovery is particularized because it is “already 13 assembled and produced” and is a “closed universe of materials.” Id. at 11 (quoting In re

14 Delphi Corp. Sec., Derivative & “ERISA” Litig., MDL No. 1725, 2007 WL 518626, at 15 *4 (E.D. Mich. Feb. 15, 2007)). 16 Defendants, in response, argue that Plaintiffs’ request is not sufficiently 17 particularized. Dkt. 91 at 6–7. They assert that Plaintiffs have failed to identify the 18 specific categories or types of documents sought or how the documents sought will be

19 relevant. Id. at 7 (quoting In re Am. Funds Sec. Litig., 493 F. Supp. 2d 1103, 1107 (C.D. 20 Cal. 2007)). 21 However, Defendants fail to engage with Plaintiffs’ cited case law. Courts have 22 regularly held that requests seeking documents produced to regulatory agencies or 1 produced in other proceedings were particularized. See, e.g., In re Royal Ahold N.V. Sec. 2 & ERISA Litig., 220 F.R.D. 246, 250 (D. Md. 2004) (finding particularity in a request 3 describing a “clearly defined universe of documents” produced to governmental,

4 regulatory, or self-regulatory agencies); Pension Tr. Fund for Operating Eng’rs v. 5 Assisted Living Concepts, Inc., 943 F. Supp. 2d 913, 915 (E.D. Wis. 2013) (agreeing that 6 requested discovery was particularized because the request was “limited solely to 7 relevant materials that have already been produced in other proceedings[.]”); In re 8 FirstEnergy Corp. Sec. Litig., No. 20-cv-03785, 2021 WL 2414763, at *3–5 (S.D. Ohio

9 June 14, 2021) (holding that the plaintiff’s “specific request for already-produced 10 discovery is sufficiently particularized.”).

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Related

In Re American Funds Securities Litigation
493 F. Supp. 2d 1103 (C.D. California, 2007)
In Re WorldCom, Inc. Securities Litigation
234 F. Supp. 2d 301 (S.D. New York, 2002)
Perkins v. Thornburgh
10 Cal. 189 (California Supreme Court, 1858)
In re Firstenergy Corp. Securities Litigation
229 F.R.D. 541 (N.D. Ohio, 2004)
Chicago, K. & S. Ry. Co. v. Kindlesparker
234 F. 1 (Sixth Circuit, 1916)

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