PATEL v. REATA PHARMACEUTICALS, INC.

CourtDistrict Court, E.D. Texas
DecidedJuly 15, 2021
Docket4:20-cv-00796
StatusUnknown

This text of PATEL v. REATA PHARMACEUTICALS, INC. (PATEL v. REATA PHARMACEUTICALS, INC.) is published on Counsel Stack Legal Research, covering District Court, E.D. Texas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
PATEL v. REATA PHARMACEUTICALS, INC., (E.D. Tex. 2021).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF TEXAS SHERMAN DIVISION

TOSHIF PATEL, Individually and § On Behalf of All Others Similarly § Situated § § v. § CIVIL NO. 4:20-CV-796-SDJ § REATA PHARMACEUTICALS, INC., § ET AL. §

MEMORANDUM OPINION AND ORDER Before the Court are the following competing motions for appointment as lead plaintiff in this proposed securities class action: (1) Motion of Russell Francis, Sr. for Appointment as Lead Plaintiff and Approval of Lead Plaintiff’s Selection of Counsel, (Dkt. #7); (2) Motion of Jason Childs for Appointment as Lead Plaintiff and Approval of His Selection of Counsel, (Dkt. #11); (3) Motion of Waterford Township General Employees Retirement System as Lead Plaintiff and Approval of Selection of Counsel, (Dkt. #13); and (4) Motion of Luke G. Massar for Appointment as Lead Plaintiff and Approval of Lead Counsel, (Dkt. #14). For the following reasons, the Court GRANTS Francis’s motion and DENIES the remaining motions. I. BACKGROUND Defendant Reata Pharmaceuticals, Inc. (“Reata”), headquartered in Plano, Texas, is a “clinical stage biopharmaceutical company that develops novel therapeutics for patients with serious or life-threatening diseases by targeting molecular pathways that regulate cellular metabolism and inflammation.” (Dkt. #1 ¶ 2). In October 2019, Reata was, and currently is, developing a drug called “omaveloxolone,” which was and remains in Phase Two1 clinical development to treat Friedreich’s ataxia (“FA”) within the United States. On October 14, 2019, during

after-market hours, Reata issued a press release announcing positive outcomes from its Phase Two “MOXIe” clinical trial of omaveloxolone. The statement provided, inter alia, that patients treated with the drug experienced a “statistically significant . . . improvement” in their condition and that “[t]he MOXIe trial . . . is the first study to demonstrate a significant improvement in neurological function in patients with FA.” (Dkt. #1 ¶ 21). The press release further indicated that Reata would seek marketing approval for the drug in the United States and internationally.

On August 10, 2020, during pre-market hours, Reata issued a press release that included the company’s second-quarter 2020 financial results and announced that “the FDA is not convinced that the MOXIe Part Two results will support a single study approval” and that Reata would “need to conduct a second pivotal trial that confirms the mFARS results of the MOXIe Part 2 study with a similar magnitude of effect.” (Dkt. #1 ¶¶ 5, 32). On the same day that Reata issued this press release,

Reata’s stock price fell nearly fifty-two dollars per share, or about thirty-three percent. (Dkt. #1 ¶ 33).

1 The FDA administers a five-step process for drug development. The Drug Development Process, U.S. FOOD & DRUG ADMIN., https://www.fda.gov/patients/learn-about- drug-and-device-approvals/drug-development-process (Jan. 4, 2018). “Clinical Research or Development”—the third step in the FDA’s process—in turn has four “phases.” Step 3: Clinical Research, U.S. FOOD & DRUG ADMIN., https://www.fda.gov/patients/drug- development-process/step-3-clinical-research (Jan. 4, 2018). Phase Two involves up to several hundred study participants suffering from the target condition and can last from several months to two years. Id. On October 15, 2020, Plaintiff Toshif Patel initiated this action against Reata, its Chief Executive Officer, J. Warren Huff, and its Chief Financial Officer, Manmeet S. Soni, on behalf of anyone who purchased or otherwise acquired Reata securities

between October 15, 2019, and August 7, 2020 (the “Class Period”). (Dkt. #1 ¶ 1). First, Patel alleges that Defendants, in announcing Reata’s ostensibly positive Phase Two clinical data, made “materially false and misleading statements regarding [Reata’s] business, operational, and compliance policies,” in violation of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 (“the Act”) and Rule 10b-5 promulgated thereunder. (Dkt. #1 ¶¶ 1, 4). Second, Patel claims that Defendants violated the Act by failing to timely disclose that the MOXIe Part Two study results

were insufficient, without additional evidence, to win marketing approval of omaveloxolone for the treatment of FA in the United States. (Dkt. #1 ¶ 4). On October 15, 2020, the same day that Patel filed the Complaint, Patel issued a Private Securities Litigation Reform Act (“PSLRA”) early notice via PRNewswire, a widely circulated national business-oriented wire service. (Dkt. #11 at 5). The notice served to advise other potential class members of the claims alleged in the Complaint

and announced that the deadline for class members to move for appointment as lead plaintiff was December 14, 2020. (Dkt. #8-2). On December 14, 2020, four separate movants sought appointment as lead plaintiff and approval of their respective choice of lead counsel under the PSLRA: Russel Francis, Sr., Jason Childs, Waterford Township General Employees Retirement System (“Retirement System”), and Luke G. Massar. (Dkt. #7, #11, #12, #13). Francis is a New York resident and individual investor with more than twenty-five years of investing experience. (Dkt. #8 at 5). Childs is a Michigan resident and individual investor with over twenty years of investing experience. (Dkt. #11 at 2). Retirement System is an institutional investor

and Michigan-based benefit plan providing benefits to current and former employees of Waterford Township, Michigan. (Dkt. #13 at 6). Massar is an individual investor and Wisconsin resident with thirty years of investing experience. (Dkt. #14-6 ¶ 2). Childs filed a Notice of Non-Opposition, (Dkt. #20), on December 28, 2020, conceding that he did not have the largest financial interest in the relief sought, as required by the PSLRA. See 15 U.S.C. § 78u–4(a)(3)(B)(iii)(I). II. LEGAL STANDARD

The PSLRA outlines the procedure for appointing a lead plaintiff in a private securities action “that is brought as a plaintiff class action pursuant to the Federal Rules of Civil Procedure.” 15 U.S.C. § 78u–4(a)(1). Within twenty days of filing a class action complaint under the PSLRA, the plaintiff(s) must ensure publication of a notice in a widely circulated business publication or wire service. 15 U.S.C. § 78u– 4(a)(3)(A)(i). The publication should advise members of the class of, inter alia: the

claims asserted in the complaint, the relevant class period, and the fact that not later than sixty days after the date of publication, any member of the purported class may move the Court to serve as lead plaintiff. Id. The Court must consider each motion for appointment as lead plaintiff and appoint the movant that is “most capable of adequately representing the interests of class members.” 15 U.S.C. § 78u– 4(a)(3)(B)(i). Under the PSLRA, courts should adopt a presumption that the most adequate plaintiff to represent the class is the person or group of persons that: (1) has filed the complaint or made a timely motion in response to a notice; (2) by the Court’s

determination, has the largest financial interest in the relief sought by the class; and (3) otherwise satisfies the requirements of Rule 23 of the

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Bluebook (online)
PATEL v. REATA PHARMACEUTICALS, INC., Counsel Stack Legal Research, https://law.counselstack.com/opinion/patel-v-reata-pharmaceuticals-inc-txed-2021.