Filbert v. REATA PHARMACEUTICALS, INC. <b><font color="red">PURSUANT TO COURT ORDER, DOCKET ONLY IN LEAD CASE 4:21cv987</font></b>

CourtDistrict Court, E.D. Texas
DecidedApril 22, 2022
Docket4:22-cv-00012
StatusUnknown

This text of Filbert v. REATA PHARMACEUTICALS, INC. <b><font color="red">PURSUANT TO COURT ORDER, DOCKET ONLY IN LEAD CASE 4:21cv987</font></b> (Filbert v. REATA PHARMACEUTICALS, INC. <b><font color="red">PURSUANT TO COURT ORDER, DOCKET ONLY IN LEAD CASE 4:21cv987</font></b>) 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.

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Filbert v. REATA PHARMACEUTICALS, INC. <b><font color="red">PURSUANT TO COURT ORDER, DOCKET ONLY IN LEAD CASE 4:21cv987</font></b>, (E.D. Tex. 2022).

Opinion

United States District Court EASTERN DISTRICT OF TEXAS SHERMAN DIVISION

TIM DOYLE, Individually and on Behalf § of All Others Similarly Situated, § § Plaintiff, § Civil Action No. 4:21-CV-00987 § MATTHEW FILBERT, Individually and § on Behalf of All Others Similarly Situated, § § Plaintiff, § Civil Action No. 4:22-CV-00012 § LABORERS’ DISTRICT COUNCIL and § CONTRACTORS’ PENSION FUND OF § OHIO, Individually and on Behalf of All § Others Similarly Situated, § § Plaintiff, § Civil Action No. 4:22-CV-00041 § v. § § REATA PHARMACEUTICALS, INC., § J. WARREN HUFF, MANMEET S. § SONI, and COLIN J. MEYER, § § Defendants. §

MEMORANDUM OPINION AND ORDER

Pending before the Court are several competing motions to consolidate, motions to be appointed lead plaintiffs, and motions for approval of lead plaintiffs’ selection of lead and liaison counsel (Dkts. #19, #20, #21, and #22 in Case No. 4:21-CV-00987; Dkts. #4, #5, and #10 in Case No. 4:22-CV-00012; Dkts. #13, #14, and #19 in Case No. 4:22-CV-00041) filed in the above- captioned cases. Pursuant to 15 U.S.C. § 78u–4(a)(3)(B)(ii) of the Securities Exchange Act of 1934 (the “Exchange Act”), as amended by the Private Securities Litigation Reform Act of 1995 (the “PLSRA”), this order addresses solely the issue of consolidation, and the Court reserves ruling on the appointment of lead plaintiffs and approval of selection of lead counsel and liaison counsel for a subsequent order. Consolidation is sought in each of the above lawsuits by the following plaintiffs and movants:

• Donald Potts (“Potts”), filed on February 19, 2022 (Dkt. #19 in Case No. 4:21-CV-00987).

• UMC Benefit Board, Inc.; US Equity Fund-P Series, a series of the Wespath Funds Trust; US Equity Index Fund-P Series, a series of the Wespath Funds Trust; Wespath Institutional Investments LLC; US Equity Fund-I Series, a series of the Wespath Funds Trust; and US Equity Index Fund-I Series, a series of the Wespath Funds Trust (collectively, “Wespath”), filed on February 18, 2022 (Dkt. #20 in Case No. 4:21-CV-00987) and March 21, 2022 (Dkt. #20 in Case No. 4:22-CV-00012; Dkt. #19 in Case No. 4:22-CV-00041).

• Laborers’ District Council; Contractors’ Pension Funds of Ohio; International Union of Operating Engineers, Local No. 793; Members Pension Benefit Trust of Ontario; and IBEW Local 353 Pension Plan (collectively, the “Labor Funds”), filed on February 18, 2022 (Dkt. #21 in Case No. 4:21-CV-00987; Dkt. #4 in Case No. 4:22-CV-00012; Dkt. #13 in Case No. 4:22-CV-00041).

• Duane Olcsvary (“Olscvary”), filed on February 23, 2022 (Dkt. #22 in Case No. 4:21-CV-987; Dkt. #5 in Case No. 4:22-CV-00012; Dkt. #14 in Case No. 4:22- CV-00041).

Having reviewed the motions and responses on the issue of consolidation, the Court finds that the motions should be GRANTED. BACKGROUND On March 1, 2021, Defendant Reata Pharmaceuticals, Inc. (“Reata”) announced that it had submitted a New Drug Application to the U.S. Food and Drug Administration (“FDA”) for bardoxolone methyl (“bardoxolone”). If approved, bardoxolone would become “the first therapy specifically indicated for treatment of [chronic kidney disease] caused by Alport’s syndrome” (Dkt. #1 at ¶ 25).1 But on December 8, 2021, the FDA’s Advisory Committee unanimously voted against approval of Reata’s application. The denial came as a shock to Reata’s investors. Back in November of 2016, “Reata told investors during an earnings conference call that ‘we have received clear guidance from [the] FDA

about requirements for approval of bardoxolone [ ] in Alport syndrome’” (Dkt. #22, Exhibit 1 at p. 8). Then in November of 2020, Reata announced that the results of a multi-year study on the efficacy of bardoxolone were “positive,” and “represent[ed] the first time that an investigational medicine ha[d] shown a significant clinical benefit in [chronic kidney] disease” (Dkt. #1 at ¶ 20). As far as investors were aware, bardoxolone worked—“the data” provided by Reata “suggest[ed] that bardoxolone treatment ha[d] beneficial long-term effects on kidney function in patients with Alport syndrome” (Dkt. #1 at ¶ 26). The bigger shock, however, was revealed within FDA briefing documents released on December 6, 2021. In stark contrast to Reata’s prior representations, investors discovered that the FDA “had repeatedly voiced concerns about the validity of the study design—specifically, that

bardoxolone’s pharmacodynamic effect on kidney function would make it difficult to assess the effectiveness of the drug” (Dkt. #22, Exhibit 1 at pp. 8–9). As a result, the FDA “did not believe that the data demonstrated that bardoxolone was effective in slowing the loss of kidney function in patients with Alport syndrome or in reducing the risk of progression to kidney failure” (Dkt. #22, Exhibit 1 at p. 8). The documents further revealed that these concerns were communicated to Reata as early as March 1, 2021. Yet, Reata never attempted to relay these concerns to its investors. Relying on Reata’s representations, investors bought and acquired millions in Reata shares and securities. Wespath “purchased 114,030 Reata shares . . . with a total [ ] expenditure of

1 Unless otherwise noted, all citations to the docket within the Background section come from filings in the first-filed case, Case No. 4:21-CV-00987. $17,184,758.77” (Dkt. #20, at p. 12); Potts and the Labor Funds purchased 12,000 and 12,289 shares of Reata common stock, respectively (Dkt. #19 at p. 3; Dkt. #21 at p. 6); and Olcsvary invested thousands in Reata securities (Dkt. #22, Exhibit 1 at p. 12). Reata’s initial share price on November 10, 2020 closed at $184.62 per share. But after the FDA released its briefing documents,

“Reata’s stock price plummeted 37%, falling from $78.69 per share to close at $48.92 per share, on unusually heavy trading volume” (Dkt. #21 at p. 9). Then, when the FDA denied Reata’s application, shares fell even further “to close at $29.11 per share—down more than 63% from the opening of trading on December 6, 2021,” just 48 hours earlier (Dkt. #21 at p. 9). As a result, millions invested in Reata was now lost, and the value of Reata’s shares mere paperweight in comparison to their once respected high. Wespath’s losses alone totaled over $10,279,158.72 (Dkt. #20 at p. 12). The Labor Funds “incurred losses of over $662,000” (Dkt. #21 at p. 6), Potts “over $558,766 in losses” (Dkt. #19 at p. 3), and Olcsvary over “$164,171 . . . on his [ ] transactions in Reata securities” (Dkt. #22, Exhibit 1 at p. 12). Beginning on December 20, 2021, investors filed several class action lawsuits against

Reata; Reata’s Chief Executive Officer, J. Warren Huff (“Huff”); Reata’s Chief Financial Officer Manmeet S. Soni (“Soni”); and Reata’s Chief Medical Officer, President, and Chairman of the Board, Colin J. Meyer (“Meyer”).2 Three lawsuits are relevant to the present motion: 4:21-CV- 987 filed on December 20, 2021 (the “Doyle action”); 4:22-CV-12 filed on January 7, 2022 (the “Filbert action”); and 4:22-CV-41 filed on January 20, 2022 (the “Laborers’ action”). Each lawsuit alleges the same material facts and allegations—that all Defendants violated § 10(b) of the Exchange Act, and Rule 10b-5 promulgated thereunder; and that individual defendants violated § 20(a) of the Exchange Act. The Doyle and Filbert actions allege the relevant class period as

2 As defined below, the Doyle and Filbert actions brought suit against Defendants Reata, Huff, and Soni, and the Laborers’ action brought suit against Defendants Reata, Huff, and Meyer. between November 9, 2020 and December 8, 2021, and the Laborers’ action alleges the relevant class period as between November 14, 2016 and December 6, 2021.

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Filbert v. REATA PHARMACEUTICALS, INC. <b><font color="red">PURSUANT TO COURT ORDER, DOCKET ONLY IN LEAD CASE 4:21cv987</font></b>, Counsel Stack Legal Research, https://law.counselstack.com/opinion/filbert-v-reata-pharmaceuticals-inc-bfont-colorredpursuant-to-txed-2022.