In Re Spero Therapeutics, Inc. Securities Litigation

CourtDistrict Court, E.D. New York
DecidedSeptember 19, 2022
Docket1:22-cv-03125
StatusUnknown

This text of In Re Spero Therapeutics, Inc. Securities Litigation (In Re Spero Therapeutics, Inc. Securities Litigation) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Spero Therapeutics, Inc. Securities Litigation, (E.D.N.Y. 2022).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF NEW YORK -----------------------------------------------------------------------x

IN RE SPERO THERAPEUTICS, INC. MEMORANDUM SECURITIES LITIGATION AND ORDER

22-CV-3125 (LDH) (RLM) 22-CV-4154 (LDH) (RLM)

-----------------------------------------------------------------------x ROANNE L. MANN, UNITED STATES MAGISTRATE JUDGE: Currently pending before this Court is the unopposed motion of Kashif Memon (“Memon”) for appointment as lead plaintiff and approval of lead counsel.1 See generally Motion of Kashif Memon for Consolidation, Appointment as Lead Plaintiff, and Approval of Lead Counsel (July 25, 2022) (“Memon Mot.”), Electronic Case Filing (“ECF”) Docket Entry (“DE”) #9; Memon’s Memorandum of Law in Support of Motion (July 25, 2022) (“Memon Mem.”), DE #9-2. For the following reasons, this Court grants Memon’s motion: Memon is hereby appointed as lead plaintiff and Memon’s choice of counsel—Pomerantz LLP (“Pomerantz”)—is approved as lead counsel.2

1 As discussed infra, another movant—Nabil Saad (“Saad”)—also timely filed a motion to be appointed lead plaintiff. Saad, however, subsequently filed a notice of non-opposition to Memon’s motion. Accordingly, the Court denies Saad’s motion as moot.

2 An order appointing lead plaintiff and approving lead counsel qualifies as a non-dispositive matter under Rule 72(a) of the Federal Rules of Civil Procedure (the “FRCP”), allowing this Court to issue a written order (i.e., a Memorandum and Order), rather than a recommended disposition (i.e., a Report and Recommendation). See Fed. R. Civ. P. 72(a). Multiple courts, including ones in this District, have concluded that such motions are non- dispositive and may be disposed of by a magistrate judge. See, e.g., Darish v. N. Dynasty Mins. Ltd., 20-cv- 5917 (ENV), 2021 WL 1026567, at *1 n.3 (E.D.N.Y. Mar. 17, 2021) (collecting cases). BACKGROUND On May 26, 2022, plaintiff Richard S. Germond (“plaintiff Germond”), who is also represented by Pomerantz, commenced this matter by filing a class action complaint against

Spero Therapeutics, Inc. (“Spero”) and individual defendants Ankit Mahadevia and Satyavrat Shukla, both of whom hold officer-level positions at the company (collectively, “defendants”). See generally Complaint (May 26, 2022) (“Compl.”), DE #1. The Complaint sets forth claims under Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 (the “Exchange Act”), 15 U.S.C. §§ 78j(b), 78t(a), and Rule 10b-5 promulgated thereunder, 17 C.F.R. § 240.10b-5, as amended by the Private Securities Litigation Reform Act of 1995 (the “PSLRA”). See Compl. ¶¶ 10, 42-57. The foregoing claims are asserted on behalf of all putative class

members who purchased or otherwise acquired Spero securities between October 28, 2021 and May 2, 2022, inclusive of both dates (the “Class Period”).3 See id. ¶ 1. Corporate defendant Spero is a “clinical-stage biopharmaceutical company, [which] focuses on identifying, developing, and commercializing treatments for multi-drug resistant . . . bacterial infections and rare diseases in the United States.” Id. ¶ 2. Spero’s “product candidates include Tebipenem Pivoxil Hydrobromide (HBr), an oral carbapenem-class

antibiotic to treat complicated urinary tract infections[.]” Id. According to the Complaint, on October 28, 2021, Spero issued a press release stating that it had submitted a new drug application for the Tebipenem HBr tablets to the U.S. Food and Drug Administration (the

3 On July 15, 2022, Memon also filed a class action complaint in this Court against defendants—styled Memon v. Spero Therapeutics, Inc. et al, 22-cv-4154 (the “Memon Action”)—which alleges substantially the same or similar facts, but asserts an enlarged class period of from May 6, 2021 until May 2, 2022, inclusive of both dates. See Complaint in 22-cv-4154 (July 15, 2022) (the “Memon Complaint”), DE #1; infra note 4. The two cases were subsequently consolidated. See infra note 5. “FDA”). See id. ¶¶ 3, 22-23.4 Subsequently, on November 10, 2021, Spero issued a press release on the Tebipenem HBr tablets and held an earnings call with investors to discuss Spero’s third-quarter 2021 results. See id. ¶¶ 24-25. On January 3, 2022, Spero issued a

second press release announcing, amongst other things, that the FDA had granted priority review designation and accepted the new drug application for said tablets. See id. ¶ 26. The Complaint alleges that the representations made by defendants in the foregoing earnings call and press releases were false and/or misleading because defendants failed to disclose that “the data submitted in support of the [new drug application for] Tebipenem HBr were insufficient to obtain FDA approval” and “accordingly, it was unlikely that the FDA would approve the Tebipenem HBr [new drug application] in its current form[.]” Id. ¶ 27. Defendants also

allegedly failed to disclose that, due to the foregoing issues, Spero would need to significantly reduce its workforce and restructure its operations. See id. On March 31, 2022, Spero issued one of two corrective disclosures in the form of a press release, which revealed that the FDA had “identified deficiencies that preclude[d] discussion of labeling and post-marketing requirements/commitments” for the Tebipenem HBr tablets. Id. ¶ 28. Following this press release, “Spero’s stock price fell $1.59 per share, or

18.27%, to close at $7.11 per share on April 1, 2022.” Id. ¶ 29. Then, on May 3, 2022, Spero announced in a second press release that the FDA had identified “substantive review issues,” and, in light of this feedback, Spero would be “immediately defer[ring] current commercialization activities for [T]ebipenem HBr[.]” Id. ¶ 30. Spero further announced that

4 The Memon Complaint, with its enlarged class period, includes references to a press release issued by Spero on May 6, 2021, which proclaimed that the company was “off to a strong start in 2021” and had “completed a pre- NDA meeting for [T]ebipenem HBr with the FDA.” See Memon Complaint ¶ 23, in 22-cv-4154. it planned to reduce its workforce by approximately 75 percent, restructure its operations to reduce costs, and reallocate resources toward other clinical development programs. See id. On the same day, “Spero’s stock price fell $3.24 per share, or 63.65%, to close at $1.85 per

share[.]” Id. ¶ 31. On July 25, 2022, after the Complaint was filed, Memon and Saad each timely moved to be appointed lead plaintiff in the instant class action.5 See generally Memon Mot., DE #9; Motion of Nabil Saad for Consolidation of Related Actions, Appointment as Lead Plaintiff, and Approval of Lead Counsel (July 25, 2022), DE #6. Memon claims to have suffered $163,918 in financial losses, see Memon Mem. at 2, DE #9-2; Memon Damages Analysis (July 25, 2022) at 6, DE #9-4, whereas Saad purports to have suffered $92,072.53 in financial

losses, see Saad Mem. at 7, DE #7; Saad Loss Chart (July 25, 2022) at 2, DE #8-3. Initially, movant Saad opposed Memon’s motion for appointment as lead plaintiff, raising questions concerning Memon’s financial interest and loss calculation. See generally Saad Opposition to Memon’s Motion (Aug. 8, 2022) (“Saad Opp.”), DE #12. More specifically, Saad asserted that Memon lacks a “bona fide financial interest” in this action because (1) Memon claims “to have sold 5,852 more shares than he certified he owned on June

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