Wang v. Ampio Pharmaceuticals, Inc.

CourtDistrict Court, D. Colorado
DecidedAugust 9, 2023
Docket1:22-cv-02105
StatusUnknown

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

Bluebook
Wang v. Ampio Pharmaceuticals, Inc., (D. Colo. 2023).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLORADO Judge William J. Martínez

Civil Action No. 22-cv-2105-WJM-MEH

CHRISTOPHER KAIN, individually and on behalf of all others similarly situated,

Plaintiff, v.

AMPIO PHARMACEUTICALS, INC., MICHAEL A. MARTINO, MICHAEL MACALUSO, and HOLLI CHEREVKA,

Defendants.

ORDER APPOINTING LEAD PLAINTIFF AND APPROVING LEAD COUNSEL

This matter is before the Court on the following motions: • Motion of Tao Wang and SynWorld Technologies Corporation (together, “Wang/SynWorld”) for Appointment as Lead Plaintiffs and Approval of Lead Plaintiffs’ Selection of Lead Counsel (ECF No. 23); • Motion of Lynn Hedeman (“Hedeman”) for Appointment as Lead Plaintiff and Approval of Lead Counsel (ECF No. 19); • Motion of Padme Management Corp. For Appointment As Lead Plaintiff and Approval of Selection of Counsel (ECF No. 18) and the Notice of Non- Opposition of Padme Management Corp. to Competing Lead Plaintiff Motions (ECF No. 28); • Notice of Motion and Motion of Punit Kohli for Appointment as Lead Plaintiff and Approval of Counsel (ECF No. 22) and the Notice of Non- Opposition to Competing Motions for Appointment as Lead Plaintiff and Approval of Counsel (ECF No. 29); and • Movant Matthew Shipley’s Motion for Appointment as Lead Plaintiff and Approval of Selection of Counsel (ECF No. 20) and the Notice of Non-

Opposition to Competing Motions (ECF No. 27). The motions are fully briefed. For the following reasons, the Court appoints Wang/SynWorld as Lead Plaintiffs and Faruqi & Faruqi, LLP (also referred to as “the Faruqi Firm”) as Lead Counsel. I. BACKGROUND1 This is a federal securities class action brought on behalf of all persons that purchased or otherwise acquired Ampio Pharmaceuticals, Inc. (“Ampio” or the “Company”) common stock between December 29, 2020 and August 3, 2022, inclusive (the “Class Period”). (¶ 1.)

Ampio is a biopharmaceutical company purportedly focused on the research, development, and advancement of immunomodulatory therapies for the treatment of pain from osteoarthritis. (¶ 13.) The Company’s lead product candidate, Ampion, purportedly has unique immunomodulatory action and anti-inflammatory effects, which may provide a treatment for individuals with inflammatory conditions including, but not limited to, severe osteoarthritis of the knee (“OAK”), osteoarthritis related to other joints (i.e., hip, shoulder, ankle and hand), and the widespread inflammation associated with COVID-19 infection commonly referred to as “Long-COVID.” (¶¶ 3, 13.)

1 Citations to (¶ __), without more, are references to the Class Action Complaint for Violations of the Federal Securities Laws and Jury Trial Demand (“Complaint”). (ECF No. 1.) From 2010 through approximately March 2022, Ampio conducted numerous clinical trials and analyses to determine Ampion’s efficacy. (¶ 4.) The complaint alleges that Ampio confidently advertised that Ampion demonstrated a statistically significant decrease in pain associated in symptomatic moderate-severe OAK on numerous

occasions. (¶ 4.) However, the Company failed to bring Ampion to market. (¶ 4.) On May 16, 2022, the Company announced that it had formed a special committee of the Ampio Board of Directors (the “Board”) to conduct internal investigations focusing specifically on the statistical analysis of Ampio’s AP-013 clinical trial and unauthorized provision of Ampion which had not yet been approved by the U.S. Food and Drug Administration (“FDA”). (¶ 5.) Then, in pre-market hours on August 3, 2022, Ampio issued a press release containing a letter to stockholders disclosing that the individual Defendants “and senior staff were aware, at the time of the per-protocol interim analysis in March 2020, that the AP-013 trial did not demonstrate efficacy for Ampion on its co-primary endpoints of pain

and function; and that these persons did not fully report the results of the AP-013 trial and the timing of unblinding of data from the AP-013 trial.” (¶ 6.) On this news, the Company’s share price dropped $0.06, or 35.38%, from the previous day’s close, on greater than usual trading volume. (¶ 6.) Plaintiffs allege that as a result of Defendants’ acts and omissions and the precipitous decline in the market value of the Company’s securities, the class members have suffered significant losses and damages. (¶ 7.) On August 17, 2022, Plaintiff Christopher Kain brought this class action against Defendants Ampio Pharmaceuticals, Michael A. Martino, Michael Macaluso, and Holli Cherevka for violations of sections 10(b) and 20(a) of the Securities Exchange Act of 1934 (the “Exchange Act”), 15 U.S.C. §78j(b) and §78t(a), and SEC Rule 10b-5, promulgated thereunder by the SEC, 17 C.F.R. §240.10b-5. (¶¶ 2, 8.) On September 8, 2022, the United States Magistrate Judge stayed this case

pending the appointment of a lead plaintiff and the filing of an amended complaint. (ECF No. 15.) II. LEGAL STANDARD The Private Securities Litigation Reform Act of 1995 (“PSLRA”) sets forth “a procedure that governs the appointment of Lead Plaintiffs in ‘each private action arising under [the Exchange Act] that is brought as a plaintiff class action pursuant to the Federal Rules of Civil Procedure.’” In re Ribozyme Pharm., Inc. Sec. Litig., 192 F.R.D. 656, 657 (D. Colo. 2000) (quoting 15 U.S.C. § 78u-4(a)(1)). Any member of the purported class may move the court to serve as Lead Plaintiff, but must do so within sixty days of the published notice of the potential class action. 15 U.S.C. § 78u-

4(3)(A)(i)(II). The Court must then appoint Lead Plaintiff no later than ninety days after the date the notice is published, or as soon as practicable after the Court has ruled on a motion to consolidate related actions. Id. § 78u-4(3)(B)(i)–(ii). In assigning a Lead Plaintiff, the PSLRA establishes “a rebuttable presumption that the ‘most adequate plaintiff’ is a person or group of persons that (1) either filed the complaint or made a motion in response to a notice, (2) has the largest financial interest in the relief sought, and (3) otherwise satisfies the requirements of Fed. R. Civ. P. 23.” Medina v. Clovis Oncology, Inc., 2016 WL 660133, at *3 (D. Colo. Feb. 18, 2016) (citing 15 U.S.C. § 78u-4(a)(3)(B)(iii)(I)(aa)–(cc)). “As for the requirement that the Lead Plaintiff otherwise satisfy the requirements of Rule 23, only two of the four requirements of Rule 23(a)—typicality and adequacy—impact the analysis of the Lead Plaintiff issue.” Wolfe v. AspenBio Pharma, Inc., 275 F.R.D. 625, 627–28 (D. Colo. 2011). The PSLRA also provides that the Lead Plaintiff “shall, subject to the approval of the court, select

and retain counsel to represent the class.” Id. § 78u-4(3)(B)(v). Accordingly, it is within the Court’s discretion to approve appropriate Lead Counsel. See In re Oppenheimer Rochester Funds Grp. Sec. Litig., 2009 WL 4016635, at *2–3 (D. Colo. Nov. 18, 2009). III. ANALYSIS While there were several motions for appointment as Lead Plaintiff listed above, after the dust settled, only two plaintiffs still vie for appointment as lead plaintiff: Hedeman (ECF No. 19) and Wang/SynWorld (ECF No. 23).

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Related

Wolfe v. Aspenbio Pharma, Inc.
275 F.R.D. 625 (D. Colorado, 2011)

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