Malkoff v. Sequenom, Inc.

District Court, S.D. California·Decided July 27, 2023·No. 3:16-cv-02054·Unknown

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF CALIFORNIA

In re SEQUENOM, INC. Lead Case No. 16-cv-02054-JAH-DDL STOCKHOLDER LITIGATION

ORDER GRANTING DEFENDANTS’ This Document Relates To: AMENDED MOTION TO DISMISS ALL ACTIONS.

INTRODUCTION In this shareholder class action lawsuit, Plaintiffs allege that Defendant Sequenom, Inc. and seven of its former board members (“Defendants”) violated Sections 14(e) and 20(a) of the Securities Exchange Act of 1934 (“Exchange Act”) by issuing a false and misleading recommendation statement advising Sequenom shareholders to tender their shares pursuant to a tender offer. Pls.’ Consolidated Amended Class Action Complaint (“AC”), Doc. No. 54.1 Specifically, Plaintiffs allege that Defendants relied on a lower set of financial projections (and excluded

1 Those seven individuals are Kenneth F. Buechler, Myla Lai-Goldman, Ronald M. Lindsay, Catherine J. Mackey, David Pendarvis, Charles P. Slacik. and Dirk van den Boom (collectively, “Individual Defendants”). The parties stipulated to the dismissal of claims against Richard A. an oncology program) as the most accurate view of the company’s prospects, and therefore misled Plaintiffs concerning the fairness of Laboratory Corporation of America Holding’s (“LabCorp”) tender offer. Pending before the Court is Defendants’ Amended Motion to Dismiss (“Mot.”) and Request for Judicial Notice (“RJN”). Doc. Nos. 123, 124. Plaintiffs opposed both. Doc. No. 126 (“Opp’n”); Doc. No. 127 (“Opp’n to RJN”). Defendants filed replies. Doc. No. 132 (“Reply”), Doc. No. 133 (“Reply to RJN”). The motion is fully briefed. The Court found this motion suitable for determination on the papers submitted and without oral argument. Civ. LR 7.1(d.1). For the reasons set forth below, the Court GRANTS Defendants’ Amended Motion to Dismiss and DISMISSES the Amended Complaint without prejudice. Sequenom was a molecular diagnostic testing and genetics analysis company. AC ¶ 2. In 2011, it launched the first noninvasive prenatal test (“NIPT”) in the United States that could screen pregnant women for Down syndrome and other chromosomal abnormalities through a blood test. Id. ¶ 39. Sequenom subsequently expanded this test (“MaterniT21 PLUS”) to detect a myriad of additional fetal chromosomal abnormalities. Id. ¶ 40. Sequenom had a “breakout year” in 2014. Id. at 8. The company sold its Bioscience segment to focus exclusively on its NIPT business and launched a new, lower cost NIPT called VisibiliT, which targeted women with average-risk pregnancies, in the international market. Id. ¶¶ 44, 48. Sequenom planned to sell VisibiliT in the United States market in 2015. Id. ¶ 49. Sequenom also entered into several agreements with other companies. In June 2014, Quest Diagnostics Inc. agreed to exclusively offer the MaterniT21 PLUS test to its network in exchange for access to Sequenom’s NIPT patents. Id. ¶¶ 45–46. Under this agreement, Quest could develop its own NIPT so long as it paid Sequenom licensing and royalty fees per test. Id. In December 2014, Sequenom entered into a pooled patents agreement with Illumina, Inc. as part of the settlement of a protracted lawsuit in which Illumina sued Sequenom for patent infringement. Id. ¶ 51. Among the terms of the agreement, Sequenom and Illumina would pool together their patents. Id. Illumina had the right to use the patent pool to develop its own NIPT kits and could also license the patents in the pool to other labs. Id. In exchange, Sequenom would receive licensee fees and royalties, as well as a lump sum payment from Illumina of $50 million upfront and at least $80 million by 2020. Id. Sequenom had a “transition year” in 2015. Id. at 11. The company launched several new tests, including VisibiliT (mentioned above), HerediT Universal (a carrier screening test), and MaterniT GENOME (a test that could analyze every chromosome). Id. ¶¶ 62, 68, 80, 118. The company cautioned investors that it expected short-term revenue loss as customers increasingly converted to licensees, but reaffirmed the company’s long-term growth potential. See, e.g., id. ¶¶ 63, 70, 79. For example, Sequenom told investors that the patent pool was growing; that it expected major growth for MaterniT GENOME; and that there was significant long- term value in the average risk market, which was significantly bigger than the high- risk market. Id. ¶ 86, 125. At a presentation to investors and analysts on September 28, 2015, one of Sequenom’s slides indicated “[o]ver $500M [in] revenues by 2020.” Ex. 10 to Mot. at 17, Doc. No. 123-12. Meanwhile, Sequenom’s financial reports for this period reflected consistently negative revenue growth. See AC ¶ 70 (2015 Q1), ¶ 77 (2015 Q2), ¶ 105 (2015 Q3), ¶ 123 (2015 Q4), ¶ 132 (2016 Q1). By the time Sequenom held its full-year 2015 earnings call, its stock was trading at $1.45 per share, down from $3.83 at the beginning of 2015. Ex. 22 to Mot. at 10–16, Doc. No. 123-24. Sequenom also decided to expand its business into the field of oncology. AC ¶¶ 57–59. In 2015, the company began a process to develop liquid biopsy oncology tests that could detect tumor cells from a blood test. Id. This involved “building a clinical foundation” and engaging medical leaders to develop a test that could eventually be submitted for validation. Id. ¶ 58. Although the process was at its early stages, Sequenom told the public that it expected long-term value for the oncology program, given that this market size was significantly higher than that of NIPT. Id. Sequenom’s Board also began taking actions to address its $130 million convertible debt, which was due in 2017 and 2018. Id. ¶ 75. The Board engaged J.P. Morgan Securities LLC (“JPM”) as its financial advisor to explore refinancing opportunities as well as opportunities for “spinning off” Sequenom’s oncology program. Id. ¶ 76, 82, 88. JPM reached out to approximately twenty-five parties and entered into confidentiality agreements with four companies, one of which was LabCorp. Schedule 14D-9, Sequenom, Inc. (“Rec.”) at 13–14, Ex. 16 to Mot., Doc. No. 123-18. By the end of the 2015, LabCorp and a few other companies had made offers to acquire all of Sequenom. Id. at 14–15; AC ¶ 108. But the Board instructed Sequenom management and JPM to not pursue any proposals for a sale of Sequenom because it wanted to eliminate its $130 million convertible debt overhang and focus on operations as a stand-alone business. AC ¶ 108. At the start of 2016, Sequenom announced a restructuring plan. Id. ¶ 116. This included reducing its workforce by approximately 20%, closing its North Carolina lab, and seeking to partner its oncology program while reducing research and development in that area. Rec. at 15–16; AC ¶ 116. In response to this news, over twenty companies expressed interest in the oncology program. Six of these companies signed confidentiality agreements and engaged in due diligence review over the period of five months. Id. ¶ 117. In the end, however, none of these parties submitted a licensing, partnering, or acquisition proposal. Amendment No. 6 to Schedule 14D-9, Sequenom, Inc. (“Am.”) at 4, Ex. 17 to Mot., Doc. No. 123-19.2 Sequenom continued to explore refinancing opportunities. AC ¶ 136. In May 2016, the CEO of LabCorp contacted Sequenom’s CEO to express interest in a potential transaction. Id. ¶ 137. On June 7, 2016, Sequenom received a proposal from a debt source for a proposed senior secured loan for up to $150 million. Id. ¶ 140. The next day, the Board asked JPM to contact companies interested in Sequenom and offer a price per share in the $3.00 range. Rec. at 17. Based on interest from LabCorp and two other companies, Sequenom opened a virtual data room with preliminary due diligence information. Id. at 18. The Board met on June 15 and 16, 2016. Sequenom management presented the Board the following revenue projections for its oncology program (“Oncology Projections”): $0 (2016), $5 million (2017), $20 m

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Malkoff v. Sequenom, Inc., (S.D. Cal. 2023).

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