Pacheco v. Guyer

CourtDistrict Court, S.D. New York
DecidedSeptember 19, 2019
Docket1:18-cv-07999
StatusUnknown

This text of Pacheco v. Guyer (Pacheco v. Guyer) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Pacheco v. Guyer, (S.D.N.Y. 2019).

Opinion

UNITED STATES DISTRICT COURT USDC SDNY SOUTHERN DISTRICT OF NEW YORK DOCUMENT Horrors nnn cera nanan ELECTRONICALLY FILED . DOC# LUIS PACHECO, Derivatively on Behalfof □□ DATE FILED: _9/19/2019 Ophthotech Corporation, : Plaintiff, : No. 18-cv-7999 (VSB) - against - : OPINION & ORDER DAVID R. GUYER, GLENN P. : SBLENDORIO, DAVID E. REDLICK, : THOMAS DYRBERG, AXEL BOLTE, : MICHAEL J. ROSS, SAMIR C. PATEL, and: NICHOLAS GALAKATOS, : Defendants. :

Appearances: Thomas G. Amon Law Office of Thomas G. Amon New York, New York Counsel for Plaintiff Jeremy Todd Adler (New York, New York) Michael G. Bongiorno (New York, New York) Timothy J. Perla (Boston, Massachusetts) Wilmer Cutler Pickering Hale & Dorr LLP Counsel for Defendants VERNON S. BRODERICK, United States District Judge: Shareholder plaintiff Luis Pacheco, derivatively on behalf of Ophthotech Corporation, brings this action against eight current and former Ophthotech directors and officers for breach of fiduciary duty, unjust enrichment, and waste of corporate assets. Before me is Defendants’ motion to dismiss the derivative complaint based upon Plaintiff's failure to make a demand on Ophthotech’s Board of Directors (the “Board”) before filing suit. Because I find that Plaintiff

has alleged particularized facts demonstrating that demand would have been futile, Defendants’ motion to dismiss is DENIED. Background1 A. The Parties

Ophthotech is a biopharmaceutical company incorporated under Delaware law, which has its “principal executive offices [] at One Penn Plaza, 35th Floor, New York, New York.” (Compl. ¶¶ 2, 15.) Plaintiff Luis Pacheco, a Florida resident, was an Ophthotech stockholder during the period of the wrongdoing complained of (March 2, 2015 through December 12, 2016 (the “Relevant Period”)), and has continued to hold Ophthotech stock as of the filing of the Complaint. (Id. ¶ 14.) Defendants are six current members of the Ophthotech Board of Directors2 (“Ophthotech Board” or “Board”) and two former members of the Board.3 (Id. ¶¶ 16–23.) At the time the Complaint was filed in August 2018, Ophthotech’s Board was comprised of seven directors— Defendants Guyer, Sblendorio, Redlick, Dyrberg, Bolte, and Ross, as well as Jane Pritchett

Henderson, the only director not named as a defendant in this action. (Id. ¶ 101.) Defendant David R. Guyer co-founded Ophthotech in 2007 and served as Chief Executive Officer (“CEO”) and Chairman of the Board until July 2017; since July 2017, he has served as Executive Chairman. (Id. ¶ 16.) Defendant Guyer is also a defendant in a related consolidated securities

1 The following factual summary is drawn from the allegations contained in the Verified Stockholder Derivative Complaint for Breach of Fiduciary Duty, Waste of Corporate Assets, and Unjust Enrichment, (“Complaint” or “Compl.”), filed August 31, 2018. (Doc. 1.) I assume the allegations set forth in the Complaint to be true for purposes of this motion. See Kassner v. 2nd Ave. Delicatessen Inc., 496 F.3d 229, 237 (2d Cir. 2007). My references to these allegations should not be construed as a finding as to their veracity, and I make no such findings. 2 The six Board members are David R. Guyer, Glenn P. Sblendorio, David E. Redick, Thomas Dyrberg, Axel Bolte, and Michael J. Ross. 3 The former Board members are Samir C. Patel and Nicholas Galakatos. class action (Micholle v. Ophthotech Corp., No. 17-cv-210 (S.D.N.Y.) (the “Securities Action”)), which alleges violations of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 (the “Exchange Act”), 15 U.S.C. §§ 78j(b), 78t(a). Defendant Samir C. Patel co-founded Ophthotech along with Guyer and served as President and Vice Chairman of the Board until January 2017;

since January 2017, Patel has acted as a consultant to Ophthotech. (Id. ¶ 22.) Patel is also a defendant in the Securities Action. (Id.) Defendant Glenn P. Sblendorio has served as President and CEO of Ophthotech since 2017, and has served as a director since May 2017. (Id. ¶ 17.) Defendant Nicholas Galakatos was an Ophthotech director from December 2009 to May 2016. (Id. ¶ 23.) David E. Redick, Thomas Dyrberg, Axel Bolte, and Michael J. Ross were outside directors at Ophthotech during the Relevant Period. (Id. ¶¶ 18–21.) B. Factual Allegations This lawsuit arises from statements made and actions taken by Defendants in conjunction with clinical trials for Fovista, a new drug developed by Ophthotech to treat macular degeneration. Many of the allegations in the Complaint are taken from the facts set forth in the

Consolidated Amended Complaint for Violations of the Federal Securities Laws (the “Consolidated Complaint”) in the related Securities Action. See Micholle, No. 17-cv-210, ECF No. 63. On September 17, 2019, I issued an Opinion & Order denying a motion to dismiss the Consolidated Complaint in the Securities Action. See id., ECF No. 89 (“Securities O&O”). In the Securities O&O, I summarized in detail the allegations set forth in the Consolidated Complaint. (See Securities O&O, Part I.) I assume familiarity with that opinion and recite here only those facts necessary to decide this motion.4

4 In the Securities O&O, I found that certain of challenged statements—i.e., those statements characterizing the successful results of the Fovista Phase 2b clinical trial—were not materially false or misleading. See Securities O&O, Part IV.A.2.a. Because I have already determined the insufficiency of the allegations relating to those statements, I will not summarize those statements again here. 1. The Fovista Clinical Trials During the Relevant Period, Ophthotech was focused on developing the drug Fovista for the treatment of wet age-related macular degeneration (“wet AMD”). (Compl. ¶ 39.) “Wet AMD” is a degenerative eye disease that occurs when areas of abnormal blood vessels and

abnormal tissue—commonly referred to as “lesions”—form in the retina and leak fluid or blood, causing patients to experience blurred vision and blind spots in their visual field. (Id. ¶¶ 39, 44.) Ophthotech designed Fovista to be used in combination with anti-vascular endothelial growth factor (“anti-VEGF”) drugs, which are commonly used to treat wet AMD. (Id. ¶ 40.) Anti- VEGF agents—including the drug Lucentis—block proteins that bind to cells on the inner lining of the abnormal blood vessels associated with wet AMD, thereby inhibiting cell growth; Fovista, by contrast, is an anti-platelet derived growth factor (“anti-PDGF”) agent designed to block proteins that bind to cells on the outer lining of the abnormal blood vessels. (Id. ¶¶ 40, 43.) In order to secure approval from the United States Food and Drug Administration, a new drug must typically undergo three phases of clinical trials. (Id. ¶¶ 41–42.) Phase 1 involves the

introduction of the drug to a small group of patients with the target disease. (Id. ¶ 42.) Phase 2 evaluates the safety and efficacy of the drug on a larger group of patients, while Phase 3 expands the safety and efficacy assessment to even more patients. (Id.) In June 2012, Ophthotech completed a Phase 2b clinical trial of Fovista (the “Phase 2b Trial”), which measured improvements in visual acuity for wet AMD patients receiving Fovista administered in combination with Lucentis (“Fovista combination therapy”), as compared to improvements when patients received Lucentis alone (“Lucentis monotherapy”). (Id. ¶ 43.) In selecting individuals to participate in the Phase 2b Trial, Ophthotech analyzed wet AMD patients’ lesions and divided patients into subgroups on the basis of whether their lesions contained “classic” or “occult” components. (Id.

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