Nguyen v. NewLink

CourtCourt of Appeals for the Second Circuit
DecidedJuly 13, 2020
Docket19-642
StatusPublished

This text of Nguyen v. NewLink (Nguyen v. NewLink) is published on Counsel Stack Legal Research, covering Court of Appeals for the Second Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Nguyen v. NewLink, (2d Cir. 2020).

Opinion

19-642 Nguyen v. NewLink

1 In the 2 United States Court of Appeals 3 For the Second Circuit 4 ________ 5 6 AUGUST TERM, 2019 7 8 ARGUED: OCTOBER 21, 2019 9 DECIDED: JULY 13, 2020 10 11 No. 19-642-cv 12 13 TREVOR ABRAMSON, Individually and on behalf of all others similarly 14 situated, 15 Plaintiff, 16 17 MICHAEL NGUYEN, Individually and on behalf of all others similarly 18 situated, KELLY NGUYEN, Individually and on behalf of all others similarly 19 situated 20 Lead Plaintiffs-Appellants, 21 22 v. 23 24 NEWLINK GENETICS CORPORATION, CHARLES J. LINK, JR., NICHOLAS N. 25 VAHANIAN, 26 Defendants-Appellees. 27 28 JOHN B. HENNEMAN, III, GORDON H. LINK, JR., 29 Defendants. 30 ________ 31 32 Appeal from the United States District Court 33 for the Southern District of New York. 34 ________ 35 2 No. 16-3734-cr

1 Before: KEARSE, WALKER, and LIVINGSTON, Circuit Judges.

2 3 ________

4 Plaintiffs Michael Nguyen and Kelly Nguyen brought this class action 5 under S.E.C. Rule 10b-5, 17 C.F.R. 240.10b-5, following the failure of Defendant 6 NewLink Genetics Corporation’s (“NewLink”) Phase 3 clinical trial for a novel 7 pancreatic cancer drug and the resulting decline in the market value of NewLink 8 shares. On appeal, Plaintiffs argue that the district court (William H. Pauley III, 9 Judge) erred in dismissing pursuant to Fed. R. Civ. P. 12(b)(6) their Rule 10b-5 10 claims alleging that NewLink and its leadership (collectively, “Defendants”) 11 materially misrepresented the efficacy of their pancreatic cancer drug, scientific 12 literature on pancreatic cancer, and the design of their Phase 3 clinical trial, and 13 these misrepresentations caused Plaintiffs financial losses. We conclude that 14 Defendants’ statements about the efficacy of their pancreatic cancer drug were 15 puffery, not material misrepresentations. We conclude, however, that Plaintiffs 16 plausibly pled material misrepresentation and loss causation for Defendants’ 17 statements about the scientific literature and the design of their clinical trial. We 18 therefore AFFIRM the district court’s dismissal of Plaintiffs’ Rule 10b-5 claim 19 regarding the 2013–2016 Assessments, VACATE the district court’s dismissal of 20 Plaintiffs’ Rule 10b-5 claims regarding the September, March, and Enrollment 21 statements, and REMAND for further proceedings consistent with this opinion.

22 ________ 23 KIM E. MILLER, Kahn Swick & Foti, LLC, New York, NY (J. Ryan 24 Lopatka, Kahn Swick & Foti, LLC, New York, NY; Lewis S. 25 Kahn and Craig J. Geraci, Kahn Swick & Foti, LLC, New 26 Orleans, LA, on the brief), for Plaintiffs-Appellants. 3 No. 19-642

1 SARAH M. LIGHTDALE, Cooley LLP, New York, NY (David H. 2 Kupfer, Cooley LLP, New York, NY; Samantha A. Kirby, 3 Cooley LLP, Palo Alto, CA, on the brief), for Defendants-Appellees.

4 ________

5 JOHN M. WALKER, JR., Circuit Judge:

6 Plaintiffs Michael Nguyen and Kelly Nguyen brought this class action 7 under S.E.C. Rule 10b-5, 17 C.F.R. 240.10b-5, following the failure of Defendant 8 NewLink Genetics Corporation’s (“NewLink”) Phase 3 clinical trial for a novel 9 pancreatic cancer drug and the resulting decline in the market value of NewLink 10 shares. On appeal, Plaintiffs argue that the district court (William H. Pauley III, 11 Judge) erred in dismissing pursuant to Fed. R. Civ. P. 12(b)(6) their Rule 10b-5 12 claims alleging that NewLink and its leadership (collectively, “Defendants”) 13 materially misrepresented the efficacy of their pancreatic cancer drug, scientific 14 literature on pancreatic cancer, and the design of their Phase 3 clinical trial, and 15 these misrepresentations caused Plaintiffs financial losses. We conclude that 16 Defendants’ statements about the efficacy of their pancreatic cancer drug were 17 puffery, not material misrepresentations. We conclude, however, that Plaintiffs 18 plausibly pled material misrepresentation and loss causation for Defendants’ 19 statements about the scientific literature and the design of their clinical trial. We 20 therefore AFFIRM the district court’s dismissal of Plaintiffs’ Rule 10b-5 claim 21 regarding the 2013–2016 Assessments, VACATE the district court’s dismissal of 22 Plaintiffs’ Rule 10b-5 claims regarding the September, March, and Enrollment 23 statements, and REMAND for further proceedings consistent with this opinion.

24 4 No. 19-642

1 BACKGROUND

2 Charles J. Link and Nicholas N. Vahanian are the co-founders of NewLink, 3 a pharmaceutical company that develops cancer treatments. At the time of the 4 events giving rise to the present litigation, Link was Chairman and Chief Executive 5 Officer of NewLink, and Vahanian was President and Chief Medical Officer.

6 Because of the huge demand for efficacious cancer drugs, in particular those 7 that can successfully treat the most intractable cancers, the market in shares of 8 firms that can potentially treat intractable cancers is highly sensitive to 9 developments in trials to establish a drug’s effectiveness and gain the Food and 10 Drug Administration’s (“FDA”) approval. Generally, the FDA requires three 11 phases of human clinical trials. After the completion of the phase 1 trial, 12 investigators are required to submit their data for approval to the FDA before 13 continuing to the next phase and launching a larger trial. The same process applies 14 when a drug candidate moves from a phase 2 trial to a larger phase 3 trial. If the 15 phase 3 trial results are sufficiently strong, investigators can submit a new drug 16 application and receive FDA approval to manufacture and sell the drug. The 17 results of each trial and the success or failure of each phase are closely watched by 18 the market, and the market reacts accordingly.

19 The present litigation stems from statements made and market losses 20 incurred during trials related to NewLink’s development of algenpantucel-L, or 21 HyperAcute Pancreas, a potential treatment for pancreatic cancer following a 22 patient’s resection (surgery to remove a tumor). 1 In 2010, NewLink completed

1The facts described herein are from the second amended complaint, which we take to be true in our review of the district court’s Rule 12(b)(6) dismissal. See Ganino v. Citizens Utilities Co., 228 F.3d 154, 161 (2d Cir. 2000). 5 No. 19-642

1 enrollment for a Phase 2 trial for HyperAcute Pancreas. One of the criteria for 2 enrollment in that trial was that subjects had to have an “[e]xpected survival 3 [greater than or equal to] 6 months.”2 Individuals with either Stage I or Stage II 4 pancreatic cancer were eligible to enroll. The Phase 2 trial did not have a control 5 group, and it was not a double-blind study. In June 2012, after at least 24 months 6 of follow-up with each patient, NewLink ended the Phase 2 trial and assessed that 7 those treated with HyperAcute Pancreas had a “survival rate,” or median life 8 expectancy, of 24.1 months.

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Nguyen v. NewLink, Counsel Stack Legal Research, https://law.counselstack.com/opinion/nguyen-v-newlink-ca2-2020.