PEPICELLI v. INNOCOLL HOLDINGS PUBLIC LIMITED COMPANY

District Court, E.D. Pennsylvania·Decided October 28, 2022·No. 2:17-cv-00341·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF PENNSYLVANIA

CIVIL ACTION IN RE INNOCOLL HOLDINGS PUBLIC - : LTD. CO. SEC. LITIG. : : No. 17-341

MEMORANDUM ag PRATTER, J, OCTOBER 2022 Over the course of its five-year lifetime, this class action litigation has absorbed thousands of attorney hours and likely demanded considerable litigation costs, but, finally, a conclusion is in sight. Shareholders sued pharmaceutical company Innocoll Holdings Public Limited Company in 2017, claiming that Innocoll had misrepresented a new product’s chances of success in the Food and Drug Administration’s approval process. Over four years later, the parties reached a settlement agreement in principle, This Court preliminarily approved the settlement on March 10, 2022, pending a final approval hearing that took place on July 6, 2022. Russel Bleiler and Carl Bayney, the Court-appointed lead plaintiffs in this securities action, have submitted an unopposed motion for final approval of the class action settlement and plan of allocation under Federal Rule of Civil Procedure 23(e), along with an unopposed motion for an award of attorneys’ fees, reimbursement of litigation expenses, and compensatory awards to lead plaintiffs. For the reasons set forth below, the Court grants both motions. BACKGROUND Innocoll is a pharmaceutical company that specializes in collagen technologies, making its initial public offering (“IPO”) in July 2014. In its amended registration statement for its IPO, Innocoll described the progress of clinical trials for XaraColl, a collagen sponge implant that contains pain medicine and is placed in surgical sites to relieve post-surgery pain. In May 2016,

Innecoll announced the results of Phase 3 clinical trials for XaraColl via press release and said on a conference call with securities analysts that there were no gating factors to filing a new drug application (“NDA”) for XaraColl with the FDA. In November 2016, Innocoll announced that it had submitted the NDA for XaraColl. On December 29, 2016, Innocol! issued a press release explaining that the FDA had issued a “Refusal to File” letter for XaraColl. Although Innocoll had tested and submitted XaraColl as a drug, the FDA determined that XaraColl should have been tested and submitted as a drug/device combination. On the day following the press release, Innocoll’s share price fell over 61%, In early 2017, shareholders sued Innocoll and individual defendants, meluding Chief Executive Officer Anthony Zook and Chief Medical Officer Lesley Russell, for violations of the Securities Exchange Act of 1934, claiming that they had misled investors who relied on the company’s positive statements about XaraColl and its chances of FDA approval. The first complaint was dismissed because the plaintiffs failed to meet the Private Securities Litigation Reform Act’s (‘PLSRA’s”) heightened pleading standard relating to the element of scienter. After the filing of an amended complaint and a stay of the action while the parties unsuccessfully pursued mediation, the parties proceeded to discovery in April 2020, The extensive discovery included review and categorization of over 400,000 pages of documents and depositions of two experts as well as of lead plaintiffs Mr. Bleiler and Mr. Bayney. While discovery was still underway, the shareholders filed a renewed motion for class certification. Just before oral argument on the motion for certification was to be held on July 6, 2021, the parties announced that they had reached a settlement in principle: Innocoll would pay $2,755 million to the shareholders, and, in exchange, the shareholders would release all claims against Innocoll relating to the alleged misrepresentations (the “Settlement”).

Under the Settlement notice program, claims administrator Strategic Claims Services (“SCS”) established a webpage, accessible at all times, which provided information relevant to the Settlement, including the current status of the Settlement, case deadlines, the online claim filing link, and the exclusion request form, SCS also maintained a toll-free telephone number through which potential settlement class members could seek further information or request the notice and claim form. SCS mailed or emailed 2,190 nominee account holders or institutional groups (including banks, brokerages, mutual funds, insurance companies, pension funds, and money

_ managers), notifying them of the Settlement and requesting that they send the postcard notice, email the summary notice, or email a link to the online notice and claim form to any customers who inight be beneficial purchasers or owners of Innocoll shares. The nominee account holders or institutional groups also had the option of providing SCS with a list of the names and mailing addresses of potential beneficial owners te SCS. Some 3,540 postcard notices were mailed by either SCS or the nominees, of which 105 were returned as undeliverable. A total of 4,465 potential settlement class members were notified of the Settlement via mailed postcard notices or via email containing a direct link to the notice and claim form. The publication notice was also disseminated twice electronically via GlobalNewswire and twice in print in Investor's Business Daily, The deadlines for settlement class members to submit claims, request exclusion from the Settlement, and object to the Settlement were June 6, 2022, June 15, 2022, and June 22, 2022 respectively, Potential Settlement class members submitted 682 claim forms, of which 123 claims were valid. July 6, 2022 Tr. 3:13-14. No member of the settlement class objected to final approval, attorneys’ fees, reimbursement of out-of-pocket expenses, or compensatory awards to the lead plaintiffs. Under the Settlement’s plan of allocation, which was formulated by lead counsel with the assistance of an experienced financial consultant, SCS will calculate class members’ recognized

. .

loss based on the time the Innocoll securities were purchased and sold, the purchase and sale price of the securities, and the estimated inflation of the price of the securities at the of purchase and sale, The Settlement amount will then be allocated to approved claimants on a pro rata basis, accounting for each class member’s recognized loss. The lead plaintiffs, Mr. Bleiler and Mr. Bayney, filed a motion for an award of attorneys’ fees, reimbursement of litigation expenses, and compensatory awards. Lead counsel seek an award of one third of the Settlement, or $918,333. Lead counsel also seek reimbursement of $296,111.74 in litigation expenses, most of which was incurred in retaining an expert who provided evidence in support of the plaintiffs’ motion for class certification, Finally, Mr. Bleiler and Mr. Bayney seek compensatory awards of $10,000 each for their dedication to pursuing this claim on behalf of the class. LEGAL STANDARDS Class actions may only be settled with court approval. Fed. R. Civ. P. 23(e). A district court may approve a settlement agreement “only after a hearing and only on finding that it is fair, reasonable, and adequate.” Fed. R. Civ. P. 23(e)(2). The Third Circuit Court of Appeals has stated its policy in favor of voluntary settlement agreements, especially in class actions and other complex litigations. Ehrheart v. Verizon Wireless, 609 F.3d 590, 594-95 (3d Cir. 2010). Nevertheless, “[t]he decision of whether to approve a proposed settlement of a class action is left to the sound discretion of the district court.” Girsh v.

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PEPICELLI v. INNOCOLL HOLDINGS PUBLIC LIMITED COMPANY, (E.D. Pa. 2022).

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