H&H Pharmaceuticals, LLC v. Cambrex Charles City, Inc.

CourtDistrict Court, D. Nevada
DecidedMarch 16, 2020
Docket2:16-cv-02946
StatusUnknown

This text of H&H Pharmaceuticals, LLC v. Cambrex Charles City, Inc. (H&H Pharmaceuticals, LLC v. Cambrex Charles City, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Nevada primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
H&H Pharmaceuticals, LLC v. Cambrex Charles City, Inc., (D. Nev. 2020).

Opinion

1 2 3 4 UNITED STATES DISTRICT COURT 5 DISTRICT OF NEVADA 6 * * *

7 H&H PHARMACEUTICALS, INC. Case No. 2:16-cv-02946-RFB-BNW

8 Plaintiff, ORDER

9 v.

10 CAMBREX CHARLES CITY, INC. CAMBREX NORTH BRUNSWICK, INC. 11

12 Defendant(s).

13 14 I. INTRODUCTION 15 Before the Court is Defendants Cambrex Charles City, Inc. and Cambrex North 16 Brunswick’s (collectively “Cambrex”) Motion for Summary Judgment. ECF No. 51. 17 II. PROCEDURAL BACKGROUND 18 Plaintiff H&H Pharmaceuticals, Inc. (“H&H”) filed its complaint on December 20, 2016. 19 ECF No. 1. In the complaint, H&H asserted claims against Cambrex for breach of contract, 20 contractual breach of implied covenant, tortious breach of implied covenant of good faith and fair 21 dealing, breach of fiduciary duty, fraudulent concealment, and negligent misrepresentation. 22 Cambrex moved to dismiss on January 27, 2017. ECF No. 9. On July 27, 2017 the Court dismissed 23 the tortious breach of implied covenant of good faith and fair dealing and breach of fiduciary duty 24 claims, and allowed for expedited discovery on the statute of limitations. ECF No. 18. Cambrex 25 answered on August 9, 2017. ECF No. 17. Cambrex moved for summary judgment on the statute 26 of limitations on December 13, 2017. ECF No. 24. On May 16, 2018, the Court denied the motion. 27 ECF No. 29. On June 27, 2019, Cambrex filed the instant motion for summary judgment. ECF No. 28 51. The motion was fully briefed. ECF Nos. 57, 58. The Court heard oral argument on the motion 1 on March 11, 2020. This written order now follows. 2 III. FACTUAL BACKGROUND 3 4 Cambrex is a contract development and manufacturing organization (“CDMO”) 5 specializing in branded and generic small molecule active pharmaceutical ingredients (“APIs”), 6 advanced intermediates, and custom development and manufacturing of controlled substances. As 7 a CDMO, Cambrex serves other companies in the pharmaceutical industry on a contract basis to 8 provide comprehensive services from drug development through drug manufacturing. Cambrex 9 10 has been developing and manufacturing APIs for over 35 years. 11 Around 1979, Jacob Hack (“Hack”) developed certain chemistry and conversion processes, 12 allegedly not available on the open marketplace and not generally publicly known, for converting 13 raw opium and concentrate of poppy straw into opiate-based raw materials by chemical extraction, 14 recovery and conversion methods (“the Conversion Methods”). On September 17, 1999, Hack and 15 16 Richard G. Herman (“Herman”) formed H&H Pharmaceuticals (“Plaintiff” or H&H”), and Hack 17 contributed the Conversion Methods to the company. 18 On June 27, 2007, Herman communicated with Richard Giles (“Giles”), then Director of 19 Business Development for Cambrex, regarding a potential business relationship between H&H 20 and Cambrex. Following the discussion between Herman and Giles, counsel for H&H and 21 22 Cambrex began negotiating the terms of a Confidentiality Agreement. The parties also discussed 23 a Bilateral Non-Disclosure Agreement (“NDA”). 24 The parties fully executed the Confidentiality Agreement on October 19, 2007. By its 25 terms, the NDA was only to take effect if H&H and Cambrex entered into a formal business 26 relationship. On or about December 11, 2007, Herman traveled to New Jersey to meet with 27 28 Cambrex representatives. The purpose of the meeting was for Herman to provide for Cambrex’s 1 consideration a set of manuals that detailed the Conversion Methods (“the Manuals”). The 2 Manuals consisted of four separately-bound manuals, which were small enough to fit in Herman’s 3 briefcase. In total, the Manuals consisted of 315 pages of materials, plus dividers, and front and 4 back covers. Herman gave the Manuals to Cambrex. 5 6 On June 13, 2008, H&H also provided to Cambrex documents concerning pro-liposome 7 technology, subject to the terms of the Confidentiality Agreement. This material included the 8 "Patent Application 60/192,465 filed April 18, 2008". 9 On October 24, 2008, Dan Giambattisto (“Giambattisto”), Vice President of Sales & 10 Business Development for Cambrex, emailed Herman to state that Cambrex decided not to pursue 11 12 development of either H&H’s opiate or pro-liposome technology. Giambattisto further stated in 13 the email that he had arranged for the Manuals to be sent back to H&H as soon as possible. 14 On October 27, 2008, Herman sent a response stating in part: “We expect Cambrex to stand 15 by the confidential agreements it has with H&H for both our Opiate Methods and Technology as 16 well as our Pro-Liposome Delivery Method to the full extent and conditions of the confidential 17 18 agreement between our two companies.” In response, Giambattisto confirmed that “Cambrex 19 [would] abide by the terms of the confidentiality agreement between the 2 companies.” 20 On or shortly after October 24, Cambrex sent soft-sided package of materials to Herman’s 21 residence via UPS Next Day Air. 22 In February 2014, Herman went through the Federal Register for purposes related to other 23 24 litigation. Herman discovered that Cambrex applied for and received DEA approval for certain 25 Schedule II narcotics, such as hydrocodone and morphine. During his review at that time, Herman 26 also noticed that Cambrex had applied for in 2007, and received approval in 2009, to import raw 27 materials including poppy straw concentrate and raw opium. 28 1 Herman became suspicious after this review, and decided to open the package containing 2 the Manuals, which had remained unopened since 2008. Upon opening the package in October 3 2016, Herman and Hack discovered that the package included a document they had never seen 4 before – a page that showed copies of the Manuals may have been made and circulated to certain 5 6 Cambrex employees. Those copies were not included in the package. There also appeared to be 7 other missing documents. In 2015 or 2016, Cambrex began to actively manufacture opiate-based 8 products. 9 H&H thus brough the instant lawsuit, asserting that Cambrex used proprietary information 10 and made copies of materials that were not destroyed, in violation of the confidentiality agreement 11 12 and to support its manufacture of opiate-based products. 13 IV. LEGAL STANDARD 14 Summary judgment is appropriate when the pleadings, depositions, answers to 15 interrogatories, and admissions on file, together with the affidavits, if any, show “that there is no 16 genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” 17 18 Fed. R. Civ. P. 56(a); accord Celotex Corp. v. Catrett, 477 U.S. 317, 322(1986). 19 When considering the propriety of summary judgment, the court views all facts and draws 20 all inferences in the light most favorable to the nonmoving party. Gonzalez v. City of Anaheim, 21 747 F.3d 789, 793 (9th Cir. 2014). 22 If the movant has carried its burden, the nonmoving party “must do more than simply show 23 24 that there is some metaphysical doubt as to the material facts …. Where the record taken as a whole 25 could not lead a rational trier of fact to find for the nonmoving party, there is no genuine issue for 26 trial.” Scott v. Harris, 550 U.S. 372, 380 (2007) (alteration in original) (internal quotation marks 27 omitted). 28 1 It is improper for the Court to resolve genuine factual disputes or make credibility 2 determinations at the summary judgment stage. Zetwick v. Cty. of Yolo, 850 F.3d 436

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