Settlement and License Agreement

Exhibit 10.2

[***] = Certain confidential information contained in this document, marked by brackets, has been omitted and filed separately with the Securities and Exchange Commission pursuant to Rule 24b-2 under the Securities Exchange Act of 1934, as amended.

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This Settlement and License Agreement (“Agreement”), effective September 14, 2015, is entered into by and between BioMarin Pharmaceutical Inc., a corporation organized and existing under the laws of the State of Delaware, having a principal place of business at 000 Xxxxxxx Xxxxxx, Xxx Xxxxxx, Xxxxxxxxxx 00000 (“BioMarin”), Merck & Cie, a Swiss corporation having a principal place of business at Xx Xxxxxxxxxxxxx 0, 0000 Xxxxxxxxxxxx, Xxxxxxxxxxx (“Merck”) (together “Plaintiffs”); and Xx. Xxxxx’x Laboratories, Ltd., a company organized under the laws of India, having a principal place of business at 8-2-337, Road Xx. 0, Xxxxxxx Xxxxx, Xxxxxxxxx, 000 000, Xxxxx and its subsidiaries, including Xx. Xxxxx’x Laboratories, Inc., a corporation incorporated under the laws of the State of New Jersey, having its principal place of business at 000 Xxxxxxx Xxxx Xxxx, Xxxxxxxxx, Xxx Xxxxxx 00000 (collectively “DRL”). Each of BioMarin, Merck, and DRL are individually referred to herein by name or the term “Party” and collectively referred to herein as “Parties.”

WHEREAS, DRL has filed Abbreviated New Drug Application No. 207685 with the United States Food and Drug Administration (“FDA”) seeking permission to market the DRL ANDA Product in the United States and its territories, including the Commonwealth of Puerto Rico (the “Territory”) before the expiration of Plaintiffs’ Orange-Book listed United States Patent Nos. 7,566,462; 7,566,714; 7,612,073; 7,727,987; 7,947,681; 8,003,126; 8,067,416; RE43,797; and 8,318,745 (collectively, the “Listed Patents”);

WHEREAS, in response to the filing of ANDA No. 207685, Plaintiffs have filed an action against DRL in the United States District Court for the District of New Jersey, captioned BioMarin Pharmaceutical Inc., et al. v. Xx. Xxxxx’x Laboratories, Inc., et al., Civil Action No. 14-CV-7203 (MAS)(TJB) (the “New Jersey Litigation”), alleging infringement of seven of the Listed Patents by DRL’s generic product;

WHEREAS, DRL has no present intention of launching the DRL ANDA Product without a court order declaring that it does not infringe the Listed Patents, except as provided herein;

WHEREAS, Plaintiffs intend to continue to assert their rights under the Listed Patents to exclude the products described in ANDA No. 207685, except as provided herein;

WHEREAS, the Parties wish to fully settle the New Jersey Litigation and all issues concerning DRL’s generic version of Kuvan® upon the terms and subject to the conditions set forth below;

WHEREAS, settlement of the New Jersey Litigation will help Plaintiffs and DRL avoid the substantial uncertainty and risk involved with prolonged litigation;

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WHEREAS, settlement of the New Jersey Litigation will permit Plaintiffs and DRL to save litigation costs, as well as adhere to the judicially-recognized mandate that encourages the settlement of litigation whenever possible;

WHEREAS, settlement of the New Jersey Litigation will permit the management of Plaintiffs and DRL to refocus on running their respective companies rather than devoting substantial time and resources to litigation;

WHEREAS, under this Agreement, DRL will have the right to enter the market for sapropterin dihydrochloride products several years prior to the expiration of the Listed Patents, thereby benefiting customers by permitting generic entry that may not have occurred were the New Jersey Litigation to proceed; and

WHEREAS, the public will benefit significantly from this final settlement, as it saves judicial resources and creates certainty for Plaintiffs and DRL;

NOW, THEREFORE, in consideration of the mutual promises and covenants contained in this Agreement and for other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the Parties agree as follows:

Article 1.Definitions.

For purposes of this Agreement, certain words and their correlatives are defined in Article 1 or in the body of this Agreement.

1.1

“Affiliate” shall mean any entity which controls, is controlled by, or is under common control with the applicable entity. For purposes of this definition, “control” shall mean: (a) in the case of corporate entities, direct or indirect ownership of at least fifty percent (50%) of the stock or shares entitled to vote for the election of directors, or otherwise having the power to control or direct the affairs of such entity; and (b) in the case of non-corporate entities, direct or indirect ownership of at least 50% of the equity interest or the power to direct the management and policies of such non-corporate entities.

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Article 2.Termination of Litigation.

2.1	The Parties stipulate to the dismissal of all claims and counterclaims in the New Jersey Litigation without prejudice, with each Party to bear its own fees and costs.

2.2	Within three (3) business days of the Effective Date, Plaintiffs shall file a stipulation of dismissal in the form attached as Exhibit A, so that the New Jersey Litigation is dismissed without prejudice in accordance with Federal Rule of Civil Procedure 41(a)(1).

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Article 3.[***]

Article 4.[***]

Article 5.[***]

Article 6.[***]

Article 7.[***]

Article 8.Confidentiality of the Agreement.

8.1

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(i)

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(ii)

In the event that a disclosure under Section 8.1(i)(b) is made, the disclosing Party shall submit the proposed disclosure in writing to the other Party at least six (6) calendar days prior to the date of the disclosure.

(iii)

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Article 9.General Provisions.

9.1

Each Party shall take or cause to be taken such further actions, and to execute, deliver, and file or cause to be executed, delivered, and filed, such further documents and instruments, and to obtain such consents, as may be reasonably required or requested in order to effectuate fully the purposes, terms, and conditions of this Agreement.

9.2	The Parties may amend or modify the provisions of this Agreement, including this provision, only by mutual agreement in writing.

9.3

No provision of this Agreement shall be waived by any act, omission, or knowledge of a Party or its agents or employees except by an instrument in writing expressly waiving such provision and signed by a duly authorized officer of the waiving Party. The failure of any Party to assert its rights under this Agreement or otherwise shall not constitute a waiver of such rights.

9.4	This Agreement (including all attachments hereto), constitutes the final, complete, and exclusive agreement and understanding of the Parties with respect to the subject matter hereof and supersedes all prior agreements or understandings, oral or written, with respect to such matters.

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9.5	All notices or communications hereunder shall be deemed to have been duly given only if made in writing, served by one of the means listed in Article 9.5(i), and directed to the individuals listed in Article 9.5(ii).

(i)

Notice or communications to a Party shall be served by personal delivery, reputable overnight express courier service (charged prepaid), or delivery by registered or certified mail (return receipt requested), at the address(es) listed in Section 9.5(ii). Such notices will be deemed to have been given on the date delivered (in the case of personal delivery or delivery by overnight courier), and on the fifth (5^th) business day following the date of postmark in the case of delivery by mail.

(ii)

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9.6

This Agreement may be executed in any number of counterparts, and execution by each of the Parties of any one of such counterparts will constitute due execution of this Agreement. Each such counterpart hereof shall be deemed to be an original instrument, and all such counterparts together shall constitute but one agreement.

9.7	Electronic execution and delivery of this Agreement by any Party shall be legal, valid, and binding to the same extent as an original signature.

9.8

If any provision of this Agreement is held invalid, illegal, or unenforceable for any reason, this holding shall not impair the validity, legality, and enforceability of the remaining provisions in any way. The Parties shall renegotiate in good faith any provision held to be invalid, illegal, or unenforceable, it being the intent of the Parties that the basic purposes of the Agreement are to be effectuated.

9.9

Each Party acknowledges that a breach of this Agreement will cause the non-breaching Party to suffer irreparable harm for which there is no adequate legal remedy. Each Party acknowledges that immediate injunctive relief is an appropriate and necessary remedy for any violation or threatened violation of this Agreement.

9.10	No Third Party shall be deemed an intended beneficiary hereunder or have any legal or equitable rights or benefits to enforce any provision of this Agreement.

9.11	None of the Parties hereto shall be considered the drafter of this Agreement or any provision thereof for the purpose of any statute, case law, or rule of construction that would or might cause any provision to be construed against the drafter thereof.

9.12

This Agreement has been negotiated between unrelated Parties who are sophisticated and knowledgeable in the matters contained in this Agreement and who have acted of their own self-interest. In addition, each Party has been represented and advised by legal counsel regarding the terms of this Agreement.

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9.13

The Parties are independent contractors and are not, and shall not represent themselves as, principal and agent, partners, joint venturers, or business associates of any kind. No Party shall attempt to act, or represent itself as having the power, to bind the other Parties or create any obligation on behalf of the other Parties. Similarly, nothing in this Agreement shall constitute or be construed as Plaintiffs’ endorsement or approval of Licensed Generic Product. DRL, and any Third Party acting in concert with DRL, shall not represent or suggest otherwise in any way, including in any labeling, promotional, or marketing material associated with Licensed Generic Product.

9.14	Mistakes of fact or law shall not constitute grounds for modification, avoidance, or rescission of the terms of this Agreement.

9.15	Each Party shall bear its own expenses that arise out of the New Jersey Litigation and/or the negotiation, execution, or performance of this Agreement.

9.16

This Agreement and any dispute arising out of or related to this Agreement shall be governed by and construed in accordance with the internal laws of the State of New Jersey, without giving effect to conflicts of law principles. With respect to any proceeding related to this Agreement, each Party irrevocably agrees and consents to the exclusive jurisdiction of the federal and state courts in New Jersey, and waives any objection to venue of any such proceeding brought in any such court.

Article 10.[***]

Article 11.[***]

[Signatures on the following pages]

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This Agreement is signed as indicated below by duly authorized representatives of BioMarin, Merck, and DRL, respectively, as of the Effective Date.


BioMarin Pharmaceutical Inc.

By:	/s/ G. Xxxx Xxxxx

Name:	G. Xxxx Xxxxx

Title:	SVP, General Counsel


Merck & Cie

By:	/s/ Xx. Xxxxxx Xxxxx

Name:	Xx. Xxxxxx Xxxxx

Title:	Managing Director


By:	/s/ Xxxxxxx Xxxxxx

Name:	Xxxxxxx Xxxxxx

Title:	Patents

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Xx. Xxxxx’x Laboratories, Inc.

By:	/s/ Xxxxxxxxxx X. Xxxxxx

Name:	Xxxxxxxxxx X. Xxxxxx

Title:	Senior Vice President, Finance


Xx. Xxxxx’x Laboratories, Ltd.

By:	/s/ Xx. Xxxxxxx Xxxxxxxxx

Name:	Xx. Xxxxxxx Xxxxxxxxx

Title:	COO

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Exhibit A

UNITED STATES DISTRICT COURT

DISTRICT OF NEW JERSEY

BioMarin Pharmaceutical Inc. and MERCK & CIE,

Plaintiffs,

XX. XXXXX’X LABORATORIES, INC. and XX. XXXXX’X LABORATORIES, LTD.,

Defendants.

Civil Action No. 3:14-cv-07203-MAS-TJB

STIPULATION OF DISMISSAL

Xxx. Xxxxxxx Xxxxx, U.S.D.J.

Xxx. Xxxxxxxx X. Xxxxxxxxxxx, U.S.M.J.

STIPULATION OF DISMISSAL, WITHOUT PREJUDICE

1.Pursuant to Rules 41(a)(1) and 41(c) of the Federal Rules of Civil Procedure, BioMarin Pharmaceutical Inc. (“BioMarin”) and Merck & Cie (“Merck”) (BioMarin and Merck are, together, the “Plaintiffs”) and Xx. Xxxxx’x Laboratories, Inc. and Xx. Xxxxx’x Laboratories, Ltd. (together, “DRL” or “Defendants”) hereby stipulate and agree that all claims, counterclaims and affirmative defenses asserted by Plaintiffs and Defendants against one another in the above-captioned consolidated action (the “Action”) are hereby dismissed without prejudice, and without costs, disbursements, or attorneys fees to any party.

2.This consolidated Action also involves claims between Plaintiffs and Par Pharmaceutical Inc. (see Case No. 3:15-cv-01706-MAS-JTB). The Clerk is directed to enter this Stipulation of Dismissal, which addresses only Plaintiffs’ and DRL’s claims for relief against one another in Case No. 3:14-cv-07203-MAS-JTB, but not the claims of Plaintiffs and Par against each other in Case No. 3:15-cv-01706-MAS-JTB. The Action will proceed on all claims as between Plaintiffs and Par.

IT IS on this ____ day of _______________, 2015:

	SO ORDERED

		XXX. XXXXXXX XXXXX, U.S.D.J.

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Settlement and License Agreement

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