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Exhibit 10.76
by and between
ALKERMES PHARMA IRELAND LIMITED
and
XXXXXXX URBAN PHARMACEUTICALS INC.
Effective as of January 1,2014
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Schedules
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This LICENSE AND SUPPLY AGREEMENT (“Agreement”), effective as of January 1, 2014 (the “Effective Date”) is by and between ALKERMES PHARMA IRELAND LIMITED, a limited liability company incorporated under the laws of Ireland (“Alkermes”). and XXXXXXX URBAN PHARMACEUTICALS INC., an Indiana corporation (“KU”).
W I T N E S E T H
WHEREAS, Alkermes is engaged, among other things, in the business of researching, development, manufacturing and commercialization of pharmaceutical products, inter alia, verapamil hydrochloride;
WHEREAS, KU is engaged, among other things, in the business of marketing and selling of pharmaceutical products;
WHEREAS UCB, Inc. (a KU Affiliate) currently maintains certain rights to market and sell certain branded and authorized generic Products (as defined below) under the UCB Agreement (defined below) which expires on December 31, 2013; and
WHEREAS, subject to the terms and conditions set forth in this Agreement, Alkermes wishes to (i) license KU certain rights to enable KU to market and sell Products (defined below) in the Territory (defined below) following the expiration of the UCB Agreement and (ii) manufacture and supply such Products to KU;
NOW, THEREFORE, the parties hereto, intending to be legally bound, hereby agree as follows:
For purposes of this Agreement, the following terms shall have the meanings set forth below:
“Activities” shall mean the manufacturing, promoting, marketing, selling and distributing of the Products in the Territory as contemplated by this Agreement,
“Affiliates” shall mean, with respect to any Person, any Persons directly or indirectly controlling, controlled by, or under common control with, such other Person,
“Alkermes” shall have the meaning set forth in the preamble.
“Annual Net Sales” shall mean, for any Year, the Net Sales for such Year.
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“Authorized Generic” shall mean a drug sold, licensed or marked under an NDA (as opposed to an ANDA) approved by the FDA under section 505(c) of the Federal Food, Drug and Cosmetics Act and marketed and distributed under a different labeler code, product code, trade name, trademark or packaging than the corresponding brand drug,
“Branded-Product” shall mean the Branded V Product and/or the Branded VPM Product
“Branded V Product” shall mean the V Product that is sold under the Trademarks licensed to KU for Product pursuant to this Agreement.
“Branded VPM Product” shall mean the VPM Product that is sold under the Trademarks licensed to KU for Product pursuant to this Agreement.
“CFR” shall mean the U.S. Code of Federal Regulations, as amended from time to time.
“CMC Section” shall mean the chemistry, manufacturing, and controls section of the NDAs as defined in 21 CFR Section 314.50 (1).
“Damages” shall mean, subject to Section 9.7, any and all actions, costs, losses, claims, liabilities, fines, penalties, demands, damages and expenses, court costs, and reasonable fees and disbursements of counsel, consultants and expert witnesses incurred by a party hereto (including interest which may be imposed in connection therewith).
“Defective” shall mean, as to any Product supplied by Alkermes hereunder, the failure of such Product to conform to the Specifications and the applicable NDA, and, in all material respects, applicable law, including, without limitation, the PDMA.
“Effective Date” shall have the meaning set forth in the preamble.
“FDA” shall mean the United States Food and Drug Administration.
“Generic V Product” shall have the meaning set forth in Section 2.6.
“Generic VPM Product” shall have the meaning set forth in Section 2.6.
“Generic VPM Operating Profits” shall mean [***].
“Generic VPM Product Profits” shall mean, [***].
“GMP” shall mean current Good Manufacturing Practices, as determined from time to time by the FDA or any other successor agency thereto.
“HSR Act” shall mean the Xxxx-Xxxxx-Xxxxxx Antitrust Improvement Act.
“Indemnified Party” shall have the meaning set forth in Section 9.2 hereof.
“Indemnifying Party” shall have the meaning set forth in Section 9.2 hereof.
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“Independent Third Party” shall mean any person other than Alkermes and KU and their respective Affiliates.
“Intellectual Property” shall mean the Trademarks. For the avoidance of doubt, Intellectual Property shall exclude any intellectual property of any nature that is owned, licensed or controlled by Affiliates or subsidiaries of Alkermes. In the event that Alkermes acquires or merges with a third party entity, Intellectual Property shall not include any Intellectual Property to the extent that such Intellectual Property relates to a product containing verapamil hydrochloride which has been approved for marketing or is in development by the said third party entity. For the avoidance of doubt, the occurrence of any such acquisition or merger shall not affect the license of the Intellectual Property granted to KU hereunder.
“Joint Marketing Committee” shall have the meaning set forth in Section 2.5.
“KU” shall have the meaning set forth in the preamble.
“Licensed Assets” shall have the meaning set forth in Section 2.1 hereof.
“NDAs” shall mean, collectively, the V NDA and the VPMNDA.
“Net Sales” shall mean, with respect to each Product, the dollar amount determined by deducting from the gross invoiced sales price billed for such Product sold by KU in the Territory to unaffiliated third parties in an arm’s length transaction, the following:
(a)trade and reasonable and customary cash discounts allowed;
(b)returns, credits, refunds, rebates, chargebacks, retroactive price adjustments, commissions and any other allowances which effectively reduce the net selling price;
(b)transportation charges or allowances, including freight pickup allowances; and
(d)any tax (excluding income tax), excise or other governmental charges upon or measured by the production, sale, transportation, delivery or use of such Product.
Such amounts shall be determined from books and records maintained in accordance with U.S. GAAP, consistently applied.
“Notice of Rejection” shall have the meaning set forth in Section 4.4(a).
“PDMA” shall mean the Prescription Drug Marketing Act of 1987, as amended from time to time, together with any rules or regulations promulgated thereunder.
“Person” shall mean a natural person, a corporation, a partnership, a trust, a joint venture, a limited liability company, any governmental authority or any other entity or organization.
“PPI” shall mean the Producer Price Index for Pharmaceutical Preparations published by the U.S. Department of Labor, Bureau of Labor Statistics for the twelve months ending on August 31st in any Year.
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“Products” shall mean, collectively, the Branded VPM Product, Branded V Product and/or Generic VPM Pro duct manufactured and supplied to KU by Alkermes under this Agreement.
“Promotional Materials” shall mean any tangible advertising and promotional labeling bearing a name (trade name or generic name) used in the promotion of the Products, including, without limitation, promotional materials produced by KU (examples include, but are not limited to, journal ads, brochures, service items, managed care pull through sheets, formulary presentations, price lists, monographs, Internet pages and telephone or television advertisements) and materials produced by outside sources (examples include, but are not limited to, medical reprints, textbooks and CME materials) to the extent funded by, created in cooperation with, reviewed, or distributed by KU. The definition of Promotional Materials shall also include press releases and other releases of information to the media regarding the Products.
“Quarter” shall mean, as the case may be, the three months ending on March 31, June 30, September 30 or December 31 in any Year.
“Specifications” shall mean, at any time and as to either Product, the specifications for such Products that are then approved by the FDA and contained in the NDA applicable to such Product, as in effect at that time.
“Technology” includes all of the intellectual property owned or controlled by Alkermes that is used in, claims or covers the manufacturing process used by Alkermes and its Affiliates to manufacture the Products supplied to KU hereunder, or any aspect of such manufacturing process.
“Territory” shall mean the fifty (50) states, the District of Columbia and the territories and possessions comprising the United States of America, including Puerto Rico.
“Trademarks” shall mean all of Alkermes’s right, title and interest in and to:
(a)those United States trademarks and trademark applications set forth on Schedule 6.4 hereto and any trademark application or trademark which constitutes an extension, registration, contribution, reissue, renewal, reexamination or continuation in part of any such trademark or trademark application; and
(b)all registrations thereof, all variations thereof and logos used in connection therewith, and all goodwill associated therewith.
“UCB Agreement” shall mean that that certain License and Supply Agreement dated 30 September 1998, as amended, relating to Products that currently exists between UCB and Alkermes (the “Agreement”) which is due to expire on December 31, 2013.
“UCB” shall mean KU’s affiliate company, UCB, Inc.
“U.S. GAAP” shall mean generally accepted accounting practices in the United States, as in effect from time to time.
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“V Product” shall mean [***].
“V NDA” shall have the meaning set forth in Section 2.1(b).
“VPM Product” shall mean [***].
“VPM NDA” shall have the meaning set forth in Section 2.1(a).
“Year” shall mean a calendar year during the term of this Agreement.
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Alkermes will supply KXJ with all of its requirements for Products and the Products samples for their subsequent use, sale, lease or transfer by KU.
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Alkermes hereby represents and warrants to KU that:
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KU represents and warrants to Alkermes that:
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Nothing contained herein will in any way restrict or impair either party’s (the “Using Party’s”) right to use, disclose or otherwise deal with any Proprietary Information of the other party which:
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in accordance with the terms set forth in this Agreement.
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If to Alkermes, as follows:
Alkermes Pharma Ireland Limited
Xxxxxxxxx Xxxxx, 0 Xxxxxxxxxx Xxxx
Xxxxxx 0
Xxxxxxx
Telephone: x000 0 000 0000
Facsimile: x000 0 000 0000
Attention: Company Secretary
With a copy to:
VP, Alliance Management
at the same address and contact details as set out above
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If to KU, as follows:
Xxxxxxx Urban Pharmaceuticals Inc.
000 Xxxxxxxx Xxxxxx, Xxxxx 000
Xxxxxxxxx, XX 00000
Facsimile: (000) 000-0000
Attention: Vice President, Sales & Marketing
or in any case to such other address or addresses as hereafter shall be furnished as provided in this Section 11.2 by any party hereto to the other party,
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[Signature page follows]
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IN WITNESS WHEREOF, the parties have caused this Agreement to be duly executed and delivered on the day and year first above written.
ALKERMES PHARMA IRELAND LIMITED
By:/s/ Xxxxx Xxxxx
Name: Xxxxx Xxxxx
Title: Director
XXXXXXX URBAN PHARMACEUTICALS INC.
By:/s/ Xxxxxx Xxxxxxxxx
Name: Xxxxxx Xxxxxxxxx
Title: President and CEO
By:/s/ Xxxx Xxxxx Xxxxxxx
Name: Xxxx Xxxxx Xxxxxxx
Title: Vice President and CEO
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Schedule 2.1(a)
to License and
Supply Agreement
NDAs
[***]
[***]
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Schedule 3.1
to License and
Supply Agreement
Product Pricing and Payment Terms
1. | Defined Terms. As used in this Schedule 3.1, the following terms shall have the respective meaning ascribed to them below. |
“Actual NSP” for a particular Product and in respect of a particular Quarter, means the [***].
“National NSP” or “NNSP” for a particular Product and in respect of a particular Year, means KU’s estimate of the Actual NSP for such Product for such Year, as determined pursuant to Section 2 of this Schedule 3.1.
“Supply Price” means Supply Price for Branded Product or Supply Price for Generic VPM Product, as the context requires.
“Supply Price for Branded Product” for a particular Branded Product and in respect of a particular Year, means [***].
“Supply Price for Generic VPM Product” for the Generic VPM Product shall [***].
2. | Determination of Notional NSP and Cost. |
(a) | Not later than [***], KU shall notify Alkermes of its proposed National NSP for each of the Branded VPM Product and the Branded V Product for the next subsequent Year. Such proposed Notional NSPs shall be discussed in good faith by the Parties, and the Parties shall agree upon the final Notional NSP for each Branded Product for such next subsequent Year not later than [***]. For example, KU shall provide its proposed Notional NSP for each Branded Product to Alkermes by [***] and the Parties shall agree upon the Notional NSP for the Branded Products for 2015 not later than [***]. |
(b) | Notwithstanding the foregoing, the Parties shall, by no later than [***], confer and agree upon the Notional NSP for 2014. |
3. | Branded VPM Product Terms. |
(a) | Subject to Section 3(c), below, each invoice submitted to KU upon delivery of an order of Branded VPM Product shall [***]. |
(b) | Each Quarterly report delivered to Alkermes pursuant to Section 3.5 of the Agreement shall set forth the Actual NSP for all Branded VPM Product sold during the Quarter to which such report relates. Based upon such Actual NSP: |
(i) | [***]. |
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(ii) | [***]. |
(c) | Anything to the contrary notwithstanding samples of Branded VPM Product shall be supplied to KU [***]. |
(d) | For the avoidance of doubt the parties agree that if for whatever reason the Branded VPM Product supplied by Alkermes to KU is not sold by KU, Alkermes shall retain the Supply Price paid for such Branded VPM Product (or if such Supply Price has not been paid, KU shall remain obligated to pay and shall pay such Supply Price to Alkermes). |
4. | Branded V Product Terms. |
(a) | Subject to Section 4(c), below, each invoice submitted to KU upon delivery of an order of Branded V Product shall reflect a price per unit equal to the then-current supply Price for the Branded V Product. |
(b) | Each Quarterly report delivered to Alkermes pursuant to Section 3.5 of the Agreement shall set forth the Actual NSP for all Branded V Product sold during the Quarter to which such report relates, Based upon such Actual NSP: |
(i) | [***]. |
(ii) | [***]. |
(c) | Anything to the contrary notwithstanding samples of Branded V Product shall be supplied to KU [***]. |
(d) | For the avoidance of doubt, the parties agree that if for whatever reason the Branded V Product supplied by Alkermes is not sold by KU, Alkermes shall retain the Supply Price paid for such Branded V Product (or if such Supply Price has not been paid, KU shall remain obligated to pay and shall pay such Supply Price to Alkermes). |
5. | Generic VPM Product Terms. |
(a) | In every Quarter during which every Branded Product in all dosages strengths is sold by KU, KU shall pay Alkermes [***]. |
(b) | In any Quarter where KU does not sell each dosage strength of each Branded Product, KU shall pay Alkermes [***]. |
(c) | Notwithstanding anything to the contrary the amount payable to Alkermes during any Quarter pursuant to Clause 5(a) or (b) above shall [***]. |
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Schedule 4.1
to License and
Supply Agreement
Batch Sizes and Minimum Volumes
(a)Branded V Product
Subject to Section 4.1(c), the minimum order for Branded V Product shall be:
Strength | Order Quantity |
[***] | [***] bottles per SKU, delivery dates need to coincide with Generic V Product. |
[***] | [***] bottles per SKU, delivery dates need to coincide with Generic V Product. |
[***] | [***] bottles per SKU, delivery dates need to coincide with Generic V Product. |
[***] | [***] bottles per SKU, delivery dates need to coincide with Generic V Product. |
(b)Branded and Generic VPM Product
If both the Branded VPM Product and the Generic VPM Product are ordered, then the minimum order shall be:
Strength | Order Quantity |
[***] | [***] bottles of Branded VPM Product, combined with [***] bottles of Generic VPM Product |
[***] | [***] bottles of Branded VPM Product, combined with [***] |
[***] | [***] bottles of Branded VPM Product, combined with [***] |
If only Branded VPM Product or Generic VPM Product is ordered, then the minimum order for whichever Product is ordered shall be:
Strength | Order Quantity |
[***] | [***] bottles of VPM Product or [***] bottles of Generic |
[***] | [***] bottles of VPM Product or [***] bottles of Generic |
[***] | [***] bottles of VPM Product or [***] bottles of Generic |
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Schedule 6.4
to License and
Supply Agreement
Intellectual Property
TRADEMARKS
VERELAN - U.S. Registration No.: 1,551,582
The Pre-Approved Forms in which this Trademark may be used by KU hereunder is as follows:
Verelan®
Verelan® capsules
Verelan® (verapamil hydrochloride capsules)