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RESIDUAL LICENSE AGREEMENT

License Agreement

RESIDUAL LICENSE AGREEMENT | Document Parties: INSITE VISION INC | AZITHROMYCIN ROYALTY SUB LLC You are currently viewing:
This License Agreement involves

INSITE VISION INC | AZITHROMYCIN ROYALTY SUB LLC

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Title: RESIDUAL LICENSE AGREEMENT
Governing Law: New York     Date: 5/12/2008
Industry: Biotechnology and Drugs     Sector: Healthcare

RESIDUAL LICENSE AGREEMENT, Parties: insite vision inc , azithromycin royalty sub llc
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Exhibit 10.5
 
RESIDUAL LICENSE AGREEMENT
 
dated as of February 21, 2008
 
between
 
AZITHROMYCIN ROYALTY SUB LLC
 
and
 
INSITE VISION INCORPORATED
 


RESIDUAL LICENSE AGREEMENT
 
This Residual License Agreement (this “ Residual License Agreement ”), dated as of February 21, 2008 (the “ Execution Date ”), is between AZITHROMYCIN ROYALTY SUB LLC, a Delaware limited liability company (the “ Issuer ”), and INSITE VISION INCORPORATED, a Delaware corporation (the “ Parent ”).
 
W I T N E S S E T H :
 
WHEREAS, the Parent owns or controls certain intellectual property rights that have been exclusively and non-exclusively licensed to Inspire pursuant to the Counterparty License Agreement for the development and commercialization of Subject Products in the Field in the Territory;
 
WHEREAS, upon a partial or entire termination of the Counterparty License Agreement, such rights will partially or entirely revert back to the Parent subject to the terms and conditions of the Counterparty License Agreement;
 
WHEREAS, the Parent and the Issuer have entered into the Purchase and Sale Agreement, pursuant to which the Parent has agreed to execute and deliver this Residual License Agreement;
 
NOW, THEREFORE, in consideration of the premises and the mutual agreements set forth herein and of other good and valuable consideration, the receipt and adequacy of which are hereby acknowledged, the parties hereto covenant and agree as follows:
 
ARTICLE I
RULES OF CONSTRUCTION AND DEFINED TERMS
 
Section 1.1   Rules of Construction and Defined Terms . The rules of construction set forth in Annex A shall apply to this Residual License Agreement and are hereby incorporated by reference into this Residual License Agreement as if set forth fully in this Residual License Agreement. Capitalized terms used but not otherwise defined in this Residual License Agreement shall have the respective meanings given to such terms in Annex A , which is hereby incorporated by reference into this Residual License Agreement as if set forth fully in this Residual License Agreement.
 
Section 1.2   Pfizer Patent Rights . Each of the Parent and the Issuer acknowledges and agrees that the Residual License does not initially, and may not in the future, include any rights to the Pfizer Patent Rights. After the Execution Date, the Parent shall use commercially reasonable efforts to obtain Pfizer’s written consent pursuant to the Pfizer License Agreement to grant the Issuer a sublicense described in Section 2.2(e) . The Issuer understands and agrees that such consent may not be obtained despite the Parent’s commercially reasonable efforts. If the Parent is able to obtain such consent and the License Effective Date occurs, then the Pfizer Patent Rights shall be automatically sublicensed to the Issuer as of the License Effective Date (or such other date as provided in such consent) under the terms and conditions of Section 2.2(e) (or such other terms as provided in such consent); provided , that (a) such sublicense will be of no greater scope than the rights and licenses granted to the Parent under the Pfizer Patent Rights pursuant to the Pfizer License Agreement, or as otherwise provided in such consent, and (b) such sublicense shall be subject to the applicable terms and conditions of the Pfizer License Agreement and such consent. If the Parent is not able to obtain such consent pursuant to this Section 1.2 and the Issuer sublicenses the Residual License to any Person other than Parent without such sublicense under the Pfizer Patent Rights, the Issuer shall indemnify, and cause such Person to indemnify, the Parent for any liability that the Parent may have to Pfizer for commercialization of the Subject Products.
 
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ARTICLE II
RESIDUAL LICENSE MATTERS
 
Section 2.1   Effectiveness . Each of the Issuer and the Parent acknowledges and agrees that the Residual License shall only become effective if and only if the Counterparty License Agreement partially or entirely terminates under the terms thereof and the Reverted IP reverts back to the Parent in respect of such partial or entire termination for the Terminated Territory prior to the earliest of the events described in the definition of the Expiration Date. Subject to the foregoing, the Residual License shall become automatically effective upon such termination for the Terminated Territory with no further action by either the Parent or the Issuer (the “ License Effective Date ”). The Issuer understands and agrees that the Residual License shall be at all times subject to any Surviving Rights. The Issuer understands and agrees that the Parent may only grant rights under the Reverted IP after the reversion of such rights back to the Parent under the terms and conditions of the Counterparty License Agreement and that no rights of Inspire may be granted by the Parent.
 
Section 2.2   Residual License Grant . Upon the License Effective Date and subject to the terms and conditions of this Residual License Agreement, the Parent automatically grants to the Issuer the following licenses during the License Term (collectively, the “ Residual License ”):
 
(a)   an exclusive license, under the AzaSite Patent Rights and the Licensed Know-How (excluding any Formulation Know-How), with the right to grant sublicenses, to develop, have developed, make, have made, use, have used, market, have marketed, commercialize, have commercialized, offer for sale, sell, have sold, import and have imported Subject Products in the Field in the Terminated Territory ;
 
(b)   a non-exclusive license, under the DuraSite Patent Rights, the Container Patent Rights and the Formulation Know-How , with the right to grant sublicenses, to develop, have developed, make, have made, use, have used, market, have marketed, commercialize, have commercialized, offer for sale, sell, have sold, import and have imported Subject Products in the Field in the Terminated Territory;
 
(c)   an exclusive license, with the right to grant sublicenses, to use the AzaSite Trademark and Licensed Domain Names in connection with the marketing, commercialization and sale of Subject Products in the Field in the Terminated Territory;
 
(d)   a non-exclusive license, with the right to grant sublicenses, to use the DuraSite Trademark in connection with the marketing, commercialization and sale of Subject Products in the Field in the Terminated Territory; and
 
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(e)   if and only if Pfizer grants its written consent under the terms and conditions of Section 1.2 and only to the extent no greater in scope than the rights and licenses granted to the Parent for the Pfizer Patent Rights pursuant to the Pfizer License Agreement (or as otherwise provided in the consent from Pfizer as provided under Section 1.2), an exclusive sublicense, with the right to grant sublicenses, to develop, have developed, make, have made, use, have used, market, have marketed, commercialize, have commercialized, offer for sale, sell, have sold, import and have imported Subject Products in the Field in the Terminated Territory.
 
Section 2.3   Interim Sublicense to the Parent .  
 
(a)   Upon the License Effective Date and subject to the terms and conditions of this Residual License Agreement, the Issuer grants the Parent, under the terms and conditions of this Section 2.3 , all the rights licensed to the Issuer under the Residual License without any retained rights (“ Interim Sublicense ”) for a three month period after the License Effective Date, or such longer period as requested by the Parent and consented to in writing by the Issuer and the Trustee in accordance with Section 9.6 (“ Interim Period ”); provided that the terms of any such sub-sublicense shall not be inconsistent with the terms of this Residual License Agreement.
 
(b)   Except as the Issuer otherwise expressly agrees in writing, the Interim Sublicense shall terminate, automatically and without further action by either the Parent or the Issuer if, at the end of the Interim Period or at any time thereafter, (a) the Parent is not actively engaged in commercially reasonable efforts to commercialize in the Field any Subject Product being commercialized by Inspire in the Terminated Territory immediately prior to the applicable Termination Date for such Terminated Territory or (b) the Parent is not a party to a definitive sub-sublicense agreement with a third party designated by the Parent (x) where the Parent used commercially reasonable efforts to procure commercially reasonable royalties and other payments as consideration for such sub-license and (y) that includes an obligation by such third party as sub-sublicensee to use commercially reasonable efforts to commercialize in the Field any Subject Product being commercialized by Inspire in the Terminated Territory immediately prior to the applicable Termination Date for such Terminated Territory (the “ Parent Sublicense ”). The Interim Sublicense will continue for the License Term for as long as the Parent performs either of the foregoing; provided that the Parent is not obligated to perform either of the foregoing. The Issuer shall not exercise the Residual License or grant any rights thereunder until the termination of the Interim Sublicense as provided herein.
 
Section 2.4   Sublicenses by the Issuer . If the Interim Sublicense terminates in accordance with Section 2.3 , the Issuer may grant a sublicense under the Residual License during the License Term subject to this Section 2.4 . In any such sublicense, the Issuer shall use commercially reasonable efforts to procure commercially reasonable royalties and other payments for the commercialization of the Subject Products under the Residual License and any such sublicense shall (i) be solely within the scope of the Residual License; (ii) be in writing and contain provisions that are not inconsistent with this Residual License Agreement and (iii) contain other customary provisions as protective of the Reverted IP as customary in the industry in an arm’s length transaction of this nature, including appropriate indemnity and other risk allocation coverage in favor of the Parent. The Issuer shall furnish to the Parent a complete copy (including any annexes, appendices, exhibits or schedules thereto) of any sublicense granted by the Issuer to any Person under the Residual License (other than the Interim Sublicense) within five Business Days of the effective date of such sublicense. Except as the parties otherwise expressly agree in writing, any sublicense granted by the Issuer under this Section 2.4 shall (A) be subject and subordinate to the terms of this Residual License Agreement and (B) provide that the sublicense will be assignable to the Parent at the end of the License Term under the same terms and the Parent shall accept such assignment as a direct license between the Parent and the sublicensee (provided that the Parent shall not be required to assume any liability incurred by the Issuer under such sublicense prior to that time). Each such sublicense granted by the Issuer under this Section 2.4 shall be herein referred to as the “ Issuer Sublicense ”.  
 
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Section 2.5   Reservation of Rights . Except as the Parent otherwise expressly agrees in writing and subject to Article VII , the Residual License shall terminate at the end of the License Term, and all rights to the Reverted IP shall then revert back to the Parent automatically and without further action by either the Parent or the Issuer. The Parent does not grant to the Issuer any technology or intellectual property rights of the Parent other than as expressly granted under this Residual License Agreement, whether by implication, estoppel or otherwise. Without limiting the foregoing, (a) the licenses and rights granted to the Issuer under this Residual License Agreement shall not include a right to offer for sale, sell or have sold Subject Products, and the Issuer expressly covenants that it shall not sell any Subject Products, in the Terminated Territory in circumstances in which the Issuer knows or reasonably should know such Subject Products will be distributed or sold outside the Terminated Territory, (b) the Parent shall retain the rights under the Reverted IP and the Pfizer Patent Rights (if granted under the terms of Section 1.2 ) to develop, have developed, make, have made, use and have used Subject Products in the Field in the Territory solely for the purposes of distribution, sale or other commercial pursuit of Subject Products outside the Territory, (c) the Parent shall retain the exclusive rights to develop, have developed, make, have made, use, have used, market, have marketed, commercialize, have commercialized, offer for sale, sell, have sold, import and have imported Subject Products outside the Field and/or outside the Territory and (d) the Parent retains all rights to pursue any of its reserved interests under the Counterparty License Agreement.
 
ARTICLE III
PAYMENTS
 
Section 3.1   Payment of Royalties . The consideration for the Residual License consists of the amounts paid by the Issuer to the Parent pursuant to the Purchase and Sale Agreement, and no further royalty payments are due from the Issuer to the Parent for the Residual License.  
 
(a)   Interim Sublicense . The Issuer acknowledges and agrees that any royalties and other payments described in (i) and (ii) below (“ License Royalties ”) will be considered Replacement Royalty Payments and shall be deposited in the Collection Account when paid by the Parent to the Issuer as provided below.  
 
(i)   In the event that the Parent directly commercializes under the Interim Sublicense, the Parent will pay the Issuer only the royalties or any other payments received by the Parent in such commercialization efforts equal to the amount of royalties and other payments that would have been payable by Inspire in each such Terminated Territory, at the time such amounts would have been payable, net of all deductions and adjustments as if the Counterparty License Agreement (as of the Termination Date) were still in effect and such commercialization was effected by Inspire as if the Subject Products were Inspire Licensed Products (as defined in the Counterparty License Agreement).  
 
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(ii)   In any sublicense under the Interim Sublicense, the Parent will use commercially reasonable efforts to procure commercially reasonable royalties and other payments for the commercialization of the Subject Products under such sublicense, provided that the Issuer understands and agrees that such royalties and other payments may not be equivalent to the royalties and other payments due from Inspire to the Parent under the Counterparty License Agreement had such agreement not terminated in the Terminated Territory. The Parent will pay the Issuer any and all royalties and any other payments received by the Parent from such sublicense under the terms of such sublicense.
 
(b)   Other than Interim Sublicense . The Issuer shall deposit, or shall cause to be deposited, in the Collection Account any and all royalties and other payments arising from the exercise of the Residual License after the termination of the Interim Sublicense, whether received by the Issuer in its own direct commercialization efforts or received by the Issuer from its sublicensees under the terms of the agreements with such sublicensees (“ Issuer Royalties ”).
 
Section 3.2   Pfizer and Other Royalties . For as long as the Issuer receives the License Royalties or the Issuer Royalties as provided under this Residual License Agreement, regardless of the party commercializing under the terms of this Residual License Agreement, the Issuer shall pay, or cause to be paid, either to the Parent for the Parent to pay the applicable third party or directly to the applicable third party, any royalties or other payments that may be due from the Parent to Pfizer and any other third parties for any commercialization of the Subject Products within the timeframes required by the Pfizer License Agreement and the agreements with such third parties, but in no event shall such royalties exceed, in the aggregate, 3.5% of Net Sales (as defined in the Counterparty License Agreement) for the applicable payment period.  
 
ARTICLE IV
BOOKS AND RECORDS
 
Section 4.1   Reports . For as long as there are License Royalties, the Parent shall provide to the Issuer, within 25 days after the end of each calendar quarter, a report setting forth for such calendar quarter the following information for each Subject Product: (a) net sales of such Subject Product by the Parent or its sublicensees on a country-by-country basis; (b) License Royalties due for such net sales; and (c) a description of how the License Royalties are calculated. For as long as there are Issuer Royalties during the License Term, the Issuer shall provide to the Parent, within 25 days after the end of each calendar quarter, a report setting forth for such calendar quarter the following information for each Subject Product: (a) net sales of such Subject Product by the Issuer or its sublicensees on a country-by-country basis; (b) Issuer Royalties paid to the Issuer for such net sales; and (c) a description of how the Issuer Royalties are calculated.
 
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Section 4.2   Books and Records . Each party shall keep and maintain, or shall cause to be kept and maintained, and shall require any sublicensee to keep and maintain, complete and accurate records and books of account in sufficient detail and form so as to enable determination and verification of any License Royalties or Issuer Royalties. Such records and books of account shall be maintained for a period of no less than two years following the calendar quarter to which they pertain. Each party shall permit such records and books of account to be examined by the other party or the other party’s duly appointed agent to the extent necessary for the other party to verify the amount of any License Royalties or Issuer Royalties payable hereunder. Such examination shall be at the expense of the examining party, during normal business hours, and upon ten days’ prior written notice to the other party.
 
ARTICLE V
REVERTED IP
 
Section 5.1   Reverted IP . To the extent owned or controlled by the Parent, any and all Reverted IP (including any inventions arising or resulting hereunder) shall remain the sole property of the Parent. Any Taxes, annuities, working fees, maintenance fees, renewal charges, extension charges or other fees or payments that are due during the License Term with respect to the prosecution or maintenance of any patents or patent applications (or reissues, extensions, substitutions, confirmations, registrations, revalidations, additions, continuations, continuations-in-part or divisions thereof or thereto or any additional protection certificate granted with respect thereto) in respect of any Reverted IP (other than due to their use or practice) shall be paid by the Parent. During the License Term, if a reissue, reexamination, interference, opposition or other proceeding before any Governmental Authority is initiated relating to any rights exclusively licensed under the Residual License, the Parent shall provide to the Issuer, to the extent it is able without any additional consent and without any adverse impact on the Parent, for its reasonable review and comment prior to filing or other submission, copies of all substantive legal documents (including any patent applications) relating to such proceeding that are owned or controlled by the Parent. The Issuer shall provide any comments within 30 days of receipt thereof (or such shorter time as may be appropriate in the circumstances), but such comments shall be advisory in nature and not binding on the Parent. Upon the Issuer’s written request, the Parent shall provide to the Issuer copies of all such documents as filed or otherwise submitted, to the extent it is able without any additional consent and without any adverse impact on the Parent.
 
ARTICLE VI
INFRINGEMENT AND LITIGATION
 
Section 6.1   Infringement and Litigation . During the License Term, each party hereto shall promptly notify the other party hereto in writing if such party hereto reasonably believes that a third party is engaging in one or more activities that infringes one or more claims of the Reverted IP in the Field in the applicable Terminated Territory. During the License Term, the Parent at its own expense shall have the first right, but not the obligation, to bring and prosecute to conclusion (or otherwise settle) any legal action for infringement of the Reverted IP in the applicable Terminated Territory or to defend any counterclaim of invalidity or action of a third party for declaratory judgment of non-infringement or interference (and the Issuer shall have the right to do the foregoing with respect to any rights exclusively owned by the Parent and exclusively licensed to the Issuer under the Residual License at its own expense if the Parent has not taken commercially reasonable steps to do so within 90 days of the notice referred to above). Any recovery or proceeds of settlement or judgment in any action brought or defended by the Parent under this Section 6.1 shall be equitably allocated between the Parent and the Issuer.
 
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ARTICLE VII
TERM AND TERMINATION
 
Section 7.1   Term and Termination . This Residual License Agreement shall be a legally binding agreement between the parties hereto as of the Execution Date and shall terminate without further notice on the Expi

 
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