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10.2 Additional Representations and Warranties of Licensor ............................................ 95
10.3 Additional Covenants of Licensor ............................................................................ 101
10.4 DISCLAIMER OF WARRANTIES ......................................................................... 101
ARTICLE 11 INDEMNITY ........................................................................................................ 101
11.1 Indemnification of Licensor ...................................................................................... 101
11.2 Indemnification of AbbVie ....................................................................................... 102
11.3 Certain Losses ........................................................................................................... 102
11.4 Notice of Claim ......................................................................................................... 103
11.5 Control of Defense .................................................................................................... 103
11.6 Special, Indirect, and Other Losses........................................................................... 105
11.7 Insurance ................................................................................................................... 105
ARTICLE 12 TERM AND TERMINATION ............................................................................. 106
12.1 Term .......................................................................................................................... 106
12.2 Termination for Material Breach .............................................................................. 107
12.3 Material Breach Related to Diligence in Major Markets .......................................... 108
12.4 Invocation of Termination for Material Breach ........................................................ 108
12.5 For Convenience ....................................................................................................... 108
12.6 Termination for Insolvency ....................................................................................... 108
12.7 Rights in Bankruptcy ................................................................................................ 108
12.8 Effects of Termination and Option Expiration ......................................................... 109
12.9 Transition .................................................................................................................. 112
12.10 Reverse Royalty ........................................................................................................ 115
12.11 Remedies ................................................................................................................... 115
12.12 Accrued Rights; Surviving Obligations .................................................................... 115
ARTICLE 13 MISCELLANEOUS ............................................................................................. 116
13.1 Force Majeure ........................................................................................................... 116
13.2 Change in Control of Licensor .................................................................................. 116
13.3 Export Control .......................................................................................................... 118
13.4 Assignment ............................................................................................................... 118
13.5 Severability ............................................................................................................... 119
13.6 Governing Law, Jurisdiction and Service ................................................................. 119
13.7 Dispute Resolution .................................................................................................... 120
13.8 Notices ...................................................................................................................... 121
13.9 Entire Agreement; Amendments............................................................................... 122
13.10 English Language...................................................................................................... 122
13.11 Equitable Relief ........................................................................................................ 123
13.12 Waiver and Non-Exclusion of Remedies .................................................................. 123
13.13 No Benefit to Third Parties ....................................................................................... 123
13.14 Further Assurance ..................................................................................................... 123
13.15 Relationship of the Parties ........................................................................................ 123
13.16 Performance by Affiliates ......................................................................................... 124
13.17 Counterparts; Facsimile Execution ........................................................................... 124
13.18 References ................................................................................................................. 124
13.19 Construction .............................................................................................................. 124
SCHEDULES
Schedule 1.69 Corporate Names
Schedule 1.90 Existing In-License Agreements
Schedule 1.127 AL003 and Backups
Schedule 1.129 AL002 and Backups
Schedule 1.150 Manufacturing Cost
Schedule 1.188 PoC Trial Parameters
Schedule 1.193 Pre Exercise Development Plan and Budget
Schedule 3.1.3 PoC Trial Report Requirements
Schedule 3.2.1 Initial Post Exercise Development Plan and Budget
Schedule 3.3.2 Antibody Approved for Additional Licensor Development Activities
Schedule 3.5.5 Pre-Approved Subcontractors
Schedule 5.7.1 Example Calculations of Third Party Payment Responsibilities
Schedule 6.4.4 FTE Rates
Schedule 7.6.5 Existing In-License Agreement Obligations
Schedule 10.2 Exceptions
Schedule 10.2.1 Existing Patents
Schedule 12.8.1(f) Enforcement and Defense of AbbVie Grantback Patents
Schedule 13.7.3 ADR Procedures
CO-DEVELOPMENT AND OPTION AGREEMENT
This Co-Development and Option Agreement (this "Agreement") is made and entered into effective as of October 16, 2017 (the "Execution Date") by and between Alector, Inc. (f/k/a Alector LLC), a Delaware corporation ("Licensor"), and AbbVie Biotechnology, Ltd., a Bermuda limited company ("AbbVie"). Licensor and AbbVie ar...
RECITALS
WHEREAS, Licensor has developed certain Licensed Antibodies (as defined herein) and Controls (as defined herein) certain intellectual property and other rights with respect to such Licensed Antibodies in the Territory (as defined herein); and
WHEREAS, Licensor wishes to grant an option to a license to AbbVie, and AbbVie wishes to take, such option to a license with respect to Licensed Antibodies under Licensor's intellectual property and other rights therein, for purposes of developing and commercializing Licensed Products (as defined herein) in the Territo...
NOW, THEREFORE, in consideration of the premises and the mutual promises and conditions hereinafter set forth, and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties, intending to be legally bound, do hereby agree as follows:
ARTICLE 1. DEFINITIONS
Unless otherwise specifically provided herein, the following terms shall have the following meanings:
1.1 "AbbVie" has the meaning set forth in the preamble hereto.
1.2 "AbbVie Background Know-How" means all Information that is (a) Controlled by AbbVie or any of its Affiliates on the Execution Date or at any time during the Term, (b) not generally known, (c) developed or invented outside the scope of this Agreement, and (d) either used by AbbVie or provided by AbbVie for use in th...
1.3 "AbbVie Background Patents" means all Patents that are (a) Controlled by AbbVie or any of its Affiliates on the Execution Date or at any time during the Term, (b) developed or invented outside the scope of this Agreement, and (c) covering subject matter either used by AbbVie or provided by AbbVie for use in the Dev...
1.4 "AbbVie Competing Product" has the meaning set forth in Section 5.10.2(a).
1.5 "AbbVie Grantback Know-How" means, as used in connection with any grant back license provided in Section 12.8.1(c), AbbVie Program Know-How and Joint Program Know-How that (a) is Controlled by AbbVie as of the effective date of the applicable termination of this Agreement (either in its entirety or with respect to ...
1.6 "AbbVie Grantback Patents" means, as used in connection with any grant back license provided in Section 12.8.1(c), AbbVie Program Patents and Joint Program Patents that (a) are Controlled by AbbVie as of the effective date of the applicable termination of this Agreement (either in its entirety or with respect to a ...
1.7 "AbbVie Incorporated Background Know-How" has the meaning set forth in Section 12.8.1(d).
1.8 "AbbVie Indemnitees" has the meaning set forth in Section 11.2.
1.9 "AbbVie Independent New Technology" means New Technology which AbbVie or its Affiliates has either acquired from a Third Party or developed outside the Collaboration Program without use or reference to the Confidential Information of Licensor, and which the Parties agree in writing will be applied to a Licensed Pro...
1.10 "AbbVie Opt In" has the meaning set forth in Section 3.3.4.
1.11 "AbbVie Opt In Exercise Date" has the meaning set forth in Section 3.3.4.
1.12 "AbbVie Opt In Product" means a Licensed Product for which AbbVie has exercised the AbbVie Opt In.
1.13 "AbbVie Program Know-How" means all Information and inventions that are, as between the Parties, conceived, discovered, developed, or otherwise made solely by or on behalf of AbbVie, its Affiliates or their Sublicensees or subcontractors as a result of performance of this Agreement. AbbVie Program Know-How express...
1.14 "AbbVie Program Patents" mean all Patents that claim inventions that, as between the Parties, are conceived, discovered, developed, or otherwise made solely by or on behalf of AbbVie, its Affiliates or their Sublicensees or subcontractors as a result of performance of this Agreement. AbbVie Program Patents express...
1.15 "Accounting Standards" means, with respect to a Party, that such Party shall maintain records and books of accounts in accordance with United States Generally Accepted Accounting Principles, consistently applied.
1.16 "Acquirer" has the meaning set forth in Section 13.2.1(a).
1.17 "Acquisition" means, with respect to a Party, a merger, acquisition (whether of all of the stock or all or substantially all of the assets of a Person or any operating or business division of a Person) or similar transaction by or with the Party, other than a Change in Control of the Party.
1.18 "Additional Development Costs" has the meaning set forth in Section 6.5.2(b)(i).
1.19 "Additional Indication" means, with respect to the Licensed Antibodies and Licensed Products, each Indication other than the Alzheimer's Indication.
1.20 "Additional Licensor Development Activities" has the meaning set forth in Section 3.3.1.
1.21 "Additional Repayment Amount" has the meaning set forth in Section 3.7.1(e).
1.22 "Adimab Agreement" has the meaning set forth in Schedule 1.90.
1.23 "Adimab Applications" has the meaning set forth in Section 10.2.5.
1.24 "Adjusted Royalty Rate" has the meaning set forth in Section 6.5.2(a).
1.25 "ADR" has the meaning set forth in Section 13.7.1.
1.26 "Adverse Ruling" has the meaning set forth in Section 12.2.
1.27 "Affiliate" means, with respect to a subject Person, any other Person that, directly or indirectly, through one (1) or more intermediaries, controls, is controlled by or is under common control with such subject Person. For purposes of this definition, "control" and, with correlative meanings, the terms "controlle...
1.28 "Agreement" has the meaning set forth in the preamble hereto.
1.29 "Alliance Manager" has the meaning set forth in Section 2.4.5.