1.31 “Know-How” means all Materials and all confidential and proprietary commercial, technical, scientific and other know-how and information, trade secrets, knowledge, technology, methods, processes, practices, formulae, instructions, skills, techniques, procedures, experiences, ideas, technical assistance, designs, drawings, assembly procedures, computer programs, specifications, data and results (including biological, chemical, pharmacological, toxicological, pharmaceutical, physical and analytical, preclinical, clinical, safety, manufacturing and quality control data and know-how, including study designs and protocols), in all cases, provided such information is confidential and proprietary, and regardless of whether patentable, in written, electronic or any other form now known or hereafter developed.
1.32 “Know-How Royalties” has the meaning set forth in Section 4.3(a).
1.33 “Late Stage Development” means, with respect to a product, that first dosing under Phase 2 Studies has been initiated.
1.34 “Law” or “Laws” means all laws, statutes, rules, regulations, orders, judgments or ordinances having the effect of law of any federal, national, multinational, state, provincial, county, city or other political subdivision.
1.35 “License Agreement” has the meaning set forth in the Preamble.
1.36 “License Agreement Effective Date” has the meaning set forth in the Preamble.
1.37 “Licensed Antibody Product” has the meaning set forth in the Development and Option Agreement.
1.38 “Licensed Genome Editing Product” has the meaning set forth in the Development and Option Agreement.
1.39 “Licensed Product” means the [***]with respect to which GreenLight has exercised the Option under the Development and Option Agreement, which consists of the Targets set forth on Appendix 1.38. For the avoidance of doubt, the term Licensed Product in respect of a given Target encompasses all variants of such Target, including the wild types, naturally occurring variants, engineered variants wherein modifications to the native amino acid sequence have been made (for example, mutated versions, derivatives or fragments) and species homologs and orthologs thereof, provided, however, that any such naturally occurring variant, engineered variant or species homolog or ortholog possesses substantially similar biological activity to such Target(s) (for example antigenicity in case of antigens). In the case of [***]GreenLight may submit multiple [***]for [***]in Appendix 1.38. In the event that GreenLight wishes to include [***]after the Effective Date these additional sequences may be submitted to the Escrow Agent for review. If the Escrow Agent determines that these [***]are not subject to Pre-Existing Restrictions (at the time of review) and are published [***] for known strains or subtypes of [***] then such [***] will be included in Appendix 1.38.
1.40 “Licensed Product Royalty Term” has the meaning set forth in Section 4.3(d).
1.41 “Licensed Technology” means all Acuitas Technology as of the License Agreement Effective Date or generated or obtained during the Term (including the Acuitas Background Technology, Acuitas Sole Technology and Acuitas’ interest in any Joint IP) necessary or useful for the research, development, manufacture, use or sale of a Licensed Product including without limitation the , patents listed, in Appendix 1.40 attached hereto to be updated from time to time.
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