Host Cell Line definition
Host Cell Line means the proprietary host cell line developed by WuXi Biologics, and designated by WuXi Biologics as the [***], that is used to make the Licensed Cell Line.
Host Cell Line means the [**] Cell Line provided by Lonza as part of the GS System and any improvements thereto;
Host Cell Line means any host cell line Controlled by Ambrx and/or its Affiliate(s) as of the Effective Date or thereafter during the Term suitable for the expression of a Compound. For clarity, the Host Cell Line contains the ReCODE/EuCODE Components, but does not contain DNA encoding a Compound and does not express Compound. Any Host Cell Line is only to be used by BMS in accordance with the terms and conditions of this Agreement for the expression of Compounds. Host Cell Lines shall be transferred to BMS pursuant to Section 6.2(c). Subject to and to the extent as provided in Section 17.8, the use of “Affiliate” in this definition shall exclude any Third Party that becomes an Affiliate due to a Change of Control Transaction involving Ambrx (or any of its Affiliates).
Examples of Host Cell Line in a sentence
WuXi Biologics shall notify Licensee in writing within [***] following the date on which WuXi Biologics completes transfection of the Host Cell Line to generate the Licensed Cell Line.
BMS shall not engineer, reverse engineer, extract or modify the ReCODE/EuCODE Components for any Host Cell Line, except to the extent as may be expressly permitted in advance in writing by Ambrx.
For the avoidance of doubt, all Intellectual Property (including rights in confidential information) in the Host Cell Line shall remain vested in Lonza but Kolltan shall be the owner of the Kolltan Cell Line.
This license granted under this Article 2 starts on the date WuXi Biologics completes transfection of the Host Cell Line to generate the applicable Licensed Cell Line (the “Commencement Date”).
More Definitions of Host Cell Line
Host Cell Line means the [**] Cell Line provided by Lonza as part of the GS System and any improvements thereto Lonza shall manufacture cGMP Product to meet the Specification, provided that there shall be no such obligation to meet the amounts stated to be target amounts or where the specification is to “report result”. Lonza shall use reasonable commercial endeavours to manufacture cGMP Product to meet the target amounts. There shall be no obligation on Lonza to meet Specification where such failure is due (in whole or in part) to acts or omissions of Kolltan or any third party after Delivery of the bulk Product. The work programme contains activities required prior to manufacture of a cGMP Batch. Changes to the Specification may affect the activities and Price for the Services.
Host Cell Line means the proprietary cell line developed by WuXi Biologics, and designated by WuXi Biologics as the CHO K1-Cell Line, that is used in the manufacture and production of Client Products for clinical trials and commercial purposes. 1.9 “Licensed Cell Line” means a transformed or transfected (using WuXi Biologics’ Construct(s)) version of the Host Cell Line that produces the Client Product. 1.10 “Licensed Know-How” means any know-how and non-public information owned or controlled by WuXi Biologics that is used or incorporated in the Process, and that is necessary to operate the Process as described in the Technology Transfer Package. The word “control” when used in connection with Licensed Know-How includes both exclusively and non-exclusively licensed know-how and non-public information, as well a right of WuXi Biologics to transfer such know-how and non-public information to Licensee. 1.11 “Materials” means the biological materials, including the Licensed Cell Line, provided to Licensee pursuant to the license granted under this Agreement. 1.12 “Media and Feeds” means any proprietary media and feeds used in the Process. 1.13 “Process” means a process for manufacture of Client Product utilizing Licensed Know-How, Materials and Media and Feeds as described in the Technology Transfer Package. 1.14 “Regulatory Approval” means any and all approvals (including pricing and reimbursement approvals), product and establishment licenses, registrations or authorizations of any kind of a Regulatory Authority necessary for the development, clinical testing, manufacture, quality testing, supply, use, storage, importation, export, transport, marketing and sale of a Client Product (or any component thereof) for use in any country or other jurisdiction.