Research License Period definition

Research License Period means, on a Research Antigen-by-Research Antigen basis, the period commencing on the date that Medarex notifies Celldex of the availability of an antigen pursuant to Section 3.2 (the “Notification Date”), and ending on the earlier of (i) twelve (12) months after the Notification Date, or if extended pursuant to Section 3.4.2, the expiration of any such extension(s), or (ii) when Celldex has taken an Exclusive Commercial License with respect to the particular Research Antigen pursuant to Section 4.3, or (iii) the termination of the Agreement.
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Research License Period means, other than as provided in Section 4.5.2, the earlier of (i) termination of the Research License for such Designated Antigen or this Agreement pursuant to Article 17 or (ii) (a) for the [***], or (b) [***].
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Research License Period means, other than as provided in Section 4.5.2, for each Designated Antigen, the earlier of (a) [ * ] , or (b) [ * ] . “Royalty Reports” has the meaning set forth in Section 11.9. “Royalty Term” means, on a Product-by-Product and country-by-country basis, the period commencing on the First Commercial Sale of a Product and ending upon [ * ] : (a) [ * ] ; or (b) (x) [ * ] , or (y) [ * ] (i) [ * ] (A) [ * ] , and (B) [ * ] . “Sales Training Expenses” has the meaning sent forth in Schedule I. “Second Collaboration Antigen” means that certain Designated Antigen with respect to which SGI exercises its Opt-In Right pursuant to Section 4.1.2. “Second Collaboration Product” means any and all products containing an ADC comprised of an Antibody that binds specifically to the Second Collaboration Antigen. “Second Exclusive Antigen” means a Designated Antigen, other than the First Exclusive Antigen or the Third Exclusive Antigen, for which Agensys exercises an Option for an Exclusive License pursuant to Section 10.1.2 of this Agreement, as set forth in S chedule C in accordance with Section 3.5 of this Agreement. “Serious Adverse Event” means any Adverse Event occurring at any dose in response to the administration of Product that: (a) results in death or threatens life; (b) results in persistent or significant disability/incapacity; (c) results in or prolongs hospitalization; (d) results in a congenital anomaly or birth defect; or (e) is otherwise medically significant. “SGI Collaboration Know-How” means any and all technical information, processes, formulae, data, inventions, methods, know- how and trade secrets, that relate to Collaboration Inventions made by or assigned to SGI under Section 15.1.3(b). “SGI Collaboration Patents” means Patents that claim the Collaboration Inventions made by or assigned to SGI under Section 15.1.3(b). “SGI Collaboration Technology” means the SGI Collaboration Patents and the SGI Collaboration Know-How. “SGI In-Licenses” means the following agreements between SGI and the indicated Third Parties: (a) the License Agreement between [ * ] and SGI dated [ * ] , as amended (the “[ * ] ”); (b) the License Agreement between [ * ] and SGI dated [ * ] , as amended (the “[ * ] ”); and (c) any other license agreement between SGI and a Third Party covering [ * ] under which Agensys is granted a sublicense under this Agreement as provided in Section 10.4.2. -16-
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Examples of Research License Period in a sentence

  • If Celldex elects to obtain a Research License from Medarex pursuant to Section 3.1 with respect to a particular Antigen, there shall be no license fee for the initial Research License Period for such Antigen.

  • The parties acknowledge and agree that Celldex shall not owe any payment for the initial twelve (12) months of a Research License Period with respect to each Research Antigen.

  • At any time during the Research License Period with respect to a particular Research Antigen, Celldex may provide written notice to Medarex that it wishes to acquire an Exclusive Commercial License to an Antibody raised against such Research Antigen and to Products containing such Antibody.

  • Upon expiration of the Research License Period for a Research Antigen, the corresponding Research License granted hereunder shall expire.

  • The initial Research License Period for a particular Research Antigen shall commence on the date that Medarex notifies Celldex that a particular Research Antigen is available for licensing by Celldex pursuant to Section 3.2 and shall expire twelve (12) months later.

  • Upon expiration of the Research License Period for a given Research Antigen, the applicable Research License shall terminate.

  • If Celldex elects to extend the Research License Period for a particular Research Antigen pursuant to Section 3.4.2, then concurrently with its notice that Celldex wishes to extend the Research License Period for such Research Antigen, Celldex shall pay to Medarex a non-refundable, non-creditable license fee of [*****] for each twelve (12) month extension.

  • The Research License Period can be extended on a case-by-case basis with the agreement of the CSC only and a maximum of up to [*].

  • If Genmab elects to extend the Research License Period for either a [***] Research Antigen or an [***] Research Antigen pursuant to Section 15.3.2(a) or 15.3.2(b), Genmab shall pay to Medarex [***] for each [***] extension per [***] Research Antigen or [***] Research Antigen.

  • Upon expiration of the Research License Period, the corresponding Research License granted hereunder shall expire.

Related to Research License Period

  • License Period means the period beginning from the Commencement Date and ending on the Termination Date.

  • Research License means a nontransferable, nonexclusive license to make and to use the Licensed Products or the Licensed Processes as defined by the Licensed Patent Rights for purposes of research and not for purposes of commercial manufacture or distribution or in lieu of purchase.

  • License Term means the duration of a License as specified in the Order.

  • Research Program Term has the meaning set forth in Section 2.2.

  • Collaboration Term has the meaning specified in Section 2.1.2 hereof.

  • Research Term has the meaning set forth in Section 3.2.

  • Research Period means the research period as described in the Commissioned Research Plan. In accordance with the provisions of this Agreement, in the event that the Agreement ended prior to the completion date of the research originally set, the date the Agreement ends shall be read as the research period.

  • Licensed Program means the executable processing programs of licensed information, which is composed of various modules in the Licensed Software package provided by the Licensor.

  • Collaboration Know-How means all Know-How and Materials discovered, created, conceived, developed or reduced to practice in the course of performing activities under the Collaboration Program (whether solely by one Party or jointly by the Parties, in each case with their Affiliates or any Third Parties or any employees, consultants or agents of any of the foregoing which perform activities under the Collaboration Program).

  • License Key means a unique key-code that enables Licensee to run Software subject to the obtained User Pack.

  • Licensed Field means all fields of use.

  • Research Use shall have the meaning given in Section 2.2.2 of this Agreement.

  • Research Program has the meaning set forth in Section 2.1.

  • Licensed Field of Use means all fields.

  • Exclusivity Period means the period beginning on the date hereof and ending on the first to occur of (a) the date six (6) months after the date hereof and (b) the mutually agreed termination of this Agreement pursuant to Section 6.01(b).

  • Licensed Programs means, collectively, NeoSystems’ and any Third Party Vendor computer software programs to be provided to Client for use on certain hardware on Client’s premises or a third party’s premises as set forth in an Agreement. The Licensed Programs shall include any fixes, work-arounds, updates, revisions, modifications, enhancements and any derivative works that are provided to Client by NeoSystems under an Agreement.

  • Licensed Fields of Use means the fields of use identified in Appendix B.

  • Collaboration Product means any pharmaceutical product in finished form that contains a Collaboration Compound, either as the sole active ingredient or in combination with one or more other active ingredients, and all present and future formulations, dosages and dosage forms thereof.

  • Collaboration has the meaning set forth in Section 2.1.

  • Sublicense Agreement means any agreement or arrangement pursuant to which Licensee (or an Affiliate or Sublicensee) grants to any third party any of the license rights granted to the Licensee under the Agreement.

  • Royalty Term has the meaning set forth in Section 8.4(b).

  • Licensee Technology means the Licensee Know-How and Licensee Patents.

  • Development Period means the period from the date of this Agreement until the Appointed Date;

  • Collaboration Technology means all Collaboration Patents and Collaboration Know-How.

  • Collaboration IP means Collaboration Know-How and Collaboration Patents.

  • Licensed Technology means the Licensed Patents and the Licensed Know-How.