Additional Applications Sample Clauses

Additional Applications. If the development and marketing of a given Licensed Product for a given Application other than (i) prostate cancer or (ii) endometriosis or uterine fibroids is proposed by PRAECIS to the Development Subcommittee (on the cost-sharing basis set forth in Section 4.5) but not approved, then PRAECIS may, but shall not be required to, carry out Development Phase activities with respect to such Licensed Product for such Application, at its own expense. If the Joint Steering Committee determines that Phase II or Phase III Clinical Trials funded by PRAECIS demonstrate safety and efficacy of such Licensed Product for such Application and that such Application is commercially viable, and Synthelabo determines that the commercialization of such Application should be pursued in the Territory, then Synthelabo shall promptly reimburse PRAECIS for *** (***%) of all Development Costs theretofore incurred by PRAECIS with respect to such Licensed Product for such Application and shall share on an equal basis all future Development Costs required for FDA Registration Approval of such 38 Licensed Product for such Application, Section 4.5 notwithstanding. Within sixty (60) days after such determination, the Development Subcommittee shall add the continued development and marketing of such Licensed Product for such Application to the Core Development Plan and/or the Supplemental Development Plan by amendment, which amendment shall be approved by the Joint Steering Committee within thirty (30) days thereafter; and Synthelabo and PRAECIS, as applicable, shall promptly and diligently pursue such continued development and marketing, in accordance with Article 4 and Article 5 hereof.
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Additional Applications. If UFRF notifies Licensee in writing with information demonstrating the potential feasibility of a particular Licensed Product, market, or application in the Licensed Field or a territory that Licensee is not pursuing (each an “Additional Application”) or that a third party is interested in pursuing an Additional Application, then Licensee shall inform UFRF in writing within [**] after the notice whether Licensee elects to develop the Additional Application, execute a Sublicense with the third party to do so, or decline to pursue the Additional Application. If Licensee elects to: (a) develop the Additional Application, then Licensee shall within [**] submit an updated Development Plan reasonably acceptable to UFRF that covers the Additional Application; (b) execute a Sublicense with the third party, then Licensee shall promptly initiate the negotiations and conclude the Sublicense on commercially reasonable terms within a reasonable period of time; and/or (c) decline to develop the Additional Application, or fails to execute a Sublicense with the third party, then, upon written notice from UFRF to Licensee, the license under the Patent Rights applicable to such Additional Application shall cease without the requirement of a further writing or, at UFRF’s option, the license thereto shall be converted to nonexclusive, and in each case, thereafter UFRF will be entitled to directly license any third party for the Additional Application under the applicable Patent Rights.
Additional Applications. 38 4.4 Regulatory Meetings.......................................39 4.5
Additional Applications. From time to time, IHP may identify additional software applications, functionality or data, which may be available via remote access. IHP will advise Physician Office of the availability of such additional applications, functionality or data, and the additional fees to be charged, if any. If additional fees are charged for access to the additional applications, functionality or data, Physician Office may either elect or decline such additional remote access privileges.
Additional Applications. (a) At any time during the Term, the Licensee may serve a notice on NSi that it wishes to obtain a separate commercial licence for an application of the Project IP within or outside the Field (Additional Application).
Additional Applications. (a) If Licensee wishes the University to file a patent application with respect to any of the Technology in any jurisdiction in which an application has not already been filed, Licensee shall identify the jurisdiction and the applicable Licensed Patent in writing to University at least 60 days prior to any bar date, and University shall have sixty (60) days after it receives such written notice in which to file such a patent application at Licensee’s expense, which the University may require be prepaid.
Additional Applications. (a) Contractor will work with CBS to identify applications for Electronic Image advertising and enhancements for use in college football game broadcasts. Contractor will cooperate with CBS to identify advertisers for any such applications. If CBS elects to include such advertising and/or enhancements in such college football games, and to the extent that advertisers acceptable to CBS can be identified by Contractor, CBS will be solely responsible for negotiating arrangements with such advertisers for their participation in Electronic Image advertising utilizing the PVI System. CBS shall be under no obligation to use the Electronic Images in any college game broadcast. If Electronic Imaging is used in college football game broadcasts, Contractor will be the sole supplier of such services.
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Additional Applications. Merck shall be responsible for preparing, filing, and prosecuting Drug Approval Applications and seeking Regulatory Approvals for the Products in all countries of the Territory outside the European Union in which Merck in good faith and in the exercise of reasonable business judgment, considers it commercially reasonable to do so, including preparing all reports necessary as part of a Drug Approval Application. All such Drug Approval Applications shall be filed in the name of Merck and a copy of each such Drug Approval Application shall be promptly provided to Kos. In connection with all Drug Approval Applications being prosecuted by Merck under this Agreement, Merck agrees to provide Kos with a copy (which may be wholly or partly in electronic form) of all filings to regulatory agencies that it makes hereunder promptly upon submission, but in no event later than **** days after written request by Kos, ****, and Kos shall, on reasonable advance notice to Merck, have the right freely to utilize such filings for its own Drug Approval Applications.
Additional Applications. Any additional applications to the in-scope of applications set forth in Appendix 2D.1 of Schedule 2D shall be subject to the then-current Vendor Blended Hourly Rate applicable for the Application Maintenance and Development Support services provided in Appendix 3.1 for the applicable Contract Year to arrive at the total additional cost for the added scope for the first twelve (12) month period following the change in scope. The Parties may make a realignment or ‘true-up’, to adjust the payment schedules of the added scope of applications with those of the baseline in- scope applications.
Additional Applications. As of the First Amendment Effective Date, the following Applications are added to the Agreement:
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