SCREENING OF ARQULE COMPOUNDS Sample Clauses

SCREENING OF ARQULE COMPOUNDS. During the Array Screening Period, Abbott shall have the right, either directly or through Abboxx'x Xxxiliates or third party contractors selected by Abbott, to perform such testing and analytical work as Abbott deems appropriate on ArQule Core Compounds received hereunder, provided that Abboxx xxxll have the right to perform composition and structural analysis only after Abboxx'x xxxeipt of confirmed chemical composition and structure and purity information pursuant to Section 5.3, and further provided that Abboxx xxxll not perform significant derivitization work on ArQule Core Compounds until Abboxx xxxes a Target Reservation for the ArQule Array containing such ArQule Core Compounds pursuant to Section 5.5. The parties agree that "significant derivitization work" shall mean any derivitization work beyond that which is reasonably necessary to allow Abboxx xx determine whether an ArQule Core Compound is sufficiently amenable to chemical modification to warrant the exercise of a Target Reservation by Abboxx.
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SCREENING OF ARQULE COMPOUNDS. ArQule hereby grants to Abbott and its Affiliates a nonexclusive, worldwide, royalty-free license (without the right to sublicense or subcontract) during the term of this Agreement and thereafter to perform such testing and analytical work as Abbott deems appropriate on ArQule Core Compounds delivered by ArQule hereunder. Notwithstanding the foregoing, Abbott may, during the term of this Agreement and thereafter, deliver ArQule Core Compounds to one or more third parties so as to allow such third parties to perform testing and analytical work on such ArQule Core Compounds provided that, prior to delivering any ArQule Core Compounds to any such third party, Abbott, ArQule and each such third party enter into a materials transfer agreement substantially in the form of the attached EXHIBIT B or such other form as may be acceptable to ArQule. At the time of delivery, ArQule will identify the Chemical Theme of each ArQule Array delivered to Abbott but not the structures of the * confidential treatment has been requested for marked portions individual ArQule Core Compounds in such ArQule Arrays. Initially, Abboxx xxxl not disclose the targets against which such ArQule Arrays are screened. If Abbott detects any Active ArQule Compound in an ArQule Array, it will promptly notify ArQule. ArQule shall then determine if such Active ArQule Compound and any Active ArQule Homolog thereto have been previously committed to a Third Party Mapping Array Partner or to a bona fide, documented internal ArQule program (including programs with academic collaborators). ArQule will disclose to Abbott (a) the structure of such Active ArQule Compound if it has not been so committed and all Active ArQule Homologs thereto (if any) that have not been so committed and (b) the structures, but not the locations in the ArQule Array, of all other ArQule Compounds in such ArQule Array and Abbott will disclose to ArQule (a) the identity of the biological target as to which activity was detected and (b) the level of activity exhibited by such Active ArQule Compound and such Active ArQule Homolog (the date of such mutual disclosure being referred to herein as the "Mutual Disclosure Date"). All such disclosed information shall be treated as Confidential Information by the receiving party in accordance with Article 8."
SCREENING OF ARQULE COMPOUNDS. During any Research Period, Monsanto shall have the right, either directly or through Monsanto's Primary Affiliates or third parties (including Secondary Affiliates who are not also Primary Affiliates) selected by Monsanto, to perform such testing as Monsanto deems appropriate on ArQule Compounds and ArQule Derivative Compounds received hereunder, provided that, prior to delivering any ArQule Compounds or ArQule Derivative Compounds to any such third party(including Secondary Affiliates who are not also Primary Affiliates), Monsanto, ArQule and each such third party(including Secondary Affiliates who are not also Primary Affiliates) enter into a Materials Transfer Agreement substantially in the form of the attached Exhibit B.
SCREENING OF ARQULE COMPOUNDS. Subject to the terms and conditions of this Agreement, ArQule hereby grants PRI and its Affiliates a nonexclusive, worldwide license (without the right to sublicense) under the ArQule Patent Rights and other rights in ArQule Technology to screen the ArQule Compounds in the Compass Array Sets and Mapping Array Sets against any Targets within the Screening Field. PRI agrees to use efforts consistent with its normal scientific practices to screen the ArQule Compounds in ----------------------------- *Confidential Treatment has been requested for the marked portion.
SCREENING OF ARQULE COMPOUNDS. During the Research Period, and subject to the screening licenses granted in Section 4.1. above, Searxx xxxll have the right, either directly or through Searxx'x Xxxmary Affiliates or third parties selected by Searxx, xx perform such testing in the Field as Searxx xxxms appropriate on ArQule Compounds and ArQule Derivative Compounds, provided that, prior to delivering any ArQule Compounds or ArQule Derivative Compounds to any such third party, Searxx, XxQule and each such third party enter into a materials transfer agreement reasonably acceptable to ArQule and including terms and conditions that are usual and customary for such agreements, and further provided that Searxx xxxll not identify the compounds provided to any third party as ArQule Compounds.
SCREENING OF ARQULE COMPOUNDS. Subject to the terms and conditions of this Agreement, ArQule hereby grants PRI and its Affiliates a nonexclusive, worldwide license (without the right to sublicense) under the ArQule Patent Rights and other rights in ArQule Technology to screen the ArQule Compounds in the Compass Array Sets and Mapping Array Sets against any Targets within the Screening Field. PRI agrees to use efforts consistent with its normal scientific practices to screen the ArQule Compounds in the Compass Array Sets and Mapping Array Sets against its Targets in the Screening Field.
SCREENING OF ARQULE COMPOUNDS. During the Research Period, Monsanto shall have the right, either directly or through Monsanto's Primary Affiliates or third parties selected by Monsanto, to perform such testing in the Field as Monsanto deems appropriate on ArQule Compounds and ArQule Derivative Compounds, provided that, prior to delivering any ArQule Compounds or ArQule Derivative Compounds to any such third party, Monsanto, ArQule and each such third party enter into a materials transfer agreement reasonably acceptable to ArQule and including terms and conditions that are usual and customary for such agreements, and further provided that Monsanto shall not identify the compounds provided to any third party as ArQule Compounds.
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Related to SCREENING OF ARQULE COMPOUNDS

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  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • Tests and Preclinical and Clinical Trials The preclinical studies and clinical trials conducted by or, to the Company’s knowledge, on behalf of the Company, that are described in the Registration Statement, the Pricing Disclosure Package and the Prospectus, as applicable, and are intended to be submitted to the U.S. Food and Drug Administration (the “FDA”) or other comparable government entities, were and, if still ongoing, are being conducted in all material respects in accordance with experimental protocols, procedures and controls pursuant to accepted professional scientific standards and all Authorizations and Applicable Laws, including, without limitation, current Good Clinical Practices and Good Laboratory Practices and any applicable rules and regulations of the jurisdiction in which such trials and studies are being conducted; the descriptions of the results of such studies and trials contained in the Registration Statement, the Pricing Disclosure Package and the Prospectus are, to the Company’s knowledge, accurate and complete in all material respects and fairly present the data derived from such studies and trials; except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package and the Prospectus, the Company is not aware of any studies or trials, the results of which the Company believes reasonably call into question the study or trial results described or referred to in the Registration Statement, the Pricing Disclosure Package and the Prospectus when viewed in the context in which such results are described and the clinical stage of development; and, except to the extent disclosed in the Registration Statement, the Pricing Disclosure Package or the Prospectus, the Company has not received any written notices or written correspondence from the FDA or any governmental entity requiring the termination or suspension of any preclinical studies or clinical trials conducted by or on behalf of the Company, other than ordinary course communications with respect to modifications in connection with the design and implementation of such trials, copies of which communications have been made available to you.

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  • Research Collaboration (a) GSK hereby grants to Anacor a non-exclusive, non-royalty bearing license under the GSK IP, solely as and to the extent necessary or important to conduct activities for which Anacor is responsible under the Research Plans during the Research Collaboration Term.

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  • Development and Regulatory Milestones With respect to each of the following milestones, Ikaria shall pay BioLineRx the corresponding payment set forth below within [**] days after the achievement by Ikaria, its Affiliates or Licensees of such milestone: MILESTONE PAYMENT

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  • Development Program A. Development Activities to be Undertaken (Please break activities into subunits with the date of completion of major milestones)

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