Common use of Additional Research Clause in Contracts

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of Janssen, conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between Xxxxxxx and CRO and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of JanssenXxxxxxx, conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen Xxxxxxx gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between Xxxxxxx and CRO and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of JanssenSponsor, conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen Sponsor gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between Xxxxxxx and CRO Sponsor and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to JanssenSponsor, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below)invention, Institution and Principal Investigator (as applicable) hereby grant to Janssen Sponsor or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of CRO or Janssen, conduct any research nor or facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen Xxxxxxx gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol Protocol, or shall be the subject of another written agreement between Xxxxxxx Institution and Principal Investigator and CRO and Institution and Principal InvestigatorXxxxxxx. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of JanssenXxxxxxx, conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen Xxxxxxx gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between Xxxxxxx and CRO and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-freeroyalty‐free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of CRO or Janssen, conduct any research nor or facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol Protocol, or shall be the subject of another written agreement between Xxxxxxx Institution and Principal Investigator and CRO and Institution and Principal InvestigatorJanssen. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.

Additional Research. Institution and Principal Investigator shall not, without the prior written consent of Janssen, conduct any research nor facilitate third parties to conduct any research not required by the Protocol on (i) Trial Subjects during the Clinical Trial (including any additional research technique, procedure, questionnaire, or observation), or (ii) biological samples collected from Trial Subjects during the Clinical Trial, or (iii) the data derived from the Clinical Trial. Hereinafter, the research described in the previous sentence shall be referred to as “Additional Research”. In any case where CRO or Janssen gives such approval, the approved Additional Research shall be considered either an amendment to the original Protocol or shall be the subject of another written agreement between Xxxxxxx and CRO Janssen and Institution and Principal Investigator. Institution and Principal Investigator shall conduct all Additional Research in compliance with all applicable regulations, including requirements for obtaining appropriate EC approval and subject informed consent. Without limiting any other remedy available by law to Janssen, if Institution and/or Principal Investigator conducts Additional Research in breach of this section, and such Additional Research results in an Invention (as defined in Section 8 below), Institution and Principal Investigator (as applicable) hereby grant to Janssen or its designee an irrevocable, worldwide, paid up, royalty-free, exclusive license, with right of sublicense, to make, have made, use, have used, sell have sold, and import any such invention that results from such Additional Research. This Section shall survive termination or expiration of this Agreement.