Common use of Clinical Trials Registry Clause in Contracts

Clinical Trials Registry. Either Party shall have the right to publish registry information and customary summaries of data and results from any Phase 1 Clinical Trials conducted by or on behalf of such Party under this Agreement, on its clinical trials registry or on a government-sponsored database such as xxx.xxxxxxxxxxxxxx.xxx, without requiring the consent of the other Party. The Parties shall reasonably cooperate if required or reasonably requested by the Party seeking such publication in order to facilitate any such publication by such Party.

Appears in 3 contracts

Samples: Master Collaboration Agreement, Master Collaboration Agreement (Prothena Corp PLC), Master Collaboration Agreement (Prothena Corp PLC)

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Clinical Trials Registry. Either Party shall For clarity, each Party, its Affiliates and its designees will have the right to publish registry information and customary summaries of data and results from any Phase 1 Clinical Trials conducted by or on behalf of such Party under this Agreementthe Licensed Products, on its clinical trials Clinical Trials registry or on a government-sponsored database such as xxx.xxxxxxxxxxxxxx.xxx, without requiring the consent of the other Partyas set forth in each Global Development Plan. The Parties shall will reasonably cooperate if required or reasonably requested by the other Party seeking such publication in order to facilitate any such publication by such Party, any of its Affiliates or any of its designees.

Appears in 1 contract

Samples: Collaboration and License Agreement (IGM Biosciences, Inc.)

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