Clinical Trial Registry Clause Samples
The Clinical Trial Registry clause requires that information about a clinical trial be registered in a publicly accessible database, such as ClinicalTrials.gov, before the trial begins. This typically involves providing key details about the study design, objectives, and eligibility criteria, ensuring transparency and accountability in clinical research. By mandating registration, the clause helps prevent selective reporting of results and promotes public trust in the integrity of clinical trials.
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Clinical Trial Registry. Prior to enrollment of the first subject in the Study, Sponsor agrees to ensure that the Study is fully registered on ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ in accordance with the requirements of the International Committee of Medical Journal Editors (ICMJE) and Public Law 110-85. Results of this Study will be reported in compliance with applicable laws.
Clinical Trial Registry. Company shall register the Study with the Clinical Trials Registry located at ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ and is committed to timely publication of the results following Study Completion, after taking appropriate action to secure intellectual property rights (if any) arising from the Study. The publication of the results of the Study will be in accordance with the Protocol.
Clinical Trial Registry. GSK shall have the right to post the results, summaries and protocols of clinical trials conducted by GSK, its Affiliates or sublicensees on Licensed Products on GSK’s clinical trial registry.
Clinical Trial Registry. Collaborator shall register the MSD Compound Study and Collaborator Clinical Trial with the clinical trials registry located at ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ (or any non-U.S. equivalent clinical trial registry), shall list MSD as a collaborator with respect to the Collaborator Clinical Trial, and shall timely publish the results following completion of the MSD Compound Study, after taking appropriate action to secure any intellectual property rights arising from the MSD Compound Study. The results of the MSD Compound Study will be published in accordance with the Protocol.
Clinical Trial Registry. Intrexon, in accordance with ▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or equivalent regulatory agency policies and procedures, shall have the right to publish all studies, clinical trials and results thereof regarding Product (but not PH20 Drug alone) on the clinical trial registries which are maintained by or on behalf of Intrexon. Portions herein identified by [*****] have been omitted pursuant to a request for confidential treatment under Rule 24b-2 of the Securities Exchange Act of 1934, as amended. A complete copy of this document has been filed separately with the Securities and Exchange Commission.
Clinical Trial Registry. BioLineRx shall register the Study with the Clinical Trials Registry located at ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ and is committed to timely publication of the results following Study Completion, after taking appropriate action to secure intellectual property rights (if any) arising from the Study. The publication of the results of the Study will be in accordance with the Protocol.
Clinical Trial Registry. Roche, in accordance with its internal policies and procedures, shall have the right to publish all studies, clinical trials and results thereof regarding Products on the clinical trial registries which are maintained by or on behalf of Roche.
Clinical Trial Registry. (a) Ultragenyx shall be responsible for registering any Clinical Trial performed pursuant to the [***] Development Plans in the appropriate clinical trial registry (e.g., ▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇) and posting the results of such Clinical Trials as required by Applicable Laws.
(b) The posting of any results to a clinical trial registry in accordance with this Section 4.4 shall be considered a “publication” and subject to the Parties’ obligations set forth in Section 14.9.
Clinical Trial Registry. The parties shall cooperate as necessary with the National Cancer Institute to have the Study registered with the ▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ website of the U.S. National Institutes of Health (or any successor thereto) before enrollment of patients for such Study.
Clinical Trial Registry. Each of SANOFI-AVENTIS and MERRIMACK shall have the obligation to the extent required by applicable Laws or regulations to publish summaries of data and results from any human clinical trials conducted by such Party under this Agreement on its clinical trials registry or on a government-sponsored database such as ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or other publicly available websites such as ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇, without requiring the consent of the other Party. The content of such publication shall be submitted to the JDC for prior approval.