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Protocol #: UCI 18125 MP 11/04/20PROTOCOL A Phase 1b multicenter study of TAS102 in combination with in patients with advanced recurrent or unresectable gastric and gastroesophageal adenocarcinoma
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Submit the completed protocol to the appropriate ethics board or institution for approval.

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Protocol UCI 18-125 is a regulatory framework that outlines specific requirements for the submission of data related to clinical trials and studies.
Researchers, institutions, and sponsors conducting clinical trials involving human subjects are required to file Protocol UCI 18-125.
To fill out Protocol UCI 18-125, complete the designated sections accurately, ensuring all required information is filled in, and follow the provided guidelines related to formatting and submission.
The purpose of Protocol UCI 18-125 is to ensure standardized reporting and compliance in clinical research, facilitating the collection of relevant data for regulatory review.
Information required to be reported includes study objectives, methodology, subject demographics, data management plans, and compliance with ethical standards.
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