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Local Protocol #: AAAP9506 NCT02632045 TITLE: A randoMized phAse II trIal of or wiTh or without Ribociclib After progression on AntIestrogeN therapy plus cyclindependent kinase 4/6 inhibition in patients
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01
Obtain the local protocol AAAP9506 documentation.
02
Read through the guidelines provided in the protocol.
03
Fill in the study title, protocol number, and relevant contact information.
04
Include information on the study design and objectives.
05
Complete the sections on inclusion and exclusion criteria for participants.
06
Outline the procedures for data collection and analysis.
07
Have relevant signatures from principal investigators and other necessary personnel.
08
Submit the completed protocol to the appropriate ethics review board or institutional review board.

Who needs local protocol aaap9506 nct02632045?

01
Researchers conducting the clinical trial referenced by NCT02632045.
02
Institutional Review Boards (IRBs) that need to review the trial protocol.
03
Clinical trial coordinators and administrators involved in the management of the trial.
04
Sponsors or funding agencies that require compliance with protocol standards.
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Local protocol aaap9506 nct02632045 is a specific clinical study protocol that outlines the methodology, objectives, and guidelines for conducting a research study registered under the National Clinical Trials identifier NCT02632045.
Researchers, institutions, or organizations conducting the clinical trial as well as any collaborators involved in the study are required to file local protocol aaap9506 nct02632045.
To fill out local protocol aaap9506 nct02632045, one must follow the guidelines provided in the protocol template, ensuring that all sections are completed with accurate information regarding study design, participant eligibility, methods, and data collection processes.
The purpose of local protocol aaap9506 nct02632045 is to provide a structured framework for conducting the clinical trial, ensuring ethical standards are met and that the study results can contribute to scientific knowledge in the relevant field.
Information that must be reported includes the study title, objectives, methodology, participant criteria, data collection methods, safety considerations, and plans for data analysis, as well as any relevant regulatory compliance details.
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