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Protocol This trial protocol has been provided by the authors to give readers additional information about their work. Protocol for: Gran J, Hagar N, Shin D, et al. Compassionate use of remdesivir
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The clinicaltrialsgovprovideddocs76protocol is the detailed plan outlining the objectives, design, methodology, statistical considerations, and organization of a clinical trial.
The sponsor or principal investigator of the clinical trial is usually responsible for filing the protocol.
The protocol should be completed following the guidelines provided by the regulatory authorities and any specific requirements of the trial sponsor.
The purpose of the protocol is to ensure the safety and well-being of trial participants, as well as to provide a framework for conducting the trial in a scientifically valid and ethical manner.
The protocol should include details on the study objectives, design, methodology, participant selection criteria, endpoints, statistical analysis plan, and procedures for ensuring the quality of the data collected.
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