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CLINICAL STUDY PROTOCOL RV144A Phase III Trial of Events Pasteur Live Recombinant MALACHI (vCP1521) Priming With Vaughn gp120 B/E (AIDS VAX B/E) Boosting in HIV uninfected Thai AdultsPrincipal Investigator:
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The clinical study protocol rv144 is a specific plan for a clinical study that describes the objectives, design, methodology, statistical considerations, and organization of a research study.
The principal investigator or sponsor of the clinical study is usually required to file the clinical study protocol rv144.
The clinical study protocol rv144 should be filled out following the guidelines and templates provided by the regulatory authorities or the Institutional Review Board.
The purpose of the clinical study protocol rv144 is to provide a detailed plan of the study to ensure that it is conducted in a scientifically sound and ethical manner.
The clinical study protocol rv144 must include information on the study objectives, study design, patient selection criteria, interventions, assessments, and statistical analysis plan.
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