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Appendix II Sample Informed Consent Form for Infant Study ParticipationIMPAACT 2008 Phase I/II Multisite, Randomized, Controlled Study monoclonal Antibody VRC01 with Combination Antiretroviral Therapy
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Phase III multisite randomized is a type of clinical trial in which participants are randomly assigned to different treatment groups at multiple sites.
Researchers conducting the clinical trial are required to file phase III multisite randomized.
Phase III multisite randomized should be filled out by providing detailed information about the trial design, participants, treatments, and outcomes.
The purpose of phase III multisite randomized is to evaluate the effectiveness and safety of a new treatment compared to standard treatment or a placebo.
Information such as the study protocol, informed consent forms, data collection methods, and statistical analysis plan must be reported on phase III multisite randomized.
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