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A Phase 2b randomized, open label, controlled, single center study in Plasmodium falciparuminfected and uninfected adults age 1855 years old in Kenya to evaluate the efficacy of the delayed, fractional
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Start by gathering all the necessary documents and information required for the phase 2b randomized trial.
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Ensure that the trial design and randomization process are properly understood.
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Identify and recruit eligible participants for the trial based on the inclusion and exclusion criteria.
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Obtain informed consent from the participants before starting the trial.
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Assign participants randomly to either the control group or the experimental group.
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Administer the intervention or treatment to the respective groups as per the trial protocol.
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Monitor and collect data on the participants' responses or outcomes during the trial.
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Analyze the collected data using appropriate statistical methods.
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Draw conclusions and report the findings of the phase 2b randomized trial.

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Phase 2b randomized is a type of clinical trial where participants are randomly assigned to different treatment groups to test the efficacy and safety of new drugs or interventions.
Researchers conducting the clinical trial are required to file a phase 2b randomized.
A phase 2b randomized form should be filled out with accurate and detailed information about the study, including participant demographics, treatment groups, outcomes measured, and adverse events.
The purpose of a phase 2b randomized trial is to gather data on the effectiveness and safety of a new treatment compared to standard care or a placebo.
Information such as participant demographics, treatment protocols, outcomes measured, adverse events, and statistical analysis methods must be reported on a phase 2b randomized.
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