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TITLE PRECLINICAL STUDY PROTOCOL NO. JAIVAC1×1_09A Phase I, Randomized, Controlled, Deescalating, SingleBlind
Clinical Trial to Evaluate the Safety and Immunogenicity of JAIVAC1
Vaccine (PfMSP119
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What is a phase i randomised?
A phase I randomised is a type of clinical trial where participants are randomly assigned to different treatment groups to evaluate the safety and dosage of a new drug.
Who is required to file a phase i randomised?
Researchers conducting the clinical trial are required to file a phase I randomised.
How to fill out a phase i randomised?
To fill out a phase I randomised, researchers need to provide detailed information about the study design, treatment groups, dosages, and safety measures.
What is the purpose of a phase i randomised?
The purpose of a phase I randomised is to determine the safety, dosage, and potential side effects of a new drug in human participants.
What information must be reported on a phase i randomised?
Information such as study design, treatment groups, dosages, safety measures, and participant demographics must be reported on a phase I randomised.
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