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Protocol Title: A Phase 2 Multi center, Randomized, Placebo Controlled, DoubleClick Study To Assess The Safety And Efficacy Of CC486 (Oral) In Combination With Pembrolizumab (Mk3475) Versus Pembrolizumab
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How to fill out placebo controlled double-blind study

01
Identify the research question or hypothesis that you want to investigate.
02
Determine the study population and inclusion/exclusion criteria.
03
Prepare the study protocol, including a detailed description of the intervention being tested and the placebo being used.
04
Recruit and randomize study participants into two groups: the treatment group and the control group.
05
Ensure that both the participants and the researchers involved in the study are blinded to the treatment allocation.
06
Administer the intervention and placebo according to the study protocol and record any adverse events or reactions.
07
Collect and analyze the data, taking into account any potential confounders or biases.
08
Interpret the results and draw conclusions based on the findings.
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Publish the study results in a peer-reviewed journal to contribute to the scientific knowledge in the field.

Who needs placebo controlled double-blind study?

01
Placebo controlled double-blind studies are needed in various fields including medicine, psychology, and pharmacology.
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Researchers, pharmaceutical companies, and regulatory bodies often require these studies to determine the effectiveness and safety of new treatments.
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Healthcare professionals and policymakers also rely on the results of placebo controlled double-blind studies to make evidence-based decisions regarding patient care and treatment guidelines.
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A placebo controlled double-blind study is a type of research study in which neither the participants nor the researchers know who is receiving the active treatment and who is receiving the placebo.
Researchers conducting clinical trials are required to conduct and file placebo controlled double-blind studies in some cases.
To fill out a placebo controlled double-blind study, researchers need to carefully design the study, recruit participants, administer treatments, collect data, and analyze results.
The purpose of a placebo controlled double-blind study is to evaluate the effectiveness and safety of a new treatment compared to placebo, while minimizing bias and ensuring the validity of the results.
Researchers must report detailed information about the study design, methods, results, and conclusions in a placebo controlled double-blind study.
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