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A PHASE II STUDY OF SECONDING THERAPY WITH REGORAFENIB PLUS IN METASTATIC PANCREATIC CANCER Case Comprehensive Cancer Center 11100 Euclid Avenue, Weren't 152 Cleveland, Ohio 441065065CASE COMPREHENSIVE
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Define the objectives and endpoints of the study.
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Design the study protocol including inclusion/exclusion criteria, study population, treatment plan, and data collection methods.
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Obtain necessary approvals from regulatory authorities and ethics committees.
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Monitor participants closely for any adverse events.
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Summarize the results and draw conclusions regarding the effectiveness and safety of the treatment.

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A phase II study is a clinical trial designed to assess the safety and efficacy of a new treatment or intervention in a larger group of patients.
Researchers and pharmaceutical companies conducting clinical trials are required to file a phase II study.
To fill out a phase II study, researchers must collect and analyze data on the safety and efficacy of the treatment under investigation.
The purpose of a phase II study is to further evaluate the safety and efficacy of a treatment or intervention identified as potentially beneficial in a phase I study.
A phase II study must report detailed data on the participants, treatment protocol, outcomes, adverse events, and statistical analysis.
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