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Page 1 of 6COGACNS2021: A Phase 2 Trial of Chemotherapy followed by ResponseBased Whole Ventricular & Spinal Canal Irradiation (WV SCI) for Patients with Localized NonGerminomatous Central Nervous
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Obtain necessary regulatory approvals before starting the study.
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Determine the target population for the study.
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Develop a study protocol outlining the objectives, methodology, and endpoints.
04
Recruit participants meeting the inclusion criteria and obtain informed consent.
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Who needs a phase ii study?

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Pharmaceutical companies developing new drugs or therapies.
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Biotechnology companies conducting research on novel treatments.
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Regulatory agencies evaluating the safety and effectiveness of a potential new treatment.
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A phase ii study is a clinical trial that evaluates the effectiveness and safety of a new drug or treatment in a larger group of people.
Drug manufacturers or researchers conducting the clinical trial are usually required to file a phase ii study.
A phase ii study can be filled out by providing detailed information about the study design, participants, treatments, and results.
The purpose of a phase ii study is to gather more information about the safety and effectiveness of a new drug or treatment before moving on to phase iii trials.
Information such as study objectives, methods, participant demographics, treatment details, and results must be reported on a phase ii study.
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