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IRB #: 44113A Phase II Study of Neoadjuvant Chemotherapy with and without Immunotherapy to CA125 (Oregovomab) followed by Hypofractionated Stereotactic Radiotherapy and Concurrent HIV Protease Inhibitor
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To fill out a phase II study, follow these steps:
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Obtain ethical approval from the relevant research ethics board.
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Recruit eligible participants and obtain informed consent.
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Regulatory authorities, such as the FDA, require phase II studies as part of the drug approval process to gather further evidence on the drug's efficacy and safety profile.

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