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PROTOCOL NO. RP65301802 An Open label, Phase II study to evaluate the efficacy and safety of Tenalisib (RP6530), a novel PI3K / dual inhibitor in adult patients with relapsed/refractory indolent NonHodgkins Lymphoma
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The study protocol is a detailed plan that outlines the objectives, methodology, and analysis of a research study.
Researchers and study sponsors are typically required to file the study protocol.
The study protocol can be filled out by providing detailed information on the study design, data collection methods, and analysis plan.
The purpose of the study protocol is to ensure transparency, credibility, and reproducibility of the research study.
Information such as study objectives, methodology, sample size calculation, statistical analysis plan, and potential biases must be reported.
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