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PROTOCOL NO. RP6530+Romidepsin1805An Open label, Phase I/II study to evaluate the safety and efficacy of Tenalisib
(RP6530), a novel PI3K / dual inhibitor given in combination with a histone
acetylate
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To fill out the clinicaltrialsgovprovideddocs00an open label phase, follow these steps:
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Read the provided documentation thoroughly to understand the requirements and guidelines of an open label phase in clinical trials.
03
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04
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Who needs clinicaltrialsgovprovideddocs00an open label phase?
01
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Researchers, scientists, pharmaceutical companies, and institutions involved in clinical research may need to fill out these documents for proper documentation and compliance.
03
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What is clinicaltrialsgovprovideddocs00an open label phase?
An open label phase is a type of clinical trial where both the researchers and the participants know which treatment is being administered.
Who is required to file clinicaltrialsgovprovideddocs00an open label phase?
Researchers conducting the clinical trial are required to file the open label phase details on clinicaltrialsgov.
How to fill out clinicaltrialsgovprovideddocs00an open label phase?
To fill out the open label phase on clinicaltrialsgov, researchers need to provide detailed information about the treatment being administered, study design, and participant eligibility criteria.
What is the purpose of clinicaltrialsgovprovideddocs00an open label phase?
The purpose of an open label phase is to evaluate the safety and efficacy of a treatment in a real-world setting.
What information must be reported on clinicaltrialsgovprovideddocs00an open label phase?
Researchers must report information on treatment administration, adverse events, participant demographics, and study outcomes on the open label phase.
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