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NI050104NI0501 inHLH10f99Clinical Study Protocol A Phase 2/3, Open label, Single Arm, Multigenre Study to Assess Safety, Tolerability, Pharmacokinetics and Efficacy of Intravenous Multiple Administrations
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What is a phase 23 open-label?
A phase 23 open-label is a type of clinical trial where both the researchers and participants are aware of the treatment being administered.
Who is required to file a phase 23 open-label?
The researchers conducting the clinical trial are required to file a phase 23 open-label.
How to fill out a phase 23 open-label?
A phase 23 open-label should be filled out accurately and completely with all the necessary information regarding the clinical trial.
What is the purpose of a phase 23 open-label?
The purpose of a phase 23 open-label is to gather information on the safety and efficacy of a treatment in a controlled setting.
What information must be reported on a phase 23 open-label?
Information such as the study protocol, participant demographics, treatment regimens, adverse events, and study outcomes must be reported on a phase 23 open-label.
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