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Multicomponent Behavioral Sleep Intervention for Insomnia in Older Adults with Mild Cognitive Impairment Informed Consent IRB Protocol Number: 832826 Approval Date: 03/30/2021Penn locate: TO: CC:30Mar2021
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What is gsk3739937 first-time-in-human ftih study?
The study gsk3739937 is a first-time-in-human (FTIH) study that involves testing a drug on humans for the first time.
Who is required to file gsk3739937 first-time-in-human ftih study?
The pharmaceutical company conducting the study is required to file the gsk3739937 first-time-in-human (FTIH) study.
How to fill out gsk3739937 first-time-in-human ftih study?
The gsk3739937 first-time-in-human (FTIH) study should be filled out according to the specific guidelines and requirements set by the regulatory authorities.
What is the purpose of gsk3739937 first-time-in-human ftih study?
The purpose of the gsk3739937 first-time-in-human (FTIH) study is to evaluate the safety, tolerability, and pharmacokinetics of the drug in humans.
What information must be reported on gsk3739937 first-time-in-human ftih study?
The gsk3739937 first-time-in-human (FTIH) study must include information on the study design, protocol, demographic data of participants, adverse events, and results of the study.
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