However, a possible obstacle to this therapy is ghrelins half-life
In addition to the foregoing IND requirements, an IRB representing each institution participating in the clinical trial must review and approve the plan for any clinical trial before it commences at that institution, and the IRB must conduct continuing review of the study at least annually
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This absence suggests that regulatory authorities have not identified major safety signals requiring specific warnings, though it does not constitute evidence of safety or efficacy for combined use
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