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Clinical Trial Summary

This is a three-period crossover phase I study designed to evaluate the relative bioavailability, food effect, safety and tolerability of SYHA1813 oral solution in healthy participants.


Clinical Trial Description

Avoid duplicating information that will be entered elsewhere, such as Eligibility Criteria or Outcome Measures. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06157918
Study type Interventional
Source Shanghai Runshi Pharmaceutical Technology Co., Ltd
Contact Clinical Trials Information Group
Phone +86-0311-69085587
Email ctr-contact@mail.ecspc.com
Status Not yet recruiting
Phase Phase 1
Start date December 12, 2023
Completion date February 28, 2024

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