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Clinical Trial Summary

This is a single centre, open-label, 5-period study in healthy male and non-pregnant and non-lactating healthy female subjects.


Clinical Trial Description

It is planned to enroll 14 subjects who will receive single oral doses of active IMP in a sequential manner over 5 periods, with a minimum of 7days between dosing in each period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04769479
Study type Interventional
Source Eidos Therapeutics, a BridgeBio company
Contact
Status Completed
Phase Phase 1
Start date March 28, 2021
Completion date September 3, 2021

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