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Clinical Trial Summary

This is a Phase 1b/IIa, single centre, non-randomised open-label uncontrolled study to assess safety, effect and PK of oral CRD-102 in patients with RHF associated with the presence of an LVAD.


Clinical Trial Description

The study will be conducted over a 40 day time period inclusive of screening and follow up time periods. Eligible subjects will receive oral CRD-102 for 14 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03217331
Study type Interventional
Source Cardiora Pty. Ltd.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 6, 2018
Completion date May 30, 2019

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