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Clinical Trial Summary

The purpose of the clinical study is to assess safety, tolerability and pharmacokinetics of RMC-035 for the prevention and treatment of acute kidney injury (AKI) in patients undergoing cardiac surgery.


Clinical Trial Description

This is a study with two parallel treatment groups where subjects are randomized to receive RMC-035 or a matching placebo in a double-blind fashion. The study will comprise of a screening visit, followed by CABG and/or valve replacement on Day 1, double-blind treatment period and a follow-up period up to Day 30. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04829916
Study type Interventional
Source Guard Therapeutics AB
Contact
Status Completed
Phase Phase 1
Start date March 16, 2021
Completion date July 15, 2021

See also
  Status Clinical Trial Phase
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