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Clinical Trial Summary

The BRight PK Study is a prospective, single-arm, open-label, non-blinded, non-randomized study, which goal is to assess the pharmacokinetic profile of the BRight drug-coated balloon at different time points after the balloon deployment. The study will enroll a maximum of 10 patients at a single site in Australia


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06065345
Study type Interventional
Source Biotronik CRC Inc.
Contact Helene KUISSU
Phone +41(0)798082147
Email helene.kuissu@biotronik.com
Status Recruiting
Phase N/A
Start date May 1, 2024
Completion date September 30, 2025

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