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Study identifier: NCT07258290 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold (RMS) System in Subjects With Coronary Artery Lesions

Condition: Coronary Disease · Heart Diseases · Cardiovascular Diseases  ·  Sponsor: Teleflex

PhaseNA
Planned participants1859
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The objective of this study is to assess the safety and efficacy of the Freesolve resorbable magnesium scaffold (RMS) in the treatment of subjects with up to two de novo lesions in native coronary arteries compared to the Xience coronary drug-eluting stent (DES) system

This description comes directly from the study's public registry record.

Talk to the study team

BIOMAG-III Project Manager  ·  1-866-246-6990  ·  biomag_us@teleflex.com

Always discuss trial participation with your own doctor first.

Locations (2)

MedStar Washington Hospital CenterWashington D.C., District of Columbia, United StatesRecruiting
Charleston Area Medical CenterCharleston, West Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07258290