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Coronary DiseaseBIOMAG-IIINCT07258290

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

A study testing Freesolve RMS and Xience DES in people with Coronary Disease and Heart Diseases, run by Teleflex at 3 sites in 2 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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 Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
Freesolve RMS and Xience DES
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,859 participants
Where
3 sitesin 2 countries
Study dates
11 Jun 2026to Jun 2033
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Clinical Inclusion Criteria:

  1. Subject is ≥ 18 years and ≤ 80 years of age
  2. Subject has provided written informed consent as approved by the Ethics Committee / Institutional Review Board (IRB) of the respective clinical site prior to the study related procedures
  3. Subject is eligible for PCI according to the applicable guidelines
  4. Subject is an acceptable candidate for coronary artery bypass surgery
  5. Subjects with stable or unstable angina pectoris, documented silent ischemia/abnormal physiologic testing or hemodynamically stable non-ST elevation myocardial infarction (NSTEMI) patients without angiographic evidence of thrombus at target lesion Note: STEMI patients may be eligible for the study for treatment of selected non-culprit lesions, if:
  • Subject and target lesion(s) meet all inclusion and no exclusion criteria and consent occurs at least ≥ 72 hours after successful treatment of the culprit lesion(s) [lesion(s) causing the acute STEMI];
  • Subject is hemodynamically stable with documented declining cardiac biomarkers;
  • Target lesion(s) to be treated are not located in the culprit vessel(s) and are not culprit lesion(s)
  1. Subject is eligible for Dual Antiplatelet Therapy (DAPT) with aspirin plus either clopidogrel, prasugrel, ticagrelor or ticlopidine
  2. Documented left ventricular ejection fraction (LVEF) ≥ 30% within 6 months prior to or during the procedure (prior to randomization)
  3. Subject is willing and able to comply with protocol requirements, including completion of study visits for the duration of the study

Angiographic Inclusion Criteria:

  1. Subjects with a maximum of two single de novo target lesions each in separate native coronary arteries
  2. Target vessel must have a reference diameter between 2.5-4.2 mm by operator visual estimation, which may be assisted by Quantitative Coronary Angiography (QCA) / Intravascular Ultrasound (IVUS) / Optical Coherence Tomography (OCT)
  3. Target lesion(s) must be ≤ 36 mm in length by operator visual estimation, which may be assisted by QCA / IVUS / OCT, (or < 20 mm for target lesion(s) to be treated with a study device < 3.0 mm in diameter) and must be amenable to treatment with a single study device
  4. Target lesion stenosis ≥ 50% and < 100% by operator visual estimation, which may be assisted by QCA / IVUS / OCT. Target lesion stenosis < 70% by visual estimation, should have clinical justification for treatment as per local standards.
  5. Target lesion must have a Thrombolysis in Myocardial Infarction (TIMI) flow ≥ 1

Clinical Exclusion Criteria:

  1. Subject is pregnant and/or breastfeeding or intends to become pregnant during the duration of the study
  2. Subject has clinical symptoms and/or electrocardiogram (ECG) changes consistent with STEMI < 72 hours prior to the index procedure Note: Hemodynamically stable non-STEMI (NSTEMI) subjects are eligible for study enrollment
  3. Subject has undergone prior PCI within the target vessel during the last 12 months prior to the index procedure or prior PCI within a non-target vessel < 72 hours prior to the index procedure
  4. Subject is on dialysis or has impaired renal function (serum creatinine > 2.5 mg/dL or 221 µmol/L, determined within 7 days prior to the index procedure)
  5. Subject has a known allergy to contrast medium that cannot be adequately premedicated, or any known allergy to aspirin, P2Y12 inhibitors, both heparin and bivalirudin, sirolimus, everolimus (or similar limus drugs), poly L-lactide, the scaffold material (magnesium, aluminum, tantalum), or Xience stent material (cobalt, chromium, tungsten, nickel, methacrylic polymer, and fluoropolymer)
  6. Subject is receiving oral or intravenous immunosuppressive therapy (inhaled steroids are permitted) or has known life-limiting immunosuppressive or autoimmune disease (e.g., human immunodeficiency virus, systemic lupus erythematosus; diabetes mellitus is permitted)
  7. Life expectancy less than 1 year
  8. Planned surgery or dental surgical procedure within 6 months after index procedure, unless DAPT can be maintained
  9. In the investigator's opinion subject will not be able to comply with the follow-up requirements
  10. Subjects under oral anticoagulation therapy (OAC) prior to index procedure unless DAPT + OAC (i.e., triple therapy) can be maintained for a minimum of 1 month
  11. Subject has had a stroke or transient ischemic attack (TIA) within 6 months prior to the index procedure
  12. Subject with active bleeding disorder, active coagulopathy, or any other reason, who is ineligible for DAPT
  13. Subject is currently participating or plans to participate in another study with an investigational device or an investigational drug
  14. Subject has known severe aortic or mitral valve stenosis/insufficiency or has previously undergone transcatheter aortic valve replacement (TAVR)

Angiographic Exclusion Criteria:

  1. Target vessel has been previously treated and the target lesion is within 5 mm proximal or distal to the previously treated lesion
  2. Left main coronary artery disease
  3. Target lesion is totally occluded (100% stenosis)
  4. Thrombus in target vessel
  5. Future planned staged PCI either in target or non-target vessel
  6. Ostial target lesion within the left anterior descending (LAD), left circumflex (LCX), or right coronary artery (RCA) (within 5.0 mm of vessel origin)
  7. Target lesion involves a side branch ≥ 2.0 mm in diameter that requires a two-device strategy after pre-dilatation
  8. Target lesion is located in or supplied by an arterial or venous bypass graft
  9. Target lesion with excessive tortuosity proximal to or within the lesion based on visual estimation or heavily calcified target lesion which cannot be adequately pre-dilated by a non-compliant and/or cutting/scoring balloon as described in angiographic exclusion criteria 10
  10. Target lesion requires treatment with a device other than the non-compliant balloon and/or cutting/scoring balloon prior to scaffold/stent placement (including but not limited to atherectomy devices, intravascular lithotripsy, drug-coated balloons, etc.)
  11. Target vessel was treated with brachytherapy any time prior to the index procedure.
  12. Unsuccessful pre-dilatation, defined as residual stenosis > 20% (by visual estimation) and/or angiographic complications (e.g., distal embolization, side branch closure, flow-limiting dissections)

Trial locations and contacts

3 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

BIOMAG-III Project Manager contact

1-866-246-6990

biomag_us@teleflex.com

3 sites in 2 countries

United States2 sites, 2 recruiting
  • Charleston Area Medical Center

    Charleston, West Virginia, 25304

    Recruiting
  • MedStar Washington Hospital Center

    Washington D.C., District of Columbia, 20010

    Recruiting

Other trials in United States

Latvia1 site, 1 recruiting
  • Pauls Stradins Clinical University Hospital

    Riga, LV-1002

    Recruiting

Other trials in Latvia

About this study

Official title: Safety and Clinical Performance of the Drug Eluting Resorbable Coronary Magnesium Scaffold System (Freesolve) in the Treatment of Subjects With de Novo Lesions in Native Coronary Arteries

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

Read the detailed description

The BIOMAG-III clinical trial is a prospective, international, multi-center, single-blinded, randomized controlled, non-inferiority trial to compare the Freesolve Sirolimus Eluting Coronary Resorbable Magnesium Scaffold (Freesolve RMS) System with the Xience Everolimus Eluting Stent (Xience DES) System. with respect to Target Lesion Failure (TLF) rate at 12 months. Subjects will be randomized in a 2:1 fashion Freesolve to Xience. A total of up to 1859 subjects will be randomized at up to 120 total sites worldwide including North America, Europe, and Asia Pacific. Clinical follow-up will be conducted at 1, 6, and 12 months and at 2, 3, 4, and 5 years post-procedure.

Being tested
Freesolve RMS, Xience DES
Keywords
Resorbable Magnesium Scaffold, Sirolimus, RMS, Drug eluting absorbable metal scaffold
Medical subject headings
Coronary Disease, Heart Diseases, Cardiovascular Diseases, Arteriosclerosis, Arterial Occlusive Diseases, Vascular Diseases, Chest Pain, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Freesolve RMSDevice

    Freesolve Sirolimus-Eluting Coronary Resorbable Magnesium Scaffold (RMS) System, a drug-eluting balloon-expandable resorbable scaffold

  • Xience DESDevice

    Xience Everolimus Eluting Stent System

Study groups in NCT07258290
Study groupRoleWhat they receive
Freesolve RMSExperimentalIntervention with a Freesolve Sirolimus Eluting Coronary Resorbable Magnesium Scaffold (RMS) System
Receives: Device: Freesolve RMS
Xience DESActive comparatorIntervention with a Xience Everolimus Eluting Stent System
Receives: Device: Xience DES

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Target Lesion Failure (TLF) rate at 12 months post-index procedure

    The primary endpoint is Target Lesion Failure (TLF) at 12 months, a composite of Cardiac Death, Target Vessel Q-wave or non-Q wave MI, or clinically driven target lesion revascularization (TLR).

    Measured: 12 months

Secondary outcomes (14)
  1. Procedure success

    Procedure success defined as achievement of < 30% final residual diameter stenosis [by Quantitative Coronary Angiography (QCA) or visual estimation] of the target lesion using the assigned study device only, without the occurrence of cardiac death, Q-wave or non-Q-wave MI, or repeat revascularization of the target lesion during the hospital stay

    Measured: Hospital Discharge (6-24 hours post-index procedure)

  2. Device Success

    Device Success defined as a final residual diameter stenosis of < 30% by QCA or visual estimation, using the assigned device only with

    • successful delivery of the device to the target lesion, and
    • appropriate device deployment, and
    • successful removal of the delivery system

    Measured: Hospital Discharge (6-24 hours post-index procedure)

  3. Target lesion failure (TLF)

    TLF is defined as a composite of Cardiac Death, Target Vessel Q-wave or non-Q-wave myocardial infarction (MI), or clinically driven Target Lesion Revascularization (TLR)

    Measured: Time Frame: 1, 6 months and 2, 3, 4 and 5 years post-index procedure

  4. Target Vessel Failure (TVF)

    Target Vessel Failure (TVF), a composite of Cardiac Death, Target Vessel Q-wave or non-Q wave MI, or clinically driven Target Vessel Revascularization (TVR)

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  5. Cardiac death

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  6. Cardiovascular death

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  7. All-cause mortality

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  8. Target vessel MI in accordance with the primary endpoint definitions for periprocedural and non-periprocedural MI

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  9. Any MI (including non-target vessel territory)

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  10. Clinically driven TLR

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  11. Clinically driven TVR

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  12. Scaffold/stent thrombosis (definite, definite/probable, probable) according to Academic Research Consortium (ARC-2) criteria for acute, sub-acute, late, very late and cumulative scaffold/stent thrombosis

    Measured: 1, 6, 12 months and 2, 3, 4 and 5 years post-index procedure

  13. Powered Secondary Endpoint 1: TLF from 1-5 Years

    A powered secondary endpoint of cumulative TLF rates between 1 and 5 years post-procedure will be evaluated.

    Measured: 1 to 5 years post-index procedure

  14. Powered Secondary Endpoint 2: TLF at 12 Months in the Diabetic Population

    A powered secondary endpoint of TLF at 12 months in the diabetic population will be evaluated.

    Measured: 12 months post-index procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Dec 2025
  2. Study start11 Jun 2026
  3. Primary completionJun 2029 (estimated)
  4. Study completionJun 2033 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
1,859 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07258290
Sponsor's protocol ID
G230176
Acronym
BIOMAG-III
Status last verified
Nov 2025
First submitted
20 Nov 2025
Last updated
31 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No: No IPD sharing is planned at this time. This study evaluates an investigational device under an FDA IDE. The sponsor may consider sharing de-identified IPD under controlled access following completion of primary endpoint analysis and regulatory review. Summary results will be reported in scientific publications and public registries.

Questions about this trial

What is this clinical trial studying?

A study testing Freesolve RMS and Xience DES in people with Coronary Disease and Heart Diseases, run by Teleflex at 3 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 31 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States, Latvia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact BIOMAG-III Project Manager (1-866-246-6990, biomag_us@teleflex.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Target Lesion Failure (TLF) rate at 12 months post-index procedure (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2026.

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