General information
  • Disease category Coronary Heart disease (BASEC)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Geneva
    (BASEC)
  • Contact Juan Fernando Iglesias juanfernando.iglesias@hug.ch (BASEC)
  • Data Source(s) BASEC: Import from 05.03.2026 ICTRP: N/A
  • Last update 05.03.2026 16:45
HumRes67905 | SNCTP000006833 | BASEC2025-D0080

Safety and clinical performance of the magnesium bioresorbable coronary stent (Freesolve) in the treatment of subjects with long de novo lesions in native coronary arteries: BIOMAG-LL

  • Disease category Coronary Heart disease (BASEC)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Geneva
    (BASEC)
  • Contact Juan Fernando Iglesias juanfernando.iglesias@hug.ch (BASEC)
  • Data Source(s) BASEC: Import from 05.03.2026 ICTRP: N/A
  • Last update 05.03.2026 16:45

Summary description of the study

This clinical trial will be conducted at 20 sites in Germany, Switzerland, Spain, Poland, Latvia, and Italy. It is planned to include 100 patients. After patients have given their consent to participate in the study, a vascular assistance device will be used. Follow-up clinical examinations will be performed at 1, 6, and 12 months, and then at 36 and 60 months after the intervention. In a smaller group of study participants, after giving their consent, the concentration of the drug released by the bioresorbable stent Freesolve will be measured. Blood samples will be used to measure the amount of drug released by the bioresorbable stent present in the blood at different times after the implantation of Freesolve in the artery. This is called pharmacokinetic evaluation. As part of the pharmacokinetic evaluation, additional blood samples will be taken before implantation and at 10 minutes, 30 minutes, and 1, 2, 3, 4, 6, 12, 24, 48, and 72 hours, as well as 7 days after the implantation of Freesolve.

(BASEC)

Intervention under investigation

In BIOMAG-LL, an extension of the size range of Freesolve (scaffold lengths of 35 and 40 mm) will be studied. The aim of the study is to evaluate the safety and clinical performance of Freesolve 35 and 40 mm in de novo coronary lesions up to 38 mm in length. Patients with clinical symptoms are referred to the investigation center for diagnostic testing. Patients who have agreed to participate and received Freesolve (35 mm and 40 mm) will be followed up at 30 days, 1, 6, 12 months, and after 36 and 60 months post-procedure. A pharmacokinetic evaluation will also be conducted in a small group of patients who have given additional consent.

(BASEC)

Disease under investigation

Coronary arteries (blood vessels in the heart) may have a narrowing that can require treatment. This narrowing can be caused by deposits on the walls of the arteries (atherosclerosis). As a result, the heart does not receive enough oxygen and nutrients, which impairs heart function. This condition is called coronary artery stenosis and can be the cause of clinical symptoms.

(BASEC)

Criteria for participation in trial
1. Subjects with a maximum of two unique lesions in two distinct coronary arteries, which must be de novo lesions and can each be covered by a single device. 2. Reference vessel diameter between 2.7 and 4.2 mm based on visual estimation, depending on the size of the scaffold used. 3. Target lesion length > 28 and ≤ 38 mm based on visual estimation, depending on the size of the scaffold used. (BASEC)

Exclusion criteria
1. The subject is pregnant and/or breastfeeding or intends to become pregnant during the study duration. 2. The subject has clinical symptoms and/or electrocardiogram (ECG) changes consistent with ST-segment elevation myocardial infarction (STEMI) less than 72 hours prior to the reference procedure. 3. Known allergies: to aspirin, P2Y12 inhibitors, heparin and bivalirudin, sirolimus (or similar drugs), poly L-lactide, or scaffold material (magnesium, aluminum, tantalum). (BASEC)

Trial sites

Geneva

(BASEC)

not available

Sponsor

BIOTRONIK AG Ackerstrasee 6, 8180 Bülach, Switzerland

(BASEC)

Contact

Contact Person Switzerland

Juan Fernando Iglesias

+41 (0)79 347 48 49

juanfernando.iglesias@hug.ch

Hopitaux Universitaires de Genève

(BASEC)

Scientific Information

not available

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Geneva

(BASEC)

Date of authorisation

05.03.2026

(BASEC)


ICTRP Trial ID
not available

Official title (approved by ethics committee)
BIOTRONIK – Safety and Clinical Performance of the Drug Eluting Resorbable MAGnesium Scaffold (Freesolve) in the Treatment of Subjects with Long de Novo Lesions in Native Coronary Arteries: BIOMAG-LL (BASEC)

Academic title
not available

Public title
not available

Disease under investigation
not available

Intervention under investigation
not available

Type of trial
not available

Trial design
not available

Inclusion/Exclusion criteria
not available

not available

Primary and secondary end points
not available

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
not available

Secondary trial IDs
not available

Results-Individual Participant Data (IPD)
not available

Further information on the trial
not available

Results of the trial

Results summary

not available

Link to the results in the primary register

not available