Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Coronary De Novo Lesions

Coronary Artery Disease Clinical Trial

Official title:

A Multicenter, Prospective, Randomized, Single-blind, Pivotal Clinical Study to Evaluate the Safety and Efficacy of GENOSS® DCB Versus SeQuent® Please NEO in Patients With Coronary De Novo Lesions

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05096442
• Other study ID #: CEP-DS1001_DN
• Status: Completed
• Phase: N/A
• Start date: September 30, 2021
• Est. completion date: November 21, 2023

Study information

• Verified date: January 2024
• Source: Genoss Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of a novel Paclitaxel-coated balloon (Genoss® DCB) by demonstrating non-inferiority to in-lesion late lumen loss at 6 months after the procedure in Korean patients with coronary de novo lesions compared with a product of the same category (SeQuent® Please NEO).

Description:

In a randomized controlled trial to compare with the same-category drug device (SeQuent® Please NEO), 204 patients with coronary de novo lesions were recruited from a total of 12 institutions, and the enrolled subjects were 1: 1 through randomization. The ratio was assigned to the test group and the control group, and each of the test or control devices was assigned to receive the procedure. The primary end point is the in-lesion late lumen loss of the target lesion at 6 months after the procedure, and the secondary end point is the target vessel failure (Composite of cardiac death, TV-MI, and ID-TVR) at 6 and 12 months after the procedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 204
• Est. completion date: November 21, 2023
• Est. primary completion date: June 28, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• Age =19 years old
• Patients requiring PCI with coronary de novo lesions
• Patients with stable angina pectoris, or unstable angina pectoris, and asymptomatic myocardial ischemia
• Women of childbearing age who agreed to use one or more of the clinically appropriate methods of contraception during the trial period.
• In case of voluntarily deciding to participate in this clinical trial by signing the informed consent form Inclusion criteria for coronary angiography
• Patients with significant coronary artery stenosis (> 50% diameter stenosis on coronary angiography)
• On coronary angiography, the length of the lesion is less than 34 mm and the diameter of the reference vessel of the coronary artery is 2.0 - 4.0mm.

Exclusion Criteria:

• Patients with ST-segment elevation myocardial infarction (STEMI)
• Patients who are contraindicated in aspirin, heparin, ticagrelor, iopromide, clopidogrel, prasugrel and paclitaxel
• Patients with platelet aggregation or disorders at risk of increased bleeding, such as gastrointestinal ulcers, which limit platelet aggregation inhibitory therapy and anticoagulant therapy
• Patients with a left ventricular ejection fraction of less than 30% on echocardiography
• Patients with renal insufficiency (eGFR<30mL/min)
• Patients with a history of cardiogenic shock
• Pregnant or lactating women
• The patients have a life expectancy of less than 12 months
• Patients who have or currently have medical conditions such as psychiatric disorders that significantly affect this clinical trial
• Patients who, in the investigator's judgment, may not be suitable for this clinical trial or may increase the risk associated with participation in the study
• Patients who are currently participating in other clinical trials or have experience participating in other clinical trials within 90 days from the screening date
• Patients who are unsuitable for the study according to the investigator judges Exclusion criteria for coronary angiography
• Patients with left main coronary lesion
• Patients with graft vessel lesion
• Patients who cannot apply pre-dilation or fail in pre-dilation to apply medical devices for clinical trials
• Patients with one of the following items after pre-dilation of the target lesion
• When FFR (Functional measurement) is measured as = 0.8 in large vessels with a reference vessel diameter exceeding 2.75mm (However, depending on the judgment of the investigator, FFR measurement may not be performed.)
• Patients who need stenting due to vascular dissection that restricts blood flow
• Residual stenosis > 30%
• TIMI flow < 3

Related Conditions & MeSH terms

• Coronary Artery Disease

Intervention

Device:
• GENOSS® DCB
Drug Coated Balloon
• SeQuent® Please NEO
Drug Coated Balloon

Locations

Country	Name	City	State
Korea, Republic of	Ulsan University Hospital	Ulsan

Sponsors (1)

Lead Sponsor	Collaborator
Genoss Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	in-lesion late lumen loss after percutaneous coronary intervention in patients with coronary de novo lesions	late lumen loss between test group and control group evaluated by quantitative coronary analysis in patients with coronary de novo lesions	Follow-up angiography at 6 months after the procedure
Secondary	Restenosis rate after percutaneous coronary intervention in patients with coronary de novo lesions	Restenosis is defined as a case where the DS(Diameter stenosis) of the reference vessel diameter is 50% or more when the successfully treated lesion is evaluated through coronary angiography.	Follow-up angiography at 6 months after procedure
Secondary	Target vessel failure(TVF)	Composite of TVF(cardiac death, TV-MI, and ID-TVR)	at 6 and 12 months after the procedure