NeoVas Bioresorbable Coronary Scaffold First-in-Man Study

Coronary Artery Disease Clinical Trial

Official title:

Clinical Evaluation of a Bioresorbable Sirolimus-eluting Coronary Scaffold in the Treatment of Patients With de Novo Coronary Artery Lesion (NeoVas): a First-in-Man Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02195414
• Other study ID #: LPM-201401
• Status: Active, not recruiting
• Phase: Phase 1
• First received: July 16, 2014
• Last updated: February 16, 2016
• Start date: July 2014
• Est. completion date: September 2019

Study information

• Verified date: December 2015
• Source: Lepu Medical Technology (Beijing) Co.,Ltd
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The NeoVas First-in-Man study is a prospective, two centers, single arm trial, which will enroll a total of 30 patients. The hypothesis of this study is to evaluate clinical feasibility, safety, and efficacy of NeoVas sirolimus-eluting bioresorbable coronary scaffold in the treatment of patients with de novo coronary lesion.

Description:

The primary endpoint is a composite endpoint of cardiac death, target vessel related myocardial infarction, and ischemia driven target lesion revascularization (TLF) at 1 month follow up. At 6 months, 1, 2, 3, 4 and 5 years follow-up, clinical endpoints include TLF (its individual components), Patient-oriented cardiac event (all cause death, all MI, and all revascularization) target vessel revascularization, scaffold thrombosis.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 31
• Est. completion date: September 2019
• Est. primary completion date: November 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Age must be between 18 and 75 years, men or unpregnant women

• Patient must have evidence of myocardial ischemia (e.g., stable angina, unstable angina)

• Total number of target lesion =1 per patient

• Target lesion must be = 20mm in length (visual estimation) and 2.75 to 3.75 mm in diameter(Online QCA)

• Target lesion is with a visually estimated stenosis of = 70% (or =50% and evidence of myocardial ischemia) with a TIMI flow of = 1

• The target lesion can be covered by one scaffold

• Patient must be an acceptable candidate for coronary artery bypass graft.

• Patient is able to verbally confirm understanding of risks, benefits and treatment of receiving the NeoVas bioresorbable coronary scaffold and he/she or his/her legally authorized representative provides written informed consent prior to any clinical investigation related procedure, as approved by the appropriate Ethics Committee of the respective clinical site.

Exclusion Criteria:

• Patients has had a known diagnosis of acute myocardial infarction (AMI) within 30 days preceding the procedure; CK and CK-MB have not returned within normal limits at the time of procedure

• Chronic total occlusion lesions(TIMI 0 grade blood flow prior to implantation), left trunk vessel lesion, ostial lesion ,multi-branch lesions needing treated, fork and bridge vessel lesions of branch vessels whose diameter =2.0mm(branch opening stenosis exceeds 40% or need balloon expansion); there is thrombus visible in the target blood vessels.

• Severe calcified lesions and twisted lesions which cannot be pre-expanded, and lesions unsuitable for delivering and expanding stents

• In-stent restenosis lesion

• Patient has undergone previous stenting anywhere within the target vessel(s) within the previous 12 months, or will require stenting within the target vessel(s) within 6 months after the study procedure; target vessels that has been planted stents over a year.

• Severe heart failure(over NYHA III grade ), or left ventricular ejection fraction(LVEF)< 40%( supersonic inspection or left ventricular radiography )

• Known renal insufficiency (e.g., eGFR <60 ml/min, or subject on dialysis)

• Patients with hemorrhage tendency, an active digestive ulcer history, a cerebral hemorrhage or subarachnoid hemorrhage history, or cerebral apoplexy within half a year, and these patients who contraindicate against platelet inhibitors and anticoagulant therefore can not bear anticoagulation treatment

• Patient has a known hypersensitivity or contraindication to aspirin, clopidogrel, heparin, contrast agent, polylactic acid or sirolimus that cannot be adequately pre-medicated

• Life expectancy < 12 months

• Patient is participating in another device or drug study that has not reached the primary endpoint of the study.

• Patient's inability to fully cooperate with the study protocol which in the investigator's opinion may limit his/her ability to participate in the study

• Patient has a heart transplant.

• Patient has current unstable arrhythmias, such as high risk ventricular premature beat and ventricular tachycardia.

• Patient is receiving or scheduled to receive chemotherapy for malignancy within 30 days prior to or after the procedure

• Patient is receiving immunosuppression therapy and has known immunosuppressive or autoimmune disease

• Patient is receiving or scheduled to receive chronic anticoagulation therapy (e.g., heparin, coumadin)

• Elective surgery is planned within the first 6 months after the procedure that will require discontinuing either aspirin or clopidogrel

• Platelet count <100,000 cells/mm3 or >700,000 cells/mm3, a WBC of <3,000 cells/mm3, or documented or suspected liver disease (including laboratory evidence of hepatitis)

• Patient has extensive peripheral vascular disease that precludes safe 6 French sheath insertion

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Disease
• Myocardial Ischemia

Intervention

Device:
• NeoVas BCS
The NeoVas First-in-Man study is a prospective, two centers, single arm trial, which will enroll a total of 30 patients. The hypothesis of this study is to evaluate clinical feasibility, safety, and efficacy of NeoVas sirolimus-eluting bioresorbable coronary scaffold in the treatment of patients with de novo coronary lesion. The primary endpoint is a composite endpoint of cardiac death, target vessel related myocardial infarction, and ischemia driven target lesion revascularization (TLF) at 1 month follow up. At 6 months, 1, 2, 3, 4 and 5 years follow-up, clinical endpoints include TLF (its individual components), Patient-oriented cardiac event (all cause death, all MI, and all revascularization) target vessel revascularization, scaffold thrombosis.

Locations

Country	Name	City	State
China	Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University	Hangzhou	Zhejiang
China	The General Hospital of Shenyang Military Region	Shenyang	Liaoning

Sponsors (1)

Lead Sponsor	Collaborator
Lepu Medical Technology (Beijing) Co.,Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Target Lesion Failure(TLF)	Target lesion failure is a composite endpoint of cardiac death, target vessel related myocardial infarction (TV-MI) and the ischemia-driven target lesion revascularization.	30 days	Yes
Secondary	Target Lesion Failure	Target lesion failure is a composite endpoint of cardiac death, target vessel related myocardial infarction (TV-MI) and the ischemia-driven target lesion revascularization.	6 months	Yes
Secondary	Target Lesion Failure		1 year	Yes
Secondary	Target Lesion Failure		2 years	Yes
Secondary	Target Lesion Failure		3 years	Yes
Secondary	Target Lesion Failure		4 years	Yes
Secondary	Target Lesion Failure		5 years	Yes
Secondary	Patient Oriented Composite Endpoint	Patients oriented composite endpoint includes all-cause death, all myocardial infarction and any revascularization.	30 days	Yes
Secondary	Patient Oriented Composite Endpoint	Patients oriented composite endpoint includes all-cause death, all myocardial infarction and any revascularization.	6 months	Yes
Secondary	Patient Oriented Composite Endpoint		1 year	Yes
Secondary	Patient Oriented Composite Endpoint		2 years	Yes
Secondary	Patient Oriented Composite Endpoint		3 years	Yes
Secondary	Patient Oriented Composite Endpoint		4 years	Yes
Secondary	Patient Oriented Composite Endpoint		5 years	Yes
Secondary	Acute Success (Clinical Device and Clinical Procedure)	Successful delivery and deployment of the Clinical Investigation scaffold at the intended target lesion and successful withdrawal of the scaffold delivery system with attainment of final residual stenosis of less than 50% of the target lesion by QCA (by visual estimation if QCA unavailable).; Successful delivery and deployment of the Clinical Investigation scaffold at the intended target lesion and successful withdrawal of the scaffold delivery system with attainment of final residual stenosis of less than 50% of the target lesion by QCA (by visual estimation if QCA unavailable) and/or using any adjunctive device without the occurrence of ischemia driven major adverse cardiac event (MACE) during the hospital stay with a maximum of first seven days post index procedure. In dual lesion setting both lesions must meet clinical procedure success.	acute	Yes
Secondary	Scaffold Thrombosis	Scaffold thrombosis will be categorized as acute (=1day), subacute (>1day =30 days) and late (>30 days).; Clinical presentation of acute coronary syndrome with angiographic evidence of scaffold thrombosis (angiographic appearance of thrombus within or adjacent to a previously treated target lesion).; In the absence of angiography, any unexplained death, or acute MI (ST segment elevation or new Q-wave)* in the distribution of the targetlesion within 30 days.	30days	Yes
Secondary	Scaffold Thrombosis		6 months	Yes
Secondary	Scaffold Thrombosis		1 year	Yes
Secondary	Scaffold Thrombosis		2 years	Yes
Secondary	Scaffold Thrombosis		3 years	Yes
Secondary	Scaffold Thrombosis		4 years	Yes
Secondary	Scaffold Thrombosis		5 years	Yes
Secondary	Angiographic Endpoint	In-segment In-scaffold, proximal and distal Late lumen loss (mm); In-segment In-scaffold, proximal and distal Minimal lumen diameter(mm); In-segment In-scaffold, proximal and distal Diameter stenosis (%) Angiographic Binary Restenosis (%).	6 months	No
Secondary	Angiographic Endpoint		2 years	No
Secondary	Angiographic Endpoint		5 years	No
Secondary	OCT Endpoint	proportion of covered struts, malapposed struts; neointimal hyperplasia (NIH) area, volume; NIH volume obstruction.	6 months	No
Secondary	OCT Endpoint		2 years	No
Secondary	OCT Endpoint		5 years	No
Secondary	IVUS Endpoint	mean/minimal vessel area, mean/minimal lumen area, mean/minimal stent area	6 months	No
Secondary	IVUS Endpoint		2 years	No
Secondary	IVUS Endpoint		5 years	No
Secondary	MSCT Endpoint	mean/minimal vessel area, mean/minimal lumen area, mean/minimal stent area	1 year	No
Secondary	MSCT Endpoint		3 years	No