A Clinical Study of MT1002 in Subjects With Acute Coronary Syndrome Undergoing PCI

NCT ID: NCT06533358

Last Updated: 2024-08-01

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-02-27
• Study Completion Date: 2025-07-31

Brief Summary

An Open-label, Sequential Dose Escalation/De-escalation Clinical Trial of MT1002 in Subjects With Acute Coronary Syndrome Undergoing PCI.

Detailed Description

MT1002 is a novel 32-amino acid synthetic peptide aimed to combine molecular functions of both a direct thrombin inhibitor and a platelet glycoprotein IIb/IIIa receptor antagonist, indicated for use as an antithrombotic and anticoagulant in patients with ACS and in patients undergoing PCI.

This study is an Open-label, sequential dose escalation/de-escalation clinical trial of MT1002 in subjects with acute coronary syndrome undergoing PCI. First dose cohort is 0.60 mg/kg (initial loading dose, intravenous bolus) + 1.2 mg/kg/h*4 h (maintenance dose, intravenous infusion). The Safety Review Committee makes decisions on subsequent dose adjustments. Dose escalation/de-escalation and stopping rules have been put in place to ensure the safety of the patients in this study.

Conditions

Acute Coronary Syndrome

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

MT1002 Injection

MT1002 is infused once only, once for 4h

Group Type: EXPERIMENTAL

MT1002 Injection

Intervention Type: DRUG

MT1002 is infused once only, once for 4h. MT1002 is for subjects with acute coronary syndrome undergoing PCI

Interventions

MT1002 Injection

MT1002 is infused once only, once for 4h. MT1002 is for subjects with acute coronary syndrome undergoing PCI

Intervention Type: DRUG

Other Intervention Names

No other name

Eligibility Criteria

Inclusion Criteria

1. Male and female aged 18-85 years old (both 18 and 85 years old)

2. Diagnosis of acute coronary syndrome (ACS)

3. Subjects who will undergo PCI during hospitalization

4. Able to understand and willing to sign written informed consent prior to undertaking any study-related activities

5. Females of childbearing potential must have a negative pregnancy test result prior to enrollment or be postmenopausal for at least 1 year, or permanently sterilized for ≥ 6 weeks. For women of childbearing potential and men with female partners of childbearing potential, effective contraception must be used if they are sexually active from the time of informed consent until 90 days after MT1002 administration

Exclusion Criteria

1. cardiogenic shock, or cardiopulmonary resuscitation (CPR）

2. Suspicious aortic dissection, pericarditis, endocarditis

3. Has any history of intracranial hemorrhage or structural abnormalities

4. Transient ischemic attack, stroke within 6 months

5. History of gastrointestinal or genitourinary bleeding within 1 month

6. Major surgery within 1 month

7. The following surgeries are planned within 1 month of enrollment: CABG, valve surgery, or other invasive procedures

8. Long-term treatment with non-steroidal anti-inflammatory drugs (except aspirin), cyclooxygenase (COX)-2 inhibitors, within 1 month prior to screening

9. Prior (within 7 days prior to enrollment) or planned use of thrombolytic agents, bivalirudin, or fondaparinux. 12 hours before enrollment, unfractionated heparin or low molecular weight heparin was injected subcutaneously.

10. Use of coumarin derivatives and/or factor Xa inhibitors in the past 7 days

11. Anticipated need for oral anticoagulants within 3 days of dosing

12. Severe uncontrolled hypertension persists even within 24 hours of adequate treatment

13. According to the judgment of the investigator, the subject has a high risk of bleeding, such as active bleeding, bleeding tendency, coagulation disorders, etc

14. Known associated hematologic abnormalities

15. Known to have a malignancy or comorbid other disease that may lead to protocol non-adherence with a life expectancy of < 1 year

16. Known severe liver disease

17. Known hepatitis B and hepatitis C, HIV screening serology positive, except for the low viral replication phase.

18. Known chronic kidney disease

19. Known allergy or intolerance to aspirin, clopidogrel, ticagrelor, prasugrel, bivalirudin, unfractionated heparin, P2Y12 antagonists, or contrast agents.

20. Weight: male subjects should not be less than 50.0kg, female subjects should not be less than 45.0kg, and body mass index within the range of 18.0~30.0kg/m2 (including boundary values)

21. Subjects who have previously used MT1002.

22. Unable to fully cooperate with the study protocol.

23. Has any other medical or psychiatric illness that, in the opinion of the investigator, precludes participation in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shaanxi Micot Pharmaceutical Technology Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Changsheng Ma, Medical phd

Role: PRINCIPAL_INVESTIGATOR

Beijing Anzhen Hospital Affiliated to Capital Medical University

Locations

Beijing Anzhen Hospital Affiliated to Capital Medical University

Beijing, Beijing Municipality, China

Site Status: RECRUITING

Xianyang Hospital, Yan'an University

Xi'an, Shaanxi, China

Site Status: RECRUITING

Countries

China

Central Contacts

Changsheng Ma, Medical phd

Role: CONTACT

chshma@vip.sina.com

13501373114

NA NA NA

Role: CONTACT

Facility Contacts

Changsheng Ma, Medical phd

Role: primary

chshma@vip.sina.com

13501373114

Qiufang Lian

Role: primary

Other Identifiers

MT1002-II-C04

Identifier Type: -

Identifier Source: org_study_id