MT1002 Phase II Study in ACS Patients With PCI
- Conditions
- Acute Coronary Syndrome
- Interventions
- Drug: MT1002 for Injection
- Registration Number
- NCT04723186
- Lead Sponsor
- Shaanxi Micot Technology Limited Company
- Brief Summary
This is an open-label, sequential-dose escalation/de-escalation trial testing 3 dose levels of MT1002 in patients undergoing PCI due to ACS with NSTEMI. Three doses of MT1002 will be sequentially tested in cohorts of 6 patients each to achieve target ACT.
- 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 to investigate the safety, tolerability, and efficacy of MT1002 in patients undergoing PCI due to ACS with NSTEMI.
This study is a single dose, sequential-dose escalation study in patients undergoing PCI due to ACS with NSTEMI. The first 2 doses were considered safe and well tolerated in the Phase 1 healthy subject study. The third dose to be given will be determined based on the safety and efficacy results from the first 2 doses. Dose escalation/de-escalation and stopping rules have been put in place to ensure the safety of the patients in this study.
The patients will receive a single MT1002 close to the initiation of PCI (Day 1) followed by 4 hours of IV infusion and follow-up at Day 2, Day 14, and Day 30.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 6
- Males and females ≥ 18 to 85 years of age.
- Diagnosed with NSTEMI.
- Patients who will undergo PCI during the index hospitalization for an NSTEMI.
- Ability to understand and willing to give written informed consent.
- Women of childbearing potential must have a negative pregnancy test or be post-menopausal for at least 1 year before enrollment or be permanently sterilized since ≥6 weeks. Females of childbearing potential and males with partners of childbearing potential must be using effective contraception.
- .Cardiogenic shock or prolonged cardiopulmonary resuscitation (CPR).
- Active bleeding, bleeding diathesis, coagulopathy.
- Any history of intracranial bleeding or structural abnormalities.
- Prior transient ischemic attack, prior stroke within 6 months.
- Index MI is STEMI or new left bundle branch block.
- The following planned procedures within 30 days after enrollment: staged PCI, CABG, valve surgery, or additional invasive procedures.
- Pre-existing atrial fibrillation or prolonged QTcF (470ms in men, 480ms in women).
- Anticipated requirement for oral anticoagulants before Day 30.
- CRUSADE bleeding risk score >40.
- Suspected aortic dissection.
- History of gastrointestinal or genitourinary bleeding within the previous 3 months.
- Refusal to receive blood transfusion if needed during the study.
- Major surgery in the last month.
- History of heparin-induced thrombocytopenia and bleeding diathesis.
- Severe uncontrolled hypertension.
- Prior (within 30 days prior to enrollment) or planned administration of thrombolytics, glycoprotein IIb/IIIa inhibitors, bivalirudin, or fondaparinux for the index MI.
- Known relevant hematological deviations: hemoglobin (male) < 11 g/dL, hemoglobin (female) < 10 g/dL, hematocrit < 35%, platelet count < 100,000 cells/µL.
- Use of Coumadin derivatives and/or Factor Xa inhibitor drugs within the last 7 days.
- Chronic therapy with non-steroidal anti-inflammatory drugs (NSAIDs; except aspirin) , cyclooxygenase (COX)-2 inhibitors within 1 month before screening.
- Known malignancies or other comorbid conditions with life expectancy < 1 year.
- Known severe liver disease (i.e., aspartate aminotransferase [AST], alanine aminotransferase [ALT] > 3 × ULN).
- Known positive serology for hepatitis B & C, HIV screen.
- Known chronic kidney disease with estimated glomerular filtration rate (eGFR) <30 mL/min and/or dialysis.
- Known allergy or intolerance to aspirin, clopidogrel, ticagrelor, prasugrel, bivalirudin, unfractionated heparin, P2Y12 antagonists, or contrast.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Monotherapy of MT1002, 3 doses via intravenous (IV) + infusion MT1002 for Injection Three doses of MT1002 (IV loading + continuous IV infusion) will be sequentially tested. The first dose level is 0.90 mg/kg initial loading dose (bolus intravenous injection) + 1.8 mg/kg/h (infusion) for 4 hours. The second dose level will be based on the results from the first cohort (If the dose is escalated, then the second dose level is 1.2 mg/kg initial loading dose (bolus intravenous injection) + 2.3 mg/kg/h (infusion) for 4 hours; if the dose is de-escalated, then the second dose level is 0.6 mg/kg initial loading dose (bolus intravenous injection) + 1.2 mg/kg/h (infusion) for 4 hours). The third dose will be determined based on the results from the first 2 cohorts.
- Primary Outcome Measures
Name Time Method To determine the safe and well tolerated dose of MT1002 in patients with ACS with NSTEMI and PCI. 30 days Co-Primary endpoints:
The number of patients with target ACT (200 -300 seconds \[sec\]) achieved on MT1002 (no switch to standard of care) prior/during PCI and PCI success.
Adverse event (AE) of interest: bleeding events major (Bleeding Academic Research Consortium \[BARC\] Type 3-5)
- Secondary Outcome Measures
Name Time Method To evaluate the anti-coagulation effect of MT1002 by activated partial thromboplastin time (aPTT) and activated clotting time (ACT) 30 days Coagulation parameters (ACT, aPTT, PT, TT, FIB, INR) and Percentage of patients who achieve ACT ≥ 200 sec
Major adverse cardiovascular event(s) 30 days To evaluate the anti-platelet effect of MT1002 by platelet aggregation (PA) 30 days PA
Trial Locations
- Locations (1)
IU Health - BMH
🇺🇸Muncie, Indiana, United States