Study on Safety and Effectiveness of Three Doses of Argatroban as Anticoagulant in Percutaneous Coronary Intervention (PCI)

NCT ID: NCT00508924

Last Updated: 2012-12-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 140 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-08-31
• Study Completion Date: 2006-10-31

Brief Summary

This is a phase II multi-centre study in 140 patients undergoing elective PCI to obtain the information on dose-response of argatroban in pharmacodynamic markers and to assess the anticoagulation, safety and efficacy of argatroban in reference to unfractionated heparin, in combination with dual antiplatelet therapy.

Detailed Description

This is a phase II multi-centre study in Europe in patients with stable coronary artery disease or troponin negative unstable angina undergoing elective PCI, to obtain the information on the safety and effects on various pharmacodynamic markers, of three doses of argatroban in combination with clopidogrel and aspirin, and to assess the results of argatroban and unfractionated heparin, both used in combination with clopidogrel and aspirin, on clinical outcomes, adequacy of anticoagulation, various pharmacodynamic markers (approximately 35 patients per group).

Conditions

Coronary Artery Disease; Angina, Unstable

Keywords

Argatroban; Direct thrombin inhibitor; Percutaneous coronary intervention; Activated clotting time; PCI; ACT

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

ARG250

Group Type: EXPERIMENTAL

Argatroban

Intervention Type: DRUG

ARG300

Group Type: EXPERIMENTAL

Argatroban

Intervention Type: DRUG

ARG350

Group Type: EXPERIMENTAL

Argatroban

Intervention Type: DRUG

Heparin

Group Type: PLACEBO_COMPARATOR

Heparin

Intervention Type: DRUG

Interventions

Argatroban

Intervention Type: DRUG

Argatroban

Intervention Type: DRUG

Argatroban

Intervention Type: DRUG

Heparin

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female (women of child bearing potential must have a negative pregnancy test prior to entry into the study)
• Aged over 18 years
• Diagnosis of stable coronary artery disease (CAD) or unstable angina (troponin negative, i.e. within the normal range for the study site) with low to moderate anatomic risk and a requirement for elective percutaneous coronary angioplasty or stent insertion with an approved device in one or more de novo-treated or re-stenotic lesions in native vessels
• Signed written informed consent

Exclusion Criteria

• Any condition which, in the investigator's opinion, contraindicates the use of argatroban, heparin or clopidogrel or endangers the patient if he/she participated in this study.
• Known cirrhosis, hepatitis, clinically significant hepatic disorder, or history of hepatic disorder. Hepatic disorder is defined as having levels of liver function tests (bilirubin, Aspartate Aminotransferase (Serum Glutamate Oxaloacetate Transaminase)(AST (SGOT)), Alanine Aminotransferase (Serum Glutamate Pyruvate Transaminase)(ALT (SGPT)) greater than 3.0 times above the upper limit of the normal range of local laboratory.
• Patients not currently taking aspirin
• Renal insufficiency, defined as serum creatinine greater than 2.0 mg/dL (greater than 177mmol/L)
• Platelets less than 125,000/ml
• If already taking any form of heparin prior to study enrolment, Activated Partial Thromboplastin Time(aPTT) equal or greater than 35 sec or ACT greater than 160 sec
• Use of low molecular heparin (LMWH) during 12 h prior to PCI
• If taking oral anticoagulant medication prior to study enrolment, International Normalised Ratio(INR) greater than 1.2
• Q wave MI with cardiogenic shock or thrombolytic therapy within 72 h of study dosing
• Use of Glycoprotein IIb / IIIa(GPIIb/IIIa) inhibitors within prior 3 weeks
• Documented coagulation disorder or bleeding diathesis
• Lumbar puncture within the past 2 weeks
• History of previous cerebral aneurysm, haemorrhagic stroke, or thrombotic stroke within the past 6 months
• Active, uncontrolled peptic ulcer disease or any gastrointestinal bleeding or genitourinary bleeding within 3 months prior to study enrolment
• Major surgery, serious trauma, puncture of non-compressible vessel, or biopsy of parenchymal organ within prior 2 months
• Planned staged procedure, planned rotational atherectomy, directional coronary atherectomy, brachytherapy, or thrombectomy catheters
• Planned surgical intervention other than study procedure within next 7 days
• Presence of greater than 50% stenosis of unprotected left main coronary artery
• Severe peripheral vascular disease, precluding femoral access
• History of vasculitis
• Uncontrolled hypertension defined as greater than 180/120 mmHg
• Pregnancy (exclusion by routine urine test)
• Lactating woman
• Woman of children bearing age who are or were not using accepted contraceptive methods
• Participation in other clinical trials of investigational products within 3 months prior to study enrolment
• Terminally ill patients with a life expectancy of < 3 months

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

Sponsors

Mitsubishi Tanabe Pharma Corporation

INDUSTRY

Sponsor Role: lead

Principal Investigators

Professor

Role: PRINCIPAL_INVESTIGATOR

Information at Mitsubishi Pharma Europe

Locations

Aalst, , Belgium

Bad Nauheim, , Germany

Cologne, , Germany

Dachau, , Germany

Düren, , Germany

Frankfurt, , Germany

Halle, , Germany

Mainz, , Germany

Countries

Belgium; Germany

References

Rossig L, Genth-Zotz S, Rau M, Heyndrickx GR, Schneider T, Gulba DC, Desaga M, Buerke M, Harder S, Zeiher AM; ARG-E04 study group. Argatroban for elective percutaneous coronary intervention: the ARG-E04 multi-center study. Int J Cardiol. 2011 Apr 14;148(2):214-9. doi: 10.1016/j.ijcard.2010.02.044. Epub 2010 Mar 11.

Reference Type: RESULT

PMID: 20226548 (View on PubMed)

Other Identifiers

ARG-E04

Identifier Type: -

Identifier Source: org_study_id