Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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27 January 2014 |
Main ID: |
EUCTR2009-016568-36-DE |
Date of registration:
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25/02/2010 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Randomized, double-blind, triple-dummy trial to compare the efficacy of otamixaban with Unfractionated Heparin + eptifibatide, in patients with Unstable angina/Non ST segment Elevation Myocardial infarction scheduled to undergo an early invasive strategy - TAO
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Scientific title:
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Randomized, double-blind, triple-dummy trial to compare the efficacy of otamixaban with Unfractionated Heparin + eptifibatide, in patients with Unstable angina/Non ST segment Elevation Myocardial infarction scheduled to undergo an early invasive strategy - TAO |
Date of first enrolment:
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05/05/2010 |
Target sample size:
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13220 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2009-016568-36 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: yes
Randomised: yes
Open: no
Single blind: no
Double blind: yes
Parallel group: yes
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: yes
Placebo: no
Other: no
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Phase:
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Countries of recruitment
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Austria
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Belgium
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Bulgaria
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Czech Republic
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Estonia
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France
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Germany
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Greece
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Hungary
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Italy
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Latvia
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Lithuania
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Netherlands
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Portugal
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Spain
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United Kingdom
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Contacts
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Name:
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Address:
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Germany |
Telephone:
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Email:
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medinfo.de@sanofi-aventis.com |
Affiliation:
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Sanofi-Aventis Deutschland GmbH |
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Name:
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Address:
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Germany |
Telephone:
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Email:
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medinfo.de@sanofi-aventis.com |
Affiliation:
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Sanofi-Aventis Deutschland GmbH |
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Key inclusion & exclusion criteria
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Inclusion criteria: Patient with non ST-segment elevation Acute Coronary Syndrome with the following symptoms:
I 01. Ischemic symptoms (chest pain or equivalent) at rest =10 minutes within 24 hours of randomization
AND
I 02.One of the two following criteria:
I 02A. New ST-segment depression =0.1 mV (=1 mm), or transient (<30 minutes) ST-segment elevation =0.1 mV (=1 mm) in at least 2 contiguous leads on the ECG, OR
I 02B. Elevation of cardiac biomarkers within 24 hours of randomization, defined as elevated troponin T, troponin I, or CK-MB level above upper limit of normal
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I 03. Planned to have a coronary angiography (followed, when indicated, by PCI) as early as possible (after at least 2 hours of treatment with study drug) and within 36 hours (at the latest on Day 3, if justified)
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I 04. Informed consent obtained in writing
Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Exclusion criteria: Cardiovascular
E 06. Revascularization procedure already performed for the qualifying event.
E 07. Acute ST-segment elevation MI
Related to prior or concomitant treatments
E 08. Patient having received curative dose of anticoagulant treatment (including UFH, LMWH, or bivalirudin) for more than 24 hours prior to randomization, or who have been treated by abciximab.
E 09. Inability to discontinue current anticoagulation in order to transition to Investigational Products according to the specified transition timing
Exclusion criteria related to the active comparator and/or mandatory background therapies
Related to mandatory background therapies
E 10. Patients who can not be treated by aspirin and clopidogrel (or any other oral antiplatelet agent) according to their local labeling
Related to eptifibatide
E 11. Patient who cannot be treated with eptifibatide according to the national labeling (when available).In countries where eptifibatide is not approved the reference label to be considered will be either the European labeling or the US labeling.
Related to unfractionated heparin
E 12. Patient who cannot be treated with unfractionated heparin according to the national labeling
Exclusion criteria related to the current knowledge of a sanofi-aventis compound
E 13. Allergy to otamixaban
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Acute coronary syndrome scheduled to undergo an early invasive strategy.
MedDRA version: 15.1
Level: PT
Classification code 10051592
Term: Acute coronary syndrome
System Organ Class: 10007541 - Cardiac disorders
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Intervention(s)
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Product Code: XRP0673 Pharmaceutical Form: Solution for injection INN or Proposed INN: otamixaban CAS Number: 219672-50-1 Current Sponsor code: XRP0673 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 5- Pharmaceutical form of the placebo: Solution for injection Route of administration of the placebo: Intravenous bolus use (Noncurrent)
Product Code: XRP0673 Pharmaceutical Form: Solution for infusion INN or Proposed INN: otamixaban CAS Number: 219672-50-1 Current Sponsor code: XRP0673 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 5- Pharmaceutical form of the placebo: Solution for infusion Route of administration of the placebo: Intravenous drip use (Noncurrent)
Trade Name: INTEGRILIN 2 mg/ml Product Name: INTEGRILIN Pharmaceutical Form: Solution for injection INN or Proposed INN: EPTIFIBATIDE CAS Number: 188627-80-7 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 2- Pharmaceutical form of the placebo: Solution for injection Route of administration of the placebo: Intravenous bolus use (Noncurrent)
Trade Name: INTEGRILIN 0.75 mg/ml Product Name: INTEGRILIN Pharmaceutical Form: Solution for infusion INN or Proposed INN: EPTIFIBATIDE CAS Number: 188627-80-7 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration number: 0.75- Pharmaceutical form of the placebo: Solution for infusion Route of administration of the placebo: Intravenous drip use (Noncurrent)
Trade Name: HEPARINE CHOAY 25 000 UI/5 ml Product Name: HEPARIN SODIUM Pharmaceutical Form: Concentrate for solution for injection INN or Proposed INN: HEPARIN SODIUM CAS Number: 01/08/9041 Concentration unit: IU/ml international unit(s)/millilitre Concentration type: equal Concentration number: 5000- Pharmaceutical form of the placebo: Solution for injection Route of administration of the placebo: Intravenous use
Product Code: XR
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Primary Outcome(s)
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Main Objective: To demonstrate the superior efficacy (composite of all-cause death + Myocardial infarction) of otamixaban as compared to unfractionated heparin (UFH) + eptifibatide.
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Primary end point(s): Primary efficacy endpoint: Adjudicated composite of all-cause death and new myocardial infarction (MI) from randomization (Day 1) to Day 7. This endpoint will be analyzed from randomization (Day 1) to Day 30 as a sensitivity analysis. Primary safety end point: TIMI significant bleeding (composite of TIMI major and minor) from randomization (Day 1) to Day 7
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Secondary Objective: • To demonstrate the superior efficacy ( composite of all-cause death + Myocardial infarction+ any stroke) of otamixaban as compared to UFH + eptifibatide • To document the effect of otamixaban on Rehospitalization or prolongation of hospitalization due to a new episode of myocardial ischemia/myocardial infarction as compared to UFH+ eptifibatide • To document the effect on mortality (all cause mortality) of otamixaban as compared to UFH+ eptifibatide • To document the safety of otamixaban as compared to UFH + eptifibatide • To document the effect of otamixaban on Thrombotic procedural complications during the index PCI as compared to UFH + eptifibatide • To characterize otamixaban pharmacokinetics over the entire dosing interval and to evaluate otamixaban exposure-response (safety and efficacy) in the target population
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Secondary ID(s)
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2009-016568-36-HU
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EFC6204
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Source(s) of Monetary Support
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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