Status:
COMPLETED
Intracoronary Stenting and Antithrombotic Regimen: Lesion Platelet Adhesion as Selective Target of Endovenous Revacept
Lead Sponsor:
Deutsches Herzzentrum Muenchen
Collaborating Sponsors:
Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK)
AdvanceCor GmbH
Conditions:
Stable Coronary Artery Disease
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The main objective is to evaluate the efficacy and safety of treatment with 2 doses (80 and 160 mg) of Revacept versus placebo in patients with stable coronary artery disease undergoing PCI.
Detailed Description
Revacept is a protein that is made up of an Fc fragment ("fragment crystallisable") fused to the GPVI receptor (the endogenous platelet collagen receptor). Consequently, Revacept binds to its ligand (...
Eligibility Criteria
Inclusion
- Signed written informed consent
- Men and women \>18 years of age
- Diagnosis: Clinically stable coronary artery disease
- Angiographic evidence of coronary artery disease
- Indication for PCI
Exclusion
- WOCBP who are unwilling or unable to use an acceptable method to avoid pregnancy for up to 4 weeks after receiving investigational product.
- Women who are pregnant or breastfeeding or are planning pregnancy during course of trial
- Women with a positive pregnancy test on enrolment or prior to investigational product administration.
- Patients with elevated high sensitivity cardiac troponin T levels at screening
- Patients receiving antithrombotic therapy with Prasugrel or Ticagrelor within 7 days prior to randomisation
- History of hypersensitivity, contraindication or serious adverse reaction to any component of the study drug (GPVI-Fc, sucrose, mannitol), acetylsalicylic acid or clopidogrel
- History of bleeding diathesis or active bleeding within the last 30 days
- Recent intracerebral haemorrhage or trauma within the last 3 months
- Thrombocytopenia (platelet count \<30000/mm3) at screening
- Sustained hypertension (systolic BP \>179mmHg or diastolic BP \>109mmHg) at screening
- Renal failure (estimated glomerular filtration rate \< 30ml/min and/or dialysis)
- Severe systemic disease, such as known malignancies or other comorbid conditions with life expectancy less than one year that may result in protocol non-compliance
- Unable to provide informed consent (e.g. severe dementia, or psychosis)
- Current severe liver dysfunction (transaminase level \>5-fold the upper normal range limit)
- Patients with an indication for anticoagulant therapy
- Participation in any other clinical interventional trial (drug/device) within less than 30 days prior to screening
- Any other contraindication to perform PCI
- Any planned additional PCI or surgery within 30 days after randomization
- Suspected poor capability to follow instructions and cooperate
- Prisoners or subjects who are involuntarily incarcerated
- Subjects who are compulsorily detained for treatment of either a psychiatric or physical illness (e.g. infectious disease)
Key Trial Info
Start Date :
November 20 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 26 2020
Estimated Enrollment :
334 Patients enrolled
Trial Details
Trial ID
NCT03312855
Start Date
November 20 2017
End Date
March 26 2020
Last Update
April 20 2020
Active Locations (8)
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1
Deutsches Herzzentrum München
Munich, Bavaria, Germany, 80636
2
Universitätsmedizin Berlin, Campus Benjamin Franklin
Berlin, Germany, 12203
3
Charité - Universitätsmedizin Berlin, Campus Virchow
Berlin, Germany, 13353
4
Universitätsklinikum Frankfurt, Medizinische Klinik III, Kardiologie
Frankfurt am Main, Germany, 60590