Evaluating Additional Platelet Inhibition in Patients With High Platelet Reactivity Undergoing Percutaneous Coronary Intervention

Cardiovascular Disease Clinical Trial

— APACS-HPR  

Official title:

Evaluating the Benefit of Additional Platelet Inhibition in Acute Coronary Syndrome Patients With High Platelet Reactivity Undergoing PCI

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01339026
• Other study ID #: 2010-020219-35
• Status: Terminated
• Phase: Phase 4
• First received: April 19, 2011
• Last updated: September 17, 2014
• Start date: February 2012
• Est. completion date: September 2013

Study information

• Verified date: September 2014
• Source: Royal Brompton & Harefield NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: National Health Service
• Study type: Interventional

Clinical Trial Summary

Patients admitted to hospital with chest pain due to reduced blood flow to heart muscle (diagnosis Acute Coronary Syndrome) can be treated with medication and an angioplasty ± stent procedure, which restores blood flow to the heart. Antiplatelet drugs (Aspirin and Clopidogrel) are blood thinning treatments and research has reported they reduce heart attacks, death and stroke. The investigators know some patients do not respond fully to Clopidogrel but currently patients are not tested for this.

The investigators wish to perform a trial to identify those patients who do not respond fully to Clopidogrel and randomise them to either Prasugrel (newer drug) or a higher dose of Clopidogrel.

Patients admitted to the hospitals (2 in the UK and 1 in Germany) will be asked for their consent to participate. A blood sample is tested for platelet activity.

1. Low platelet activity result means patient has responded well to Clopidogrel and will continue on the routine dose. They will be entered into an observational registry. Data will be collected of routine blood tests and investigations, medication and procedures. Their GP will be contacted at about 30 days to see if they are alive.

2. High platelet activity results means patient has not responded fully to Clopidogrel. These patients will be randomly allocated to a higher dose of Clopidogrel or new drug Prasugrel. Data will be collected of routine blood tests and investigations, medication and procedures. A hospital visit at 30±5 days is required to assess how patients are doing, medications and occurrence of any events.

Description:

STUDY DESCRIPTION This is a multinational, randomised open label study comparing Prasugrel versus Clopidogrel in ACS patients who have high platelet reactivity managed with an early invasive strategy (PCI as early as possible and no later than 72 hours from admission).

Patients identified with low platelet reactivity indicating a good response to Clopidogrel will be entered into an observational Registry.

Sites There will be three participating hospitals, two in the UK and one in Germany.

Screening All patients admitted to the hospital with suspected ACS requiring early PCI (within 3 days of admission) will be screened for entry into the trial.

The investigator and/or his/her designee will explain the study requirements and procedures and obtain consent before any study procedures are performed.

We estimate approximately 500 patients will be screened. From these a total of 140 patients will be randomised, the remaining screened patients will be entered into the registry. There will be competitive recruitment and each site is expected to randomise about 40 to 50 patients each. We estimate 7 to 8 patients randomised per month over a period of 18 months.

Routine blood tests and investigations will be carried out according to local management strategies. The angiogram and PCI procedure are part of the routine management for this patient and will be performed according to local policies and procedures.

A research blood sample will be required to determine platelet activity which has to be taken > 2hours from the standard Clopidogrel pre-PCI loading. For most patients this will be taken in the catheter laboratory around the PCI procedure. In a few patients who are loaded with Clopidogrel close to the PCI procedure the blood samples may be taken in the ward or recovery area. Depending on the platelet activity results patients will be either entered into the registry or randomly allocated to either Clopidogrel or Prasugrel.

1. Patients who are good responders to Clopidogrel (platelet reactivity <400 AUC min) will be entered into the registry.

2. Patients who are poor responders to Clopidogrel (platelet reactivity > 400AUC min) will be randomised.

REGISTRY PATIENTS Patients will continue on the standard treatment of Clopidogrel. Data will be collected of routine blood tests and investigations, medication and procedures. Additional blood samples will be taken (if patient consents) for the biomarker and genetic sub-studies. Their GP will be contacted at 30±5 days to see if they are alive.

RANDOMISED PATIENTS Randomisation Investigators will access an automated telephone or automated web service. Investigators will have to confirm patient fulfils the eligibility criteria and that consent has been obtained.

Randomised Treatment Randomised patients will be allocated to receive either open label Clopidogrel (Plavix) or Prasugrel (Efient).

Group 1: Clopidogrel (Plavix)

• Day 1 Loading 600mg

• Day 2 to 7 day: 150mg o.d.

• Day 8 to 30±5 days: 75mg o.d.

Group 2: Prasugrel (Efient)

• Day 1 loading 60mg

• Day 2 to 7 10mg o.d.

• Day 8 to 30±5 days 10mg od

Drug Supply and Storage Prasugrel, a commercially available product, will be supplied by Eli Lilly which holds the manufacturing license to produce Prasugrel. Clopidogrel (Plavix) will be purchased by the hospital Pharmacy through normal purchasing arrangements. All study drugs should be stored in an appropriate locked room, under the control of the Hospital Pharmacist or the Investigator, in the conditions described in the package insert.

Hospital Admission to Discharge

• Patients will be followed until they are discharged home.

• Blood samples taken for platelet activity at 1, 4 and 24 hours, and pre-discharge.

• Blood sample for the biomarker substudy will be taken pre-PCI procedure at 24 hours and at discharge.

• Blood sample for the genetic substudy will be taken at baseline or if not possible pre-discharge.

• Patients will have instructions on how to contact the research team if they have any questions or concerns.

One Month Follow UP RCT Patients in the RCT will be required to attend the hospital for a follow up visit at 30±5 days from date of randomisation. Patients will be assessed by the investigator or his/her designee for heart rate and blood pressure, medication tolerance and compliance, occurrence of adverse events and clinical endpoints, blood sample for platelet activity. At this time the investigator will discuss with the patient their treatment options after this period.

Sub-studies There are two sub-studies proposed (i) biomarker and (ii) genetic. Blood samples will be taken and stored locally before shipment to a core lab in Germany.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 44
• Est. completion date: September 2013
• Est. primary completion date: September 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. ACS patients with intent for PCI <72 hours from admission.

2. Prior clopidogrel loading within 24h before planned PCI or chronic (>24 hours) treatment with clopidogrel

3. High platelet reactivity (HPR) PA > 400 AU min by multiplate analyser ("poor responders")

4. Initial platelet function sample at least 2 hours after pre PCI loading dose

5. Consent

Exclusion Criteria:

1. Patients <18 years and >75 years

2. Body weight <60kg

3. Pretreatment with prasugrel within 7 days of randomisation

4. History of stroke or transient ischaemic attack

5. Patients with increased bleeding risk e.g.

• recent major trauma or surgery

• gastrointestinal bleeding or active peptic ulceration

• Platelet count <100,000 / mm3 at the time of screening

• Internationally Normalized Ratio (INR)> 1.5 at the time of screening

6. Hb<10g/dL

7. Intracranial neoplasm, arteriovenous malformation or aneurysm.

8. Severe hepatic impairment (Child Pugh class C)

9. Intention to use the following medications

• oral anticoagulation

• other antiplatelet therapy (including GPIIb/IIIa inhibitors) besides aspirin

• nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase-2 (COX-2) inhibitors

10. Female patients who are pregnant, planning pregnancy, not using reliable contraception or who are breastfeeding

11. Known allergy, hypersensitivity or other contraindications to prasugrel or clopidogrel

Study Design

Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Coronary Syndrome
• Cardiovascular Disease
• Cardiovascular Diseases

Intervention

Drug:
• Prasugrel
Day 1 loading 60mg Day 2 to 7 10mg o.d. Day 8 to 30 days 10mg od
• Plavix
Clopidogrel (Plavix) Day 1 Loading 600mg Day 2 to 7 day: 150mg o.d. Day 8 to 30 days: 75mg o.d.

Locations

Country	Name	City	State
Germany	Universitätsklinikum Tübingen	Tübingen

Sponsors (2)

Lead Sponsor	Collaborator
Royal Brompton & Harefield NHS Foundation Trust	University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Platelet Reactivity	The primary endpoint will compare the proportion of patients with improved platelet response (i.e. decreased platelet reactivity under the cut-off value of 400 Au.min) in the prasugrel re-loading arm compared to the clopidogrel re-loading arm at 4 hours after randomization in patients with initial high platelet reactivity	4 hours post loading dose	No
Secondary	Platelet reactivity in response to randomised study drug	To compare the proportion of patients with improved platelet response between the treatment arms at hospital discharge/7 days and at 30 days.	7 days/hospital discharge and 30 days	No
Secondary	Extent of myocardial damage	To compare the AUC for CK and troponin at 24 hours between the treatment arms	24 hours	No
Secondary	MACE	To compare the rates major adverse events (death, myocardial infarction, stroke, repeated revascularization) at 30 days between the treatment arms	30 days	No
Secondary	Bleed	To compare the rate of major bleedings at 30 days between the treatment arms	30 days	Yes