Multicentre, Prospective Randomized Open Label, Blinded-endpoint (PROBE) Controlled Trial of Thrombolysis With Low Dose Tenecteplase (TNK-tPA) Versus Standard of Care in Minor Ischemic Stroke With Proven Acute Symptomatic Occlusion

Who is this study for? Adult patients with Acute Ischemic Stroke
What treatments are being studied? Tenecteplase
Status: Completed
Location: See all (61) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This trial will enroll patients that have been diagnosed with a transient ischemic attack (TIA) or minor stroke that has occurred within the past 12 hours. Anyone diagnosed with a minor stroke faces the possibility of long-term disability and even death, regardless of treatment. Stroke symptoms such as weakness, difficulty speaking and paralysis may improve or worsen over the hours or days immediately following a stroke. TEMPO-2 is a minor stroke trial for patients presenting within 12 hours of their symptom onset. Patients will be randomized to TNK-tPA or standard of care. In the intervention group TNK-tPA is given as a single, intravenous bolus (0.25mg/Kg) immediately upon randomization. Maximum dose 50mg. The control group will receive antiplatelet agent(s) as decided by the treating physician. Antiplatelet agent(s) choice will be at the treating physician's discretion. TEMPO-2 Coordinating Centre is located in Calgary, AB, Canada. There will be approximately 50 sites participating worldwide. Dr. Shelagh Coutts is the Principal Investigator.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Acute ischemic stroke in an adult patient (18 years of age or older)

• Onset (last-seen-well) time to treatment time ≤ 12 hours.

• TIA or minor stroke defined as a baseline NIHSS ≤ 5 at the time of randomization. Patients do not have to have persistent demonstrable neurological deficit on physical neurological examination.

• Any acute intracranial occlusion or near occlusion (TICI 0 or 1) (MCA, ACA, PCA, VB territories) defined by non-invasive acute imaging (CT angiography or MR angiography) that is neurologically relevant to the presenting symptoms and signs. Multiphase CTA or CT perfusion are required for this study. An acute occlusion is defined as TICI 0 or TICI 1 flow.1 Practically this can include a small amount of forward flow in the presence of a near occlusion AND, Delayed washout of contrast with pial vessels on multiphase CTA in a region of brain concordant with clinical symptoms and signs OR, Any area of focal perfusion abnormality identified using CT or MR perfusion - e.g. transit delay (TTP, MTT or T Max), in a region of brain concordant with clinical symptoms and signs.

• Pre-stroke independent functional status - structured mRS ≤2.

• Informed consent from the patient or surrogate.

• Patients can be treated within 90 minutes of the first slice of CT or MRI. Scans can be repeated to meet this requirement; if there is no change neurologically then only a CT head need be repeated for assessment of extent and depth of ischemia.

Locations
Other Locations
Australia
Royal Adelaide Hospital
Adelaide
Box Hill Hospital
Box Hill
Calvary Public Hospital Bruce
Canberra
Gold Coast University Hospital
Gold Coast
Royal Melbourne Hospital
Melbourne
Fiona Stanley Hospital
Murdoch
John Hunter Hospital
Newcastle
Austria
Medical University of Vienna (Coordinating Centre)
Vienna
St. John's of God Hospital Vienna
Vienna
Brazil
Hospital de Clínicas de Botucatu
Botucatu
Instituto Hospital de Base do Distrito Federal
Brasília
Hospital Universitário Maria Aparecida Pedrossian
Campo Grande
Hospital Celso Ramos Florianopolos
Celso Ramos
Hospital Geral de Fortaleza
Fortaleza
Clinica Neurologica e Neurocirurgica de Joinville Ltda
Joinville
Porto Alegre Hospital
Porto Alegre
Santa Casa de Porto Alegre
Porto Alegre
Hospital de Clínicas de Ribeirão Preto
Ribeirão Preto
Americas Medical City
Rio De Janeiro
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
São Paulo
Hospital São Paulo UNIFESP
São Paulo
Irmandade Da Santa Casa de Misericordia de Sao Paulo
São Paulo
Hospital Estadual Central
Vitória
Canada
University of Calgary/Foothills Medical Centre
Calgary
University of Alberta
Edmonton
Hamilton Health Sciences Centre
Hamilton
Kingston General Hospital
Kingston
London Health Sciences Centre
London
McGill University
Montreal
Royal Columbian Hospital
New Westminster
Ottawa General Hospital
Ottawa
CHU de Québec-Université Laval
Quebec City
University of Saskatchewan/ Royal University Hospital
Saskatoon
St. Michael's Hospital
Toronto
Sunnybrook Health Sciences Centre
Toronto
Toronto Western
Toronto
Vancouver General Hospital
Vancouver
Victoria General Hospital
Victoria
Finland
University Central Hospital HUCH
Helsinki
Ireland
Beaumont Hospital
Dublin
Mater Misericordiae University Hospital Dublin
Dublin
New Zealand
Christchurch Hospital
Christchurch
Singapore
National Neuroscience Institute Tan Tock Seng Hospital
Singapore
Singapore General Hospital
Singapore
Spain
Complejo Jospitalario Universitario A Coruna
A Coruña
Vall d'Hebron Institut de Recerca
Barcelona
Vall d'Hebron Institut de Recerca (VHIR)
Barcelona
Hospital Universitari Doctor Josep Trueta
Girona
Clinc University Hospital Valladolid
Valladolid
United Kingdom
Royal Victoria Hospital
Belfast
Queen Elizabeth Hospital
Birmingham
Addenbrooke Hospital
Cambridge
Queen Elizabeth University Hospital
Glasgow
Charring Cross Hospital
London
Countess of Chester
London
Kings College Hospital
London
St George's University Hospitals NHS Foundation trust
London
Stoke University of North Midlands
London
University College London Hospital
London
Nottingham University Hospital
Nottingham
John Radcliffe Hospital
Oxford
Time Frame
Start Date: 2015-04-01
Completion Date: 2024-04-10
Participants
Target number of participants: 1274
Treatments
Experimental: Tenecteplase (tNK)
Experimental: TNK-tPA (0.25mg/kg) given as a single, intravenous bolus immediately upon randomization. Experimental treatment will be administered as a single intravenous bolus over 1-2 minutes as per the standard manufacturers' instructions for use. Tenecteplase, a genetically engineered mutant tissue plasminogen activator, has a longer half-life, is more fibrin specific, produces less systemic depletion of circulating fibrinogen, and is more resistant to plasminogen activator inhibitor than alteplase.
Active_comparator: Control (Antiplatelet Agents)
Control: Patients will be treated with standard of care based antiplatelet treatment - choice at the discretion of the investigator. Low dose aspirin (single agent) will be the choice of most physicians, some will chose to use the combination of aspirin and clopidogrel. As this is a multi-centre, international trial where local practices will vary, rather than mandating a specific antiplatelet agent, we will allow the local investigator to chose which antithrombotic regime should be used. Standard of care medication(s) should be given immediately upon randomization.
Related Therapeutic Areas
Sponsors
Leads: University of Calgary

This content was sourced from clinicaltrials.gov

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