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Active HORIZON European Commission

PROGNOSIS IMPROVEMENT OF UNPROVOKED VENOUS THROMBOEMBOLISM USING PERSONALIZED ANTICOAGULANT THERAPY

€9.96M EUR

Funder European Commission
Recipient Organization Centre Hospitalier Regional Et Universitaire de Brest
Country France
Start Date Dec 01, 2023
End Date Nov 30, 2028
Duration 1,826 days
Number of Grantees 17
Roles Participant; Associated Partner; Third Party; Coordinator
Data Source European Commission
Grant ID 101095698
Grant Description

Venous thromboembolism (VTE) is a frequent and life-threatening disease. In 50% of cases, VTE occurs in the absence of any major risk factors (unprovoked VTE).

In these patients, when anticoagulation is stopped after 3 months of anticoagulation, more than 35% will develop recurrent VTE. Consequently, international guidelines recommend to treat these patients indefinitely. However, such practice exposes them to a substantial increase risk of bleeding.

Nevertheless, after several years of anticoagulation in all patients with unprovoked VTE, the risk of anticoagulant-related bleeding is expected to exceed the risk of recurrent VTE after stopping treatment.

In addition, extending anticoagulation indefinitely in all patients with unprovoked VTE exposes 65% of patients to an unjustified high risk of bleeding, who would never have experienced recurrent VTE after stopping treatment.In this setting, optimal duration and management of anticoagulation remains a pivotal and unresolved challenging issue which has the potential to markedly improve long-term prognosis of unprovoked VTE.

Based on quantitative and qualitative approaches, MORPHEUS will for the first time integrate (i) clinical, laboratory and imaging biomarkers (personalized medicine) and (ii) socio-anthropological markers (patient-centred model) into sets of prediction rules for optimizing anticoagulant management integrated in a shared decision-making process.

The ultimate goal of the European MORPHEUS project will be to develop and validate a time-dependent multi-component tool integrated in a shared decision-making process regarding anticoagulant treatment duration in patients with unprovoked VTE.

The whole MORPHEUS program, leaded by a consortium of outstanding European researchers in the field of VTE, will constitute a major breakthrough compared with the present standard of care in patients with unprovoked VTE with major scientific, public health, economic, and societal impacts.

All Grantees

Academisch Ziekenhuis Leiden; Ecrin European Clinical Research Infrastructure Network; Institut National de la Sante Et de la Recherche Medicale; Kungliga Tekniska Hoegskolan; Region Syddanmark; Universite de Geneve; Universite de Bretagne Occidentale; Todaytomorrow B.V.; Kobenhavns Universitet; Fundacion Para la Investigacion Biomedica Del Hospital Universitario Ramon Y Cajal; Servicio Madrileno de Salud; Warszawski Uniwersytet Medyczny; Agencia Estatal Consejo Superior de Investigaciones Cientificas; Universite de Bordeaux; Universite Paris Cite; Universitaetsmedizin Der Johannes Gutenberg-Universitaet Mainz; Centre Hospitalier Regional Et Universitaire de Brest

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