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Rituximab in patients with acute myocardial infarction: a phase 2 placebo-controlled randomised clinical trial

Descripción del proyecto

Un fármaco para la leucemia se utiliza también contra la insuficiencia cardíaca

El infarto agudo de miocardio (IAM) provoca una disfunción ventricular izquierda y una insuficiencia cardíaca en casi el 50 % de los pacientes. Tras ensayos preclínicos exhaustivos, el proyecto financiado con fondos europeos RITA-MI 2 pretende darle un nuevo uso a un fármaco existente, el rituximab, empleado actualmente contra las neoplasias linfáticas y los trastornos autoinmunitarios, como la artritis reumatoide. El rituximab es un anticuerpo monoclonal que se centra de forma selectiva en linfocitos B maduros que expresan el CD20. La idea consiste en detener o limitar la remodelación cardíaca dañina que ocurre tras un IAM y fomentar la recuperación de la función cardíaca. RITA-MI 2 evaluará los efectos de la reducción de los linfocitos B en pacientes con IAM en un ensayo clínico de fase 2b.

Objetivo

RITA-MI 2 will assess the impact of a novel therapeutic strategy targeting patients’ immune response on the recovery of heart function after myocardial infarction (MI) in a phase 2 clinical trial.

Cardiovascular diseases (CVD) represent a major cause of morbidity and mortality worldwide. Despite important advances in the treatment of acute MI, the occurrence of MI still results in left ventricular dysfunction in up to 50% of patients, which leads to the development of heart failure. Left ventricular dysfunction is the strongest predictor of adverse outcome after acute MI, and is associated with a 3 to 4-fold increase in mortality risk. In Westernised countries, heart failure is responsible for 1-2% of all health expenditure, which is mostly driven by repeated hospital admissions. Therefore, there is a considerable need for new therapies to limit the burden of CVD.
This application builds on a ground-breaking discovery by a unique team of clinicians and scientists who provided extensive validation for their findings through a series of basic, pre-clinical and translational research. Our goal is to translate this discovery into benefit for patients. The new therapy is based on selective targeting of a specific immune cell subset, mature B lymphocytes, with the aim to limit deleterious cardiac remodelling and improve heart function recovery post-MI. Of note, the drug that targets this pathway, i.e. CD20 monoclonal antibody (mAb) rituximab, is available for testing in a re-purposing scheme, allowing for rapid initiation of proof-of-concept clinical trials. The PIs of the present proposal have successfully completed a phase 1/2a clinical trial (RITA-MI, NCT03072199), which established the safety of rituximab treatment at the acute phase of MI.

RITA-MI 2 will conduct a phase 2b randomised double-blind placebo-controlled CT to assess the impact of B cell depletion with the CD20 mAb rituximab on left ventricular dysfunction and cardiac remodelling after acute MI.

Convocatoria de propuestas

H2020-SC1-BHC-2018-2020

Consulte otros proyectos de esta convocatoria

Convocatoria de subcontratación

H2020-SC1-2020-Two-Stage-RTD

Régimen de financiación

RIA - Research and Innovation action

Coordinador

INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
Aportación neta de la UEn
€ 258 750,00
Dirección
RUE DE TOLBIAC 101
75654 Paris
Francia

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Región
Ile-de-France Ile-de-France Paris
Tipo de actividad
Research Organisations
Enlaces
Coste total
€ 258 750,00

Participantes (13)