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Lamin A/C Gene Mutation clinical trials

View clinical trials related to Lamin A/C Gene Mutation.

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NCT ID: NCT04904393 Recruiting - Heart Failure Clinical Trials

Subanalysis in Patients With CARDIoLAMinopathy Enrolled to REPORT-CCM Registry

CARDILAM-CCM
Start date: March 8, 2021
Phase:
Study type: Observational

Observational, retrospective registry with acute and chronic endpoints

NCT ID: NCT03860454 Recruiting - Clinical trials for Lamin A/C Gene Mutation

The Deep Phenotype of Lamin A/C Cardiomyopathy

Start date: March 7, 2019
Phase:
Study type: Observational

This study seeks to discover clinically useful tests to improve the diagnosis of a rare and serious heart muscle disease caused by mutations in a gene called 'Lamin'. Patients born with lamin gene mutations have apparently healthy hearts initially, they begin experiencing symptoms in their twenties or thirties, and by age 45 the majority have undergone a heart transplant, experienced a major cardiac complication, or have died. Sudden heart rhythm abnormalities are a major cause of sudden death so earlier diagnosis can save lives by enabling timely treatment or implantation of specialised pacemakers (defibrillators). In clinical practice, diagnosis of lamin heart disease currently relies on the genetic test. Very little is known about the detailed imaging features of the hearts of patients with lamin heart disease although advanced echocardiography and cardiac MRI now offer the opportunity to study the health of the heart without the need for radiation.

NCT ID: NCT03439514 Terminated - Clinical trials for Dilated Cardiomyopathy

A Study of ARRY-371797 (PF-07265803) in Patients With Symptomatic Dilated Cardiomyopathy Due to a Lamin A/C Gene Mutation

REALM-DCM
Start date: April 17, 2018
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo-controlled study in patients with dilated cardiomyopathy (DCM) due to a mutation of the gene encoding the lamin A/C protein (LMNA). The study will further evaluate a dose level of study drug (ARRY-371797) that has shown preliminary efficacy and safety in this patient population. After the primary analysis has been performed, eligible patients may receive open-label treatment with ARRY-371797.