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Study identifier: NCT07606274 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Recruiting

A Study With NVC-001 in Patients With LMNA-related Dilated Cardiomyopathy (SUNBEAM-LMNA)

Condition: LMNA-Related Dilated Cardiomyopathy  ·  Sponsor: Nuevocor Pte. Ltd.

PhasePhase 1/Phase 2
Planned participants21
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where8 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This study is designed to evaluate the safety and tolerability of NVC-001 in adults with LMNA-related dilated cardiomyopathy (LMNA-DCM). The study will also assess exploratory measures of efficacy.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Key Inclusion Criteria: 1. Adult ≥18 years old, able to provide informed consent 2. Clinical diagnosis of LMNA-related dilated cardiomyopathy (DCM) with LV systolic dysfunction 3. Pathogenic or likely pathogenic LMNA mutation confirmed by a CLIA-certified/CAP-accredited laboratory 4. NYHA Functional Class I, II, or III 5. LVEF \>25% and ≤45% by echocardiography 6. Implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy-defibrillator )CRT-D) implanted \>3 months prior to consent Key Exclusion Criteria: 1. Any chronic medical condition that, in the Investigator's opinion, would compromise participant safety or compliance 2. Hospitalization as an inpatient for the following conditions within 3 months prior to signing the ICF: Heart failure, Persistent/refractory ventricular arrhythmia requiring external defibrillation, or multiple/recurrent cardioversion/defibrillation by ICD Indication for, or history of, LV assist device or cardiac transplantation due to end-stage cardiac dysfunction 3. Current or anticipated need for chronic IV inotropic therapy

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (8)

University of Alabama in BirminghamBirmingham, Alabama, United StatesNot Yet Recruiting
Cedars-Sinai Medical CenterLos Angeles, California, United StatesRecruiting
Brigham and Women's HospitalBoston, Massachusetts, United StatesNot Yet Recruiting
University of MichiganAnn Arbor, Michigan, United StatesNot Yet Recruiting
Mayo ClinicRochester, Minnesota, United StatesRecruiting
The Christ HospitalCincinnati, Ohio, United StatesNot Yet Recruiting
The Ohio State UniversityColumbus, Ohio, United StatesNot Yet Recruiting
Houston Methodist HospitalHouston, Texas, United StatesRecruiting

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