A Study With NVC-001 in Patients With LMNA-related Dilated Cardiomyopathy (SUNBEAM-LMNA)
Nuevocor Pte. Ltd. · NCT07606274
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 1, Phase 2
- Target enrollment
- 21
- US sites recruiting
- 3
- Study start
- June 16, 2026
- Record last updated
- August 7, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: NVC-001 - Low Dose; NVC-001 - Intermediate Dose; NVC-001 - High Dose
Conditions: LMNA-Related Dilated Cardiomyopathy
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Adult ≥18 years old, able to provide informed consent
- Clinical diagnosis of LMNA-related dilated cardiomyopathy (DCM) with LV systolic dysfunction
- Pathogenic or likely pathogenic LMNA mutation confirmed by a CLIA-certified/CAP-accredited laboratory
- NYHA Functional Class I, II, or III
- LVEF >25% and ≤45% by echocardiography
- Implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy-defibrillator )CRT-D) implanted >3 months prior to consent
Key Exclusion Criteria
- Any chronic medical condition that, in the Investigator's opinion, would compromise participant safety or compliance
- 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
- Current or anticipated need for chronic IV inotropic therapy
Recruiting US locations
Cedars-Sinai Medical Center
Los Angeles, CA 90048
Site contact: Nuevocor Clinical Trial Team · 310-248-8300 · info@nuevocor.com
Mayo Clinic
Rochester, MN 55905
Site contact: Nuevocor Clinical Trial Team · 507-422-5433 · info@nuevocor.com
Houston Methodist Hospital
Houston, TX 77030
Site contact: Nuevocor Clinical Trial Team · 281-222-9983 · info@nuevocor.com
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