Hypoplastic Left Heart Syndrome
Conditions
Keywords
Pediatrics, HLHS
Brief summary
This study is intended to evaluate the safety and feasibility of intramyocardial injection of allogeneic mesenchymal cells during the Bi-Directional Cavopulmonary Anastomosis (BDCPA) surgery for hypoplastic left heart syndrome (HLHS) pediatric patients.
Detailed description
This is an open label study, intended as a safety and efficacy assessment prior to a full comparator study. In this Phase I study, cells administered will be delivered in 6-10 intramyocardial injections that will be tested in 20 patients and 10 patients will be controls with a total of 30 HLHS patients. A total of 30 patients with HLHS will be enrolled in a staged enrollment process. In this open-labeled study, a maximum of 20 patients will eventually receive intramyocardial injection of the allogeneic mesenchymal stem cells and 10 control patients with no cell injection. The enrollment of the patients will occur in two stages groups: Group A and Group B. In Group A, 10 consecutive HLHS patients will be initially enrolled in the allogenic MSCs treatment arm to determine feasibility and safety. After 6 months of the last enrolled patient in Group A, all Group A patients will be assessed in order to determine whether it is feasible and safe, including the harvesting, processing, and administering of the allogeneic MSCs. Thereafter, Group B will start enrolling a total of 20 HLHS patients which will be randomized to the treatment and control arms in a 1:1 ratio, respectively, in order to have 10 allogeneic MSCs-treated patient and 10 control patients. At the completion of this Phase I clinical study, the total enrolled cohort will be 20 patients treated with allogeneic MSCs and 10 patients in the control arm.
Interventions
DRUGAllo-hMSCs
Allogeneic Human Mesenchymal Stem Cells
DRUGPlacebo
Placebo
Sponsors
Longeveron Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Masking description
HLHS patients which will be randomized to the treatment and control arms in a 1:1 ratio
Intervention model description
20 patients and 10 patients will be controls with a total of 30 HLHS patients.
Eligibility
Sex/Gender
ALL
Age
No minimum to 30 Days
Healthy volunteers
No
Inclusion criteria
* Subjects with hypoplastic left heart syndrome (all types) requiring BDCPA surgery.
Exclusion criteria
* Have HLHS and restrictive or intact atrial septum. * Be undergoing the Norwood procedure that do not have HLHS. * Have significant coronary artery sinusoids. * Require mechanical circulatory support prior to surgery. * Have an underlying evidence of arrhythmia requiring anti-arrhythmia therapy. * Parent or guardian unwilling or unable to comply with necessary follow-up(s) * Be serum positive for HIV, hepatitis BsAg (B Surface Antigen) or viremic hepatitis C. * Be unsuitable for inclusion in the study, in the opinion of the investigator. * Need for concomitant surgery for aortic coarctation or tricuspid valve repair.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Monitor major adverse cardiac events | 1 month after injection | Monitoring of events includes death, sustained/symptomatic ventricular tachycardia requiring intervention with inotropic support, aggravation of heart failure, new myocardial infarction, unplanned cardiovascular operation for cardiac tamponade and infection in the first month after injection, and serially afterwards. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Composite Change from baseline in right ventricular function, right ventricular end-diastolic volume, right ventricular end-systolic volume, right ventricular end-systolic diameter and tricuspid regurgitation | baseline, 24 weeks and 1 year | as measured by serial echocardiograms and MRI scans. |
| Number of participants with incidence of mortality or need for transplantation after the BDCPA operation | One year after injections | Assessed through the number of participants with adverse events, hospitalizations, or transplantations. |
| Composite Changes in somatic growth velocity over time (weight, height, head circumference) from the BDCPA operation | 12 months post operative | Changes in weight, height, and head circumference will be measured |
| Assessment of Co-morbidity | up to 12 months follow-up | Assessment of cardiovascular mortality, all-cause morbidity, Cardiovascular morbidity, re-hospitalizations, need for transplantation. |
Countries
United States
Outcome results
None listed