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Phase 2 N=37 Randomized Single-blind Treatment

PercutaneOus StEm Cell Injection Delivery Effects On Neomyogenesis in Dilated CardioMyopathy (The POSEIDON-DCM Study)

Non-ischemic Dilated Cardiomyopathy

Enrolled (actual)
37
Serious AEs
32.4%
Results posted
Feb 2018
Primary outcome: Primary: Incidence of Any Treatment-emergent Serious Adverse Events (TE-SAEs) — 1; 0; 0; 1 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Autologous hMSCs (Biological); Allogeneic hMSCs (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Joshua M Hare
Primary completion
Aug 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Incidence of Any Treatment-emergent Serious Adverse Events (TE-SAEs)
1; 0; 0; 1; 0; 1
SECONDARY
Measurement of Changes in Peak VO2
16.0; 17.9; 15.5; 17.6; 16.4; 20.1
SECONDARY
Measurement of Changes in 6 Minute Walk
416.4; 427.2; 384.2; 438.7; 32.3; 35.1
SECONDARY
Measurement of Changes in Global Ejection Fraction
25.2; 37.6; 32.3; 35.1
SECONDARY
Measurement of Changes in New York Heart Association (NYHA)
6; 4; 8; 9; 2; 5
SECONDARY
Measurement of Changes in Minnesota Living With Heart Failure (MLHF) Questionnaire
30.5; 38.0; 35; 18; 9.0; 12.0

Summary

The technique of transplanting progenitor cells into a region of damaged myocardium, termed cellular cardiomyoplasty1, is a potentially new therapeutic modality designed to replace or repair necrotic, scarred, or dysfunctional myocardium2-4. Ideally, graft cells should be readily available, easy to culture to ensure adequate quantities for transplantation, and able to survive in host myocardium; often a hostile environment of limited blood supply and immunorejection. Whether effective cellular regenerative strategies require that administered cells differentiate into adult cardiomyocytes and couple electromechanically with the surrounding myocardium is increasingly controversial and recent evidence suggests that this may not be required for effective cardiac repair. Most importantly, transplantation of graft cells should improve cardiac function and prevent adverse ventricular remodeling. To date, a number of candidate cells have been transplanted in experimental models, including fetal and neonatal cardiomyocytes5, embryonic stem cell-derived myocytes6, 7, tissue engineered contractile grafts8, skeletal myoblasts9, several cell types derived from adult bone marrow10-15, and cardiac precursors residing within the heart itself16. There has been substantial clinical development in the use of whole bone marrow and skeletal myoblast preparations in studies enrolling both post-infarction patients, and patients with chronic ischemic left ventricular dysfunction and heart failure. The effects of bone-marrow derived mesenchymal stem cells (MSCs) have also been studied clinically. Currently, bone marrow or bone marrow-derived cells represent highly promising modality for cardiac repair. The totality of evidence from trials investigating autologous whole bone marrow infusions into patients following myocardial infarction supports the safety of this approach. In terms of efficacy, increases in ejection fraction are reported in the majority of the trials. Non-ischemic dilated cardiomyopathy is a common and problematic condition; definitive therapy in the form of heart transplantation is available to only a tiny minority of eligible patients. Cellular cardiomyoplasty for chronic heart failure has been studied less than for acute MI, but represents a potentially important alternative for this disease.

Eligibility Criteria

Major Inclusion Criteria:

  • Be ≥ 18 and 5.9cm in male subjects, an LVEDD of > 5.6cm in female subjects or left ventricular end diastolic volume index > 125 mL/m2
  • Be able to undergo an MRI or CT.

Major Exclusion Criteria:

  • Baseline glomerular filtration rate equal or 550 ms on screening ECG.
  • AICD firing in the past 30 days prior to the procedure
  • Be eligible for or require coronary artery revascularization.
  • Diabetic with poorly controlled blood glucose levels and/or evidence of proliferative retinopathy.
  • Have a hematologic abnormality as evidenced by hematocrit 1.3) not due to a reversible cause.
  • Known, serious radiographic contrast allergy.
  • Known allergies to penicillin or streptomycin.
  • Organ transplant recipient.
  • Have a history of organ or cell transplant rejection
  • Clinical history of malignancy within 5 years (i.e., patients with prior malignancy must be disease free for 5 years), except curatively-treated basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma.
  • Non-cardiac condition that limits lifespan to < 1 year.
  • On chronic therapy with immunosuppressant medication.
  • Serum positive for HIV, hepatitis BsAg, or viremic hepatitis C.
  • Female patient who is pregnant, nursing, or of child-bearing potential and not using effective birth control.
  • Have a history of drug or alcohol abuse within the past 24 months.
  • Be currently participating (or participated within the previous 30 days) in an investigational therapeutic or device trial.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01392625). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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