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Study to Assess Efficacy and Safety of CDR132L in Patients With Reduced Left Ventricular Ejection Fraction After Myocardial Infarction (HF-REVERT)

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ClinicalTrials.gov Identifier: NCT05350969
Recruitment Status : Recruiting
First Posted : April 28, 2022
Last Update Posted : August 2, 2022
Sponsor:
Information provided by (Responsible Party):
Cardior Pharmaceuticals GmbH

Brief Summary:

This is a Phase 2, multicenter, randomized, parallel, 3-arm, placebo-controlled study to assess efficacy and safety of CDR132L in patients with reduced Left Ventricular Ejection Fraction (LVEF) (≤ 45%) after myocardial infarction (MI). This study consists of a screening period (to occur at least 3 days after MI diagnosis), a 6-month double-blind period, and a 6-month extension period with the End of Study (EOS) Visit at Day 360/Month 12.

Two dosages of CDR132L will be tested against placebo on their effects on patients, who just had a heart attack in addition to standard care. The aim of the study is to show that CDR132L is safe and effective to improve heart failure in such patients.


Condition or disease Intervention/treatment Phase
Myocardial Infarction, Acute Heart Failure, Left Sided Drug: CDR132L Drug: Placebo to CDR132L Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 280 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Masking Description: Pharmacy staff is unblinded. They will hand-over prepared investigational medicinal product (IMP) in light-protected syringe.
Primary Purpose: Treatment
Official Title: Phase 2, Multicenter, Randomized, Parallel, 3-arm, Placebo-controlled Study to Assess Efficacy and Safety of CDR132L in Patients With Reduced Left Ventricular Ejection Fraction (≤ 45%) After Myocardial Infarction
Actual Study Start Date : June 27, 2022
Estimated Primary Completion Date : June 30, 2024
Estimated Study Completion Date : November 30, 2024

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Attack

Arm Intervention/treatment
Experimental: CDR132L 5 mg
CDR132L 5 mg/kg body weight intravenous in single dose on Day 1, Day 29 and Day 57
Drug: CDR132L
CDR132L is a synthetic antisense oligonucleotide (ASO) and a selective inhibitor of microRNA-132-3p (miR-132). miR-132 in cardiomyocytes is a central switch affecting the expression of genes that are crucially involved in maladaptive cardiac remodeling, transformation, and pathological cardiac growth (hypertrophy), contributing to adverse cardiac remodeling and heart failure (HF).1-5 Aberrant expression of miR-132 in cardiac cells is causally associated with cardiac remodeling and HF progression.

Experimental: CDR132L 10 mg
CDR132L 10 mg/kg body weight intravenous in single dose on Day 1, Day 29 and Day 57
Drug: CDR132L
CDR132L is a synthetic antisense oligonucleotide (ASO) and a selective inhibitor of microRNA-132-3p (miR-132). miR-132 in cardiomyocytes is a central switch affecting the expression of genes that are crucially involved in maladaptive cardiac remodeling, transformation, and pathological cardiac growth (hypertrophy), contributing to adverse cardiac remodeling and heart failure (HF).1-5 Aberrant expression of miR-132 in cardiac cells is causally associated with cardiac remodeling and HF progression.

Placebo Comparator: Placebo
Placebo intravenous in single dose on Day 1, Day 29 and Day 57
Drug: Placebo to CDR132L
Placebo to CDR132L




Primary Outcome Measures :
  1. Echocardiography (ECHO) [ Time Frame: 6 months ]
    Percent change from baseline (screening to occur at least 3 days after MI diagnosis as measured by ECHO [central laboratory]) in Left Ventricular End-Systolic Volume (LVESVI) at Month 6.



Information from the National Library of Medicine

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Ages Eligible for Study:   30 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Main Inclusion Criteria:

  1. Male or female patients, aged ≥ 30 to ≤ 80 years at the date of signing informed consent which is defined as the beginning of the Screening Period.
  2. Spontaneous acute mycardial infarction (AMI) (type I) based on the universal MI definition with randomization to occur no later than 14 days after index event diagnosis.
  3. Patient with a LVEF ≤ 45% as measured by ECHO after MI diagnosis (STEMI or NSTEMI).
  4. Patient with previous MI events in history can be included.
  5. Patient with body weight of ≤ 120 kg.
  6. N-terminal pro B-type natriuretic peptide level ≥ 125 pg/ml and < 8000 pg/ml at screening.
  7. Patient with STEMI/NSTEMI who underwent percutaneous coronary intervention for this event.

Exclusion Criteria:

  1. A woman of childbearing potential (WOCBP).
  2. Patient with HF of non-ischemic origin; e.g., myocarditis, alcoholic cardiomyopathy.
  3. Patient with New York Heart Association (NYHA) class IV at screening or randomization.
  4. Patient has any planned cardiac intervention (angiogram without angioplasty is acceptable) or any other planned surgery after the Screening Period.
  5. Patient has severe valvular heart disease.
  6. Patient has systolic BP < 90 mmHg or > 180 mmHg, diastolic BP < 50 mmHg or > 110 mmHg, and/or heart rate < 50 or > 100 beats/minute at screening or randomization.
  7. Patient with an estimated glomerular filtration rate < 30 mL/min/1.73 m2 or on dialysis.
  8. Patient with hepatic insufficiency classified as Child-Pugh B or C.
  9. Patient has medical history of disease(s) affecting the blood-brain-barrier, e.g., stroke within 6 months or multiple sclerosis.
  10. Patient has medical history of bleeding disorders or has thrombocytopenia (platelets < 100,000/μL).
  11. Patient has poorly controlled diabetes as determined by the Investigator.
  12. Patient has a history or presence of any of the following cardiac conditions: known structural cardiac abnormalities beyond HF, family history of long QT syndrome, cardiac syncope, or recurrent, idiopathic syncope.
  13. Any clinically significant abnormalities, at the discretion of the Investigator, in rhythm, conduction, or morphology of resting ECG that pose an additional safety risk to patients.
  14. Patient with active "severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)" infection confirmed as per the local testing guidelines at screening.
  15. Patient is not to be enrolled into the study if they received any prohibited therapy within 3 months of screening.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05350969


Contacts
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Contact: Cardior Clinical Team +49511338599 ext 30 clinical@cardior.de

Locations
Show Show 58 study locations
Sponsors and Collaborators
Cardior Pharmaceuticals GmbH
Investigators
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Principal Investigator: Johann Bauersachs, Prof. Dr. Hannover Medical School
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Responsible Party: Cardior Pharmaceuticals GmbH
ClinicalTrials.gov Identifier: NCT05350969    
Other Study ID Numbers: CDR132L-P2-01
2021-006040-27 ( EudraCT Number )
First Posted: April 28, 2022    Key Record Dates
Last Update Posted: August 2, 2022
Last Verified: August 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Heart Failure
Myocardial Infarction
Infarction
Heart Diseases
Cardiovascular Diseases
Ischemia
Pathologic Processes
Necrosis
Myocardial Ischemia
Vascular Diseases