Cardior Announces CE Marking of CardiorHealth miR-132 PCR Kit Used in Ongoing HF-REVERT Phase 2 Clinical Study
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Thursday, September 8, 2022
Science, Cardiology, Biotechnology, Research, Pharmaceutical, Health, Medical Devices, Clinical Trials, Patient, LVEF, Degenerative disease, RNA transfection, RNA, Safety, Gene, Medication, Heart, Echocardiography, Heart failure, Blood, Myocardial infarction, Quality of life, CSO, PCR, Fibrosis, European Heart Journal, Standard of care, Therapy, SOC, Founder, MiR-132, HF, CE, ECHO, Trial of the century, Medical device, EU
By using the CardiorHealth miR-132 PCR kit, Cardior ensures consistent measurement of miR-132 levels following CDR132L treatment across all clinical trial centers as an indicator of the target engagement and the compounds mechanism of action.
Key Points:
- By using the CardiorHealth miR-132 PCR kit, Cardior ensures consistent measurement of miR-132 levels following CDR132L treatment across all clinical trial centers as an indicator of the target engagement and the compounds mechanism of action.
- Cardior is developing CDR132L as a therapeutic candidate to improve cardiac systolic and diastolic function in patients with heart failure.
- The CardiorHealth miR-132 PCR kit is the first PCR kit designed to monitor the treatment with a non-coding RNA-based therapeutic.
- CE mark approval of the kit was based on the clinical evaluation of the test in patients receiving various doses of CDR132L or placebo, where the kit demonstrated comparable results to a similar testing protocol used in Cardiors Phase 1b clinical study.