drugset / Trial / NCT05953831

Reverse Remodeling Effects of CDR132L in Patients With Heart Failure With Mildly Reduced or Preserved Ejection Fraction and Cardiac Hypertrophy

NCT05953831 ↗

Phase 2 Withdrawn Cardior Pharmaceuticals GmbH
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2, multicenter, randomized, double-blind, placebo-controlled study including approximately 130 randomized HF patients with heart failure with mildly reduced or preserved ejection fraction (LVEF ≥45%), to assess efficacy and safety of CDR132L on reverse remodeling. In this study, patients with HFpEF (EF ≥50%) or HFmrEF (LVEF 45-49%) will be included.

Timeline

Start
2024-04-30
Primary completion
2025-09-30
Completion
2025-09-30

Outcome

Outcome not reported

Stopped: “Transfer of study responsibility and planning”

Drugs

EvaluationDrugModalityDoseRoute
Subject CDR132L Antisense oligonucleotide 4.52 mg/kg Intravenous