A Phase 2, randomized, double-blind, placebo-controlled trial to evaluate the efficacy, safety, and tolerability of CRD-4730 in patients with heart failure with reduced ejection fraction (HFREF) (CALIBRATE-HF)

Registry ID
2025-525033-31-00
Source registry
CTIS
Status
Authorised
Phase
PHASE2
Study type
INTERVENTIONAL
Sponsor
Cardurion Pharmaceuticals Inc.
Enrollment
102
Last update
2026-08-14

Conditions

Primary outcomes

Composite Z-score calculated as the average of Z-scores for the change from baseline at 24 weeks for the following 6 endpoints: NT-proBNP (log-transformed), Left ventricular end-diastolic volume index (LVEDVI), Left ventricular end-systolic volume index (LVESVI), E/e′ ratio, Global longitudinal strain (GLS), Left atrial volume index (LAVI).

Locations

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