At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Tolerability and CK-1827452 Plasma Concentrations During Intravenous and Immediate-Release Oral CK-1827452 in Patients With Ischemic Cardiomyopathy and Angina
In Brief
A Phase 2 clinical trial evaluating CK-1827452 24mg and 6 mg iv infusion, CK-1827452 12.5mg capsule, and 4 other interventions for Heart Failure and 2 related conditions. Completed, enrolled 94 participants across 14 sites in 2 countries.
Detailed Summary
This study investigates whether symptom-limited exercise capacity in ischemic cardiomyopathy patients with angina is deleteriously affected by treatment with CK-1827452.
Study Details
Timeline
Interventions
I.V. infusion for 2 hours at 24mg/hr followed by 18 hours at 6mg/hr
12.5mg oral immediate release capsule
I.V. infusion for 2 hours at 48mg/hr followed by 18 hours at 11mg/hr
25mg oral immediate release capsule
Matching placebo iv infusion
Matching placebo oral immediate release capsule