drugset / Trial / NCT02695420
Safety, PK, and Efficacy of Omecamtiv Mecarbil in Japanese Subjects With Heart Failure With Reduced Ejection Fraction
RandomizedParallel-groupQuadruple-blindTreatment
Summary
* To evaluate pharmacokinetics (PK) of omecamtiv mecarbil in Japanese subjects with heart failure (HF) with reduced ejection fraction * To evaluate the safety and tolerability of oral omecamtiv mecarbil
Timeline
- Start
- 2016-04-14
- Primary completion
- 2017-04-06
- Completion
- 2017-05-08
Outcome
Met primary endpoint
release “the Phase 2 clinical trial of omecamtiv mecarbil in Japanese patients with heart failure has met its pharmacokinetic primary endpoint” cytokinetics.com ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Omecamtiv Mecarbil | Small molecule | 25 mg | Oral |
| Subject | Omecamtiv Mecarbil | Small molecule | 37.5 mg | Oral |
| Subject | Omecamtiv Mecarbil | Small molecule | 50 mg | Oral |