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Completed Phase 2 Interventional

Study to Evaluate the Safety and Efficacy of IV Infusion Treatment With Omecamtiv Mecarbil in Subjects With Left Ventricular Systolic Dysfunction Hospitalized for Acute Heart Failure (ATOMIC-AHF)

ClinicalTrials.gov ID: NCT01300013

Public ClinicalTrials.gov record NCT01300013. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 11:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of IV Infusion Treatment With Omecamtiv Mecarbil in Subjects With Left Ventricular Systolic Dysfunction Hospitalized for Acute Heart Failure

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of the study is to evaluate the effect of 48 hours of intravenous (IV) omecamtiv mecarbil compared with placebo on dyspnea in subjects with left ventricular systolic dysfunction hospitalized for acute heart failure. This is a multicenter, randomized, double-blind, placebo-controlled study with 3 dose cohorts enrolled sequentially in order of ascending dose strength of omecamtiv mecarbil. In each cohort, subjects are randomized 1:1 to omecamtiv mecarbil or placebo.

Study identification

NCT ID
NCT01300013
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cytokinetics
Industry
Enrollment
614 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2011 (Type not available)
Primary completion
Apr 2013 (Actual)
Completion
Sep 2013 (Actual)
Last update posted
Jul 27, 2021

2011 – 2013

United States locations

U.S. sites
45
U.S. states
22
U.S. cities
41
Facility City State ZIP Site status
Research Site Mobile Alabama 36608 —
Research Site Inglewood California 90301 —
Research Site La Jolla California 92037 —
Research Site San Francisco California 94121 —
Research Site Danbury Connecticut 06810 —
Research Site Newark Delaware 19718 —
Research Site Atlantis Florida 33462 —
Research Site Clearwater Florida 33756 —
Research Site Fort Lauderdale Florida 33308 —
Research Site Miami Florida 33133 —
Research Site Orlando Florida 32803 —
Research Site Atlanta Georgia 30322 —
Research Site Chicago Illinois 60611 —
Research Site Peoria Illinois 61636 —
Research Site Baltimore Maryland 21201 —
Research Site Detroit Michigan 48201 —
Research Site Detroit Michigan 48202 —
Research Site Novi Michigan 48374 —
Research Site Minneapolis Minnesota 55417 —
Research Site St Louis Missouri 63110 —
Research Site Lincoln Nebraska 68506 —
Research Site Newark New Jersey 07103 —
Research Site Cortlandt Manor New York 10567 —
Research Site Roslyn New York 11576 —
Research Site The Bronx New York 10467 —
Research Site Chapel Hill North Carolina 27599 —
Research Site Charlotte North Carolina 28204 —
Research Site Durham North Carolina 27705 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Cincinnati Ohio 45219 —
Research Site Cincinnati Ohio 45220 —
Research Site Cincinnati Ohio 45267 —
Research Site Cleveland Ohio 44109 —
Research Site Columbus Ohio 43210 —
Research Site Fairfield Ohio 45014 —
Research Site Oklahoma City Oklahoma 73120 —
Research Site Portland Oregon 97239 —
Research Site Charleston South Carolina 29425 —
Research Site Greenville South Carolina 29605 —
Research Site Memphis Tennessee 38120 —
Research Site Nashville Tennessee 37203 —
Research Site Nashville Tennessee 37232-8802 —
Research Site Tullahoma Tennessee 37388 —
Research Site Houston Texas 77030 —
Research Site Murray Utah 84107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 105 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01300013, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 27, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01300013 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →