NotablePrimary endpoints: details revised at 1 of 1 entryShow 4 more changesShow less
Trial sites expanded: 205 → 208 locations
Eligibility criteria expanded, about 29 words
Secondary endpoints: details revised at 2 of 7 entries
Publications: details revised at 1 of 1 entry
MinorTrial sites expanded: 201 → 205 locationsv25
MinorStudy sites: 199 to 201v24
MinorTrial sites expanded: 196 → 199 locationsv23
MinorTrial sites expanded: 191 → 196 locationsv22
MinorTrial sites expanded: 188 → 191 locationsv21
MinorStudy sites: 187 to 188v20
MinorStudy sites: 185 to 187v19
MinorStudy sites: 183 to 185v18
MinorStudy sites: 181 to 183
Eligibility criteria expanded, about 136 words
v17
MinorStudy sites: 177 to 181v16
MinorStudy sites: 171 to 177v15
MinorStudy sites: 169 to 171v14
MinorStudy sites: 84 to 169v13
MinorStudy sites: 77 to 84v12
MinorStudy sites: 72 to 77v11
MinorStudy sites: 63 to 72v10
MinorStudy sites: 50 to 63v9
MinorStudy sites: 33 to 50v8
MinorStudy sites: 18 to 33v7
MinorStudy sites: 13 to 18v6
MinorStudy sites: 9 to 13v5
MinorStudy sites: 7 to 9v4
MinorStudy sites: 5 to 7v3
MinorStudy sites: 1 to 5v2Show 4 more changesShow less
Start date changed from estimate of Dec 2024 to Dec 19, 2024
Eligibility criteria shortened, about 21 words
Secondary endpoints revised (7)
Study description expanded, about 15 words
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to find out if the investigational drug called omecamtiv mecarbil can reduce the risk of the effects of heart failure, like hospitalization, transplantation, or death in patients with heart failure and severely reduced ejection fraction.