At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 40 enrolled
Drug / intervention
Entresto™ 49Mg-51 mg tabletdrug
Likely dose
Entresto™ 49Mg-51 mg tabletfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Proof of Concept Study to Determine the Efficacy of Entresto™ in HFpEF Based on Circulating Neprilysin Levels: The Circulating NEP and NEP Inhibition (CNEPi) Study
In Brief
A Phase 4 clinical trial evaluating Entresto™ 49Mg-51 mg tablet for Heart Failure With Preserved Ejection Fraction. Completed, enrolled 40 participants across 1 site.
Detailed Summary
To determine biomarker responses to Entresto™in patients with Heart Failure with preserved Ejection Fraction (HFpEF) and who have high or low serum neprilysin (NEP) levels.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsNational Institute on Aging (NIA)
Timeline
Phase 4CompletedFinished
20192020202120222023202420252026
First PostedApr 2018
Enrollment StartJun 2018
Primary CompletionMar 2021
TodayJul 2026
First PostedApr 24, 2018
Enrollment StartJun 25, 2018
Primary CompletionMar 23, 2021
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 8.2 years ago
Interventions
Entresto™ 49Mg-51 mg tabletdrug
Entresto™ 49Mg-51 mg will be given twice daily orally for 5 weeks