Drugs / sacubitril/valsartan
last change Jun 2023 re-read 3 minutes ago

sacubitril/valsartan

Developed for
heart failure
Investigated by
Novartis Pharmaceuticals

Trials 1

202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 4 NCT04491136 Nov 2020 → Jun 2023 heart failure Novartis Pharmaceuticals Terminated Missed primary

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2020-03-18 Novartis Pharmaceuticals Results Novartis announces NEJM publication of three pivotal trials showing durable and potent efficacy of inclisiran, an investigational first-in-class siRNA cholesterol-lowering therapy novartis.com ↗
The primary endpoints were achieved in all three trials.
2016-06-22 Novartis Pharmaceuticals Results Timely use of Novartis' Entresto could prevent or postpone over 28,000 US deaths per year among HFrEF patients, according to an expert analysis in JAMA Cardiology novartis.com ↗
They compared Entresto to the ACE-inhibitor enalapril and found Entresto was associated with more than a year longer average survival time, and that it was cost-effective compared to enalapril when these medications were used with other standard of care therapies.
2016-04-02 Novartis Pharmaceuticals Results New analyses show Novartis' Entresto(TM) reduced cardiovascular death or hospitalization for heart failure, consistently benefitting patients with reduced ejection fraction regardless... novartis.com ↗
In a second analysis, patients taking Entresto had about a 20% reduction in CV death or heart failure hospitalization compared to those taking enalapril, regardless of background therapy[1],[2]

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as sacubitril/valsartan “Oral sacubitril/valsartan at the dosage of investigators discretion, whit a target dose of 200mg bid for the next 6 months of this study” NCT04491136 ↗
Route Oral “Oral sacubitril/valsartan at the dosage of investigators discretion, whit a target dose of 200mg bid for the next 6 months of this study” NCT04491136 ↗