Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol

Standard

Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol. / Ray, Kausik K; Landmesser, Ulf; Leiter, Lawrence A; Kallend, David; Dufour, Robert; Karakas, Mahir; Hall, Tim; Troquay, Roland P T; Turner, Traci; Visseren, Frank L J; Wijngaard, Peter; Wright, R Scott; Kastelein, John J P.

in: NEW ENGL J MED, Jahrgang 376, Nr. 15, 13.04.2017, S. 1430-1440.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Ray, KK, Landmesser, U, Leiter, LA, Kallend, D, Dufour, R, Karakas, M, Hall, T, Troquay, RPT, Turner, T, Visseren, FLJ, Wijngaard, P, Wright, RS & Kastelein, JJP 2017, 'Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol', NEW ENGL J MED, Jg. 376, Nr. 15, S. 1430-1440. https://doi.org/10.1056/NEJMoa1615758

APA

Ray, K. K., Landmesser, U., Leiter, L. A., Kallend, D., Dufour, R., Karakas, M., Hall, T., Troquay, R. P. T., Turner, T., Visseren, F. L. J., Wijngaard, P., Wright, R. S., & Kastelein, J. J. P. (2017). Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol. NEW ENGL J MED, 376(15), 1430-1440. https://doi.org/10.1056/NEJMoa1615758

Vancouver

Ray KK, Landmesser U, Leiter LA, Kallend D, Dufour R, Karakas M et al. Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol. NEW ENGL J MED. 2017 Apr 13;376(15):1430-1440. https://doi.org/10.1056/NEJMoa1615758

Bibtex

@article{b039b8361caf4b4889e7191ddda5459d,
title = "Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol",
abstract = "BACKGROUND: In a previous study, a single injection of inclisiran, a chemically synthesized small interfering RNA designed to target PCSK9 messenger RNA, was found to produce sustained reductions in low-density lipoprotein (LDL) cholesterol levels over the course of 84 days in healthy volunteers.METHODS: We conducted a phase 2, multicenter, double-blind, placebo-controlled, multiple-ascending-dose trial of inclisiran administered as a subcutaneous injection in patients at high risk for cardiovascular disease who had elevated LDL cholesterol levels. Patients were randomly assigned to receive a single dose of placebo or 200, 300, or 500 mg of inclisiran or two doses (at days 1 and 90) of placebo or 100, 200, or 300 mg of inclisiran. The primary end point was the change from baseline in LDL cholesterol level at 180 days. Safety data were available through day 210, and data on LDL cholesterol and proprotein convertase subtilisin-kexin type 9 (PCSK9) levels were available through day 240.RESULTS: A total of 501 patients underwent randomization. Patients who received inclisiran had dose-dependent reductions in PCSK9 and LDL cholesterol levels. At day 180, the least-squares mean reductions in LDL cholesterol levels were 27.9 to 41.9% after a single dose of inclisiran and 35.5 to 52.6% after two doses (P<0.001 for all comparisons vs. placebo). The two-dose 300-mg inclisiran regimen produced the greatest reduction in LDL cholesterol levels: 48% of the patients who received the regimen had an LDL cholesterol level below 50 mg per deciliter (1.3 mmol per liter) at day 180. At day 240, PCSK9 and LDL cholesterol levels remained significantly lower than at baseline in association with all inclisiran regimens. Serious adverse events occurred in 11% of the patients who received inclisiran and in 8% of the patients who received placebo. Injection-site reactions occurred in 5% of the patients who received injections of inclisiran.CONCLUSIONS: In our trial, inclisiran was found to lower PCSK9 and LDL cholesterol levels among patients at high cardiovascular risk who had elevated LDL cholesterol levels. (Funded by the Medicines Company; ORION-1 ClinicalTrials.gov number, NCT02597127 .).",
keywords = "Aged, Anticholesteremic Agents/administration & dosage, Cardiovascular Diseases/prevention & control, Cholesterol, LDL/blood, Dose-Response Relationship, Drug, Double-Blind Method, Female, Humans, Hypercholesterolemia/drug therapy, Injections, Subcutaneous, Male, Middle Aged, Proprotein Convertase 9/antagonists & inhibitors, RNA, Small Interfering/administration & dosage, Risk Factors, Transaminases/blood",
author = "Ray, {Kausik K} and Ulf Landmesser and Leiter, {Lawrence A} and David Kallend and Robert Dufour and Mahir Karakas and Tim Hall and Troquay, {Roland P T} and Traci Turner and Visseren, {Frank L J} and Peter Wijngaard and Wright, {R Scott} and Kastelein, {John J P}",
year = "2017",
month = apr,
day = "13",
doi = "10.1056/NEJMoa1615758",
language = "English",
volume = "376",
pages = "1430--1440",
journal = "NEW ENGL J MED",
issn = "0028-4793",
publisher = "Massachussetts Medical Society",
number = "15",

}

RIS

TY - JOUR

T1 - Inclisiran in Patients at High Cardiovascular Risk with Elevated LDL Cholesterol

AU - Ray, Kausik K

AU - Landmesser, Ulf

AU - Leiter, Lawrence A

AU - Kallend, David

AU - Dufour, Robert

AU - Karakas, Mahir

AU - Hall, Tim

AU - Troquay, Roland P T

AU - Turner, Traci

AU - Visseren, Frank L J

AU - Wijngaard, Peter

AU - Wright, R Scott

AU - Kastelein, John J P

PY - 2017/4/13

Y1 - 2017/4/13

N2 - BACKGROUND: In a previous study, a single injection of inclisiran, a chemically synthesized small interfering RNA designed to target PCSK9 messenger RNA, was found to produce sustained reductions in low-density lipoprotein (LDL) cholesterol levels over the course of 84 days in healthy volunteers.METHODS: We conducted a phase 2, multicenter, double-blind, placebo-controlled, multiple-ascending-dose trial of inclisiran administered as a subcutaneous injection in patients at high risk for cardiovascular disease who had elevated LDL cholesterol levels. Patients were randomly assigned to receive a single dose of placebo or 200, 300, or 500 mg of inclisiran or two doses (at days 1 and 90) of placebo or 100, 200, or 300 mg of inclisiran. The primary end point was the change from baseline in LDL cholesterol level at 180 days. Safety data were available through day 210, and data on LDL cholesterol and proprotein convertase subtilisin-kexin type 9 (PCSK9) levels were available through day 240.RESULTS: A total of 501 patients underwent randomization. Patients who received inclisiran had dose-dependent reductions in PCSK9 and LDL cholesterol levels. At day 180, the least-squares mean reductions in LDL cholesterol levels were 27.9 to 41.9% after a single dose of inclisiran and 35.5 to 52.6% after two doses (P<0.001 for all comparisons vs. placebo). The two-dose 300-mg inclisiran regimen produced the greatest reduction in LDL cholesterol levels: 48% of the patients who received the regimen had an LDL cholesterol level below 50 mg per deciliter (1.3 mmol per liter) at day 180. At day 240, PCSK9 and LDL cholesterol levels remained significantly lower than at baseline in association with all inclisiran regimens. Serious adverse events occurred in 11% of the patients who received inclisiran and in 8% of the patients who received placebo. Injection-site reactions occurred in 5% of the patients who received injections of inclisiran.CONCLUSIONS: In our trial, inclisiran was found to lower PCSK9 and LDL cholesterol levels among patients at high cardiovascular risk who had elevated LDL cholesterol levels. (Funded by the Medicines Company; ORION-1 ClinicalTrials.gov number, NCT02597127 .).

AB - BACKGROUND: In a previous study, a single injection of inclisiran, a chemically synthesized small interfering RNA designed to target PCSK9 messenger RNA, was found to produce sustained reductions in low-density lipoprotein (LDL) cholesterol levels over the course of 84 days in healthy volunteers.METHODS: We conducted a phase 2, multicenter, double-blind, placebo-controlled, multiple-ascending-dose trial of inclisiran administered as a subcutaneous injection in patients at high risk for cardiovascular disease who had elevated LDL cholesterol levels. Patients were randomly assigned to receive a single dose of placebo or 200, 300, or 500 mg of inclisiran or two doses (at days 1 and 90) of placebo or 100, 200, or 300 mg of inclisiran. The primary end point was the change from baseline in LDL cholesterol level at 180 days. Safety data were available through day 210, and data on LDL cholesterol and proprotein convertase subtilisin-kexin type 9 (PCSK9) levels were available through day 240.RESULTS: A total of 501 patients underwent randomization. Patients who received inclisiran had dose-dependent reductions in PCSK9 and LDL cholesterol levels. At day 180, the least-squares mean reductions in LDL cholesterol levels were 27.9 to 41.9% after a single dose of inclisiran and 35.5 to 52.6% after two doses (P<0.001 for all comparisons vs. placebo). The two-dose 300-mg inclisiran regimen produced the greatest reduction in LDL cholesterol levels: 48% of the patients who received the regimen had an LDL cholesterol level below 50 mg per deciliter (1.3 mmol per liter) at day 180. At day 240, PCSK9 and LDL cholesterol levels remained significantly lower than at baseline in association with all inclisiran regimens. Serious adverse events occurred in 11% of the patients who received inclisiran and in 8% of the patients who received placebo. Injection-site reactions occurred in 5% of the patients who received injections of inclisiran.CONCLUSIONS: In our trial, inclisiran was found to lower PCSK9 and LDL cholesterol levels among patients at high cardiovascular risk who had elevated LDL cholesterol levels. (Funded by the Medicines Company; ORION-1 ClinicalTrials.gov number, NCT02597127 .).

KW - Aged

KW - Anticholesteremic Agents/administration & dosage

KW - Cardiovascular Diseases/prevention & control

KW - Cholesterol, LDL/blood

KW - Dose-Response Relationship, Drug

KW - Double-Blind Method

KW - Female

KW - Humans

KW - Hypercholesterolemia/drug therapy

KW - Injections, Subcutaneous

KW - Male

KW - Middle Aged

KW - Proprotein Convertase 9/antagonists & inhibitors

KW - RNA, Small Interfering/administration & dosage

KW - Risk Factors

KW - Transaminases/blood

U2 - 10.1056/NEJMoa1615758

DO - 10.1056/NEJMoa1615758

M3 - SCORING: Journal article

C2 - 28306389

VL - 376

SP - 1430

EP - 1440

JO - NEW ENGL J MED

JF - NEW ENGL J MED

SN - 0028-4793

IS - 15

ER -