WebInclisiran, sold under the brand name Leqvio, is a medication for the treatment of people with atherosclerotic cardiovascular disease (ASCVD), ASCVD risk-equivalents, and … WebApr 12, 2024 · The ORION-10 trial was a randomized, double-blind, placebo-controlled, parallel-group, phase 3 study involving 1561 US patients with ASCVD (with LDL-C > 70 …
Long-term efficacy and safety of inclisiran in patients with …
WebSep 4, 2024 · PARIS – A small interfering RNA drug, inclisiran, safely halved LDL cholesterol levels in more than 800 patients in a phase 3, multicenter study, in a big step toward this drug coming onto the market and offering an alternative way to harness the potent cholesterol-lowering power of PCSK9 inhibition. – A small interfering RNA drug, inclisiran WebNov 5, 2015 · This outcome measure evaluated the individual responsiveness of participants to inclisiran (single and double dose) in the mITT population as defined by an LDL-C level of <25 mg/deciliter [dL] at Day 90 and Day 180. Number of Participants With Greater Or Equal To 50% LDL-C Reduction From Baseline At Day 180 [ Time Frame: Baseline, Day 180 ] biography of mary robinson
A Randomized Study to Evaluate the Effect of an "Inclisiran First
WebFeb 23, 2024 · This clinical study was designed to assess the efficacy, safety, and tolerability of long-term dosing of inclisiran and evolocumab given as subcutaneous injections in participants with high cardiovascular risk and elevated low-density lipoprotein cholesterol (LDL-C). Detailed Description: WebJan 5, 2024 · Conclusions: In this phase 1 trial, no serious adverse events were observed with inclisiran. Doses of 300 mg or more (in single or multiple doses) significantly reduced levels of PCSK9 and LDL cholesterol for at least 6 months. (Funded by Alnylam Pharmaceuticals and the Medicines Company; ClinicalTrials.gov number, NCT02314442 … WebInclisiran was administered once every 28 days by subcutaneous injection into the scapular and mid‐dorsal areas, with injection sites rotated for each dose. Atorvastatin was administered to alert animals once daily by oral gavage. Dosing occurred over 85 days, followed by a 90‐day post‐treatment observation period (i.e., recovery phase). biography of matt haig