BACKGROUND : Alirocumab reduces low-density lipoprotein cholesterol (LDL-C) levels by up to 61%. The ODYSSEY Open-Label Extension study investigated the effect of alirocumab in patients with heterozygous familial hypercholesterolaemia (HeFH) over 144 weeks. METHODS : Eligible patients with HeFH had completed an earlier double-blind, randomised, placebo-controlled parent study. Patients were initiated on 75 mg alirocumab Q2W subcutaneous (SC) unless baseline LDL-C was > 8.9 mmol/l, in which case they received 150 mg alirocumab Q2W. Dose titration to 150 mg Q2W was at the investigator’s discretion. RESULTS : The study enrolled 167 patients and the parent study mean (± SD) baseline LDL-C level was 3.65 ± 1.9 mmol/l. Mean LDL-C lev...
Background: Alirocumab, a monoclonal antibody that inhibits proprotein convertase subtilisin- kexin ...
BACKGROUND Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/ke...
# The Author(s) 2014. This article is published with open access at Springerlink.com Background Indi...
Background and aims: ODYSSEY OLE (open-label extension; NCT01954394) included patients diagnosed wit...
AbstractBackgroundPCSK9 inhibition with alirocumab significantly reduced LDL-C levels in trials of u...
Background: Patients with heterozygous familial hypercholesterolemia (HeFH) who completed the double...
Aims To assess long-term (78 weeks) alirocumab treatment in patients with heterozygous familial hype...
Background: Homozygous familial hypercholesterolemia (HoFH) is characterized by extremely elevated l...
BACKGROUND: The alirocumab expanded use program provided open-label access to alirocumab before its ...
Background: ODYSSEY OLE (NCT01954394) was an open-label extension (OLE) study for patients with hete...
Background: Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/kexi...
Background Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/kexi...
AbstractObjectivesDespite maximally tolerated statin therapy, many patients with high cardiovascular...
Background: Mutations in the genes for the low-density lipoprotein receptor (LDLR), apolipoprotein B...
Background - The PCSK9 antibody alirocumab (75 mg every 2 weeks; Q2W) as monotherapy reduced low-den...
Background: Alirocumab, a monoclonal antibody that inhibits proprotein convertase subtilisin- kexin ...
BACKGROUND Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/ke...
# The Author(s) 2014. This article is published with open access at Springerlink.com Background Indi...
Background and aims: ODYSSEY OLE (open-label extension; NCT01954394) included patients diagnosed wit...
AbstractBackgroundPCSK9 inhibition with alirocumab significantly reduced LDL-C levels in trials of u...
Background: Patients with heterozygous familial hypercholesterolemia (HeFH) who completed the double...
Aims To assess long-term (78 weeks) alirocumab treatment in patients with heterozygous familial hype...
Background: Homozygous familial hypercholesterolemia (HoFH) is characterized by extremely elevated l...
BACKGROUND: The alirocumab expanded use program provided open-label access to alirocumab before its ...
Background: ODYSSEY OLE (NCT01954394) was an open-label extension (OLE) study for patients with hete...
Background: Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/kexi...
Background Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/kexi...
AbstractObjectivesDespite maximally tolerated statin therapy, many patients with high cardiovascular...
Background: Mutations in the genes for the low-density lipoprotein receptor (LDLR), apolipoprotein B...
Background - The PCSK9 antibody alirocumab (75 mg every 2 weeks; Q2W) as monotherapy reduced low-den...
Background: Alirocumab, a monoclonal antibody that inhibits proprotein convertase subtilisin- kexin ...
BACKGROUND Alirocumab is a fully human monoclonal antibody to proprotein convertase subtilisin/ke...
# The Author(s) 2014. This article is published with open access at Springerlink.com Background Indi...