Literature DB >> 30293878

Long-term safety and efficacy of alirocumab in patients with heterozygous familial hypercholesterolemia: An open-label extension of the ODYSSEY program.

Michel Farnier1, G Kees Hovingh2, Gisle Langslet3, Robert Dufour4, Marie T Baccara-Dinet5, Chantal Din-Bell6, Garen Manvelian7, John R Guyton8.   

Abstract

BACKGROUND AND AIMS: ODYSSEY OLE (open-label extension; NCT01954394) included patients diagnosed with heterozygous familial hypercholesterolemia (HeFH), receiving maximally tolerated statins, who had completed one of four Phase 3 double-blind parent studies (all 18 months' duration), with the aim to assess longer-term safety and efficacy of alirocumab.
METHODS: Patients received starting dose alirocumab 75 mg every 2 weeks (Q2W; patients from FH I, FH II, and LONG TERM) or alirocumab 150 mg Q2W (patients from HIGH FH). Low-density lipoprotein cholesterol (LDL-C) levels were blinded to the patient and physician until Week 8; from Week 8, LDL-C levels were communicated to physicians. From Week 12, dose adjustment from 75 to 150 mg Q2W, or vice versa, was possible per physician's clinical judgment according to patient's LDL-C levels.
RESULTS: Patients who had received alirocumab (n = 655) compared with placebo (n = 330) in the parent studies exhibited similar rates of treatment-emergent adverse events (TEAEs; 87.3% vs. 83.9%) during OLE (2.5 years median alirocumab exposure). Overall, 33 patients (3.4%) experienced TEAEs leading to permanent treatment discontinuation. At Week 8, alirocumab reduced mean LDL-C by 44.2% (reduction from 151.9 mg/dL at parent study baseline to 84.9 mg/dL); reduction in LDL-C was consistent to Week 96 of OLE. Reductions in lipid parameters were similar regardless of treatment allocation in the parent study.
CONCLUSIONS: In patients with HeFH, no unexpected long-term safety concerns were observed with alirocumab compared with previously published data; durability of LDL-C-lowering over 3 years (including 1.5 years of parent trials) was demonstrated.
Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Alirocumab; Cardiovascular disease; Lipid-lowering therapy; Low-density lipoprotein cholesterol; Open-label extension; PCSK9

Mesh:

Substances:

Year:  2018        PMID: 30293878     DOI: 10.1016/j.atherosclerosis.2018.08.036

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  9 in total

1.  Long-term safety and efficacy of alirocumab in South African patients with heterozygous familial hypercholesterolaemia: the ODYSSEY Open-Label Extension study.

Authors:  Dirk J Blom; Johannes Breedt; Lesley J Burgess; Iftikhar O Ebrahim; Graham Ellis; Prashilla Soma; Eugene van der Walt; Poobalan Naidoo; Alet van Tonder; Frederick J Raal
Journal:  Cardiovasc J Afr       Date:  2019-09-11       Impact factor: 1.167

2.  A spotlight on alirocumab in high cardiovascular risk patients with type 2 diabetes and mixed dyslipidemia: a review on the emerging data.

Authors:  Khyatiben Rana; Jessica Reid; Joshua N Rosenwasser; Todd Lewis; Mae Sheikh-Ali; Rushab R Choksi; Rebecca F Goldfaden
Journal:  Diabetes Metab Syndr Obes       Date:  2019-09-19       Impact factor: 3.168

Review 3.  Management of Familial Hypercholesterolemia: Current Status and Future Perspectives.

Authors:  David T W Lui; Alan C H Lee; Kathryn C B Tan
Journal:  J Endocr Soc       Date:  2020-08-21

4.  Treatment adherence and effect of concurrent statin intensity on the efficacy and safety of alirocumab in a real-life setting: results from ODYSSEY APPRISE.

Authors:  Maciej Banach; José Luis López-Sendon; Maurizio Averna; Bertrand Cariou; Megan Loy; Garen Manvelian; Isabela Batsu; Yann Poulouin; Daniel Gaudet
Journal:  Arch Med Sci       Date:  2021-10-29       Impact factor: 3.318

5.  LDL-Cholesterol-Lowering Therapy.

Authors:  Angela Pirillo; Giuseppe D Norata; Alberico L Catapano
Journal:  Handb Exp Pharmacol       Date:  2022

Review 6.  Diagnosis and Treatment of Heterozygous Familial Hypercholesterolemia.

Authors:  Mary P McGowan; Seyed Hamed Hosseini Dehkordi; Patrick M Moriarty; P Barton Duell
Journal:  J Am Heart Assoc       Date:  2019-12-16       Impact factor: 5.501

Review 7.  Efficacy and safety of PCSK9 monoclonal antibodies: an evidence-based review and update.

Authors:  Rasha Kaddoura; Bassant Orabi; Amar M Salam
Journal:  J Drug Assess       Date:  2020-08-11

Review 8.  Proprotein convertase subtilisin/kexin type 9 inhibition in cardiovascular disease: current status and future perspectives.

Authors:  Kyung Hoon Cho; Young Joon Hong
Journal:  Korean J Intern Med       Date:  2020-08-28       Impact factor: 2.884

9.  PCSK9 Inhibitors in a German Single-Center Clinical Practice: Real-World Treatment of Patients at High Cardiovascular Risk Over 68 Weeks.

Authors:  Tim Hollstein; Ursula Kassner; Thomas Grenkowitz; Friederike Schumann; Thomas Bobbert; Elisabeth Steinhagen-Thiessen
Journal:  Am J Cardiovasc Drugs       Date:  2021-01       Impact factor: 3.571

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.