Utilisation Trend of Long-Acting Insulin Analogues including Biosimilars across Europe: Findings and Implications.


Journal

BioMed research international
ISSN: 2314-6141
Titre abrégé: Biomed Res Int
Pays: United States
ID NLM: 101600173

Informations de publication

Date de publication:
2021
Historique:
received: 26 03 2021
accepted: 06 08 2021
entrez: 22 10 2021
pubmed: 23 10 2021
medline: 9 2 2022
Statut: epublish

Résumé

Diabetes mellitus rates and associated costs continue to rise across Europe enhancing health authority focus on its management. The risk of complications is enhanced by poor glycaemic control, with long-acting insulin analogues developed to reduce hypoglycaemia and improve patient convenience. There are concerns though with their considerably higher costs, but moderated by reductions in complications and associated costs. Biosimilars can help further reduce costs. However, to date, price reductions for biosimilar insulin glargine appear limited. In addition, the originator company has switched promotional efforts to more concentrated patented formulations to reduce the impact of biosimilars. There are also concerns with different devices between the manufacturers. As a result, there is a need to assess current utilisation rates for insulins, especially long-acting insulin analogues and biosimilars, and the rationale for patterns seen, among multiple European countries to provide future direction. Typically increasing use of long-acting insulin analogues across Europe including both Western and Central and Eastern European countries reflects perceived patient benefits despite higher prices. However, activities by the originator company to switch patients to more concentrated insulin glargine coupled with lowering prices towards biosimilars have limited biosimilar uptake, with biosimilars not currently launched in a minority of European countries. A number of activities were identified to address this. Enhancing the attractiveness of the biosimilar insulin market is essential to encourage other biosimilar manufacturers to enter the market as more long-acting insulin analogues lose their patents to benefit all key stakeholder groups. There are concerns with the availability and use of insulin glargine biosimilars among European countries despite lower costs. This can be addressed.

Sections du résumé

BACKGROUND BACKGROUND
Diabetes mellitus rates and associated costs continue to rise across Europe enhancing health authority focus on its management. The risk of complications is enhanced by poor glycaemic control, with long-acting insulin analogues developed to reduce hypoglycaemia and improve patient convenience. There are concerns though with their considerably higher costs, but moderated by reductions in complications and associated costs. Biosimilars can help further reduce costs. However, to date, price reductions for biosimilar insulin glargine appear limited. In addition, the originator company has switched promotional efforts to more concentrated patented formulations to reduce the impact of biosimilars. There are also concerns with different devices between the manufacturers. As a result, there is a need to assess current utilisation rates for insulins, especially long-acting insulin analogues and biosimilars, and the rationale for patterns seen, among multiple European countries to provide future direction.
RESULTS RESULTS
Typically increasing use of long-acting insulin analogues across Europe including both Western and Central and Eastern European countries reflects perceived patient benefits despite higher prices. However, activities by the originator company to switch patients to more concentrated insulin glargine coupled with lowering prices towards biosimilars have limited biosimilar uptake, with biosimilars not currently launched in a minority of European countries. A number of activities were identified to address this. Enhancing the attractiveness of the biosimilar insulin market is essential to encourage other biosimilar manufacturers to enter the market as more long-acting insulin analogues lose their patents to benefit all key stakeholder groups.
CONCLUSIONS CONCLUSIONS
There are concerns with the availability and use of insulin glargine biosimilars among European countries despite lower costs. This can be addressed.

Identifiants

pubmed: 34676266
doi: 10.1155/2021/9996193
pmc: PMC8526244
doi:

Substances chimiques

Biosimilar Pharmaceuticals 0
Hypoglycemic Agents 0
Insulin, Long-Acting 0
Insulin Glargine 2ZM8CX04RZ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9996193

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021 Brian Godman et al.

Déclaration de conflit d'intérêts

The authors have no relevant conflicts of interest to declare. However, a number of the coauthors work for health authorities or are advisers to them.

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Auteurs

Brian Godman (B)

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK.
Division of Public Health Pharmacy and Management, School of Pharmacy, Sefako Makgatho Health Sciences University, Pretoria, South Africa.
School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, Malaysia.

Magdalene Wladysiuk (M)

Chair of Epidemiology and Preventive Medicine, Medical College, Jagiellonian University, Krakow, Poland.
HTA Consulting, Starowiślna Str. 17/3, 31-038 Krakow, Poland.

Stuart McTaggart (S)

Public Health Scotland, Gyle Square, 1 South Gyle Crescent, Edinburgh, UK.

Amanj Kurdi (A)

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK.
Division of Public Health Pharmacy and Management, School of Pharmacy, Sefako Makgatho Health Sciences University, Pretoria, South Africa.
Department of Pharmacology, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Eleonora Allocati (E)

Istituto di Ricerche Farmacologiche 'Mario Negri' IRCCS, Milan, Italy.

Mihajlo Jakovljevic (M)

Department of Global Health Economics and Policy, University of Kragujevac, Kragujevac, Serbia.
Institute of Comparative Economic Studies, Faculty of Economics, Hosei University Tokyo, Tokyo, Japan.

Francis Kalemeera (F)

Department of Pharmacy Practice and Policy, Faculty of Health Sciences, University of Namibia, Windhoek, Namibia.

Iris Hoxha (I)

Department of Pharmacy, Faculty of Medicine, University of Medicine, Tirana, Albania.

Anna Nachtnebel (A)

Dachverband der Österreichischen Sozialversicherungen, Kundmanngasse 21, AT-1030 Vienna, Austria.

Robert Sauermann (R)

Dachverband der Österreichischen Sozialversicherungen, Kundmanngasse 21, AT-1030 Vienna, Austria.

Manfred Hinteregger (M)

Dachverband der Österreichischen Sozialversicherungen, Kundmanngasse 21, AT-1030 Vienna, Austria.

Vanda Marković-Peković (V)

Faculty of Medicine, Department of Social Pharmacy, University of Banja Luka, Banja Luka, Bosnia and Herzegovina.

Biljana Tubic (B)

Faculty of Medicine, Department of Medicinal Chemistry, University of Banja Luka, Banja Luka, Bosnia and Herzegovina.
Agency for Medicinal Product and Medical Devices of Bosnia and Herzegovina, 78000 Banja Luka, Bosnia and Herzegovina.

Guenka Petrova (G)

Faculty of Pharmacy, Department of Social Pharmacy and Pharmacoeconomics, Medical University of Sofia, Sofia, Bulgaria.

Konstantin Tachkov (K)

Faculty of Pharmacy, Department of Social Pharmacy and Pharmacoeconomics, Medical University of Sofia, Sofia, Bulgaria.

Juraj Slabý (J)

State Institute for Drug Control, Prague, Czech Republic.

Radka Nejezchlebova (R)

State Institute for Drug Control, Prague, Czech Republic.

Iva Selke Krulichová (IS)

Department of Medical Biophysics, Faculty of Medicine in Hradec Králové, Charles University, Simkova 870, 500 03 Hradec Králové, Czech Republic.

Ott Laius (O)

State Agency of Medicines, Nooruse 1, 50411 Tartu, Estonia.

Gisbert Selke (G)

Wissenschaftliches Institut der AOK (WIdO), Rosenthaler Straße 31, 10178 Berlin, Germany.

Irene Langner (I)

Wissenschaftliches Institut der AOK (WIdO), Rosenthaler Straße 31, 10178 Berlin, Germany.

András Harsanyi (A)

Department of Health Policy and Health Economics, Eotvos Lorand University, Budapest, Hungary.

András Inotai (A)

Syreon Research Institute and Semmelweis University, Center of Health Technology Assessment, Budapest, Hungary.

Arianit Jakupi (A)

Faculty of Pharmacy, UBT Higher Education Institute, Pristina, Kosovo.

Svens Henkuzens (S)

Independent Consultant, Riga, Latvia.

Kristina Garuolienė (K)

Department of Pathology, Forensic Medicine and Pharmacology, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Jolanta Gulbinovič (J)

Department of Pathology, Forensic Medicine and Pharmacology, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Patricia Vella Bonanno (PV)

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK.
Department of Health Services Management, University of Malta, Valletta, Malta.

Jakub Rutkowski (J)

HTA Consulting, Starowiślna Str. 17/3, 31-038 Krakow, Poland.

Skule Ingeberg (S)

Medicines Committee, Oslo University Hospitals, Oslo, Norway.

Øyvind Melien (Ø)

Medicines Committee, Oslo University Hospitals, Oslo, Norway.

Ileana Mardare (I)

Faculty of Medicine, Public Health and Management Department, "Carol Davila" University of Medicine and Pharmacy Bucharest, 050463 Bucharest, Romania.

Jurij Fürst (J)

Health Insurance Institute, Miklosiceva 24, SI-1507 Ljubljana, Slovenia.

Sean MacBride-Stewart (S)

Pharmacy Services, Greater Glasgow and Clyde (NHS GGC), Glasgow, UK.

Carol Holmes (C)

NHS Lothian, Edinburgh, UK.

Caridad Pontes (C)

Drug Department, Catalan Health Service, Gran Via de les Corts Catalanes, 08007 Barcelona, Spain.
Department of Pharmacology, Therapeutics and Toxicology, Universitat Autònoma de Barcelona, Barcelona, Spain.

Corinne Zara (C)

Drug Department, Catalan Health Service, Gran Via de les Corts Catalanes, 08007 Barcelona, Spain.

Marta Turu Pedrola (MT)

Drug Department, Catalan Health Service, Gran Via de les Corts Catalanes, 08007 Barcelona, Spain.

Mikael Hoffmann (M)

NEPI-Nätverk för läkemedelsepidemiologi, Stockholm, Sweden.

Vasileios Kourafalos (V)

National Organization for the Provision of Healthcare Services (EOPYY), Athens, Greece.

Alice Pisana (A)

Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

Rita Banzi (R)

Istituto di Ricerche Farmacologiche 'Mario Negri' IRCCS, Milan, Italy.

Stephen Campbell (S)

Centre for Primary Care and Health Services Research, School of Health Sciences, University of Manchester, Manchester M13 9PL, UK.
NIHR Greater Manchester Patient Safety Translational Research Centre, School of Health Sciences, University of Manchester, Manchester, UK.

Bjorn Wettermark (B)

Department of Pharmacy, Disciplinary Domain of Medicine and Pharmacy, Uppsala University, Uppsala, Sweden.

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