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Real-world persistence and adherence to glucagon-like peptide-1 receptor agonists among obese commercially insured adults without diabetes.
Gleason, Patrick P; Urick, Benjamin Y; Marshall, Landon Z; Friedlander, Nicholas; Qiu, Yang; Leslie, R Scott.
Afiliação
  • Gleason PP; Prime Therapeutics, LLC, Eagan, MN.
  • Urick BY; Prime Therapeutics, LLC, Eagan, MN.
  • Marshall LZ; Prime Therapeutics, LLC, Eagan, MN.
  • Friedlander N; Prime Therapeutics, LLC, Eagan, MN.
  • Qiu Y; Prime Therapeutics, LLC, Eagan, MN.
  • Leslie RS; Prime Therapeutics, LLC, Eagan, MN.
J Manag Care Spec Pharm ; 30(8): 860-867, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38717042
ABSTRACT

BACKGROUND:

In 2014, the US Food and Drug Administration approved the first glucagon-like peptide-1 (GLP-1) receptor agonist product, liraglutide injection, for obesity treatment. Many GLP-1 obesity treatment clinical trials report significant weight loss and medication adherence at more than 85%. Little is known about the real-world GLP-1 obesity treatment adherence, persistence, and switch rates.

OBJECTIVE:

To measure GLP-1 therapy persistence, adherence, and switch rates in a real-world cohort of members without diabetes using these drugs for obesity treatment.

METHODS:

Integrated pharmacy and medical claims data from 16.5 million average monthly commercially insured membership were used to identify obese members without diabetes newly initiating GLP-1 therapy between January 1, 2021, and December 31, 2021. Members were required to be continuously enrolled 1-year before and after the GLP-1 therapy start date and aged 19 years of age or older. Persistence was measured as no greater than or equal to 60-day gap with allowance for GLP-1 switching. Adherence was measured as the proportion of days covered (PDC) and members with a PDC greater than or equal to 80% were considered adherent. GLP-1 product switching was also assessed descriptively.

RESULTS:

4,066 commercially insured obese members without diabetes that newly initiated GLP-1 therapy met all study criteria. The mean age was 46 years, and 81% were female. Overall, GLP-1 persistence was 46.3% at 180 days and 32.3% at 1 year. The highest and lowest persistence rates at 1 year were observed for semaglutide (Ozempic) at 47.1% and liraglutide (Saxenda) 19.2%, respectively. Average PDC during the 1-year assessment was 51.0% with 27.2% adherent to therapy and 11.1% switched GLP-1 drugs.

CONCLUSIONS:

This GLP-1 weight loss treatment real-world analysis, among obese individuals without diabetes, found poor 1-year persistence and adherence and low rates of switching between products. These findings will aid in assessing products cost-effectiveness, understanding obesity care management program needs, forecasting future GLP-1 use and cost trends, and negotiating GLP-1 pharmaceutical manufacturer value-based purchasing agreements.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adesão à Medicação / Liraglutida / Receptor do Peptídeo Semelhante ao Glucagon 1 / Obesidade Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Manag Care Spec Pharm Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adesão à Medicação / Liraglutida / Receptor do Peptídeo Semelhante ao Glucagon 1 / Obesidade Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Manag Care Spec Pharm Ano de publicação: 2024 Tipo de documento: Article