Pancreatitis Incidence in the Exenatide BID, Exenatide QW, and Exenatide QW Suspension Development Programs: Pooled Analysis of 35 Clinical Trials.

Exenatide Pancreatitis Pooled analysis

Journal

Diabetes therapy : research, treatment and education of diabetes and related disorders
ISSN: 1869-6953
Titre abrégé: Diabetes Ther
Pays: United States
ID NLM: 101539025

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 18 01 2019
pubmed: 12 5 2019
medline: 12 5 2019
entrez: 12 5 2019
Statut: ppublish

Résumé

Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are widely used for treatment of type 2 diabetes mellitus; however, there have been concerns that GLP-1RA treatment may be associated with an increased incidence of pancreatitis. This study aimed to evaluate the incidence of pancreatitis in a pooled population of type 2 diabetes trials from the clinical development program of the GLP-1RA exenatide as well as to describe patient-level data for all reported cases. The primary analysis examined pooled data among patients with type 2 diabetes from the controlled arms of 35 trials (ranging from 4 to 234 weeks' duration) in the integrated clinical databases for exenatide twice daily, once weekly, and once-weekly suspension, excluding comparator arms with other incretin-based therapies. The exposure-adjusted incidence rate (EAIR) of pancreatitis was calculated for exenatide and non-exenatide (non-incretin-based therapy or placebo) treatment groups. Patient-level data were described for all pancreatitis incidences. The primary analysis included 5596 patients who received exenatide and 4462 in the non-exenatide group. The mean duration of study medication exposure for the exenatide and non-exenatide treatment groups was 57.0 and 47.9 weeks, respectively. Pancreatitis was diagnosed in 14 patients (exenatide, n = 8; non-exenatide, n = 6), of whom 13 recovered with or without sequelae. The pancreatitis EAIR was 0.1195 events per 100 patient-years [95% confidence interval (CI), 0.0516-0.2154] in the exenatide group versus 0.1276 events per 100 patient-years (95% CI 0.0468-0.2482) in the non-exenatide treatment group. The EAIR ratio for the exenatide versus non-exenatide treatment group was 0.761 (95% CI 0.231-2.510). In this pooled analysis of 10,058 patients among studies comparing exenatide with other glucose-lowering medications or placebo, pancreatitis was rare. The EAIRs of pancreatitis were low and similar between exenatide and non-exenatide treatment groups. No evidence of an association between exenatide and pancreatitis was observed. Bristol-Myers Squibb and AstraZeneca. Plain language summary available for this article.

Identifiants

pubmed: 31077072
doi: 10.1007/s13300-019-0627-1
pii: 10.1007/s13300-019-0627-1
pmc: PMC6612359
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1249-1270

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Auteurs

Marion L Vetter (ML)

Bristol-Myers Squibb, Lawrenceville, NJ, USA.
Janssen Pharmaceutical Companies of Johnson & Johnson, Philadelphia, PA, USA.

Kristina Johnsson (K)

AstraZeneca, Mölndal, Sweden. kristina.m.johnsson@astrazeneca.com.

Elise Hardy (E)

AstraZeneca, Gaithersburg, MD, USA.

Hui Wang (H)

AstraZeneca, Gaithersburg, MD, USA.
Fisher Clinical Research Institute, San Jose, CA, USA.

Nayyar Iqbal (N)

AstraZeneca, Gaithersburg, MD, USA.

Classifications MeSH