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Once-weekly insulin icodec compared with daily basal insulin analogues in type 2 diabetes: Participant-level meta-analysis of the ONWARDS 1-5 trials.
Bajaj, Harpreet S; Ásbjörnsdóttir, Björg; Bari, Tanvir J; Begtrup, Kamilla; Vilsbøll, Tina; Rosenstock, Julio.
Afiliación
  • Bajaj HS; Endocrine and Metabolic Research, LMC Healthcare, Brampton, Canada.
  • Ásbjörnsdóttir B; Novo Nordisk A/S, Søborg, Denmark.
  • Bari TJ; Novo Nordisk A/S, Søborg, Denmark.
  • Begtrup K; Novo Nordisk A/S, Søborg, Denmark.
  • Vilsbøll T; Clinical Research, Steno Diabetes Center Copenhagen, University of Copenhagen, Herlev, Denmark.
  • Rosenstock J; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Diabetes Obes Metab ; 26(9): 3810-3820, 2024 Sep.
Article en En | MEDLINE | ID: mdl-38951942
ABSTRACT

AIM:

To perform a participant-level post hoc meta-analysis of Phase 3a trials in type 2 diabetes (T2D) to characterize the hypoglycaemia safety and glycaemic efficacy of once-weekly insulin icodec (icodec). MATERIALS AND

METHODS:

All ONWARDS 1-5 randomized participants were pooled as overall T2D, insulin-naive, an insulin-experienced subgroups, and by once-daily trial comparator (degludec or glargine U100). The main outcomes included incidence and rates of clinically significant and severe hypoglycaemia. Additional endpoints included change in glycated haemoglobin (HbA1c) from baseline and HbA1c target achievement without clinically significant or severe hypoglycaemia.

RESULTS:

The meta-analysis comprised 3765 participants (1882 icodec vs. 1883 comparators). In the overall T2D pool, clinically significant hypoglycaemia incidence was similar in the icodec group versus the comparator group (17.9% vs. 16.2%, odds ratio [OR] 1.14, 95% confidence interval [CI] 0.94, 1.38); however, rates were low but significantly higher in the icodec group (1.15 vs. 1.00 episodes/participant-year of exposure, estimated rate ratio 1.51 [95% CI 1.24, 1.85]). Fewer severe hypoglycaemic episodes occurred with icodec than with comparators (8 vs. 18). A greater reduction in HbA1c occurred with icodec versus comparators, irrespective of subgroup (estimated treatment difference range [-0.10 to -0.29%]; all p < 0.05). Across subgroups, except for the insulin-experienced subgroup, the odds of achieving HbA1c <53 mmol/mol (7.0%) without clinically significant or severe hypoglycaemia were greater with icodec than with comparators (OR range 1.30-1.55; all p < 0.05).

CONCLUSIONS:

Icodec was associated with a similar incidence but higher rates of clinically significant hypoglycaemia (equating to one additional hypoglycaemic episode every 6 years) and fewer severe hypoglycaemic episodes versus comparators. Our findings also confirmed the greater efficacy of icodec that was demonstrated in the ONWARDS trial programme.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hemoglobina Glucada / Esquema de Medicación / Insulina de Acción Prolongada / Diabetes Mellitus Tipo 2 / Insulina Glargina / Hipoglucemia / Hipoglucemiantes Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hemoglobina Glucada / Esquema de Medicación / Insulina de Acción Prolongada / Diabetes Mellitus Tipo 2 / Insulina Glargina / Hipoglucemia / Hipoglucemiantes Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2024 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido