Kommersiellt obunden läkemedelsinformation riktad till läkare och sjukvårdspersonal

Liraglutid

Klassificering: C

Preparat: Saxenda, Victoza, Xultophy®

ATC kod: A10AE56, A10BJ02

Substanser: liraglutid

Sammanfattning

Större HbA1c-minskning samt har setts hos kvinnor jämfört med män vid behandling med liraglutid. Högre andel gastrointestinala biverkningar och fler hypoglykemiepisoder hos kvinnor har även rapporterats.

Högre exponering av liraglutid har setts hos både flickor/kvinnor jämfört med pojkar/män, men inga kliniskt relevanta könsskillnader i farmakokinetik har påvisats.

Additional information

For type 1 diabetes mellitus when diagnosed under the age of 15, the prevalence between boys and girls is similar. In adult populations of patients with both type 1 and 2 diabetes, the differences between the sexes in prevalence seem to vary depending on several factors such as incidence of disease, age groups and ethnicities studied.  Studies indicate that men in the early middle age display a higher prevalence of type 2 diabetes mellitus compared with women in the same age group [1]. In a nationwide population-based pharmaco-epidemiological study in Sweden, the total age-standardized prevalence of pharmacologically and non-pharmacologically treated diabetes (2012) was 56% for men and 39% for women [2].

Pharmacokinetics and dosing

The pharmacokinetics of a single-dose liraglutide has been investigated in healthy men and women in a clinical trial (16 men, 16 women). When adjusted for body weight, pharmacokinetics of liraglutide were similar in men and women [3].

A population pharmacokinetic analysis based on two different trials with liraglutide treatment (811 men, 2112 women), showed that liraglutide exposure was 24% lower in men than in women of comparable body weight (mean AUC ratio 0.76, [90% CI; 0.74, 0.78]). This corresponds to 32% greater exposure in women compared with men at comparable body weight. Since the 90% CI for this effect was outside of the bioequivalence limits, a patient’s sex was considered to have a pharmacokinetically relevant effect on liraglutide exposure [4].

The FDA prescribing information states that based on the results of a population pharmacokinetic analyses, women have 25% lower weight-adjusted clearance of liraglutide compared with men [5]. The European product information states that patient’s sex had no clinically meaningful effect on the pharmacokinetics of liraglutide based on the results of population pharmacokinetic data analysis of men and women, and a pharmacokinetic study in healthy subjects [6]. However, both the European and American product information state that based on the pharmacokinetics of liraglutide, no dosage adjustment according to sex is necessary [5, 6].

Safety, tolerability and pharmacokinetics of liraglutide in adolescents (12-17 years) with obesity was assessed in a 5-week randomized, double-blind, placebo-controlled trial (7 boys, 14 girls). A joint analysis that included data from a similar study with liraglutide in adults with obesity (3 adolescent males, 10 adolescent females, 18 adult males, 11 adult females) was performed. Liraglutide exposure was 23% lower in male participants than in female participants (0.77 [0.65; 0.92], 90%CI) [7].

In a pharmacokinetic and exposure-response meta-analysis (1137 PK observations from 116 patients), the influence of patient sex was on liraglutide exposure in pediatric patients with diabetes type 2, was evaluated. Relative exposure of liraglutide was lower in boys than in girls (ratio: 0.72 [95% CI: 0.62; 0.85]) [8].

Effects

In the pivotal efficacy phase 3 trials for liraglutide and when clinically treating diabetes type 2 patients, liraglutide is used as an adjunct treatment to metformin. Evaluation of liraglutide’s sex differences in effect and safety is therefore complicated due to the lack of liraglutide monotherapy studies.The efficacy and safety of liraglutide versus glimepiride (as adjunct treatments to metformin), in achieving glycemic control was assessed in Italian patients with type 2 diabetes mellitus (75 men, 104 women). The women with liraglutide had stronger reduction in HbA1c level than men (-1.5 vs -0.75). The study also showed the impact of female sex in predicting a better glycemic response to liraglutide even after adjustment for age, duration of diabetes, and BMI. There were no sex differences in body weight, waist circumference, or blood pressure [9].

Adverse effects

In a post-hoc analysis of the DURATION-6 study (comparing exenatide once weekly and liraglutide in 499 men and 412 women), the incidence of gastrointestinal adverse events (AEs) was analyzed in 245 men and 205 women with liraglutide. A greater proportion of women than men reported gastrointestinal AEs from liraglutide (48.3% in women vs 35.5% in men, p<0.01) [10].

Reproductive health issues

Regarding teratogenic aspects, please consult Janusmed Drugs and Birth Defects (in Swedish, Janusmed fosterpåverkan).

Försäljning på recept

Fler män än kvinnor hämtade ut läkemedel innehållande liraglutid (ATC-kod A10BJ02) på recept i Sverige år 2020, totalt 17 423 män och 14 596 kvinnor. Det motsvarar 3,4 respektive 2,8 personer per tusen invånare. Andelen som hämtat ut läkemedel var högst i åldersgruppen 65-79 år hos båda könen. I åldersgruppen 49 år och yngre läkemedel innehållande liraglutid i genomsnitt 2,3 gånger vanligare hos kvinnor och i åldersgruppen 50 år och äldre 1,4 gånger vanligare hos män [11].

Uppdaterat: 2021-09-27

Litteratursökningsdatum: 2021-06-15

Referenser

  1. Gale EA, Gillespie KM. Diabetes and gender. Diabetologia. 2001;44(1):3-15. PubMed
  2. Jansson SP, Fall K, Brus O, Magnuson A, Wändell P, Östgren CJ et al. Prevalence and incidence of diabetes mellitus: a nationwide population-based pharmaco-epidemiological study in Sweden. Diabet Med. 2015;32(10):1319-28. PubMed
  3. Damholt B, Golor G, Wierich W, Pedersen P, Ekblom M, Zdravkovic M. An open-label, parallel group study investigating the effects of age and gender on the pharmacokinetics of the once-daily glucagon-like peptide-1 analogue liraglutide. J Clin Pharmacol. 2006;46:635-41. PubMed
  4. Overgaard RV, Petri KC, Jacobsen LV, Jensen CB. Liraglutide 30 mg for Weight Management: A Population Pharmacokinetic Analysis. Clin Pharmacokinet. 2016;55(11):1413-1422. PubMed
  5. Food and Drug Administration (FDA). Prescribing information - Victoza (liraglutide). Drugs@FDA [www]. [updated 2017-08-01, cited 2021-07-08]. länk
  6. Victoza (liraglutide). Summary of Product Characeristics. European Medicines Agency (EMA) [updated 2021-11-02, cited 2021-07-08]
  7. Danne T, Biester T, Kapitzke K, Jacobsen SH, Jacobsen LV, Petri KCC et al. Liraglutide in an Adolescent Population with Obesity: A Randomized, Double-Blind, Placebo-Controlled 5-Week Trial to Assess Safety, Tolerability, and Pharmacokinetics of Liraglutide in Adolescents Aged 12-17 Years. J Pediatr. 2017;181:146-153e3. PubMed
  8. Petri KCC, Hale PM, Hofman PL, Jacobsen LV. Liraglutide pharmacokinetics and exposure-response in pediatric patients with type 2 diabetes. J Pediatr Endocrinol Metab. 2020;33(10):1289-1292. PubMed
  9. Chiefari E, Capula C, Vero A, Oliverio R, Puccio L, Liguori R, Pullano V, Greco M, Foti D, Tirinato D, Vero R, Brunetti A. Add-On Treatment with Liraglutide Improves Glycemic Control in Patients with Type 2 Diabetes on Metformin Therapy. Diabates Technol Ther. 2015;17(7):468-74. länk
  10. Horowitz M, Aroda VR, Han J, Hardy E, Rayner CK. Upper and/or lower gastrointestinal adverse events with glucagon-like peptide-1 receptor agonists: Incidence and consequences. Diabates Obes Metab. 2017;16(5):672-681. länk
  11. Statistikdatabas för läkemedel. Stockholm: Socialstyrelsen. 2020 [cited 2021-03-10.] länk

Författare: Diana Rydberg, Linnéa Karlsson Lind

Faktagranskat av: Carl-Olav Stiller

Godkänt av: Karin Schenck-Gustafsson