Real-world effectiveness and safety of fixed-ratio combination insulin glargine 100 u/ml plus lixisenatide in adults with type 2 diabetes (T2DM): subanalysis of the international, multicentre, prospective observational study SUCCESS in the Russian po

AIM: To evaluate the impact a fixed-ratio combination of insulin glargine(100U/ml) and lixisenatide(iGlarLixi) on the glycemic control in Russian study T2D population uncontrolled on OAD ± insulin therapy in real-world settings. MATERIALS AND METHODS : The Russian subanalysis of international, multicentre, prospective, observational SUCCESS study included 160 T2DM patients who had initiated iGlarLixi within 1 month prior to study inclusion from 11 regions of the Russian Federation. The primary endpoint — HbA 1c change from baseline to month 6. Secondary endpoints: HbA 1c change after 12 months, achievement of target HbA 1c levels after 6 and 12 months; change in FPG and PPG, change in body weight after 6 and 12 months, iGlarLixi dose dynamics. Safety endpoints: adverse events, serious adverse events, adverse events of special interest, frequency of hypoglycemia during the study period. RESULTS : The average age of patients in the Russian population was 60.8±9.4 years; average duration of T2DM was 11.4 years, mean HbA 1c — 9.3±1.5%; mean BMI 33.3 kg/m 2 . Prior to the study, most patients were on 2 (36.3%) and 3 OADs (27.5%), 32.5% — on insulin therapy. The mean change of HbA 1c at month 6 was -1.81%, and -2.03% at month 12. 51.3% patients achieved individual HbA 1c targets at month 12, 46.7% of patients achieved the HbA 1c target without hypoglycemia and weight gain. The decrease of body weight in 12 months was -3.3±4.4 kg. During the study period, 17 cases of hypoglycemia were recorded (0.11 events per patient-year); 1 severe hypoglycemia (0.01 events per patient-year). The total number of adverse events (AEs) was 43(26.9%), serious AEs - 10 (6.3%). CONCLUSION : According to the results of this prospective real world sub-group analysis, initiation of iGlarLixi in Russian adults with T2DM uncontrolled on OADs ± insulin significantly improves glycemic control with low risk of hypoglycemia and no body weight increase.

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Journal
Diabetes Mellitus
Published
2024-11-21
DOI
https://doi.org/10.14341/dm13236
Primary Topic
Diabetes Treatment and Management
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article
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article

Real-world effectiveness and safety of fixed-ratio combination insulin glargine 100 u/ml plus lixisenatide in adults with type 2 diabetes (T2DM): subanalysis of the international, multicentre, prospective observational study SUCCESS in the Russian po

M. I. Kharakhulakh, Д. А. Авалиани, Roza Atanesyan, Sergey N. Vorobyev et al.
Diabetes Mellitus
Diabetes Treatment and Management
article

Real-world effectiveness and safety of fixed-ratio combination insulin glargine 100 u/ml plus lixisenatide in adults with type 2 diabetes (T2DM): subanalysis of the international, multicentre, prospective observational study SUCCESS in the Russian po

M. I. Kharakhulakh, Д. А. Авалиани, Roza Atanesyan, Sergey N. Vorobyev, M. A. Prudnikova, Ekaterina L. Zaitseva, Marina V. Shestakova, Т. В. Саприна, Olga K. Vikulova, Н. В. Андреева, Н. Г. Мокрышева, S. D. Movsesyan, Yu. P. Kasatkina, A. A. Perevyazka, I. A. Krivosheyeva
article en

Abstract

AIM: To evaluate the impact a fixed-ratio combination of insulin glargine(100U/ml) and lixisenatide(iGlarLixi) on the glycemic control in Russian study T2D population uncontrolled on OAD ± insulin therapy in real-world settings. MATERIALS AND METHODS : The Russian subanalysis of international, multicentre, prospective, observational SUCCESS study included 160 T2DM patients who had initiated iGlarLixi within 1 month prior to study inclusion from 11 regions of the Russian Federation. The primary endpoint — HbA 1c change from baseline to month 6. Secondary endpoints: HbA 1c change after 12 months, achievement of target HbA 1c levels after 6 and 12 months; change in FPG and PPG, change in body weight after 6 and 12 months, iGlarLixi dose dynamics. Safety endpoints: adverse events, serious adverse events, adverse events of special interest, frequency of hypoglycemia during the study period. RESULTS : The average age of patients in the Russian population was 60.8±9.4 years; average duration of T2DM was 11.4 years, mean HbA 1c — 9.3±1.5%; mean BMI 33.3 kg/m 2 . Prior to the study, most patients were on 2 (36.3%) and 3 OADs (27.5%), 32.5% — on insulin therapy. The mean change of HbA 1c at month 6 was -1.81%, and -2.03% at month 12. 51.3% patients achieved individual HbA 1c targets at month 12, 46.7% of patients achieved the HbA 1c target without hypoglycemia and weight gain. The decrease of body weight in 12 months was -3.3±4.4 kg. During the study period, 17 cases of hypoglycemia were recorded (0.11 events per patient-year); 1 severe hypoglycemia (0.01 events per patient-year). The total number of adverse events (AEs) was 43(26.9%), serious AEs - 10 (6.3%). CONCLUSION : According to the results of this prospective real world sub-group analysis, initiation of iGlarLixi in Russian adults with T2DM uncontrolled on OADs ± insulin significantly improves glycemic control with low risk of hypoglycemia and no body weight increase.

Diabetes MellitusVol. 27(5)
Rostov State Medical University (RU), Siberian State Medical University (RU), Endocrinology Research Center (RU), Consultative and Diagnostic Center (RU), City Clinical Hospital (RU)
Openalex Percentile: Top 67%
Diabetes Treatment and Management
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