Literature DB >> 34567926

Real-world evidence for long-term safety and effectiveness of ipragliflozin in treatment-naïve versus non-naïve Japanese patients with type 2 diabetes mellitus: subgroup analysis of a 3-year post-marketing surveillance study (STELLA-LONG TERM).

Hiroshi Maegawa1, Kazuyuki Tobe2, Ichiro Nakamura3, Satoshi Uno4.   

Abstract

BACKGROUND: STELLA-LONG TERM was a 3-year post-marketing surveillance study that evaluated the long-term safety and effectiveness of ipragliflozin in Japanese patients with type 2 diabetes mellitus (T2DM). This subgroup analysis examined the safety and effectiveness of ipragliflozin in treatment-naïve and non-naïve patients.
MATERIALS AND METHODS: Patients were stratified into two subgroups: treatment-naïve (patients who had not received any antidiabetic drugs before starting ipragliflozin monotherapy) and non-naïve (all other patients). Patients who had added or switched antidiabetic drugs during follow-up were excluded from the analysis from that point. The incidence of adverse drug reactions (ADRs) and changes from baseline in glycosylated hemoglobin (HbA1c), body weight, fasting plasma glucose (FPG) and laboratory parameters were assessed.
RESULTS: Of the 11,051 patients in the safety analysis set, 1980 patients (17.92%) were treatment-naïve and 9071 (82.08%) were non-naïve. In the safety analysis set, treatment-naïve patients reported significantly lower incidences of ADRs (10.81% vs 20.87%; p < 0.001) and serious ADRs (0.86% vs 2.09%; p < 0.001) compared with non-naïve patients, as well as significantly lower incidences of polyuria/pollakiuria, volume depletion-related events, skin complications and renal disorders. In the effectiveness analysis, sustained and significant reductions from baseline to 36 months were observed in HbA1c, FPG and body weight in both treatment-naïve and non-naïve patients (all p < 0.001 vs baseline).
CONCLUSIONS: Over 3 years, ipragliflozin was better tolerated in treatment-naive than in non-naive Japanese patients with T2DM and had similar efficacy in these populations. Therefore, ipragliflozin is a useful first-line treatment option for patients with T2DM. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov: NCT02479399. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13340-021-00501-w. © The Japan Diabetes Society 2021.

Entities:  

Keywords:  Ipragliflozin; Japan; Post-marketing surveillance study; Sodium–glucose transporter 2 inhibitors; Type 2 diabetes mellitus

Year:  2021        PMID: 34567926      PMCID: PMC8413411          DOI: 10.1007/s13340-021-00501-w

Source DB:  PubMed          Journal:  Diabetol Int        ISSN: 2190-1678


  32 in total

1.  Safety and effectiveness of ipragliflozin in Japanese patients with type 2 diabetes mellitus and impaired renal function: subgroup analysis of a 3-year post-marketing surveillance study (STELLA-LONG TERM).

Authors:  Kazuyuki Tobe; Hiroshi Maegawa; Ichiro Nakamura; Satoshi Uno
Journal:  Diabetol Int       Date:  2020-11-23

2.  Efficacy and safety of dapagliflozin monotherapy in people with Type 2 diabetes: a randomized double-blind placebo-controlled 102-week trial.

Authors:  C J Bailey; E C Morales Villegas; V Woo; W Tang; A Ptaszynska; J F List
Journal:  Diabet Med       Date:  2014-11-22       Impact factor: 4.359

3.  A Phase IIb, randomized, placebo-controlled study of the SGLT2 inhibitor empagliflozin in patients with type 2 diabetes.

Authors:  E Ferrannini; L Seman; E Seewaldt-Becker; S Hantel; S Pinnetti; H J Woerle
Journal:  Diabetes Obes Metab       Date:  2013-03-04       Impact factor: 6.577

4.  Metabolic consequences of acute and chronic empagliflozin administration in treatment-naive and metformin pretreated patients with type 2 diabetes.

Authors:  Elza Muscelli; Brenno Astiarraga; Elisabetta Barsotti; Andrea Mari; Freimut Schliess; Leszek Nosek; Tim Heise; Uli C Broedl; Hans-Juergen Woerle; Ele Ferrannini
Journal:  Diabetologia       Date:  2015-12-24       Impact factor: 10.122

5.  Empagliflozin monotherapy with sitagliptin as an active comparator in patients with type 2 diabetes: a randomised, double-blind, placebo-controlled, phase 3 trial.

Authors:  Michael Roden; Jianping Weng; Jens Eilbracht; Bruno Delafont; Gabriel Kim; Hans J Woerle; Uli C Broedl
Journal:  Lancet Diabetes Endocrinol       Date:  2013-09-09       Impact factor: 32.069

6.  Ipragliflozin: first global approval.

Authors:  Raewyn M Poole; Rosselle T Dungo
Journal:  Drugs       Date:  2014-04       Impact factor: 9.546

Review 7.  Drug treatment of type 2 diabetes mellitus in patients for whom metformin is contraindicated.

Authors:  Brian K Irons; Molly G Minze
Journal:  Diabetes Metab Syndr Obes       Date:  2014-01-18       Impact factor: 3.168

8.  Baseline Glycated Hemoglobin Values Predict the Magnitude of Glycemic Improvement in Patients with Type 1 and Type 2 Diabetes: Subgroup Analyses from the DIAMOND Study Program.

Authors:  Liana K Billings; Christopher G Parkin; David Price
Journal:  Diabetes Technol Ther       Date:  2018-07-25       Impact factor: 6.118

9.  Management of Hyperglycemia in Type 2 Diabetes, 2018. A Consensus Report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD).

Authors:  Melanie J Davies; David A D'Alessio; Judith Fradkin; Walter N Kernan; Chantal Mathieu; Geltrude Mingrone; Peter Rossing; Apostolos Tsapas; Deborah J Wexler; John B Buse
Journal:  Diabetes Care       Date:  2018-10-04       Impact factor: 19.112

10.  Effects of ipragliflozin on glycemic control, appetite and its related hormones: A prospective, multicenter, open-label study (SOAR-KOBE Study).

Authors:  Hiroshi Miura; Kazuhiko Sakaguchi; Yuko Okada; Tomoko Yamada; Natsu Otowa-Suematsu; Anna So; Hisako Komada; Yushi Hirota; Takeshi Ohara; Yasuo Kuroki; Kenta Hara; Tomokazu Matsuda; Minoru Kishi; Akihiko Takeda; Kazuki Yokota; Yoshikazu Tamori; Wataru Ogawa
Journal:  J Diabetes Investig       Date:  2019-03-28       Impact factor: 4.232

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