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Endocrine Abstracts (2024) 99 EP337 | DOI: 10.1530/endoabs.99.EP337

1Shivam Hospital, Ahmedabad, India; 2Maya Hospital & Maternity Centre, Department of General Medicine, Kanpur, India; 3GSVM Medical College, Department of Medicine, Kanpur, India; 4Medstar Speciality Hospital, Bangalore, India; 5Moti lal Nehru Medical College, Department of Medicine, Prayagraj, India; 6District Civil Hospital, Aurangabad, India; 7Hormone Care, Aurangabad, India; 8Global Hospital and Research Institute, Department of Diabetology, Pune, India; 9Priyadarshini Nursing Home, Mumbai, India; 10S. P. Medical College & A.G of Hospitals, Bikaner, India; 11M.V. Hospitals and Research Center, Department of Medicine, Lucknow, India; 12Victoria Hospital, Department of General Medicine, Bangalore, India; 13Janta Hospital, Varanasi, India; 14Maharaja Agrasen superspeciality Hospital, Department of General Medicine, Jaipur, India; 15Nilratan Sircar Medical College and Hospital, Kolkata, India; 16Medical College and Hospital, Kolkata, India; 17Citizen hospital, Bangalore, India; 18Pagarav Hospital & ICU, Department of Medicine, Gandhinagar, India; 19BGS Global Institute of Medical Sciences, Department of General Medicine, Bangalore, India; 20SMS hospital, Department of Medicine, Jaipur, India; 21Grant Govt. Medical College and Sir J. J. Group of Hospital, Department of Internal Medicine, Mumbai, India; 22Sun Pharma Laboratories Limited, India Clinical Research, Mumbai, India; 23Ex Sun Pharma Laboratories Limited, India Clinical Research, Mumbai, India; 24Sun Pharma Laboratories Limited, Head Medical Affairs, Clinical Research, India & EM, Mumbai, India; 25Ex Sun Pharmaceutical Industries Limited, Medical Affairs and India Clinical Research, Mumbai, India


Background and Objective: Fixed-dose combination (FDC) of dapagliflozin+metformin+sulfonylurea with complementary mechanisms can provide effective glycaemic control, preserve beta-cell function, improved compliance without risk of weight gain, and reno-protective action in type 2 diabetes mellitus (T2DM) patients. This subgroup analysis assessed efficacy and safety of triple-drug FDC vs (vs) two-drug combination in T2DM Indian patients aged <45 years and 45-65 years.

Method: This is a subgroup analysis of phase 3, open-label, four-arm, active-controlled study (CTRI/2022/06/043249) in T2DM patients (glycated haemoglobin [HbA1c] 8%-11%) taking metformin 1000 mg 2000 mg/day and glimepiride 2 mg/day at screening. Patients received FDC of dapagliflozin+glimepiride+metformin IR tablet twice-daily (BID) (5 mg+1 mg+500 mg [test-1]/5 mg+1 mg+1000 mg [test-2]) OR co administration of glimepiride tablet + metformin IR BID (1 mg+1 tablet of 500 mg [comparator-1]/1 mg+2 tablets of 500 mg [comparator-2]) for 16 weeks. Post Week 16, up titrated dose of glimepiride (2 mg) in respective treatments was provided to patients with HbA1c ≥7% in each arm. This subgroup analysis evaluated glycaemic and safety parameters from Baseline till Week 28 in two age subgroups; subgroup 1 (S1:age <45 years) and subgroup 2 (S2:age 45-65 years).

Results: At baseline, 223 patients aged <45 years (S1) and 310 patients aged 45-65 years (S2). Adjusted mean change (SE) in HbA1c in S1 was statistically significant in test-1 vs comparator-1 [2.48% (0.14%) vs 1.64% (0.14%), P<0.0001) and in test-2 vs comparator-2 [-2.31% (0.13%) vs -1.65% (0.13%), P=0.0004) at Week 16. Adjusted mean change (SE) in HbA1c in S2 was statistically significant in test-1 vs comparator-1 (2.1% (0.12%) vs -1.63% (0.12%), P=0.0043)] and in test-2 vs comparator-2 [-2.18% (0.12%) vs -1.75% (0.12%), P=0.0116] at Week 16. In S1, proportion of patients achieving HbA1c <7% were significantly higher in test-1 vs comparator-1 (74.5% vs 46.9%, P=0.0047) and test-2 vs comparator-2 (85.5% vs 58.1%, P=0.0011) at Week 16. In S2, proportion of patients achieving HbA1c <7% were significantly higher in test-1 vs comparator-1 (70.1% vs 46.8%, P=0.0032) and test-2 vs comparator-2 (73.7% vs 47.1%, P=0.0011) at Week 16. Significant reduction in HbA1c, fasting and post prandial blood glucose was observed from Baseline to Weeks 12 and 16 in each arm in both subgroups. No patient reported hypoglycaemia or required rescue medication. Both treatments were well tolerated.

Conclusion: Triple FDCs of dapagliflozin+glimepiride+metformin IR tablets showed statistically significant reduction in HbA1c from Baseline to Week 16 as compared to dual combinations in T2DM patients of both age groups (<45 years and 45-65 years) and is a treatment option for all age groups.

Volume 99

26th European Congress of Endocrinology

Stockholm, Sweden
11 May 2024 - 14 May 2024

European Society of Endocrinology 

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