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June 9, 2026Diabetes1 citations

1254-OR: Orforglipron vs. Dapagliflozin in Type 2 Diabetes Inadequately Controlled with Metformin

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MWMICHELLE D. WELCHTFTHOMAS A. FORSTWJWEIPING JIA

Key Points

  • The study evaluates the efficacy and safety of orforglipron versus dapagliflozin in individuals with type 2 diabetes inadequately controlled by metformin.
  • 40-week, phase 3, open-label, randomized trial with 962 participants
  • Participants were randomized to receive either orforglipron (3, 12, or 36 mg) or dapagliflozin (10 mg)
  • Primary endpoint was the change in HbA1c from baseline at week 40
  • All orforglipron doses exhibited superior reductions in HbA1c compared to dapagliflozin at week 40
  • Orforglipron 12 mg and 36 mg showed significant body weight reduction compared to dapagliflozin
  • Orforglipron 36 mg also demonstrated greater reductions in triglycerides, non-HDL-C, and systolic blood pressure

Abstract

Introduction and Objective: ACHIEVE-2 (NCT06192108) assessed the efficacy and safety of orforglipron (OFG), an oral non-peptide GLP-1 receptor agonist (RA), versus dapagliflozin (DAPA), an SGLT2 inhibitor, in people with T2D inadequately controlled with metformin. Methods: This 40-week, phase 3, open-label (OFG dose-blinded), randomized study included adults with T2D (HbA1c ≥7.0 to ≤10.5%) taking metformin (≥1500 mg/day) with a BMI ≥23.0 kg/m2. Participants were randomized 1:1:1:1 to once daily OFG 3, 12, 36 mg, or DAPA 10 mg. The primary endpoint was change from baseline in HbA1c at week 40. Key secondary endpoints are listed in the Table. Results: The 962 randomized participants had a mean baseline age 56 years, HbA1c 8.1%, T2D duration 8.0 years, and BMI 32.6 kg/m2. At week 40, all OFG doses were superior to DAPA in reducing HbA1c; OFG 12 and 36 mg were superior for reductions in body weight (BW); and OFG 36 mg was superior for reductions in triglycerides, non-HDL-C and systolic blood pressure. The most frequent adverse events (AEs) associated with OFG were mild to moderate gastrointestinal (GI) AEs occurring mostly during dose escalation. Treatment discontinuations due to GI AE were 5.8-8.3% with OFG and 0.4% with DAPA. No severe hypoglycemia episodes were reported. Conclusion: Compared with dapagliflozin, orforglipron demonstrated superior glycemic control, BW reduction and improvements in cardiometabolic parameters, with a safety profile consistent with the GLP-1 RA class. Disclosure M.D. Welch: Stock/Shareholder; Current; Abbott, Eli Lilly and Company. Speaker's Bureau; Current; Eli Lilly and Company, Amgen Inc. T.A. Forst: Speaker's Bureau; Current; AstraZeneca. Advisory Panel; Current; Bayer AG. Speaker's Bureau; Current; Boehringer Ingelheim International GmbH, Daiichi Sankyo, Lilly, Novo Nordisk. W. Jia: None. P. Orozco del Pino: Employee; Current; Eli Lilly and Company. M. Denning: Employee; Current; Eli Lilly and Company. W. Wu: Employee; Current; Eli Lilly and Company. R. Liu: None. J. Li: Employee; Current; Eli Lilly and Company. M. Eifu: None. Y. Chen: None.

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Cite This Study

WELCH et al. (2026) studied this question.

synapsesocial.com/papers/6a27adb0a963992e16267c82https://doi.org/10.2337/db26-1254-or
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