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ANDREW: A Multicenter, Prospective, Observational Study in Patients with Type 2 Diabetes on Persistent Treatment with
Antonio C Bossi1, Valentina De Mori2, Cristiana Scaranna3
1ASST Bergamo Ovest, Treviglio, BG, Italy. antonio_bossi@asst-bgovest.it.
Summary
Real-world data show dulaglutide effectively improves glycemic control and reduces weight in type 2 diabetes patients. This long-acting glucagon-like peptide-1 receptor agonist (GLP-1RA) offers sustained benefits up to 24 months.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Dulaglutide, a long-acting glucagon-like peptide-1 receptor agonist (GLP-1RA), is used for type 2 diabetes (T2D).
- Real-world effectiveness data are crucial for understanding treatment outcomes beyond clinical trials.
Purpose of the Study:
- To evaluate the real-world effectiveness of dulaglutide in T2D patients.
- To assess glycemic control and body weight changes over 24 months.
- To examine the durability of dulaglutide's treatment effects.
Main Methods:
- A multicenter, prospective, observational study (ANDREW) was conducted.
- 1584 T2D patients initiated once-weekly dulaglutide (0.75 or 1.5 mg).
- Data were collected on glycemic control (HbA1c, FPG) and weight parameters up to 24 months.
Main Results:
- At 12 months, significant reductions in HbA1c (-10 mmol/mol), FPG (-24.9 mg/dL), body weight (-3.4 kg), and waist circumference (-3.3 cm) were observed (p < 0.0001).
- Among patients completing 24 months (n=270), initial improvements in HbA1c and FPG stabilized after 12 months.
- Treatment discontinuation occurred in 170 patients before the 12-month endpoint.
Conclusions:
- Dulaglutide is an effective treatment for T2D, demonstrating significant improvements in glycemic control and body weight in real-world settings.
- The study confirms findings from randomized controlled trials regarding the metabolic and weight-related benefits of dulaglutide.
- Sustained benefits require ongoing patient support for lifestyle modifications alongside GLP-1RA therapy.

