What is the recommended dose of Trulicity (dulaglutide) for glycemic control?

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Last updated: November 17, 2025View editorial policy

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Trulicity (Dulaglutide) Dosing for Glycemic Control

For adults with type 2 diabetes, start Trulicity at 0.75 mg subcutaneously once weekly, then increase to 1.5 mg once weekly for additional glycemic control, with further dose escalations in 1.5 mg increments every 4 weeks as needed, up to a maximum of 4.5 mg weekly. 1

Adult Dosing Algorithm

Initial dose: 0.75 mg subcutaneously once weekly 1

First escalation: Increase to 1.5 mg once weekly if additional glycemic control is needed 1

Subsequent escalations: If further glycemic control is required, increase in 1.5 mg increments (to 3 mg, then 4.5 mg) after at least 4 weeks on the current dose 1

Maximum dose: 4.5 mg subcutaneously once weekly 1

Pediatric Dosing (Age ≥10 Years)

Initial dose: 0.75 mg subcutaneously once weekly 1

Maximum dose: 1.5 mg once weekly (after at least 4 weeks on 0.75 mg if additional control needed) 1

  • Pediatric patients are limited to a maximum of 1.5 mg weekly, unlike adults who can escalate to 4.5 mg 1

Renal Dosing Considerations

No dose adjustment required for any level of renal impairment 2

  • Dulaglutide does not require dose adjustment in mild, moderate, or severe renal impairment 2
  • Unlike exenatide or lixisenatide, dulaglutide is safe in patients with eGFR <30 mL/min/1.73 m² 2
  • Monitor eGFR when initiating or escalating doses, particularly in patients with chronic kidney disease who report severe gastrointestinal reactions 2
  • In the AWARD-7 trial, dulaglutide demonstrated efficacy and safety in patients with moderate-to-severe chronic kidney disease (stages 3-4) 3

Administration Details

Timing: Once weekly, any time of day, with or without food 1

Route: Subcutaneous injection in abdomen, thigh, or upper arm; rotate injection sites with each dose 1

Missed dose protocol: If a dose is missed, administer as soon as possible if ≥3 days (72 hours) remain until the next scheduled dose; if <3 days remain, skip the missed dose 1

Critical Contraindications and Warnings

Absolute contraindications: 1

  • Personal or family history of medullary thyroid carcinoma (MTC)
  • Multiple Endocrine Neoplasia syndrome type 2 (MEN 2)
  • Serious hypersensitivity reaction to dulaglutide

Important precautions:

  • Not studied in patients with history of pancreatitis; consider alternative agents in this population 1
  • Not recommended in patients with severe gastrointestinal disease or severe gastroparesis 1
  • Should not be used in type 1 diabetes mellitus 1

Perioperative Management

For elective surgery: Consider holding dulaglutide for one week before procedures due to delayed gastric emptying effects, though evidence on aspiration risk with long-term use remains uncertain 2

  • The half-life of dulaglutide ranges from 4.5 to 4.7 days depending on dose 2
  • GLP-1 receptor agonists are associated with delayed gastric emptying, raising theoretical concerns about pulmonary aspiration risk 2

Common Adverse Effects

Gastrointestinal effects are the most frequently reported adverse events 4, 5, 3:

  • Nausea (14-20% vs 5% with insulin glargine) 3
  • Diarrhea (16-17% vs 7% with insulin glargine) 3
  • Vomiting 4

Hypoglycemia risk: Low inherent risk (4.3-4.4 events per patient-year vs 9.6 with insulin glargine) 5, 3

Rare but serious: Acute pancreatitis has been reported, though uncommon 6

Clinical Efficacy Context

  • Dulaglutide demonstrated non-inferiority to liraglutide 1.8 mg daily and superiority to metformin, sitagliptin, exenatide, and insulin glargine in glycemic control 4, 7
  • The REWIND trial showed significant reduction in major adverse cardiac events (MACE) at median 5.4 years follow-up 5
  • Dulaglutide 1.5 mg (but not 0.75 mg) consistently reduces body weight from baseline 4
  • In patients with moderate-to-severe CKD, dulaglutide reduced decline in eGFR compared to insulin glargine 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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