Dulaglutide (Trulicity)
Long-acting GLP-1 receptor agonist consisting of two GLP-1 analogs fused to a human IgG4 Fc fragment, giving a ~5-day half-life suitable for once-weekly SC injection. Approved for type 2 diabetes and cardiovascular risk reduction; REWIND established benefit in a broad T2D population. Dosing 0.75-4.5 mg SC weekly.
Projected serum levels — 1.5 mg, weekly
Maintenance schedule: 1.5 mg weekly (subcutaneous).
Loading schedule: 2.5 mg on day 1, then 1.5 mg weekly — reaching therapeutic levels sooner.
Modeled steady state after ~14 days: peak ≈ 1.1 mg, trough ≈ 0.58 mg body load. Population-based estimate over 42 days for a 1.5 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.
Key facts
- Category
- Peptide
- Route modeled
- Subcutaneous
- Model confidence
- inferred
- Half-life
- 5 days
- Common dose
- 1.5 mg
- Suggested maximum
- 4.5 mg/day
- Reference dose range
- 0.75–4.5 mg (single dose)
- Suggested cadence
- weekly
- Validated against
- 0.75 mg sc — Cmax 0.11 mg/L at 48 h
Documented interactions
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Liraglutide (Victoza/Saxenda) + Dulaglutide (Trulicity)
Dulaglutide (Trulicity) and Liraglutide (Victoza/Saxenda) both push the glp1 receptor in the same direction.
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Retatrutide (Reta) + Dulaglutide (Trulicity)
Dulaglutide (Trulicity) and Retatrutide (Reta) both push the glp1 receptor in the same direction.
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Semaglutide (Ozempic/Wegovy) + Dulaglutide (Trulicity)
Dulaglutide (Trulicity) and Semaglutide (Ozempic/Wegovy) both push the glp1 receptor in the same direction.
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Sitagliptin (Januvia) + Dulaglutide (Trulicity)
Dulaglutide (Trulicity) and Sitagliptin (Januvia) both push the glp1 receptor in the same direction.
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Tirzepatide (Mounjaro/Zepbound) + Dulaglutide (Trulicity)
Dulaglutide (Trulicity) and Tirzepatide (Mounjaro/Zepbound) both push the glp1 receptor in the same direction.
Serum checks 5 modeled interaction pairings for dulaglutide (trulicity) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.
Research behind this entry
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Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial
REWIND RCT of 9901 T2D patients across the CV risk spectrum showed weekly dulaglutide reduced major adverse CV events by 12% over 5.4 years, notably in a predominantly primary-prevention population.
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Efficacy and safety of dulaglutide added onto pioglitazone and metformin versus exenatide in type 2 diabetes in a randomized controlled trial (AWARD-1)
AWARD-1 RCT of 976 T2D patients demonstrated once-weekly dulaglutide was superior to twice-daily exenatide for HbA1c reduction over 26 weeks.
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Dulaglutide: a review of its pharmacology and clinical pharmacokinetics
Review characterizing dulaglutide's ~47% absolute bioavailability after SC injection, elimination half-life of ~4.7 days, and degradation via general protein catabolism.
3 published studies referenced in the app, each with a plain-language summary.