Liraglutide (Victoza/Saxenda)

Peptideprescriptionsubcutaneous · inferred

GLP-1 receptor agonist approved for type 2 diabetes (Victoza, 1.8 mg) and chronic weight management (Saxenda, 3.0 mg). Albumin-bound with half-life of ~13 hours, dosed once daily. Enhances glucose-dependent insulin secretion, suppresses glucagon, and reduces appetite.

Projected serum levels — 1.8 mg, once daily

Liraglutide (Victoza/Saxenda)
Liraglutide (Victoza/Saxenda) modeled serum levels, 1.8 mg once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 2 days. 0 0.50 1 1.5 2 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 2
Liraglutide (Victoza/Saxenda) modeled serum levels with a loading dose of 2.8 mg, then 1.8 mg once daily The first dose is larger so levels approach steady state faster. 0 0.50 1 1.5 2 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule

Maintenance schedule: 1.8 mg once daily (subcutaneous).

Loading schedule: 2.8 mg on day 1, then 1.8 mg once daily — reaching therapeutic levels sooner.

Modeled steady state after ~2 days: peak ≈ 1.7 mg, trough ≈ 0.92 mg body load. Population-based estimate over 15 days for a 1.8 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
13 h
Common dose
1.8 mg
Suggested maximum
3 mg/day
Reference dose range
0.90–3 mg (single dose)
Suggested cadence
once daily
Validated against
1.8 mg sc — Cmax 0.14 mg/L at 9 h

Documented interactions

  • danger
    Levothyroxine (Synthroid) + Liraglutide (Victoza/Saxenda) Protein binding

    Liraglutide (Victoza/Saxenda) may displace Levothyroxine (Synthroid) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • danger
    Tacrolimus (Prograf) + Liraglutide (Victoza/Saxenda) Protein binding

    Liraglutide (Victoza/Saxenda) may displace Tacrolimus (Prograf) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • danger
    Warfarin (Coumadin) + Liraglutide (Victoza/Saxenda) Protein binding

    Liraglutide (Victoza/Saxenda) may displace Warfarin (Coumadin) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free…

  • warning
    Apigenin + Liraglutide (Victoza/Saxenda) Protein binding

    Apigenin may displace Liraglutide (Victoza/Saxenda) from plasma protein binding sites, transiently raising free drug concentration.

  • warning
    Aripiprazole (Abilify) + Liraglutide (Victoza/Saxenda) Protein binding

    Liraglutide (Victoza/Saxenda) may displace Aripiprazole (Abilify) from plasma protein binding sites, transiently raising free drug concentration.

  • warning
    Armour Thyroid (Desiccated Thyroid Extract) + Liraglutide (Victoza/Saxenda) Protein binding

    Liraglutide (Victoza/Saxenda) may displace Armour Thyroid (Desiccated Thyroid Extract) from plasma protein binding sites, transiently raising free drug concentration.

Serum checks 143 modeled interaction pairings for liraglutide (victoza/saxenda) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. Liraglutide in Type 2 Diabetes Mellitus: Clinical Pharmacokinetics and Pharmacodynamics Kapitza C et al. · Clinical Pharmacokinetics, 2015 DOI

    Comprehensive pharmacokinetic review establishing liraglutide elimination half-life of 13 hours, 55% absolute bioavailability, and >98% albumin binding supporting once-daily dosing.

  2. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management (SCALE Obesity) Pi-Sunyer X et al. · New England Journal of Medicine, 2015 DOI

    Pivotal SCALE trial showing liraglutide 3.0 mg daily produced 8.0% mean weight loss vs 2.6% with placebo over 56 weeks in adults with obesity.

  3. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER) Marso SP et al. · New England Journal of Medicine, 2016 DOI

    Landmark cardiovascular outcomes trial demonstrating liraglutide reduced the rate of first occurrence of major adverse cardiovascular events by 13% versus placebo.

3 published studies referenced in the app, each with a plain-language summary.