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Research & Educational Use Only. Liraglutide is FDA-approved as Saxenda (obesity) and Victoza (T2DM) and requires a prescription. Not medical advice. Consult a healthcare professional.
GLP-1 Receptor AgonistEvidence Grade: A (FDA-Approved, LEADER/SCALE Trials)

Liraglutide (Saxenda / Victoza) Protocol Guide

Liraglutide is an acylated GLP-1 receptor agonist with 97% amino acid homology to native human GLP-1. FDA-approved as Victoza (1.8mg) for type 2 diabetes and Saxenda (3.0mg) for chronic weight management, it was the first GLP-1 agonist to demonstrate cardiovascular risk reduction (LEADER trial: 13% MACE reduction, 22% CV death reduction). Liraglutide slows gastric emptying, enhances glucose-dependent insulin secretion, suppresses glucagon, and reduces appetite via hypothalamic signaling. This protocol covers the 0.6-3.0mg daily titration, GI management, and metabolic monitoring.

Protocol Overview

Compound
Liraglutide (Saxenda 3.0mg / Victoza 1.8mg)
Category
GLP-1 Receptor Agonist
Mechanism
GLP-1R agonism: glucose-dependent insulin secretion, glucagon suppression, delayed gastric emptying, hypothalamic appetite reduction, cardioprotection
MW
3,751 Da
Half-Life
~13 hours (daily dosing required)
Form
Pre-filled pen (6mg/mL solution)
Route
Subcutaneous
Frequency
Once daily
Cycle
Ongoing (chronic therapy)

Dosing — Titration Schedule

WeekDoseIndicationNotes
Week 10.6 mg/dayBothGI adaptation phase
Week 21.2 mg/dayBothAppetite effects begin
Week 31.8 mg/dayVictoza max / Saxenda titrationT2DM therapeutic dose reached
Week 42.4 mg/daySaxenda titrationContinue if tolerated
Week 5+3.0 mg/daySaxenda maintenanceFull weight management dose

Inject at any time of day, with or without food, at the same time each day. Abdomen, thigh, or upper arm. If a titration step is not tolerated, remain at that dose for an additional week before advancing. If 3.0mg is not tolerated after extended titration, 2.4mg may be used as maintenance.

Timeline

Week 1-2
GI adaptation (nausea most common). Mild appetite suppression. Early glycemic improvement in T2DM patients.
Week 4-8
Meaningful appetite reduction at 3.0mg. 2-4% body weight loss. Reduced food cravings and portion sizes. Improved fasting glucose.
Week 12-26
5-8% total body weight loss (SCALE trial average). Improved HbA1c. Reduced waist circumference. Improved blood pressure and lipid markers.
Week 26-56
Maximum weight loss plateau (~8% average, up to 13% in high responders). Sustained cardiovascular benefits. Continued metabolic improvement.

Side Effects & Stacking

Side Effects

  • Nausea (40% initially, improves with titration)
  • Diarrhea or constipation
  • Headache (early, transient)
  • Injection site reactions (mild)
  • Hypoglycemia (mainly if combined with sulfonylureas/insulin)
  • Increased heart rate (4-6 bpm average)
  • Rare: pancreatitis, gallbladder disease
  • Contraindicated: personal/family history of MTC or MEN2

Stacking

  • BPC-157: GI support during nausea phase
  • MOTS-C: Metabolic synergy
  • NAD+: Cellular energy and metabolic support
  • GHK-Cu: Skin elasticity during weight loss
  • Do NOT combine with: Semaglutide, Tirzepatide, or Retatrutide (same class)

Blood Work

PanelMarkersTiming
MetabolicFasting glucose, HbA1c, fasting insulinBaseline, Week 12, 26
LipidsFull lipid panel, ApoB, triglyceridesBaseline, Week 12, 26
PancreaticLipase, amylaseBaseline, if symptoms arise
ThyroidTSH, calcitonin (if risk factors)Baseline
BasicCBC, CMP, kidney functionBaseline, Week 12
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Related Resources

Adipotide Protocol AOD-9604 Protocol Tesofensine Protocol Semaglutide vs Liraglutide Dosing Calculator Reconstitution Calculator Bloodwork Planner Stack Checker Peptide Catalog
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