Victoza vs Zepbound

liraglutide (GLP-1 receptor agonist) vs tirzepatide (Dual GIP and GLP-1 receptor agonist) — a complete side-by-side comparison.

Novo NordiskEli Lilly

Victoza weight loss

3.2%

Zepbound weight loss

22.5%

Victoza dosing

Once daily

Zepbound dosing

Once weekly

Reviewed by Dr. Elena Vance, DOLast reviewed 19 sources cited

Summary

Victoza (liraglutide) and Zepbound (tirzepatide) are both injectable incretin therapies, but they target different conditions and represent different generations of incretin pharmacology. Victoza, approved in 2010, was an early single-receptor GLP-1 agonist that established cardiovascular benefit in type 2 diabetes (LEADER trial). Zepbound, approved in 2023, is a modern dual GIP and GLP-1 receptor agonist developed specifically for chronic weight management. There is no head-to-head trial comparing them because the FDA labels and clinical questions do not overlap. Patients researching both brands are typically mapping the broader GLP-1 landscape rather than choosing between them as alternatives.

Different FDA-Approved Indications

Victoza is approved as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes, for type 2 diabetes in patients aged 10 and older, and for cardiovascular risk reduction in adults with type 2 diabetes and established cardiovascular disease. Zepbound is approved for chronic weight management in adults with BMI ≥30 or ≥27 with at least one weight-related comorbidity, and in December 2024 the FDA added a moderate-to-severe obstructive sleep apnea indication for adults with obesity. Zepbound is not approved for type 2 diabetes — that indication for the same tirzepatide molecule lives with Mounjaro. Victoza is not approved for chronic weight management — that indication for the same liraglutide molecule lives with Saxenda at the higher 3.0 mg daily dose.

Mechanism, Dose, and Administration

Victoza is liraglutide, a single GLP-1 receptor agonist with a roughly 13-hour half-life that requires daily injection. Doses range from 0.6 mg starter through 1.2 mg to a maximum of 1.8 mg, titrated weekly. Zepbound is tirzepatide, a dual GIP and GLP-1 receptor agonist with a half-life near five days, injected subcutaneously once weekly. Doses titrate every four weeks from 2.5 mg starter through 5, 7.5, 10, 12.5, and 15 mg as tolerated. Zepbound is also available in single-dose vials through LillyDirect at reduced self-pay pricing alongside the standard auto-injector pens. Victoza pens require refrigeration before first use and may be stored at room temperature for 30 days after.

Efficacy in Their Respective Labeled Conditions

Victoza 1.8 mg daily in LEADER produced average A1C reduction of 1.1 percentage points and weight loss of 2.8 kg over a median 3.8 years, with a 13 percent reduction in major adverse cardiovascular events compared with placebo in patients with established CVD. The cardiovascular indication followed those results. Zepbound 15 mg weekly in SURMOUNT-1 produced average weight loss of 22.5 percent of baseline body weight (25.3 kg absolute) over 72 weeks. SURMOUNT-OSA demonstrated meaningful reductions in apnea-hypopnea events alongside weight loss in patients with obesity and obstructive sleep apnea, supporting the December 2024 OSA indication. The trials measured different primary endpoints in different populations, so cross-comparing the numbers directly is misleading.

Coverage and Practical Considerations

Victoza is covered broadly by commercial plans and Medicare Part D for type 2 diabetes with prior authorization, and the launch of generic liraglutide in 2024 has further reduced costs. Zepbound coverage is restrictive: many commercial plans exclude weight-management medications, and Medicare Part D does not cover Zepbound for weight loss alone under federal law. The December 2024 OSA indication and the cardiovascular trial results that may eventually emerge are the coverage levers under construction. For patients with type 2 diabetes who have weight as a secondary concern, Mounjaro (same tirzepatide as Zepbound, labeled for diabetes) is the relevant comparator to Victoza rather than Zepbound itself. The choice between Victoza and Zepbound starts and ends with which condition the patient and prescriber are treating.

Victoza vs Zepbound: Full Comparison

FeatureVictoza(liraglutide)Zepbound(tirzepatide)
Active Ingredientliraglutidetirzepatide
Drug ClassGLP-1 receptor agonistDual GIP and GLP-1 receptor agonist
ManufacturerNovo NordiskEli Lilly
FDA Approved2010-01-252023-11-08
Approved Indications
  • Type 2 diabetes mellitus (adjunct to diet and exercise)
  • Reduction of major adverse cardiovascular events in adults with type 2 diabetes and established cardiovascular disease
  • Type 2 diabetes in patients aged 10+ years
  • Chronic weight management in adults with BMI ≥30 or ≥27 with at least one weight-related comorbidity (adjunct to diet and exercise)
  • Treatment of moderate-to-severe obstructive sleep apnea in adults with obesity (December 20, 2024)
Routesubcutaneous injectionsubcutaneous injection
FrequencyOnce dailyOnce weekly
Starting Dose0.6 mg daily2.5 mg weekly
Maintenance Dose1.2 mg or 1.8 mg daily5 mg, 10 mg, or 15 mg weekly
Max Dose1.8 mg daily15 mg weekly
Weight Loss (%)3.2%22.5%
A1C Reduction1.1%N/A (not indicated for diabetes)
Key TrialLEADER (188 weeks)SURMOUNT-1 / SURMOUNT-5 (head-to-head vs semaglutide) (72 weeks)
List Price$950-$1,100/month$1,060-$1,176/month
With Insurance$25-$150/month (varies by plan)$25-$250/month (varies; weight-loss coverage is limited)
Savings Card$25/month (Novo Nordisk savings card, commercially insured)$25/month (Lilly savings card, commercially insured)

Side Effects: Victoza vs Zepbound

Side EffectVictozaZepbound
Nausea28%24-33%
Diarrhea17%18-25%
Vomiting11%10-18%
Headache9%Not reported
Decreased appetite9%Not reported
Dyspepsia7%7-10%
Constipation6%13-17%
Pancreatitis (rare)<1%<1%
Abdominal painNot reported10-14%
Injection site reactionNot reported3-7%
Hair lossNot reported5-6%
Gallbladder eventsNot reported1.6%

Severity scale: 1 (mild) to 5 (serious). Based on FDA prescribing information and clinical trial data.

Related Comparisons

Frequently Asked Questions

Sources & References

FDA & Regulatory

  1. Victoza FDA Drugs@FDA approval record FDA
  2. Zepbound FDA Drugs@FDA approval record FDA

Clinical Trial Records

  1. LEADER clinical trial record ClinicalTrials.gov
  2. SURMOUNT-1 / SURMOUNT-5 (head-to-head vs semaglutide) clinical trial record ClinicalTrials.gov

Peer-Reviewed Literature

  1. Marso SP et al. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER). N Engl J Med 2016;375:311-322 New England Journal of Medicine
  2. Jastreboff AM et al. Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1). N Engl J Med 2022;387:205-216 New England Journal of Medicine
  3. Malhotra A et al. Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity (SURMOUNT-OSA). N Engl J Med 2024;391:1193-1205 New England Journal of Medicine

Safety Communications

  1. FDA approves first medication for obstructive sleep apnea (Zepbound OSA indication, December 20, 2024) FDA

Manufacturer Information

  1. Victoza patient and healthcare provider website Novo Nordisk
  2. Zepbound patient and healthcare provider website Eli Lilly
  3. Lilly lowers price of Zepbound single-dose vials (December 1, 2025) Eli Lilly Investor Relations
  4. SURMOUNT-5: Zepbound superior weight loss over Wegovy (May 11, 2025) Eli Lilly Investor Relations

Reference Entries

  1. Liraglutide entry on Wikipedia Wikipedia
  2. Tirzepatide entry on Wikipedia Wikipedia

Additional References

  1. Victoza (liraglutide) FDA prescribing information (Novo Nordisk)
  2. Zepbound (tirzepatide) FDA prescribing information (Eli Lilly)
  3. LEADER cardiovascular outcomes trial (Marso SP, et al. N Engl J Med. 2016;375(4):311-322)
  4. SURMOUNT-1 trial (Jastreboff AM, et al. N Engl J Med. 2022;387(3):205-216)
  5. SURMOUNT-OSA trial (Malhotra A, et al. N Engl J Med. 2024;391(13):1193-1205)

This content is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions. See our full medical disclaimer.