Comparison of GLP-1 Agonists
(full update August 2024)
This chart compares GLP-1 agonists (including the “twincretin” tirzepatide) in regard to A1c reduction, weight loss, dosing, tolerability, clinical outcomes (e.g., cardiac or kidney benefit), how supplied, cost, and storage. For a review of class adverse effects, see footnote f.
Drug/ A1c decrease/ Weight loss |
Availability Costb Storagec |
Dosing (subcutaneous injection in ADULTS unless otherwise specified)c |
Comments (e.g., clinical outcomes, tolerability) |
Dulaglutide (Trulicity) A1c: -1.09% (mean across trials)1 Weight loss: |
Single dose pen (autoinjector): 0.75, 1.5, 3 (US), 4.5 mg (US) US: $977.42 Canada: ~$250 (1.5 mg/week) Store at 2oC to 8oC, or room temp (≤30oC) for ≤14 days. |
Initial: 0.75 mg once weekly. Max: may increase to 1.5 mg once weekly, then by 1.5 mg weekly every four weeks to a max of 4.5 mg once weekly. Comparative dose: see footnote g. Missed dose: If <72 hours remain until the next scheduled dose, skip the missed dose. If ≥72 hours remain, administer the missed dose.c If ≥3 doses are missed, consider restarting with ≤1.5 mg.15 |
Added to standard DM treatment in patients with CV disease or risk factors, over ~5.4 years reduced the composite of nonfatal MI, nonfatal stroke, and death from CV or unknown causes (NNT = 71).4 For individual outcomes, only nonfatal stroke was significantly reduced. Reduced a composite of new macroalbuminuria, 30% decrease in eGFR, or need for dialysis/transplant (NNT= 40), driven by prevention of macroalbuminuria (exploratory analysis).5 Discontinuation due to adverse GI effects |
Exenatide (Byetta [US]) A1c: -0.7% (10 mcg BID monotherapy)a,c Weight loss: -1.5 kg (10 mcg BID monotherapy)a,c |
Sixty (60)-dose pen: (needles not included) US: $849.95 Store at 2oC to 8oC. In-use pens can be stored at ≤25oC for up to 30 days. |
Initial: 5 mcg BID within 60 min before the two main meals (≥6 hours apart). Max: may increase to 10 mcg BID after four weeks. Comparative dose: see footnote g. Missed dose: skip missed dose Kidney impairment: Not recommended if CrCl <30 mL/min. Use 10 mcg BID with caution if CrCl 30 to 50 mL/min. Use caution in kidney transplant. |
Discontinuation due to adverse GI effects |
Exenatide (Bydureon BCise [US]) A1c: -0.64% (adults); -0.71% (pediatrics)a,c Weight loss: 0.92 kg |
Single dose pen (autoinjector): US: $827.45 Store at 2oC to 8oC, or room temp (≤30oC) for ≤4 weeks. |
For patients 10 years and older: 2 mg once every seven days Comparative dose: see footnote g. Kidney impairment: Not recommended if eGFR <45 mL/min/1.73 m2. Use caution in kidney transplant. Missed dose: If <72 hours remain until the next scheduled dose, skip the missed dose. If ≥72 hours remain, administer the missed dose. |
Once-weekly exenatide added to standard DM therapy in patients with or without CV disease had a neutral CV effect, but was associated with a reduction in death from any cause compared to placebo (NNT = 341).6 Discontinuation due to adverse GI effects: ~1 in 22 patients.3 Highest rate of injection site reactions among once-weekly GLP-1s.3 Required mixing immediately before injection. |
Liraglutide (Saxenda) Indicated for weight loss. Weight loss: 3.7 to 5.2 kg |
Dial-a-dose pen: 18 mg/3 mL (pen needles not included) US: $1,349.02 Canada: ~$450 Store at 2oC to 8oC. In-use pens can be stored at room temp (≤30oC) for ≤30 days. |
For patients 12 years and older: 3 mg once daily (start with 0.6 mg once daily, increase dose weekly by 0.6 mg to goal of 3 mg once daily). For adults, discontinue after 16 weeks if <4% (after 12 weeks if ≤5% [Canada]) weight loss achieved. Comparative dose: see footnote g. Missed dose: Skip the missed dose. If more than three days have elapsed since the last dose, retitrate starting with 0.6 mg once daily (US). |
See Victoza, below for information on clinical outcomes in type 2 DM. ~44% to 62% of patients met weight loss goal (≥5%) at 56 weeks compared to 16% to 34% with placebo. Discontinuation due to adverse effects: ~1 in 11 patients.c |
Liraglutided (Victoza) A1c: -1.04% (adults); -1.06 (pediatrics)1,a,c Weight loss: 1.33 kg1 |
Dial-a-dose pen: 18 mg/3 mL (needles not included) US: $815.27 Canada: $336.10 Store at 2oC to 8oC. In-use pens can be stored at room temp (≤30oC) for ≤30 days. |
For patients 10 years and older: Initial: 0.6 mg once daily for one week, then 1.2 mg once daily. (Pediatric patients may achieve control with 0.6 mg once daily.) Max: may increase to 1.8 mg once daily after one week. Comparative dose: see footnote g. Missed dose: Skip the missed dose. If more than three days have elapsed since the last dose, retitrate starting with 0.6 mg once daily (US). |
Added to standard care in patients with type 2 DM with CV disease or at high CV risk over ~4 years reduced:7
Discontinuation due to adverse GI effects |
Semaglutide (Ozempic) A1c: -1.4% Weight loss
|
Multi-dose pen: 0.25 or 0.5 mg (four 0.25 mg doses or two 0.5 mg doses), 1 mg (4 doses), 2 mg (4 doses [US]) (includes needles) US: $1,291.36 Canada: Store at 2oC to 8oC. In-use pens can be stored at room temp (≤30oC) for ≤56 days. |
Initial: 0.25 mg once weekly for four weeks, then 0.5 mg once weekly, Max: may increase to 1 mg once weekly after four weeks. After four weeks on the 1 mg dose, may increase to 2 mg once weekly. Comparative dose: see footnote g. Missed dose: if <48 hours remain until the next scheduled dose, skip the missed dose. If >48 remain, administer the missed dose. If two or more consecutive doses are missed, consider starting with 0.25 mg once weekly.c Some experts would restart with 1 mg if one or two doses are missed, 0.5 mg if three or four doses are missed, or 0.25 mg if ≥5 doses are missed.15 |
In type 2 DM patients with CV disease, CKD, or CV risk factors, reduced the combined endpoint of CV death, nonfatal MI, or nonfatal stroke (NNT = 44 for ~ 2 years). For individual outcomes, only nonfatal stroke was significant. A composite of new onset macroalbuminuria or doubling of SCr plus eGFR ≤45 mL/min/1.73 m2, need for dialysis/transplant, or death from kidney causes was reduced (NNT = 44), driven by prevention of macroalbuminuria.8 In type 2 DM with CKD, reduced a composite of major kidney events (kidney failure, ≥50% reduction in eGFR, kidney or CV death) (NNT = 20 over 3 years). Kidney function declined more slowly, and the risks of major CV events and all-cause mortality were reduced.21 Discontinuation due to adverse GI effects (1 mg): ~1 in 10 patients3 |
Semaglutide (Rybelsus) A1c: -1.1% (as monotherapy, 14 mg/day)a,c Weight loss |
3 mg, 7 mg, or US: 968.52 Canada: 233.38 |
Initial: 3 mg once daily at least 30 minutes before the first food, beverage, or other oral medications of the day, with ≤120 mL of water (~half a glass). After 30 days, increase the dose to 7 mg once daily. Max: After 30 days on the 7 mg dose, may increase to 14 mg once daily. Comparative dose: patients taking Rybelsus Missed dose: skip the missed dose |
ORAL semaglutide in patients with type 2 DM and CV disease, CKD, or CV risk factors had a neutral CV effect.9 Discontinuation due to adverse GI effects: ~1 in 15 patientsc |
Semaglutide (Wegovy) Indicated for weight loss. Weight loss: ~10.6 to 12.7 kg (2.4 mg once weekly at one year)13,14 |
Single-dose pen (autoinjector): 0.25, 0.5, 1, 1.7, US: $1,349.02 Canada: $419.73 Store at 2oC to 8oC. Can be stored at room temp (≤30oC) for ≤28 days. |
For patients 12 years and older: 0.25 mg once weekly, increased every four weeks to 0.5 mg, 1 mg, 1.7 mg, then 2.4 mg once weekly. Canada: consider stopping if the patient is not showing progress after 12 weeks on the maintenance dose. Comparative dose: see footnote g. Missed dose: if <48 hours remain until the next scheduled dose, skip the missed dose. If >48 hours remain, administer the missed dose. If two or more consecutive doses are missed, consider restarting with 0.25 mg once weekly.c Some experts would restart with 1 mg if one or two doses are missed, 0.5 mg if three or four doses are missed, and 0.25 mg if ≥5 doses are missed.15 |
Reduces CV risk (prevents 1 event for every 67 patients treated for ~ 3 years.10 67% to 85% of patients met weight loss goal (≥5%) at 52 weeks compared to 30% to 48% with placebo.13,14 Discontinuation due to adverse effects: ~ 1 in 15 patientsc |
Tirzepatidee (Mounjaro) A1c: -2.1%1,a Weight loss: 6.18 kg (as monotherapy, 15 mg/week).a,c |
Single-dose vial or pen (autoinjector [US]): 2.5, 5, 7.5, 10, 12.5 (US), (vial does not includes needles or syringe) US: $1,069.08 Canada: ~$97 (10 mg vial) Store at 2oC to 8oC. Can be stored at room temp (≤30oC) for ≤21 days. |
Initial: 2.5 mg once weekly for four weeks, then 5 mg once weekly. Max: may increase by 2.5 mg/week every four weeks to a max of 15 mg once weekly. Comparative dose: see footnote g. Missed dose: If <72 hours remain until the next scheduled dose, skip the missed dose. If ≥72 hours remain, administer the missed dose.c If ≥3 doses are missed, consider restarting with ≤5 mg once weekly.15 |
May delay oral contraceptive absorption. Advise switching to a non-oral contraceptive or adding a barrier contraceptive for four weeks after initiation or a dosage increase.c Discontinuation due to adverse GI effects |
Tirzepatidee (Zepbound [US]) Indicated for weight loss. Weight loss: ~18.8 kg |
Single-dose vial or pen: 2.5, 5, 7.5, 10, 12.5, 15 mg (vials do not include syringe or needle) US: $1,059.87 Store at 2oC to 8oC. Can be stored at room temp (≤30oC) for ≤21 days. |
Start with 2.5 mg once weekly, increase dose every 4 weeks to 5 mg, 7.5 mg, 10 mg, 12.5 mg, then Comparative dose: see footnote g. Missed dose: If <72 hours remain until the next scheduled dose, skip the missed dose. If ≥72 hours remain, administer the missed dose.c If ≥3 doses are missed, consider restarting with ≤5 mg once weekly.15 |
May delay oral contraceptive absorption. Advise switching to a non-oral contraceptive or adding a barrier contraceptive for four weeks after initiation or a dosage increase.c Discontinuation due to adverse effects: ~ 1 in 15 patients Though no specific guidance is available, stopping after 12 weeks if <5% weight loss achieved is reasonable based on guidelines.11 85% to 91% of patients met weight loss goal (≥5%) at 72 weeks compared to 35% with placebo.12 |
Abbreviations: BID = twice daily; CKD = chronic kidney disease; CV = cardiovascular; DM: diabetes mellitus; eGFR = estimated glomerular filtration rate; GI = gastrointestinal; HF = heart failure; MI = myocardial infarction; NNT = number needed to treat; SCr = serum creatinine
- Diabetes indication: mean A1c and weight reduction compared to placebo, as an add-on to other diabetes medication (unless monotherapy is specified). Weight loss indication: mean weight loss with lifestyle changes and/or diet. Weight loss is the amount above that seen with placebo. Weight loss varies based on lifestyle modification, baseline weight, etc.
- Wholesale acquisition cost (US) per month of maximum dose (or dose specified). US medication pricing by Elsevier, accessed July 2024. Canadian cost is wholesale. Prices for products that are dosed weekly represent a 28-day supply. Prices for products that are dosed daily represent a 30-day supply.
- US product information used in creation of this chart: Trulicity (December 2022), Byetta (December 2022), Bydureon BCise (May 2023), Saxenda (April 2023), Victoza (July 2023), Ozempic (September 2023), Rybelsus (January 2024), Wegovy (March 2024), Mounjaro (July 2023), Zepbound (March 2024). Canadian product monographs used in creation of this chart: Trulicity (July 2024), Saxenda (April 2024), Victoza (March 2024), Ozempic (March 2024), Rybelsus (February 2024), Wegovy (March 2024), Mounjaro (July 2024)
- Liraglutide is available in combination with insulin degludec (Xultophy).
- Tirzepatide is a GLP-1 agonist and glucose-dependent insulinotropic polypeptide (GIP) agonist (i.e., a “twincretin”).
- Adverse effects:c (Note that in the US, these medications must be dispensed with a Medication Guide.)
- GI side effects are common during dose escalation (e.g., nausea, vomiting, diarrhea). Resulting volume depletion may lead to acute kidney injury. GLP-1 agonists have been associated with bowel obstruction.17 Educate patients about the potential for ileus.20
- These GI side effects, and delayed gastric emptying, entail special considerations in surgical patients. See our chart, Perioperative Management of Diabetes.
- These drugs carry warnings about gallbladder disease (low risk) and pancreatitis (association unclear).3,19,20,c Stop if pancreatitis is suspected, and do not restart if pancreatitis is confirmed. There have been reports of pancreatic cancer in patients using GLP-1 agonists, but current evidence does not support causality.19
- These drugs are contraindicated in patients with a personal or family history of medullary thyroid cancer or patients with multiple endocrine neoplasia type 2. They cause thyroid C-cell tumors in mice.
- Rapid improvement in glycemic control is associated with diabetic retinopathy complications.
- Risk of hypoglycemia is low as monotherapy.
- Monitor for depression and suicidal ideation in patients taking these drugs for weight loss. Discontinue if symptoms develop.
- Don’t combine with other GLP-1 agonists. Generally, avoid use in patients taking a dipeptidylpeptidase-4 inhibitor (e.g., saxagliptin), as combining these two classes of medications is unlikely to improve weight loss or glycemic control and is not cost-effective.18
- Comparative dosing based on glycemic efficacy.15 Consider a lower starting dose if GI tolerability is a priority.16
- exenatide 5 mcg BID ~liraglutide 0.6 mg/week ~semaglutide 3 mg orally once daily
- dulaglutide 0.75 mg/week ~ exenatide 10 mcg BID ~ liraglutide 1.2 mg/week ~ semaglutide 0.25 mg/week ~ semaglutide 7 mg orally once daily
- dulaglutide 1.5 mg/week ~ exenatide 2 mg/week ~ liraglutide 1.8 mg/week ~ semaglutide 0.5 mg/week ~ semaglutide 14 mg orally once daily ~ tirzepatide 2.5 mg/week
- dulaglutide 4.5 mg/week ~ semaglutide 1 mg/week
- semaglutide 2 mg/week ~ tirzepatide 5 mg/week
References
- Yao H, Zhang A, Li D, et al. Comparative effectiveness of GLP-1 receptor agonists on glycaemic control, body weight, and lipid profile for type 2 diabetes: systematic review and network meta-analysis. BMJ. 2024 Jan 29;384:e076410.
- Trujillo JM, Nuffer W, Smith BA. GLP-1 receptor agonists: an updated review of head-to-head clinical studies. Ther Adv Endocrinol Metab. 2021 Mar 9;12:2042018821997320.
- Trujillo J. Safety and tolerability of once-weekly GLP-1 receptor agonists in type 2 diabetes. J Clin Pharm Ther. 2020 Sep;45 Suppl 1(Suppl 1):43-60.
- Gerstein HC, Colhoun HM, Dagenais GR, et al. Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial. Lancet. 2019 Jul 13;394(10193):121-130.
- Gerstein HC, Colhoun HM, Dagenais GR, et al. Dulaglutide and renal outcomes in type 2 diabetes: an exploratory analysis of the REWIND randomised, placebo-controlled trial. Lancet. 2019 Jul 13;394(10193):131-138.
- Holman RR, Bethel MA, Mentz RJ, et al. Effects of Once-Weekly Exenatide on Cardiovascular Outcomes in Type 2 Diabetes. N Engl J Med. 2017 Sep 28;377(13):1228-1239.
- Marso SP, Daniels GH, Brown-Frandsen K, et al. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes. N Engl J Med. 2016 Jul 28;375(4):311-22.
- Marso SP, Bain SC, Consoli A, et al.Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med. 2016 Nov 10;375(19):1834-1844.
- Husain M, Birkenfeld AL, Donsmark M, et al. Oral Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med. 2019 Aug 29;381(9):841-851.
- Lincoff AM, Brown-Frandsen K, Colhoun HM, et al. Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes. N Engl J Med. 2023 Dec 14;389(24):2221-2232.
- Apovian CM, Aronne LJ, Bessesen DH, et al. Pharmacological management of obesity: an endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2015 Feb;100(2):342-62. Erratum in: J Clin Endocrinol Metab. 2015 May;100(5):2135-6.
- Jastreboff AM, Aronne LJ, Ahmad NN, et al. Tirzepatide Once Weekly for the Treatment of Obesity. N Engl J Med. 2022 Jul 21;387(3):205-216.
- Wilding JPH, Batterham RL, Calanna S, et al. Once Weekly Semaglutide in Adults with Overweight or Obesity. N Engl J Med. 2021 Mar 18;384(11):989-1002.
- Wadden TA, Bailey TS, Billings LK, et al. Effect of Subcutaneous Semaglutide vs Placebo as an Adjunct to Intensive Behavioral Therapy on Body Weight in Adults With Overweight or Obesity: The STEP 3 Randomized Clinical Trial. JAMA. 2021 Apr 13;325(14):1403-1413.
- Whitley HP, Trujillo JM, Neumiller JJ. Special Report: Potential Strategies for Addressing GLP-1 and Dual GLP-1/GIP Receptor Agonist Shortages. Clin Diabetes. 2023 Summer;41(3):467-473.
- Almandoz JP, Lingvay I, Morales J, Campos C. Switching Between Glucagon-Like Peptide-1 Receptor Agonists: Rationale and Practical Guidance. Clin Diabetes. 2020 Oct;38(4):390-402.
- Sodhi M, Rezaeianzadeh R, Kezouh A, Etminan M. Risk of Gastrointestinal Adverse Events Associated With Glucagon-Like Peptide-1 Receptor Agonists for Weight Loss. JAMA. 2023 Nov 14;330(18):1795-1797.
- Lajthia E, Bucheit JD, Nadpara PA, et al. Combination therapy with once-weekly glucagon like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes: a case series. Pharm Pract (Granada). 2019 Oct-Dec;17(4):1588.
- Egan AG, Blind E, Dunder K, et al. Pancreatic safety of incretin-based drugs--FDA and EMA assessment. N Engl J Med. 2014 Feb 27;370(9):794-7. Erratum in: N Engl J Med. 2014 Jun 5;370(23):2253.
- American Diabetes Association Professional Practice Committee. 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes-2024. Diabetes Care. 2024 Jan 1;47(Suppl 1):S158-S178. doi: 10.2337/dc24-S009. Erratum in: Diabetes Care. 2024 Jul 1;47(7):1238.
- Perkovic V, Tuttle KR, Rossing P, et al. Effects of Semaglutide on Chronic Kidney Disease in Patients with Type 2 Diabetes. N Engl J Med. 2024 Jul 11;391(2):109-121.
Cite this document as follows: Clinical Resource, Comparison of GLP-1 Agonists. Pharmacist’s Letter/Pharmacy Technician’s Letter/Prescriber Insights. August 2024. [400862]
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