Peptide Comparison
DulaglutidevsLiraglutide
Once-weekly GLP-1 receptor agonist Fc-fusion protein (Trulicity) that reduces HbA1c by 1.5–1.9%, promotes 3–4.6 kg weight loss, and demonstrated cardiovascular event reduction in the REWIND trial — available in convenient pre-filled autoinjector with no reconstitution required
FDA-approved once-daily GLP-1 receptor agonist (Victoza/Saxenda) that reduces HbA1c by 0.9–1.6%, promotes 5–10% body weight loss, and demonstrated a 13% reduction in major adverse cardiovascular events in the landmark LEADER trial of 9,340 patients
At a Glance
Quick
comparison
Dose Range
Dulaglutide
0.75–4.5 mg
Liraglutide
0.6–3.0 mg
Frequency
Dulaglutide
Once weekly
Liraglutide
Once daily
Administration
Dulaglutide
Subcutaneous injection
Liraglutide
Subcutaneous injection
Cycle Length
Dulaglutide
Ongoing/indefinite
Liraglutide
Ongoing/indefinite
Onset Speed
Dulaglutide
Gradual (3-4 weeks)
Liraglutide
Gradual (3-4 weeks)
Evidence Level
Dulaglutide
Strong human trials (Phase 3 or FDA approved)
Liraglutide
Strong human trials (Phase 3 or FDA approved)
Efficacy
Benefit
ratings
Metabolic
Weight Management
Healing & Recovery
Technical Data
Compound
specifications
Dulaglutide
Molecular Formula
C2646H4044N704O836S18 (complete fusion protein homodimer)
Molecular Weight
~63 kDa (~59,670 Da per chain)
Half-Life
~5 days (terminal elimination); Tmax ~48 hours; steady state in 2–4 weeks; accumulation ratio 1.56 at 1.5 mg
Bioavailability
47–65% after subcutaneous injection (dose-dependent); apparent clearance 0.142 L/h
CAS Number
923950-08-7
Liraglutide
Molecular Formula
C172H265N43O51
Molecular Weight
3,751 Da
Half-Life
~13 hours (enabling once-daily dosing); Tmax 8–12 hours; steady state in 3–5 days
Bioavailability
~55% after subcutaneous injection; >98% plasma protein binding to albumin via C16 fatty acid moiety
CAS Number
204656-20-2
Protocols
Dosing
tiers
Dulaglutide
Liraglutide
Applications
Best
suited for
Dulaglutide
Type 2 diabetes patients seeking convenient once-weekly dosing with strong glycemic control
Dulaglutide is particularly well-suited for individuals focused on type 2 diabetes patients seeking convenient once-weekly dosing with strong glycemic control. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Patients with established cardiovascular disease or multiple CV risk factors seeking REWIND-proven cardioprotection
Dulaglutide is particularly well-suited for individuals focused on patients with established cardiovascular disease or multiple cv risk factors seeking rewind-proven cardioprotection. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Overweight or obese T2DM patients requiring both weight loss and HbA1c reduction
Dulaglutide is particularly well-suited for individuals focused on overweight or obese t2dm patients requiring both weight loss and hba1c reduction. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Pediatric patients aged 10–17 with type 2 diabetes (approved indication)
Dulaglutide is particularly well-suited for individuals focused on pediatric patients aged 10–17 with type 2 diabetes (approved indication). Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Liraglutide
Type 2 diabetes patients with HbA1c >7% requiring both glycemic control and weight management
Liraglutide is particularly well-suited for individuals focused on type 2 diabetes patients with hba1c >7% requiring both glycemic control and weight management. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Obese individuals (BMI ≥30) or overweight (BMI ≥27) with weight-related comorbidities seeking FDA-approved pharmacotherapy
Liraglutide is particularly well-suited for individuals focused on obese individuals (bmi ≥30) or overweight (bmi ≥27) with weight-related comorbidities seeking fda-approved pharmacotherapy. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Patients with established cardiovascular disease or high cardiovascular risk seeking cardioprotective diabetes therapy
Liraglutide is particularly well-suited for individuals focused on patients with established cardiovascular disease or high cardiovascular risk seeking cardioprotective diabetes therapy. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Patients on metformin requiring add-on therapy with favorable weight and cardiovascular profile
Liraglutide is particularly well-suited for individuals focused on patients on metformin requiring add-on therapy with favorable weight and cardiovascular profile. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.
Safety Profile
Side
effects
Dulaglutide
Common
- Nausea
- Diarrhea and abdominal pain
- Vomiting
- Decreased appetite
Uncommon
- Injection site reactions and fatigue
Serious
- Acute pancreatitis
- Gallbladder disease
Liraglutide
Common
- Nausea
- Diarrhea
- Vomiting
- Decreased appetite and headache
Uncommon
- Injection site reactions
Serious
- Acute pancreatitis
- Gallbladder disease
Research Status
Safety
& evidence
Dulaglutide
Evidence Level
Strong human trials (Phase 3 or FDA approved)
FDA Status
FDA approved for this use
Safety Overview
Dulaglutide is an FDA-approved GLP-1 receptor agonist carrying a black box warning for thyroid C-cell tumor risk, based on rodent data showing increased medullary thyroid cancer (MTC) in rat models. This risk is contraindicated in patients with personal or family history of MTC or multiple endocrine neoplasia type 2. Nausea occurs in 20-40% of patients, particularly dose-dependent and most severe at initiation; gastrointestinal side effects (vomiting, diarrhea) are common. Pancreatitis has been reported in 0.1-0.2% of patients—discontinue immediately if severe abdominal pain develops. Rapid weight loss can trigger gallstone formation. Dehydration risk is significant, especially with concurrent SGLT2 inhibitors. Injection site reactions are mild but frequent.
Contraindications
- xPersonal or family history of medullary thyroid carcinoma (MTC) — black box warning based on rodent thyroid C-cell tumor data
- xMultiple Endocrine Neoplasia syndrome type 2 (MEN 2)
- xKnown serious hypersensitivity to dulaglutide or any excipient
- xType 1 diabetes mellitus or diabetic ketoacidosis (not indicated)
Liraglutide
Evidence Level
Strong human trials (Phase 3 or FDA approved)
FDA Status
FDA approved for this use
Safety Overview
Liraglutide (Victoza, Saxenda) is FDA-approved with extensive safety data from 15+ years of clinical use in diabetes (GLP-1 agonist) and obesity indications. Gastrointestinal side effects (nausea, vomiting, diarrhea) occur in 30-40% of patients during dose escalation but diminish significantly after 2-3 weeks of stable dosing. Black box warnings include risk of medullary thyroid carcinoma and pancreatitis, though absolute incidence remains rare. Injection site reactions are minimal. The compound shows no hepatotoxicity, nephrotoxicity, or major drug interactions at approved doses.
Contraindications
- xPersonal or family history of medullary thyroid carcinoma (MTC) — black box warning based on rodent thyroid C-cell tumor findings
- xMultiple Endocrine Neoplasia syndrome type 2 (MEN 2)
- xKnown hypersensitivity to liraglutide or any excipients
- xPregnancy (Saxenda indication) — contraindicated; effective contraception required
Decision Guide
Which is
right for you?
Choose Dulaglutide if...
- Type 2 diabetes patients seeking convenient once-weekly dosing with strong glycemic control
- Patients with established cardiovascular disease or multiple CV risk factors seeking REWIND-proven cardioprotection
- Overweight or obese T2DM patients requiring both weight loss and HbA1c reduction
- Pediatric patients aged 10–17 with type 2 diabetes (approved indication)
Choose Liraglutide if...
- Type 2 diabetes patients with HbA1c >7% requiring both glycemic control and weight management
- Obese individuals (BMI ≥30) or overweight (BMI ≥27) with weight-related comorbidities seeking FDA-approved pharmacotherapy
- Patients with established cardiovascular disease or high cardiovascular risk seeking cardioprotective diabetes therapy
- Patients on metformin requiring add-on therapy with favorable weight and cardiovascular profile