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Peptide Database

Goals
Fat LossMuscle BuildingInjury HealingAnti-AgingCognitive EnhancementSleep OptimizationImmune SupportGut HealingSkin RejuvenationSexual Health
Peptides
Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PNC-27
Cancer Research
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 32
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Peptide Comparison

MazdutidevsSurvodutide

Dual GLP-1/glucagon receptor agonist delivering up to 20% weight loss with superior glycemic control in clinical trials.

Dual GLP-1/glucagon receptor agonist for obesity and metabolic liver disease

Weight ManagementWeight Management

At a Glance

Quick
comparison

Dose Range

Mazdutide

3 mg–9 mg mg

Survodutide

2.4 mg–6 mg mg

Frequency

Mazdutide

Once daily

Survodutide

Once daily

Administration

Mazdutide

Subcutaneous injection

Survodutide

subcutaneous injection

Cycle Length

Mazdutide

Ongoing/indefinite

Survodutide

Ongoing/indefinite

Onset Speed

Mazdutide

Moderate (1-2 weeks)

Survodutide

Moderate (1-2 weeks)

Evidence Level

Mazdutide

Strong human trials (Phase 3 or FDA approved)

Survodutide

Strong human trials (Phase 3 or FDA approved)

Efficacy

Benefit
ratings

Mazdutide
Survodutide

Weight Loss

Mazdutide98%
Survodutide0%

Blood Sugar Control

Mazdutide96%
Survodutide8%

Metabolic Health

Mazdutide90%
Survodutide9%

Weight Management

Mazdutide0%
Survodutide9%

Technical Data

Compound
specifications

Mazdutide

Molecular Formula

C210H322N46O67

Molecular Weight

4563.1 Da

Half-Life

Approximately 8 days

Bioavailability

Subcutaneous bioavailability characteristic of acylated peptide analogs

CAS Number

2259884-03-0

Survodutide

Molecular Formula

C192H289N47O61

Molecular Weight

4,231.6 Da

Half-Life

~7 days (enabling once-weekly dosing)

Bioavailability

Optimized for subcutaneous administration with C18 acylation

CAS Number

2805997-46-8

Applications

Best
suited for

Mazdutide

Individuals seeking substantial weight loss exceeding 15% body weight

Mazdutide is particularly well-suited for individuals focused on individuals seeking substantial weight loss exceeding 15% body weight. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Adults with type 2 diabetes requiring superior glycemic management

Mazdutide is particularly well-suited for individuals focused on adults with type 2 diabetes requiring superior glycemic management. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Patients with obesity-related metabolic comorbidities

Mazdutide is particularly well-suited for individuals focused on patients with obesity-related metabolic comorbidities. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Those seeking dual-mechanism metabolic therapy

Mazdutide is particularly well-suited for individuals focused on those seeking dual-mechanism metabolic therapy. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Survodutide

Significant body weight reduction in obesity

Survodutide is particularly well-suited for individuals focused on significant body weight reduction in obesity. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

MASH/NASH resolution and liver fibrosis improvement

Survodutide is particularly well-suited for individuals focused on mash/nash resolution and liver fibrosis improvement. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Type 2 diabetes management with concurrent weight loss goals

Survodutide is particularly well-suited for individuals focused on type 2 diabetes management with concurrent weight loss goals. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Enhanced metabolic outcomes through dual receptor engagement

Survodutide is particularly well-suited for individuals focused on enhanced metabolic outcomes through dual receptor engagement. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Safety Profile

Side
effects

Mazdutide

Common

  • Nausea
  • Diarrhea
  • Decreased Appetite

Uncommon

  • Vomiting
  • Injection Site Reactions

Serious

  • Acute Pancreatitis
  • Acute Cholecystitis and Biliary Disease
  • Severe Nausea and Gastrointestinal Intolerance

Survodutide

Common

  • Nausea
  • Vomiting
  • Diarrhea
  • Decreased Appetite

Uncommon

  • Constipation and Abdominal Pain

Serious

  • Acute Pancreatitis

Research Status

Safety
& evidence

Mazdutide

Evidence Level

Strong human trials (Phase 3 or FDA approved)

FDA Status

Research compound

Safety Overview

Mazdutide (Roche/Carmot GLP-1/GCG/GIP triple agonist) completed Phase Ib with generally favorable safety profile but dose-limiting gastrointestinal side effects. Nausea/vomiting occur in 40-50% of subjects at higher doses; weight loss averaging 12-18% observed. Pancreatitis risk monitoring required; calcitonin elevation consistent with GCG activation. Heart rate increases 5-8 bpm; no serious cardiac safety signals. Developmental program focuses on tolerability optimization.

Contraindications

  • xPersonal or family history of medullary thyroid carcinoma or MEN2 syndrome
  • xKnown hypersensitivity to mazdutide or any formulation excipients
  • xHistory of severe pancreatitis
  • xSevere renal impairment (eGFR <15 mL/min) without clinical data

Survodutide

Evidence Level

Strong human trials (Phase 3 or FDA approved)

FDA Status

Research compound

Safety Overview

Survodutide data comes from Phase 2 obesity and MASH trials with dose-dependent gastrointestinal side effects (nausea up to 75% at highest doses, diarrhea, vomiting) that mirror GLP-1 receptor agonist class effects but occur with greater frequency due to additional glucagon receptor activation increasing energy expenditure. Pancreatitis risk exists as with all GLP-1 agonists—baseline lipase evaluation and patient education on warning signs (persistent upper abdominal pain) are essential. Medullary thyroid carcinoma risk, though theoretical based on GLP-1 class, contraindicates use in MEN 2 or personal thyroid cancer history.

Contraindications

  • xPersonal or family history of medullary thyroid carcinoma (GLP-1 class warning)
  • xMultiple Endocrine Neoplasia syndrome type 2 (MEN 2)
  • xKnown hypersensitivity to survodutide or excipients
  • xHistory of pancreatitis (caution advised with GLP-1 receptor agonists)

Decision Guide

Which is
right for you?

Choose Mazdutide if...

  • Individuals seeking substantial weight loss exceeding 15% body weight
  • Adults with type 2 diabetes requiring superior glycemic management
  • Patients with obesity-related metabolic comorbidities
  • Those seeking dual-mechanism metabolic therapy

Choose Survodutide if...

  • Significant body weight reduction in obesity
  • MASH/NASH resolution and liver fibrosis improvement
  • Type 2 diabetes management with concurrent weight loss goals
  • Enhanced metabolic outcomes through dual receptor engagement
Mazdutide vs Survodutide — Peptide Comparison | Peptide Initiative