COMPLETE KIT INCLUDEDbacteriostatic water, syringes, protocol and guide with every order

Certified by ISSCA in Peru and Colombia•ISSCA World Peptide ConferencePERU 2026•Certified by ISSCA in Peru and Colombia•ISSCA World Peptide ConferencePERU 2026•Certified by ISSCA in Peru and Colombia•ISSCA World Peptide ConferencePERU 2026•Certified by ISSCA in Peru and Colombia•ISSCA World Peptide ConferencePERU 2026•

Research guide · Metabolic Support

Survodutide — research protocol

Dual GLP-1/glucagon receptor agonist studied for advanced weight management and metabolic regulation.

Evidence boundary

This guide summarizes study areas and sources associated with the compound. BioPeptideX does not convert experimental information into a clinical regimen or recommend an individual dose, frequency, route or duration.

Catalog presentations

10mg

Concentration table

Mathematical reference only; this is not a dosing recommendation.

Resulting concentration5.00 mg/mL
On a U-100 syringe · 1 unit contains0.050 mg

Research areas

  • Dual GLP-1 + Glucagon receptor agonist
  • Next-generation metabolic research compound
  • Lyophilized powder for maximum stability
  • 99% HPLC verified purity

Most-cited research protocols

Educational information based on research protocols and literature; it does not replace guidance from a healthcare professional.

Survodutide is an investigational once-weekly subcutaneous peptide developed for weight loss and MASH. It acts as a dual GLP-1 and glucagon receptor agonist, currently not FDA-approved as of June 2026.

DoseFrequencyDurationRoute
Phase 2 obesity trial (lowest studied dose)0.6 mgonce weekly46 weeksSubcutaneous injection
Phase 2 obesity trial (mid dose)2.4 mgonce weekly46 weeksSubcutaneous injection
Phase 2 obesity trial (top dose)4.8 mgonce weekly46 weeksSubcutaneous injection
Phase 3 SYNCHRONIZE-1 trialVaried, with a slower, more flexible dose increaseonce weekly76 weeksSubcutaneous injection

Cycle: Dose escalation during the first 20 weeks, then steady for 26 weeks (Phase 2); slower and more flexible dose increase in Phase 3.

Benefits and research observations: Side effects were most common during the initial 20-week dose-increase phase, then improved as weight loss continued through 76 weeks, primarily from fat tissue.

Handling and storage

Store unreconstituted product according to its label and maintain the cold chain where applicable. After any preparation, follow only validated instructions for the specific product and diluent. Do not use if packaging is damaged or the solution shows particles or unexpected changes.

Warnings

Do not use this page for self-diagnosis or self-medication. Pregnancy, breastfeeding, minors, cancer history, allergies, active disease and concurrent treatments require individual professional evaluation.

Published sources

  1. 1.le Roux CW, et al. Lancet Diabetes Endocrinol, 2024.
  2. 2.Sanyal AJ, et al. NEJM, 2024.