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Specimen Atlas of Research Peptides81 plates · MIT
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69Plate 69Reviewed 2026-04-27

Survodutide

GLP-1/Glucagon Dual Agonist

also known as BI 456906

Dual GLP-1/glucagon receptor agonist developed by Boehringer Ingelheim and Zealand Pharma, currently in Phase 3 trials (SYNCHRONIZE program) for obesity and metabolic dysfunction-associated steatohepatitis (MASH). Phase 2 data demonstrated significant weight loss through reduced energy intake and increased energy expenditure. Acts centrally via circumventricular organs and peripherally on hepatic and pancreatic receptors. Once-weekly subcutaneous administration.

§ I

At a glance

Frequency
Once weekly
Development stage
Phase 3
Dual target
GLP-1/GCGR
Route

SQ · Once Weekly

§ II

Mechanism

Edit ↗

Primary target — GLP-1 receptor and glucagon receptor (GCGR) [yathindra-2026][zimmermann-2026].

Pathway — Central: CVOs → hypothalamic appetite regulation. Peripheral: GLP-1R → incretin effect; GCGR → hepatic lipid metabolism, energy expenditure [zimmermann-2026][long-2026].

Downstream effect — Decreased energy intake, increased energy expenditure, improved glucose homeostasis, hepatic fat reduction [zimmermann-2026][yathindra-2026].

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Standard doseNot yet disclosed (Phase 3 ongoing)SYNCHRONIZE Phase 3 program underway. [rubino-2026]
FrequencyOnce weekly
RouteSubcutaneous [yathindra-2026]
Evidence basisPhase 2 RCT (obesity) · Phase 3 ongoing
Phase 2 findingsSignificant weight loss and metabolic marker improvement [yathindra-2026]
MASH indicationUnder investigation for MASH-cirrhosis [patil-2026][andonie-2026]
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to Survodutide's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ IV

Evidence

Edit ↗
Strength
75/100
phase 2

Phase 2 RCT in obesity · Phase 3 SYNCHRONIZE program ongoing

OutcomeFinding
Primary fat targetTotal body weight, visceral adipose tissue
Weight loss mechanismDual action: decreased energy intake + increased energy expenditure [zimmermann-2026]
Phase 2 efficacySignificant weight loss demonstratedSpecific percentage not disclosed in abstracts.
Metabolic markersImprovements in ALT, AST, LDL levels; significant ALT reduction (MD -22.10 vs placebo) [yathindra-2026][abulehia-2026][andonie-2026]
MRI-PDFF reductionHepatic fat reduction demonstrated in MASH trials [andonie-2026]
Network meta-analysisFavorable efficacy profile vs other glucagon receptor agonists
Hepatic requirementHepatic GCGR required for maximal weight loss and metabolic effects [long-2026]
Energy expenditureIncreased energy expenditure contributes to weight loss [zimmermann-2026]
Comparative efficacyNetwork meta-analysis shows competitive efficacy in GRA class
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
GI symptomsmild
Diarrhea, nausea, fatigue — class effect of GLP-1 agonists
Safety profile
Network meta-analysis: comparable safety to other GRAs
Serious adverse events
Monitored in Phase 2/3; no unique safety signals reported
Injection site reactionsmild
Expected with subcutaneous administration
Glucagon-related effectsmoderate
Potential for tachycardia, increased blood pressure — theoretical glucagon effect
Absolute contraindications
  • Personal or family history of medullary thyroid carcinoma (class effect)
  • Multiple endocrine neoplasia syndrome type 2
Relative contraindications
  • Severe GI disease (inflammatory bowel disease, gastroparesis)
  • History of pancreatitis
  • Cardiovascular disease (monitor closely for glucagon effects)
§ VI

Administration

Edit ↗
  1. 01
    Reconstitution

    Specific reconstitution protocol not yet publicly disclosed. Follow manufacturer instructions upon approval.

  2. 02
    Injection site

    Subcutaneous — abdomen, thigh, or upper arm. Rotate sites weekly to minimize injection site reactions.

  3. 03
    Timing

    Once weekly, same day each week. Can be administered at any time of day, with or without meals.

  4. 04
    Storage

    Store refrigerated (2–8 °C) until use. Do not freeze. Protect from light. Specific reconstituted storage duration pending labeling.

  5. 05
    Needle

    Subcutaneous injection with appropriate gauge needle (typically 27–31G). Use sterile technique.

Appendix

Sources

46%

of 54 rendered claims carry a resolvable citation.

  1. [abulehia-2026]
    Abulehia 2026Comparative Efficacy and Safety of Glucagon Receptor Agonists on Metabolic Outcomes: A Network Meta-Analysis of Randomised Controlled Trials.
    journal, 2026
  2. [andonie-2026]
    Andonie 2026Comparative Analysis of Glucagon Receptor Agonists vs. Resmetirom in MASLD and MASH: Network Meta-Analysis of Clinical Trials.
    journal, 2026
  3. [elmendorf-2026]
    Elmendorf 2026IUPHAR review: From foe to friend: Repurposing glucagon to treat obesity and type 2 diabetes.
    journal, 2026
  4. [long-2026]
    Long 2026Hepatic GCGR is required for the superior weight loss and metabolic effects of a structurally related analogue of the dual GCGR/GLP-1R agonist survodutide in mice.
    journal, 2026
  5. [patil-2026]
    Patil 2026Metabolic Dysfunction-Associated Steatohepatitis (MASH)-Cirrhosis Clinical Trials: Lessons Learned and Future Directions.
    journal, 2026
  6. [rubino-2026]
    Rubino 2026Optimization of patient and site engagement in the SYNCHRONIZE™ phase 3 clinical trial program for survodutide in obesity through clinical trial simulation.
    journal, 2026
  7. [yathindra-2026]
    Yathindra 2026A review of survodutide: a new dual acting agonist.
    journal, 2026
  8. [zimmermann-2026]
    Zimmermann 2026Survodutide acts through circumventricular organs in the brain and activates neuronal regions associated with appetite regulation.
    journal, 2026
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-core · 29 fields uncited — open contributions