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Published Phase 2 human RCT

Survodutide

Survodutide

A plain-language overview of survodutide — what it is, its once-weekly subcutaneous route, and its investigational (non-approved) regulatory status — with the reconstitution and mg-to-units arithmetic handled separately on the survodutide dosage calculator.

Peptide Calculator X

Reconstitution / draw volume / syringe units / supply-chain

Arithmetic + reference toolNot medical advice
Inputs
Research context
Product form
Target dose
Weight unit
Syringe barrel
Draw to
50units
0.5 mL5 mg/mL2.5 mg / dose
1 mL syringe - 100 u/mLFits
50 u050100 u
ARITHMETIC OK - VERIFY CLINICALLY

Arithmetic checks out. Confirm clinically, against the label, and against the actual vial before any use.

10 mg
4
0 mg
28 days
-
-

Independent check - dose mg / concentration mg/mL = volume. U-100 units = mL x 100.

Reconstitution planner

Reverse: pick a dose and the units you want it to read, then calculate diluent to add.

Reverse
Desired dose
1 mL
10 mg/mL
4
Formula and source context only. Not medical advice; verify with a clinician, product label, pharmacist, or approved research protocol. Do not use this tool to infer sterility, potency, purity, stability, compatibility, or an appropriate dose. Catalog and supply-chain data: finnrick.com/products - research date 2026-06-24.

Survodutide: reference record

Survodutide - regulatory status, route, frequency and published range
Regulatory statusInvestigational; no FDA/UK/EU marketing approval
RouteSubcutaneous
Dosing frequencyOnce weekly
Published range0.6–4.8 mg
Evidence basisPublished Phase 2 human RCT
Common vial sizes10

Sources

  • PubMed - PMID 38330987Basis for the regulatory status, route, frequency and published range in the table above. Source last checked 2026-06-24

What is Survodutide?

Survodutide is an investigational injectable peptide acting at both the GLP-1 and glucagon receptors, studied for weight management in early-phase clinical trials.

Is Survodutide FDA-approved?

No. Survodutide is investigational with no FDA, UK or EU marketing approval. The published figures come from a clinical trial rather than an approved label.

How is Survodutide given?

Subcutaneously, once weekly, in the published Phase 2 dose-finding trial, with escalation carried out over an extended period under protocol control.

What are the known safety concerns with Survodutide?

The trial escalation was supervised, and the published range is not a personal titration schedule. Long-term safety has not been established through an approval process.

Phase 2 dose-finding tested 0.6, 2.4, 3.6 and 4.8 mg weekly with 20-week escalation

Study range only; no approved commercial concentration or label.

Trial escalation was controlled; the published range is not a personal titration schedule.

Supply-chain quality · Finnrick

Avg quality score

6.8

/10

Purity range

98.39

99.95

%

Qty divergence

±

20

%

Vendors · samples

7

·

27

Common vial sizes

10

mg

Test window

Apr 2025 - May 2026

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