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MariTide (maridebart cafraglutide)_Dosage, benefits & legal status

Also known as maridebart cafraglutide, AMG 133, MariTide

Published July 22, 2026 · Updated August 14, 2026

An experimental once-a-month obesity shot.

Weight lossGLP-1 agonist / GIP antagonistInvestigational
Dose140 up to 420 mg per month (trial doses)
FrequencyMonthly
RouteUnder the skin (subcutaneous)
StatusInvestigational
CycledNot cycled in the trials

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

01

What is MariTide (maridebart cafraglutide)?

Plain language first. The technical label stays, but it never stands alone.

Overview

It combines appetite signals in one long-lasting molecule you inject only once a month. It is still experimental.

The technical version

MariTide is an unusual design, an antibody linked to two GLP-1 peptides that also blocks the GIP receptor.

What it's used for

An experimental once-a-month obesity shot, offering strong early weight loss with the convenience of monthly dosing.

02

How does MariTide (maridebart cafraglutide) work?

What it does in the body, and where.

MariTide is structurally unlike anything else here: an antibody with two GLP-1 peptides attached, which blocks one receptor while activating another.

  1. 01
    It activates GLP-1
    The peptide halves do the familiar appetite work.
  2. 02
    It blocks GIP rather than activating it
    This is the strange part. Tirzepatide activates GIP; this blocks it, and both approaches produce weight loss. The reason is genuinely not settled.
  3. 03
    The antibody body makes it last weeks
    Antibodies clear slowly, which is what allows monthly rather than weekly injection.
  4. 04
    Still investigational
    Phase 2 is complete, phase 3 is running.
Receptors
HITSGLP-1GIP blocked2

Hits 2 receptors at once.

03

What else is it used for?

Each use below carries its own evidence level. Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

  • Weight loss with once-a-month dosingInvestigational
  • Type 2 diabetesInvestigational

The published record

Research index

53

Records indexed for MariTide (maridebart cafraglutide)

41 in humans, 5 of them original studies.

27 registered trials, 2 with posted results.

Browse the records

In animalsPro
In the labPro
ReviewsPro
Senior author sharePro

Counted from Europe PMC indexing, not read by a person. Human means indexed under humans, which includes reviews and work on human cells. Original studies exclude reviews and lab work on human cells.Last updated 12 September 2026.

MariTide (maridebart cafraglutide) vial rendering
Compound field notes

At a glance

Four things to know about MariTide (maridebart cafraglutide)

01

Evidence

Investigational

02

Category

Weight loss and metabolic

03

Common vial

Varies

04

Half-life

About 21 days

04

How much, and do you cycle it?

The range, and whether you take breaks.

140 up to 420 mg per month (trial doses), monthly. Not cycled in the trialsTrial dose

Given continuously for the whole study period: MARITIME-1, 72 weeks. The dose is stepped up at the start, which is a ramp rather than a cycle, and no trial in this class built in a planned break.

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

About 21 daysTrial protocol

A peptide joined to an antibody, which is what makes monthly dosing possible.

Source: Jastreboff AM, et al. NEJM 2025, PMID 40549887, MARITIME-1

You can compare this against the whole library to see where it sits.

06

How do I dose and price it?

Enter your vial and your dose. Pick a mix. We show the draw and the cost.

The vial holds a fixed amount of drug. Adding more water does not make more drug, it just spreads it thinner, so you draw a bigger number on the syringe for the same dose.

Your vial size (mg)
Printed on the vial.
What you paid per vial
$
Used for cost per dose only.
Your dose (mg)
Commonly referenced range: 140 up to 420 mg per month (trial doses)Trial dose

Choose your mix

your own mL
units · —
Enter your own volume

Measuring the water1 mL = one full 100-unit syringe.

Your draw

2800 / 100 units
2800 units will not fit in a 100-unit syringe. It would take 28 separate draws, or you can mix with less water so it fits in one.
07

How do you store it?

Before mixing, and after.

Dry powder in the freezer or fridge. Once mixed, fridge, and use within about a month.

Unmixed lyophilized MariTide (maridebart cafraglutide) keeps for a long time cold. Once you add water the clock starts: most reconstituted vials hold up for roughly 28 to 30 days at fridge temperature. Keep it out of light, and do not freeze it after mixing.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.
Handling note

This compound is in clinical trials and is not sold in a standard vial, so there is no common vial size to show. Trial doses are given as prepared by the study, and the reconstitution calculator does not apply. Doses up to 420 mg a month are more than forty times the 10 mg reference vial.

Who should avoid it

Check these before anything else.
  • No formal contraindications established
  • Pregnancy

Stop and get help

These are emergencies. Seek care.
  • Vomiting or dry-heaving that will not stop, especially with signs of dehydration
  • Signs of an allergic reaction such as face or throat swelling, hives, or trouble breathing

Common effects

Expected, and usually mild.
  • Almost everyone in the trial had a stomach effect: nausea, vomiting, constipation, retching, or diarrhea
  • Up to 27% stopped because of it, though slower dose increases cut that to about 8%
  • No effect on bone density was found

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is MariTide (maridebart cafraglutide) approved?

And where the numbers on this page come from.

No. MariTide (maridebart cafraglutide) is not approved anywhere and is currently in company-run clinical trials. There is no legal route to obtain it outside a trial.

  • Approval status
    Investigational
  • Route
    Under the skin (subcutaneous)
  • Checked
    September 2026

What has happened recently

We have not yet written a full regulatory note for this compound. The status above is current as of the date shown.

You can compare this against the whole library, or read how to check a seller.


Guides for this compound

Sources

Last reviewed 8 September 2026

Beyond these, 53 records are indexed. Browse the records