Maridebart cafraglutide

BInvestigational (phase 3)GLP-1 and incretin agonists →MariTideAMG 133MariTide peptide
In one paragraphMaridebart cafraglutide, or MariTide, is an antibody that blocks the GIP receptor with two GLP-1-agonist peptides attached, injected once a month. In a 592-person phase 2 trial published in the New England Journal of Medicine in 2025, people with obesity lost 12–16% at 52 weeks against 2.5% on placebo. Gut side effects were common, less so with dose escalation. Phase 3 trials are running; it is not approved anywhere.
Overall gradeB Probable
Human trials1 phase 2 RCT (n=592); phase 3 running
Outcomes graded3
Last reviewed23 September 2026
EvidenceWhat it isHow it worksUnknownsMolecule & PKRegulationQuestionsReferences

What the human research shows

A well-run phase 2 with an unusual pharmacology — it blocks the receptor tirzepatide activates — and a monthly schedule. Grade B rather than C because the trial was large for its phase and fully published; the effect size sits below the weekly incretins so far.

MetabolicCardioMuscleHealingNeuroImmuneSexualSkinAgeing

Evidence profile0–5

  • Metabolic & weightB3.5
  • Cardiovascular—0.0
  • Muscle & growth—0.0
  • Healing & repair—0.0
  • Neuro & sleep—0.0
  • Immune & inflammation—0.0
  • Sexual & hormonal—0.0
  • Skin & appearance—0.0
  • Ageing & longevity—0.0
Each score is confidence × effect size, taken from the best-evidenced benefit in that domain: the grade (A–D) sets the confidence, the measured effect sets the size. Hover a domain to see the outcomes behind it. Adverse effects are excluded and listed separately below.
OutcomeGradeEffect sizeHuman studiesWhere the evidence comes from
Body weight (obesity)BProbableLarge1 phase 2 RCT (465 in the obesity cohort, 52 wk)Six dosing regimens of 140–420 mg every four or eight weeks. Intention-to-treat loss ranged from 12.3% to 16.2% against 2.5% on placebo. In the 127-person diabetes cohort, 8.4–12.3% against 1.7%.1
Blood glucose (HbA1c) in type 2 diabetesBProbableLargeSame RCT, diabetes cohort (n=127)HbA1c fell 1.2–1.6 points against 0.1 on placebo.1
GI side effectsadverseBProbableLargeSame RCTNausea and vomiting were frequent, particularly without dose escalation; the regimens that started low and stepped up were better tolerated, which is why phase 3 uses escalation.1
AMultiple good human trials, consistentBSome human trials, mostly consistentCFew or weak human studiesDAnimal or anecdotal onlyeffect size · red = adverse

Literature searched to 23 September 2026. Human studies only; animal and cell work informs the mechanism section and nothing else.

Registered trials

ClinicalTrials.gov lists 28 interventional studies naming Maridebart cafraglutide as an intervention — 11 completed, 5 recruiting, and 2 with results posted to the registry.

A registration is not a result. Anyone can register a study, and many never report — so this list shows what has been attempted, not what has been shown. The graded evidence above is the answer to whether something works.

20 further studies are registered. Participant counts marked * are the sponsor's estimate, not a final enrolment. Source: ClinicalTrials.gov, read directly from the registry and refreshed weekly.

What it is

MariTide is a conjugate: a monoclonal antibody that antagonises the GIP receptor, with two GLP-1 receptor agonist peptides chemically linked to it. The antibody's long half-life is what allows monthly — possibly less frequent — injection. It is strictly a peptide–antibody hybrid, included here because the active pharmacology is peptide and because it is one of the most-searched names in the category.

Amgen is running the MARITIME phase 3 programme in obesity, with and without diabetes.

How it is thought to work

The GLP-1 peptides do what semaglutide does. The antibody part blocks GIP signalling — the opposite of tirzepatide, which activates it. That both strategies reduce weight is one of the open puzzles of the field; long-term GIP agonism may desensitise the receptor, making the two approaches less different than they look.

What is still unknown

  • Whether monthly dosing holds weight loss as well as weekly drugs over years.
  • Long-term effects of chronic GIP receptor blockade, which no approved drug does.
  • Immunogenicity of the antibody with repeated dosing.

The molecule and how long it lasts

Identity

A monoclonal antibody conjugated to two GLP-1 peptides — no small-molecule record

Pharmacokinetics
Route
Subcutaneous, every 4 weeks
Half-life
About 14–16 days for the intact molecule (21–24 days total)

From a published human pharmacokinetic study: Véniant MM, et al. A GIPR antagonist conjugated to GLP-1 analogues promotes weight loss with improved metabolic parameters in preclinical and phase 1 settings. Nat Metab 2024;6:290–303

Regulatory status

European Union
Not authorised

Investigational.

United States
Not approved

Investigational; phase 3 running. Products sold as 'MariTide' online are not the trial drug and cannot be, given the manufacturing involved.

United Kingdom
Not licensed

No MHRA licence.

Australia
Not on the ARTG

Investigational only.

Canada
Not authorised

No Drug Identification Number.

Sport (WADA)
Prohibited at all times

Unapproved anywhere, so S0 (non-approved substances).

Questions people actually ask

Is MariTide a peptide?
Partly. Two GLP-1 peptides are attached to an antibody. The antibody gives it the month-long half-life; the peptides do the metabolic work.
How does MariTide compare with tirzepatide?
Lower weight loss so far (up to 16% at 52 weeks versus tirzepatide's 21% at 72), given monthly rather than weekly, and with the opposite action at the GIP receptor. No direct comparison exists.
Can you buy MariTide?
No. It is an investigational antibody conjugate made by Amgen; nothing sold online under the name is the real molecule.

One page per claimed effect

References

  1. 1
    Jastreboff AM, et al. Once-monthly maridebart cafraglutide for the treatment of obesity — a phase 2 trial.N Engl J Med, 2025592 enrolled; obesity and obesity-diabetes cohorts; 52 weeks. NCT05669599.

Change log

  • 2026-09-23Initial publication from the NEJM phase 2. Grade B.