GLP-1 Receptor Agonists

Maridebart cafraglutide: indexed trial records

Records checked

Compiled and citation-checked by GLP-1 Receptor Agonists editorial desk

Qualified clinical review None on record

Withheld from the index. This page sets out the indexed clinical-record picture for Maridebart cafraglutide.

Every compound in scope is marked high impact and none has a qualified clinical reviewer recorded, so this page is built, checked and served with a noindex directive and left out of the sitemap. Nothing on it has been removed or softened. Recording a named reviewer publishes it unchanged on the next build. How the gate works.

This page carries 5 of the 13 records the literature query returned for Maridebart cafraglutide, selected by citation count and preferring records that name the compound in their title. It is a selection, not a complete index.

Every row below resolves to a real identifier and names the study model the indexer assigned. The record class is read from the publication type on the record itself. Nothing here states what a record found.

At a glance

Class
Incretin receptor agonists
Receptor targets as recorded
GLP-1 receptor, GIP receptor
Records indexed here
5
Records returned by the query
13
Publication years covered
2024–2026
Query retrieved
2026-10-12

Shape of the indexed record set

Record classRecords
Phase 21
Phase 11
Review or synthesis2
Not a registered trial record1
Study model as assignedRecords
human trial2
other2
rodent1

Study model is the indexer’s own assignment, taken from the MeSH population headings and the publication type. It is not a judgement about how well a record was conducted.

Endpoint coverage

EndpointRecords for this compoundRecords across all compounds in scope
Body weight and adiposity5108
Glycaemic control3117
Cardiovascular030
Renal010
Hepatic19
Neurological018

Derived record-set tier

Preparation or mixture (INFERRED, derived from record counts)
Basis: PubChem returned no compound record for this name, so the subject is a preparation, protein or mixture rather than a defined small molecule; identity fields are unsourced.
This label counts record types. It is not an assessment of clinical efficacy, of safety, of study quality or of consensus, and it does not rank one compound above another.

What the corpus does not carry for this compound

  • Identity fields with no source retrieved: cas, pubchem_cid, uniprot_id, molecular_formula, molecular_weight, sequence.
  • Reported half-life: no source retrieved, so the value reads Unknown.
  • Amounts reported in the cited literature: no row recorded.
  • Adverse effects reported in the cited literature: no row recorded.
  • Long-form mechanism: not written, because no source was read in full.
  • Records the query returned that this corpus does not carry: 8.

An absent row records the absence of a retrieved report, never the absence of the thing itself.

Application register

A query of the FDA Drugs@FDA application register on 2026-10-09 returned no application records for this compound name. This compound is not approved by the FDA for human use.[1]

Scope statement: this records the result of a single automated query against the openFDA drugsfda endpoint on the stated date. It is not legal advice and is not a jurisdiction-by-jurisdiction legality assessment.

The records

Phase 2 — 1 record

No.IdentifierYearRecordModelSubject headings
4pmid:405498872025Once-Monthly Maridebart Cafraglutide for the Treatment of Obesity - A Phase 2 Trial
The New England journal of medicine · Clinical Trial, Phase II, Multicenter Study
human trialHumans; Diabetes Mellitus, Type 2; Obesity; Weight Loss; Receptors, Gastrointestinal Hormone; Anti-Obesity Agents; Immunoconjugates; Body Mass Index

Phase 1 — 1 record

No.IdentifierYearRecordModelSubject headings
5pmid:383169822024A GIPR antagonist conjugated to GLP-1 analogues promotes weight loss with improved metabolic parameters in preclinical and phase 1 settings
Nature metabolism · research-article, Clinical Trial, Phase I
human trialAnimals; Humans; Mice; Obesity; Weight Loss; Peptides; Male; Glucagon-Like Peptide 1

Review or synthesis — 2 records

No.IdentifierYearRecordModelSubject headings
1pmid:410548012026Novel GLP-1-based Medications for Type 2 Diabetes and Obesity
Endocrine reviews · Review
otherAnimals; Humans; Diabetes Mellitus, Type 2; Obesity; Hypoglycemic Agents; Glucagon-Like Peptide 1; Glucagon-Like Peptides; Glucagon-Like Peptide-1 Receptor Agonists
3pmid:421666832026The Paradox and Future of GLP-1/GIP Combination Therapies: Efficacy and Mechanisms
Annual review of nutrition · Review
otherAnimals; Humans; Obesity; Gastric Inhibitory Polypeptide; Receptors, Gastrointestinal Hormone; Anti-Obesity Agents; Drug Therapy, Combination; Glucagon-Like Peptide 1

Not a registered trial record — 1 record

No.IdentifierYearRecordModelSubject headings
2pmid:412872122026A metabolic comparison of GIPR agonism versus GIPR antagonism in male mice
Diabetes, obesity & metabolism · Comparative Study, research-article
rodentLiver; Adipose Tissue; Animals; Mice, Inbred C57BL; Mice; Insulin Resistance; Obesity; Body Weight

Where this page sits

Receptor targets

All compounds in scope: the trial index. Coverage by endpoint: the endpoint index.

Review status

Review tier
High impact
State
Pending qualified review
Compiled by
automated pipeline
Qualified clinical review
None on record

Why this tier was assigned

  • 2 indexed record(s) are interventional human trials
  • the class covers weight-management and metabolic prescribing, the highest-risk consumer subject in this corpus

Checks the pipeline performed

  • every cited source id resolves to a sources[] row on the entity
  • every identifier is a well-formed PMID or DOI
  • study model derived only from assigned MeSH headings and publication types
  • banned-phrase lint over rendered HTML including title, meta, alt and JSON-LD
  • unknown values render as the literal word Unknown

Checks the pipeline did not perform

  • no full text was read
  • no clinical appraisal of any study
  • no assessment of whether the indexed set is representative of the literature

A high_impact profile with qualified_review null must not be published as indexable. Compilation and linting are not clinical validation.

Sources

  1. Drugs@FDA application register query for this compound, no application records returned. U.S. Food and Drug Administration, openFDA drugsfda endpoint (2026). fda:maritide
  2. Discovery of AMG 133, a Glucose-Dependent Insulinotropic Polypeptide Receptor Antagonist and Glucagon-Like Peptide 1 Receptor Agonist Antibody-Drug Conjugate for the Treatment of Obesity. Journal of medicinal chemistry (2026). pmid:41941715
  3. Design and therapeutic rationale of antibody-peptide conjugates: insights from maridebart cafraglutide (AMG133) and emerging applications. Antibody therapeutics (2026). pmid:42592044
  4. Phase I results for AMG 133. Nature reviews. Endocrinology (2024). pmid:38388678
  5. Once-Monthly Maridebart Cafraglutide for the Treatment of Obesity - A Phase 2 Trial. The New England journal of medicine (2025). pmid:40549887
  6. Once-Monthly Maridebart Cafraglutide in Obesity - A Phase 2 Trial. The New England journal of medicine (2025). pmid:41337722
  7. Once-Monthly Maridebart Cafraglutide in Obesity - A Phase 2 Trial. Reply. The New England journal of medicine (2025). pmid:41337724