Evidence map›Paper›PMID 41907544›Full record

ReviewFrontiers in endocrinology2026

The melanocortin receptors as targets for general obesity: contextualizing clinical failures and analyzing future perspectives.

Claudia R Prindle, Thomas L Bennett, Benjamin H Rajewski, Kade J Kelley, Anna C Impastato, Russell Potterfield, Daniel L Marks, Jordan Y Delev

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Claudia R Prindle *Endevica Bio, Northbrook, IL, United States.
Thomas L Bennett *Endevica Bio, Northbrook, IL, United States.
Benjamin H Rajewski *Endevica Bio, Northbrook, IL, United States.
Kade J KelleyEndevica Bio, Northbrook, IL, United States.
Anna C ImpastatoEndevica Bio, Northbrook, IL, United States.
Russell PotterfieldEndevica Bio, Northbrook, IL, United States.
Daniel L MarksEndevica Bio, Northbrook, IL, United States.
Jordan Y DelevEndevica Bio, Northbrook, IL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The melanocortin system is a genetically conserved and clinically validated target for the treatment of obesity. Hundreds of studies establish the role of the melanocortin receptors, particularly the melanocortin-4 receptor, in food intake, weight control, and energy expenditure. Over the last several decades, the pharmaceutical industry pursued melanocortin-4 receptor-selective agonists for the treatment of general obesity. Many candidates failed to demonstrate meaningful weight loss in the clinic due to potency, selectivity or side effect profiles, leading pharmaceutical companies to dismiss the use of melanocortin compounds for treating general obesity. Recent advancements in the field demonstrate the importance of modulating both melanocortin-3 and -4 receptors for optimal weight loss and offer solutions to mitigate undesired side effects associated with melanocortin agonism. Considering these discoveries, it is imperative to review past clinical attempts and compare them with programs currently in development. A thorough understanding of the shortcomings of past clinical programs will enable the development of novel melanocortin therapeutics for the treatment of general obesity.

Indexed as

Anti-Obesity AgentsObesityReceptor, Melanocortin, Type 4Receptors, MelanocortinAnimalsEnergy MetabolismHumansAnti-Obesity AgentsReceptor, Melanocortin, Type 4Receptors, Melanocortinfood intakemelanocortin-3 receptormelanocortin-4 receptormelanocortin-4 receptor agonistmelanocortin (MC)metabolismobesityweight loss

Identifiers

PMID41907544
PMCPMC13017269

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.