Evidence map›Paper›PMID 42977781›Full record

ReviewInnere Medizin (Heidelberg, Germany)2026

[New oral anti-obesity drugs: the future or second choice?]

H Hauner

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Innere Medizin (Heidelberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

H HaunerSeniorprofessur der Else Kröner-Fresenius-Stiftung, Institut für Klinische Ernährungsmedizin, School of Medicine and Health, Technische Universität München, Am Olympiacampus 11, 80809, München, Deutschland. hans.hauner@tum.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity and its comorbidities represent a growing worldwide health challenge. To date, lifestyle modification is the most frequently used treatment modality, but offers only limited success in terms of both the extent and maintenance of weight loss. Potent injectable incretin mimetics such as semaglutide and tirzepatide were recently introduced as novel pharmacological options for improved and clinically meaningful weight management. In 2026, the first two oral glucagon-like peptide‑1 (GLP-1)-based agents, namely oral semaglutide and orforglipron, were approved and are promoted as alternative drug choices for additional weight loss, allowing people with obesity to make their own choice from a broader spectrum of therapeutics. This review describes the current state of knowledge on these new medications for the treatment of obesity. A variety of other oral drugs is currently under development and will substantially expand obesity management in the coming years.

Indexed as

Diabetes mellitus, type 2Glucagon-like peptide‑1 receptor agonistsOrforglipronSemaglutide/oral administrationWeight loss

Identifiers

PMID42977781

What OpenQuestion holds

Textmetadata
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.