Evidence map›Paper›PMID 37592798›Full record

ArticleCurrent drug metabolism2023

Simone I Schulz, Dieter Lang, Gabriele Schmuck, Michael Gerisch, Michaela Bairlein, Robert Fricke, Heino Stass

Open access · greenAbstract read
In one paragraph

Article in Current drug metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 42% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

7 authors at 1 institution in 1 country.

Simone I SchulzBayer AG, 42096 Wuppertal, Germany.
Dieter LangBayer AG, 42096 Wuppertal, Germany.ORCID 0000-0002-2968-638X
Gabriele SchmuckBayer AG, 42096 Wuppertal, Germany.
Michael GerischBayer AG, 42096 Wuppertal, Germany.
Michaela BairleinBayer AG, 42096 Wuppertal, Germany.
Robert FrickeBayer AG, 42096 Wuppertal, Germany.
Heino StassBayer AG, 42096 Wuppertal, Germany.
Bayer (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNifurtimox is an effective treatment for patients with Chagas disease, but knowledge of its biotransformation and excretion is limited.

objectiveThis study aimed to better understand the fate of oral nifurtimox

methodsWe investigated the exposure and excretion pathways of [

resultsIn rats, orally administered nifurtimox was rapidly absorbed (t

conclusionThis contemporary analysis of the complex metabolite profile and associated exposures emerging after oral dosing of nifurtimox in rats and humans, together with the expected low risk for clinically relevant DDIs, expands the understanding of this important anti-trypanosomal drug.

Indexed as

Chagas DiseaseNifurtimoxAdministration, OralAnimalsBiotransformationCytochrome P-450 Enzyme SystemDrug InteractionsHumansRatsCytochrome P-450 Enzyme SystemNifurtimoxbiotransformationChagas diseasedrug dispositiondrug-drug interactionsmetabolitesNifurtimoxstability

Identifiers

PMID37592798
PMCPMC10661964
OpenAlexW4385968540

What OpenQuestion holds

Textmetadata
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.