Evidence map›Paper›PMID 42320973›Full record

ArticleDrug testing and analysis2026

Investigations Into the Metabolism and Elimination of Tesofensine in Human Urine.

O Krug, A Thomas, M Thevis

Abstract read
In one paragraph

Article in Drug testing and analysis, 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

3 authors.

O KrugInstitute of Biochemistry, Center for Preventive Doping Research (ZePräDo), German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0008-5517-7571
A ThomasInstitute of Biochemistry, Center for Preventive Doping Research (ZePräDo), German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0003-1199-0743
M ThevisInstitute of Biochemistry, Center for Preventive Doping Research (ZePräDo), German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-1535-6451

Funding

Federal Ministry of the Interior and CommunityManfred-Donike Institute for Doping Analysis
6 · The paper itself

Abstract

Tesofensine (NS-2330) is a pharmacologically active compound with weight-reducing effects in obese patients. Although still under regulatory review, it has been marketed online as a dietary supplement promoted for weight management and metabolic enhancement. Due to its impact on body weight, tesofensine could be relevant in competitive sports, particularly in weight-class disciplines and sports where power-to-weight ratio is decisive. It is classified under "S6 stimulants" on the World Anti-Doping Agency's Prohibited List and is prohibited in-competition only, making detailed knowledge of its metabolism and excretion essential for anti-doping purposes. Although the pharmacological effects and elimination of tesofensine and one dealkylated metabolite were described previously, elimination profiles and structural information on additional metabolites have been limited. In this study, in vitro metabolism experiments were conducted, followed by investigation of urinary metabolism and elimination in six volunteers after ingestion of 483 μg tesofensine as a dietary supplement. Urine was collected for up to 600 h, prepared by solid-phase extraction, and analyzed by LC-HRMS. Four principal metabolites were identified: three dealkylated metabolites (M1-M3) and one hydroxylated and glucuronidated metabolite (M4), supported by MS/MS dissociation patterns. The validated analytical method for human urine showed an LOD of 0.01 ng/mL, 34% recovery, and 8% interday imprecision. Marked interindividual variability was observed, with peak concentrations of 1-4 ng/mL after 4-46 h and detection windows up to 500 h. The findings enhance analytical procedures and suggest that recommended dosing is unlikely to result in concentrations constituting an Adverse Analytical Finding (AAF) under currently applicable stimulant minimum reporting levels.

Indexed as

Anti-Obesity AgentsBridged Bicyclo Compounds, HeterocyclicAdultDietary SupplementsDoping in SportsHumansLiquid Chromatography-Mass SpectrometryMaleTandem Mass SpectrometryAnti-Obesity AgentsBridged Bicyclo Compounds, HeterocyclicTesofensinein vitroin vivoLC–MSmetabolismtesofensineurine

Identifiers

PMID42320973
PMCPMC13532915

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.