Evidence map›Paper›PMID 42547066›Full record

ArticleDrug testing and analysis2026

Quantification of the Carboxylated LGD-4033 Long-Term Metabolite in Human Micro-Dose Excretion Study Urine Samples.

Panagiotis Sakellariou, Sebastian Marcel Schröder, Jasmin Thelen, Linus Korsmeier, Sven Guddat, Christian Görgens, Andreas Thomas, Mario 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

8 authors.

Panagiotis SakellariouInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0005-1005-738X
Sebastian Marcel SchröderInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.
Jasmin ThelenInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.
Linus KorsmeierInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.
Sven GuddatInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.
Christian GörgensInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-6061-0407
Andreas ThomasInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0003-1199-0743
Mario ThevisInstitute of Biochemistry/Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-1535-6451

Funding

World Anti-Doping Agency 25T04MT
6 · The paper itself

Abstract

Selective androgen receptor modulators (SARMs), such as LGD-4033, are frequently detected in doping control samples and pose significant challenges for result interpretation, particularly at low concentration levels potentially arising from contamination. In this study, a quantitative method for the determination of the carboxylated long-term metabolite (M5-b) of LGD-4033 in human urine was developed and applied to samples obtained from controlled micro-dose administration studies. Urine samples from single- and multiple-dose administration studies (1, 10, and 50 μg) were analyzed following enzymatic hydrolysis and solid-phase extraction using LC-HRMS/MS. Quantification was enabled by the use of a recently synthesized certified reference material, allowing, for the first time, the generation of quantitative excretion data for long-term metabolite under micro-dose conditions. The results demonstrated the rapid formation of long-term metabolite and a clear dose-dependent increase in urinary concentrations. Extended detection windows were observed for all dosing regimens, with long-term metabolite remaining detectable for several days after single-dose administration and for substantially longer periods following consecutive administration (5 days). Accumulation effects during multiple-dose intake resulted in sustained urinary concentrations and prolonged detectability. The quantitative data generated in this study provide an important basis for improved interpretation of adverse analytical findings involving LGD-4033 and support a more evidence-based distinction between different intake scenarios.

Indexed as

PyridinesSubstance Abuse DetectionDoping in SportsHumansLimit of DetectionLiquid Chromatography-Mass SpectrometryNitrilesPyrrolidinesSolid Phase ExtractionTandem Mass Spectrometry4-(2-(2,2,2-trifluoro-1-hydroxyethyl)pyrrolidin-1-yl)-2-(trifluoromethyl)benzonitrileNitrilesPyridinesPyrrolidinesdopingLGD‐4033ligandrolmetabolismSARMs

Identifiers

PMID42547066
PMCPMC13628428

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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.