Evidence map›Paper›PMID 40906309›Full record

ArticleClinical drug investigation2025

The Effect of Multiple Oral Doses of a Glycine Transporter 1 Inhibitor, Iclepertin (BI 425809), on the Steady-state Pharmacokinetics of a Combined Oral Contraceptive Containing Ethinylestradiol and Levonorgestrel: a Phase I Clinical Trial in Healthy Females.

Shilpa Madari, Yesilda Balavarca, Yury Shatillo, Corey Reuteman-Fowler, Michael Desch

Registry-linked trialAbstract readClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in Clinical drug investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05613777 (The Effect of Multiple Doses of BI 425809 on the Pharmacokinetics of Multiple Doses of a Combination of Ethinylestradiol and Levonorgestrel Following Oral Administration in Healthy Premenopausal Female Subjects), which is not on this 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.

NCT05613777 phase1completednot on this map

The Effect of Multiple Doses of BI 425809 on the Pharmacokinetics of Multiple Doses of a Combination of Ethinylestradiol and Levonorgestrel Following Oral Administration in Healthy Premenopausal Female Subjects (an Open-label, Two-period, Fixed Sequence Design Trial With run-in Period)

TypeinterventionalSponsorBoehringer IngelheimRan2022 to 2023Enrolled19ConditionsHealthyArmsMicrogynon®, Iclepertin
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

5 authors.

Shilpa MadariBoehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA.
Yesilda BalavarcaStaburo GmbH, München, Germany.
Yury ShatilloBoehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.
Corey Reuteman-FowlerBoehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA.
Michael DeschBoehringer Ingelheim Pharma GmbH & Co. KG, Birkendorfer Strasse 65, 88400, Biberach an der Riss, Germany. michael.desch@boehringer-ingelheim.com.ORCID http://orcid.org/0000-0003-0205-1592

Funding

Boehringer Ingelheim 1346-0036
6 · The paper itself

Abstract

backgroundIclepertin is a selective inhibitor of glycine transporter 1 recently investigated as a novel treatment for cognitive impairment associated with schizophrenia. Iclepertin is a potential mild inducer of liver cytochrome P450 3A4, which metabolises ethinylestradiol and levonorgestrel, which are used in combined oral contraceptives (OCs).

objectivesThis trial investigated the potential drug interaction effect of steady-state iclepertin on the steady-state pharmacokinetics of combined OCs.

methodsThis phase I, non-randomised, open-label, two-period, fixed-sequence trial was conducted in healthy pre-menopausal female volunteers aged 18-35 years. In period 1, participants received a combined OC (ethinylestradiol 30 µg/levonorgestrel 150 µg once daily; reference treatment). In period 2, participants received a combined OC and iclepertin 10 mg once daily (test treatment). Primary pharmacokinetic endpoints of ethinylestradiol or levonorgestrel in plasma at steady state over a uniform dosing interval τ were area under the concentration-time curve (AUC

resultsIn total, 19 participants entered the trial; 17 were treated (periods 1 and 2). Steady-state pharmacokinetics of ethinylestradiol and levonorgestrel were similar with and without iclepertin; geometric mean ratios for AUC

conclusionIclepertin 10 mg had no meaningful effect on the pharmacokinetics of ethinylestradiol and levonorgestrel, suggesting that these drugs can be administered concomitantly.

trial registrationClinicalTrials.gov (NCT05613777; registered on 18 October 2023).

Indexed as

Contraceptives, Oral, CombinedEthinyl EstradiolGlycine Plasma Membrane Transport ProteinsLevonorgestrelAdministration, OralAdolescentAdultDrug CombinationsDrug InteractionsFemaleHealthy VolunteersHumansLiver-Specific Organic Anion Transporter 1PiperazinesSulfonesYoung Adult(4-(3-fluoro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl)(5-methanesulfonyl-2-(2,2,2-trifluoro-1-methylethoxy)phenyl)methanoneContraceptives, Oral, CombinedDrug CombinationsEthinyl Estradiolethinyl estradiol, levonorgestrel drug combinationGlycine Plasma Membrane Transport ProteinsLevonorgestrelLiver-Specific Organic Anion Transporter 1PiperazinesSLCO1B1 protein, humanSulfones

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Registered trials

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.