Evidence map›Paper›PMID 41055137›Full record

ArticleClinical pharmacology and therapeutics2026

Population Pharmacokinetics and Exposure-Response Analyses of Momelotinib, Its Active Metabolite (M21), and Total Active Moiety in Myelofibrosis.

Benjamin Rich, Meenakshi Srinivasan, Yu Liu Ho, Sandra A G Visser, Geraldine Ferron-Brady, Georgios Vlasakakis

Abstract read
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Article in Clinical pharmacology and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Benjamin RichInnoMx, Outremont, Quebec, Canada.ORCID 0009-0004-2903-5554
Meenakshi SrinivasanGSK, Waltham, Massachusetts, USA.ORCID 0000-0002-2718-4335
Yu Liu HoGSK, Collegeville, Pennsylvania, USA.ORCID 0009-0005-0074-1938
Sandra A G VisserGSK, Collegeville, Pennsylvania, USA.ORCID 0009-0008-2186-7195
Geraldine Ferron-BradyGSK, Collegeville, Pennsylvania, USA.ORCID 0000-0001-5703-8315
Georgios VlasakakisGSK, Collegeville, Pennsylvania, USA.ORCID 0000-0002-7390-9712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Momelotinib, a Janus kinase (JAK) 1/JAK2/activin A receptor type 1 inhibitor, is approved for the treatment of myelofibrosis with anemia. These analyses characterized the population pharmacokinetics of momelotinib and its active metabolite M21 following administration of the commercial tablet formulation in patients with myelofibrosis from phase II/III trials and other participants from phase I trials (N = 661). Predicted covariate effects on momelotinib, M21, and total active moiety (TAM)-representing the combined potency-weighted exposures of momelotinib and M21-exposures following 200-mg once-daily dosing were evaluated using a simulation-based approach. Using sequential modeling, momelotinib was described by a two-compartment model with six transit absorption compartments and first-order elimination, and M21 by a two-compartment model with first-order elimination. Hepatic function, concomitant CYP3A4 inducers, and concomitant OATP1B1/1B3 inhibitors were significant momelotinib covariates, while baseline creatinine clearance and hepatic function were significant M21 covariates, with cumulative effects on TAM. Exposure-response relationships between the average TAM concentration under actual dosing and key efficacy and safety end points were assessed using data from the 24-week randomized period of three phase III trials in patients with myelofibrosis (N = 417). After relevant covariate adjustment, significant positive relationships were identified with spleen volume reduction and transfusion independence (the latter specifically in JAK inhibitor-experienced patients), but not symptom improvement. Greater TAM exposure was significantly associated with lower odds of grade 3/4 anemia and higher odds of any-grade peripheral neuropathy, although the latter was infrequently observed in phase III trials. There was no significant relationship with grade ≥ 3 thrombocytopenia or any-grade diarrhea.

Indexed as

BenzamidesJanus Kinase InhibitorsPrimary MyelofibrosisProtein Kinase InhibitorsPyrimidinesPyrrolidinesAdultAgedBridged-Ring CompoundsClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicFemaleHumansJanus Kinase 1Janus Kinase 211-(2-pyrrolidin-1-ylethoxy)-14,19-dioxa-5,7,26-triazatetracyclo(19.3.1.1(2,6).1(8,12))heptacosa-1(25),2(26),3,5,8,10,12(27),16,21,23-decaeneBenzamidesBridged-Ring CompoundsJanus Kinase 1Janus Kinase 2Janus Kinase InhibitorsN-(cyanomethyl)-4-(2-((4-(4-morpholinyl)phenyl)amino)-4-pyrimidinyl)benzamideProtein Kinase InhibitorsPyrimidinesPyrrolidines

Identifiers

PMID41055137
PMCPMC12882756

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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.