Evidence map›Paper›PMID 31876117›Full record

Trial reportClinical pharmacology in drug development2020

Population Pharmacokinetics of Paliperidone Palmitate (Once-Monthly Formulation) in Japanese, Korean, and Taiwanese Patients With Schizophrenia.

Hiroko Shimizu, Martine Neyens, Marc De Meulder, Srihari Gopal, Yuko Tsukamoto, Mahesh N Samtani, Bart Remmerie

Abstract readClinical Trial, Phase IClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Clinical pharmacology in drug development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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.

Hiroko ShimizuJanssen Pharmaceutical K.K, Tokyo, Japan.
Martine NeyensJanssen Research and Development, a division of Janssen Pharmaceuticals NV, Beerse, Belgium.
Marc De MeulderJanssen Research and Development, a division of Janssen Pharmaceuticals NV, Beerse, Belgium.
Srihari GopalJanssen Research and Development LLC, Raritan, New Jersey, USA.
Yuko TsukamotoJanssen Pharmaceutical K.K, Tokyo, Japan.
Mahesh N SamtaniJanssen Research and Development LLC, Raritan, New Jersey, USA.
Bart RemmerieJanssen Research and Development, a division of Janssen Pharmaceuticals NV, Beerse, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The paliperidone pharmacokinetics after intramuscular administration of once-monthly paliperidone palmitate in Japanese patients were studied in 3 phase 1 studies and in 2 phase 3 studies performed in Japan, Korea, and Taiwan. These data (Japanese, n = 509; Korean, n = 31; Taiwanese, n = 47) were used to describe the paliperidone palmitate pharmacokinetics in Japanese, to compare with non-Japanese, and to validate the historical population pharmacokinetic (Pop-PK) model for paliperidone palmitate, developed using data from studies in patients with schizophrenia outside Japan. The final historical Pop-PK model, including all significant patient covariates of Japanese studies, was used to simulate paliperidone plasma concentration-time data using nonlinear mixed effects, followed by comparison with actual data. Visual predictive checks displayed considerable overlap between predicted and actual plasma concentrations; the majority of observations were within the 90% prediction interval. Japanese, Korean, and Taiwanese patients had comparable plasma concentrations. Covariate distributions demonstrated comparatively lower median body mass index in Japanese, Korean, and Taiwanese patients versus rest-of-world population. Prediction errors for the data set used for external validation were within cutoff values, confirming accuracy/precision of the model. Paliperidone pharmacokinetics were adequately predicted for Japanese studies using the historical Pop-PK model, confirming its robustness. Pharmacokinetics in Japanese, Korean, and Taiwanese patients with schizophrenia were comparable with rest-of-world population.

Indexed as

AdultAgedAntipsychotic AgentsBody Mass IndexCase-Control StudiesDopamine D2 Receptor AntagonistsFemaleHalf-LifeHumansInjections, IntramuscularJapanMaleMiddle AgedPaliperidone PalmitatePredictive Value of TestsRepublic of KoreaAntipsychotic AgentsDopamine D2 Receptor AntagonistsPaliperidone PalmitateSerotonin 5-HT2 Receptor Antagonistslong-acting injectablepaliperidone palmitatepharmacokinetics

Identifiers

PMID31876117
PMCPMC7028061

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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.