Evidence map›Paper›PMID 42623271›Full record

Trial reportThe international journal of neuropsychopharmacology2026

Weight and metabolic changes in patients with schizophrenia treated with paliperidone palmitate 6-month formulation versus paliperidone palmitate 3-month formulation: a post-hoc analysis.

Mark Guirguis, Robert Karl Knight, Panna Sanga, John Han, Silvana Galderisi

2 registry-linked trialsAbstract readRandomized Controlled TrialClinical Trial, Phase IIIComparative Study
In one paragraph

Trial report in The international journal of neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are 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.

NCT03345342 phase3completednot on this map

A Double-blind, Randomized, Active-controlled, Parallel-group Study of Paliperidone Palmitate 6-Month Formulation

TypeinterventionalSponsorJanssen Research & Development, LLCRan2017 to 2020Enrolled841ConditionsSchizophreniaArmsPP6M, PP3M 350 mg eq., PP3M 525 mg eq., PP1M, Placebo
NCT04072575 phase3completednot on this map

Single-arm, Open-label Extension to a Double-blind, Randomized, Active-controlled, Parallel-group Study of Paliperidone Palmitate 6-Month Formulation

TypeinterventionalSponsorJanssen Research & Development, LLCRan2019 to 2022Enrolled178ConditionsSchizophreniaArmsPP6M injection Dose 1, PP6M injection Dose 2
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.

Mark GuirguisJohnson & Johnson Innovative Medicine, LLC, Titusville, NJ, United States.ORCID 0009-0002-1085-7430
Robert Karl KnightJohnson & Johnson Innovative Medicine, LLC, Titusville, NJ, United States.ORCID 0009-0006-7595-2286
Panna SangaJohnson & Johnson Innovative Medicine, LLC, Titusville, NJ, United States.ORCID 0000-0003-0903-2925
John HanJohnson & Johnson Innovative Medicine, LLC, Titusville, NJ, United States.ORCID 0009-0001-9806-674X
Silvana GalderisiUniversity of Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0002-1592-7656

Funding

Janssen Research and Development, LLC
6 · The paper itself

Abstract

objectiveTo determine the effect that paliperidone palmitate 6-month long-acting injectable formulation (PP6M) had on metabolic parameters including body weight (BW), and blood lipid profiles, a post-hoc analysis was conducted to assess changes in BW from baseline to the end of study based on age, body mass index (BMI), and changes in blood lipid profiles during a 12-month, phase 3, double-blind (DB) clinical study. Long term effects of PP6M on BW and BMI were further explored during a 24-month extension study in which participants were treated exclusively with PP6M.

methodIn the 12-month DB phase, participants were randomized to receive PP6M or paliperidone palmitate 3-month long-acting injectable formulation (PP3M). The mean change in BW and abnormal weight percent change from baseline were calculated at endpoint by age, gender, and BMI. Additionally, treatment-emergent shifts from baseline for the four key lipid parameters (fasting low density lipoprotein [LDL], fasting triglycerides [TG], fasting total cholesterol [TC], and fasting high density lipoprotein [HDL]) during DB were assessed. Following this study, participants were given the opportunity to transition to a 24-month extension study and be treated with PP6M. The mean change and percent change in BW, and the mean change in BMI from DB baseline to the end of the extension study (36 months total) were calculated.

resultsParticipants who were treated with PP6M showed numerically less weight gain, BMI, waist circumference, and more weight decrease compared to PP3M group during 12-month DB phase, though the proportion of participants reporting an abnormal change (≥7% change) in BW did not significantly differ between PP3M and PP6M. The weight differences were more pronounced in the younger age group (18-25 years) and those who were overweight (BMI: 25 to <30 kg/m2. Numerical differences in favor of PP6M were found in fasting blood lipids (HDL, LDL, TG, and TC). The changes in BW and BMI over time remained consistent throughout the 24-month extension, favoring PP6M in each instance.

conclusionsThis post-hoc analysis demonstrated that PP6M was comparable to PP3M in terms of metabolic parameters; however, it may have a beneficial effect on weight gain, especially in young patients.

trial registrationPost-Hoc Analysis of Studies NCT03345342 and NCT04072575 (ClinicalTrials.gov). Significant outcomes The findings from this study have highlighted that participants who were treated with the 6-month long-acting injectable formulation of paliperidone exhibited less weight gain during treatment overall, and significantly less weight gain in adolescents and young adults. Importantly, this trend continued over the course of long-term treatment, regardless of age. Participants treated with the 6-month formulation also had fewer shifts in blood lipids outside of the normal range and had more favorable changes in body mass index and waist circumference. These results suggest that when considering metabolic dysregulation as a factor in choosing a long-acting injectable antipsychotic, the 6-month formulation is a viable alternative to the 3-month formulation, particularly in younger patients with schizophrenia. Limitations Because this is a post hoc analysis and the study was not powered to test weight and metabolic changes, most endpoints were summarized descriptively and the statistical test was limited to the main endpoint (abnormal percent weight gain and loss).

Indexed as

Antipsychotic AgentsBody WeightPaliperidone PalmitateSchizophreniaAdolescentAdultBody Mass IndexDelayed-Action PreparationsDouble-Blind MethodFemaleHumansLipidsMaleMiddle AgedYoung AdultAntipsychotic AgentsDelayed-Action PreparationsLipidsPaliperidone Palmitatebody mass indexlong-acting injectablepaliperidone palmitateschizophreniaweight gain

Identifiers

PMID42623271
PMCPMC13533545

What OpenQuestion holds

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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.