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Record W4407387012 · doi:10.1093/ijnp/pyae059.273

SAFETY AND EFFICACY OF DIFFERENT INITIAL DOSES OF LURASIDONE IN THE SCHIZOPHRENIA TREATMENT: A RANDOMIZED, OPEN-LABEL, MULTI- CENTER STUDY

2025· article· en· W4407387012 on OpenAlexaboutno aff
Qi Liu, Qi Wu, Xin Yu

Bibliographic record

VenueThe International Journal of Neuropsychopharmacology · 2025
Typearticle
Languageen
FieldMedicine
TopicPharmaceutical studies and practices
Canadian institutionsnot available
Fundersnot available
KeywordsLurasidoneSchizophrenia (object-oriented programming)Open labelMedicineRandomized controlled trialPharmacologyPsychiatryInternal medicineAntipsychotic

Abstract

fetched live from OpenAlex

Abstract Background Schizophrenia is a group of serious mental illnesses and antipsychotics are the primary clinical treatment. Lurasidone, a second-generation antipsychotic drug, was approved in China in 2019 for the treatment of adult schizophrenia with a maximum dose of 80 mg/d. The safety and efficacy of different initial doses of lurasidone in treating acute schizophrenia remain unclear, especially whether the discontinuation rate due to adverse events (AEs) increases with higher initial dose. Aim To compare the safety and efficacy of different initial doses of lurasidone in the treatment of acute schizophrenia. Methods A 6-week, randomized, open-label, multi-center study was conducted and eligible subjects were randomized to receive either a 40 mg/d or 80 mg/d initial dose of lurasidone in a 1:1 ratio. The dose could be adjusted or maintained after 7 days of fixed-dose initial treatment. The primary safety endpoint was the discontinuation rate due to AEs at the end of treatment. Other safety evaluations included adverse events, weight change and laboratory tests. The efficacy was assessed by the proportion of responders at week1/ week2 and changes in PANSS total score and Lindenmayer 5-factor scores / Clinical Global Impression-Severity (CGI-S) scale score/ Calgary Depression Scale for Schizophrenia (CDSS) score from baseline to week 6. Results A total of 197 patients were enrolled in the full analysis set (FAS) and the safety set (SS). There was no significant difference in the discontinuation rate due to AEs between the two treatment groups (3.03% in 40 mg/d initiation group vs 5.10% in 80 mg/d initiation group, P = 0.707). 193 AEs occurred in 65 subjects (65.7%) in 40 mg/d initiation group and 185 AEs occurred in 71 subjects (72.4%) in 80 mg/d initiation group. Notably, the 40 mg/d initiation group had a higher percentage of patients experiencing clinically significant weight gain compared to the 80 mg/d initiation group (12.1% vs 4.1%). The proportion of responders was similar between the two groups at week 1 (39.39% vs 40.82%, P = 0.839) and showed a numerical, but not statistically significant advantage for the 80 mg/d initiation group at week 2 (52.53% vs 57.14%, P = 0.515). Compared to the baseline, significant improvements were observed in the PANSS total score (P <0.001) and 5-factor scores (P <0.001), CGI-S scale score (P <0.001), and CDSS score (P <0.01) at all visit points in both treatment groups. Additionally, treatment with 80 mg/d initial dose of lurasidone was associated with significantly greater improvement on 5- factor cognitive score at visit 2-4 compared to the 40 mg/d initial dose. Conclusion Both the 40 mg/d or 80 mg/d initial doses of lurasidone are safe and effective for the treatment of acute schizophrenia. Furthermore, the 80 mg/d initial dose does not result in a significantly higher discontinuation rate due to AEs compared to the 40 mg/d initial dose. References 1.Jingping Z., et al., Guidelines for schizophrenia Prevention and Treatment in China (2nd Edition). 2015. 2.Yumei W., et al., Safety and effectiveness of lurasidone in the treatment of Chinese schizophrenia patients: An interim analysis of post-marketing surveillance. World J Psychiatry. 2023.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.127
Threshold uncertainty score0.246

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.082
GPT teacher head0.464
Teacher spread0.382 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
Has abstractyes

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