Abstract | PURPOSE/BACKGROUND: METHODS/PROCEDURES: The diagnosis of TRS was based on clinical history and lack of improvement in psychopathology during a 6-week open trial of lurasidone 80 mg/d (phase 1). This was followed by a randomized, double-blind, 24-week trial of lurasidone, comparing 80- and 240-mg/d doses (phase 2). FINDINGS/RESULTS: Significant non-dose-related improvement in the Positive and Negative Syndrome Scale-Total and subscales and in 2 of 7 cognitive domains, speed of processing and executive function, were noted. Twenty-eight (41.8%) of 67 patients in the combined sample improved ≥20% in the Positive and Negative Syndrome Scale-Total. Of the 28 responders, 19 (67.9%) first reached ≥20% improvement between weeks 6 and 24 during phase 2, including some who had previously failed to respond to clozapine. IMPLICATIONS/CONCLUSIONS:
|
Authors | Herbert Y Meltzer, Daniel B Share, Karu Jayathilake, Ronald M Salomon, Myung A Lee |
Journal | Journal of clinical psychopharmacology
(J Clin Psychopharmacol)
2020 May-Jun
Vol. 40
Issue 3
Pg. 240-249
ISSN: 1533-712X [Electronic] United States |
PMID | 32332459
(Publication Type: Clinical Trial, Phase II, Journal Article, Randomized Controlled Trial)
|
Chemical References |
- Antipsychotic Agents
- Lurasidone Hydrochloride
|
Topics |
- Adult
- Antipsychotic Agents
(adverse effects, therapeutic use)
- Double-Blind Method
- Drug Resistance
(drug effects)
- Female
- Humans
- Lurasidone Hydrochloride
(adverse effects, therapeutic use)
- Male
- Psychiatric Status Rating Scales
- Schizophrenia
(drug therapy)
- Schizophrenic Psychology
- Treatment Outcome
|