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A Multicenter, Inpatient, Phase 2, Double-Blind, Placebo-Controlled Dose-Ranging Study of LY2140023 Monohydrate in Patients With DSM-IV Schizophrenia
Abstract
The primary objective of this study was to test the hypothesis that 1 or more dose levels of LY2140023 monohydrate, an oral prodrug of the potent metabotropic glutamate (mGlu) 2/3 receptor agonist LY404039, given to patients with schizophrenia for 4 weeks would demonstrate significantly greater efficacy than placebo. The HBBI study was a multicenter, randomized, double-blind, parallel, placebo- and active-controlled trial. Male and female patients aged 18 to 65 years who met the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria for schizophrenia were randomized in a 2:2:2:2:2:1 ratio to receive 5-, 20-, 40-, or 80-mg LY2140023 monohydrate twice daily, placebo twice daily, or placebo (am) and 15 mg of olanzapine (pm) daily. Efficacy was defined as the change from baseline on the Positive and Negative Syndrome Scale (PANSS) total score assessed at 4 weeks. The primary analysis did not show that any of the 4 LY2140023 monohydrate doses were more efficacious than placebo as measured by the PANSS total score. Similarly, olanzapine did not significantly separate from placebo. A higher-than-anticipated treatment effect (14.6-point improvement) in the placebo group was observed on PANSS total score. LY2140023 monohydrate was generally well tolerated, although 4 patients reported the serious adverse event of convulsion. LY2140023 monohydrate-treated patients showed little change in dopamine-related adverse events and weight. The results of the HBBI study are considered to be inconclusive because LY2140023 monohydrate and the active control olanzapine did not separate from placebo in the treatment of patients with acutely exacerbated schizophrenia. Additional efficacy, safety, and tolerability testing are needed.
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“Only 2 of 6 completed monotherapy trials are currently published49,50 but without results of neurocognitive testing.”
From Clinical trials of potential cognitive-enhancing drugs in schizophrenia: what have we learned so far? (2013) · cites this paper as [50]
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Metadata
- Authors
- Kinon, B. J., Zhang, L., Millen, B. A., Osuntokun, O. O., Williams, J. E., Kollack-Walker, S., Jackson, K., Kryzhanovskaya, L., & Jarkova, N.
- Affiliations
- Eli Lilly (United States) (US)
- Corresponding author
- Kinon, Bruce J.
- Zhang, Lu
- Millen, Brian A.
- Osuntokun, Olawale O.
- Williams, Judy E.
- Jackson, Kimberley
- Kryzhanovskaya, Ludmila
- Venue
- Journal of Clinical Psychopharmacology
- Published
- 2011-06
- Volume
- 31
- Issue
- 3
- Pages
- 349-355
- ISSN
- 0271-0749 (ISSN-L)
- OpenAlex
- W2312770619
- Cited by
- 256
- References
- 15
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 9 · 2023: 4 · 2022: 17 · 2021: 9 · 2020: 10 · 2019: 13 · 2018: 12 · 2017: 13 · 2016: 19 · 2015: 28 · 2014: 29 · 2013: 34 · 2012: 39
- FWCI
- 24.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Clinical Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Eli Lilly and Company
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Keywords
- prodrugs, schizophrenia, acute exacerbation of schizophrenia, olanzapine, dose-ranging, PANSS, convulsions, weight change, drug safety and tolerability
- MeSH terms
- Olanzapine, Assessment of Medication Adherence, Adolescent, Adult, Aged, Amino Acids, Benzodiazepines, Dose-Response Relationship, Drug, Double-Blind Method, Female, Humans, Inpatients, Male, Middle Aged, Prodrugs, Psychiatric Status Rating Scales, Schizophrenia, Antipsychotic Agents, Drug Monitoring, Receptors, Metabotropic Glutamate, Diagnostic and Statistical Manual of Mental Disorders, Medication Adherence
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