Efficacy and safety of adjunctive treatment with the fatty acid amide hydrolase inhibitor JNJ-42165279 in participants with major depressive disorder with anxious distress: A double-blind, placebo-controlled, randomised study

dc.contributor.authorSchmidt, Mark E.
dc.contributor.authorGargano, Cynthia
dc.contributor.authorZhou, Xianhuang
dc.contributor.authorPalmer, James A.
dc.contributor.authorSaad, Ziad S.
dc.contributor.authorVieta i Pascual, Eduard, 1963-
dc.contributor.authorDrevets, Wayne C.
dc.contributor.authorStuyckens, Kim
dc.contributor.authorPandina, Gahan
dc.date.accessioned2026-06-02T14:56:59Z
dc.date.available2026-06-02T14:56:59Z
dc.date.issued2026-05-01
dc.date.updated2026-06-02T14:57:01Z
dc.description.abstractJNJ-42165279 is a potent, selective inhibitor of fatty acid amide hydrolase (FAAH), the enzyme responsible for degradation of the endocannabinoid N-arachidonoylethanolamide (anandamide), which plays a role in regulation of fear and anxiety responses. This double-blind, randomised, placebo-controlled, phase 2a study assessed the efficacy, safety and pharmacodynamics of adjunctive treatment with JNJ-42165279 in participants with major depressive disorder (MDD) with anxious distress and inadequate response to selective serotonin reuptake inhibitors (SSRI) or serotonergic/noradrenergic reuptake inhibitors (SNRI). Eligible participants (18-64 years; N = 153) were randomised (1:1) to receive JNJ-42165279 (25 mg) or placebo orally once daily and were maintained on their current SSRI/SNRI treatment. The primary endpoint was the change from baseline at week 6 in the 17-item Hamilton Depression Rating Scale (HDRS17). The study results did not show a significant treatment effect of adjunctive JNJ-42165279 on the primary endpoint versus placebo (least square mean difference [standard error]: -0.2 [1.04]; one-sided p=0.416) in the enriched intent-to-treat population. Findings for the key secondary efficacy endpoints also did not demonstrate an additional benefit of adjunctive JNJ-42165279 treatment over placebo. Treatment with JNJ-42165279 produced substantial increases in the mean concentrations of fatty acid amides in plasma, and the plasma JNJ-42165279 and anandamide levels were strongly correlated. The safety results were consistent with the known safety profile of JNJ-42165279. Overall, adjunctive treatment with JNJ-42165279 at the dose tested did not provide significant benefit in reducing depression/anxiety symptoms versus placebo but showed no new safety signals in participants with MDD and anxious distress.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec766989
dc.identifier.issn0924-977X
dc.identifier.pmid41616640
dc.identifier.urihttps://hdl.handle.net/2445/229843
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.euroneuro.2026.112771
dc.relation.ispartofEuropean Neuropsychopharmacology, 2026, vol. 106
dc.relation.urihttps://doi.org/10.1016/j.euroneuro.2026.112771
dc.rightscc-by (c) Schmidt, Mark E. et al., 2026
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationDepressió psíquica
dc.subject.classificationEnzims
dc.subject.classificationAnsietat
dc.subject.otherMental depression
dc.subject.otherEnzymes
dc.subject.otherAnxiety
dc.titleEfficacy and safety of adjunctive treatment with the fatty acid amide hydrolase inhibitor JNJ-42165279 in participants with major depressive disorder with anxious distress: A double-blind, placebo-controlled, randomised study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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