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.author | Schmidt, Mark E. | |
| dc.contributor.author | Gargano, Cynthia | |
| dc.contributor.author | Zhou, Xianhuang | |
| dc.contributor.author | Palmer, James A. | |
| dc.contributor.author | Saad, Ziad S. | |
| dc.contributor.author | Vieta i Pascual, Eduard, 1963- | |
| dc.contributor.author | Drevets, Wayne C. | |
| dc.contributor.author | Stuyckens, Kim | |
| dc.contributor.author | Pandina, Gahan | |
| dc.date.accessioned | 2026-06-02T14:56:59Z | |
| dc.date.available | 2026-06-02T14:56:59Z | |
| dc.date.issued | 2026-05-01 | |
| dc.date.updated | 2026-06-02T14:57:01Z | |
| dc.description.abstract | JNJ-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.extent | 8 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.idgrec | 766989 | |
| dc.identifier.issn | 0924-977X | |
| dc.identifier.pmid | 41616640 | |
| dc.identifier.uri | https://hdl.handle.net/2445/229843 | |
| dc.language.iso | eng | |
| dc.publisher | Elsevier B.V. | |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1016/j.euroneuro.2026.112771 | |
| dc.relation.ispartof | European Neuropsychopharmacology, 2026, vol. 106 | |
| dc.relation.uri | https://doi.org/10.1016/j.euroneuro.2026.112771 | |
| dc.rights | cc-by (c) Schmidt, Mark E. et al., 2026 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.source | Articles publicats en revistes (Medicina) | |
| dc.subject.classification | Depressió psíquica | |
| dc.subject.classification | Enzims | |
| dc.subject.classification | Ansietat | |
| dc.subject.other | Mental depression | |
| dc.subject.other | Enzymes | |
| dc.subject.other | Anxiety | |
| dc.title | 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.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion |
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