BENITIONSClinical Trial Intelligence

A Study of CLE-100 (Oral Esketamine) as an Adjunctive Treatment to Standard Antidepressants for Major Depressive Disorder

2期 已完成 NCT06340958

适应症Adjunctive Treatment of Major Depressive Disorder
分期2期
申办方Clexio Biosciences Ltd.
状态已完成
受试者人数99 人
干预(药物)CLE-100
开始日期2024年3月18日
完成日期2025年6月6日
结果公布日2026年6月23日

摘要

The study is a Phase 2, double-blind, randomized, placebo-controlled study in Major Depressive Disorder (MDD) participants with an inadequate response to standard antidepressants The objective of the study is to assess CLE-100 (oral esketamine) for the treatment of MDD in participants currently treated with an oral antidepressant medication and who have an inadequate response to at least 2 antidepressants.

Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Score

29 days · units on a scale

CLE-100-11.66 ± 1.50 units on a scale
Placebo-8.70 ± 1.55 units on a scale
p-value0.15
Least square (LS) mean difference-2.96 (95% CI -7.01–1.09)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。