A Study to Assess the Efficacy and Safety of REL-1017 as Adjunctive Treatment for Major Depressive Disorder (MDD)
| Заболевание | Major Depressive Disorder, Depression |
|---|---|
| Фаза | Фаза 3 |
| Спонсор | Levomecor Inc. |
| Статус | Прекращено |
| Участники | 236 участн. |
| Вмешательство | REL-1017 |
| Дата начала | 30.03.2021 |
| Дата завершения | 31.12.2024 |
| Публикация результатов | 10.07.2026 |
Кратко
This is an outpatient, 2-arm, Phase 3, multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of REL-1017 once daily (QD) as an adjunctive treatment of Major Depressive Disorder. Study participants will continue to take their current antidepressant therapy in addition to the study drug or placebo for the duration of the treatment period.
Change From Baseline to Day 28 in MADRS Total Score
| REL-1017 | -14.81 ± 1.00 Scores on a scale (MADRS10) |
|---|---|
| Placebo | -13.9 ± 1.01 Scores on a scale (MADRS10) |
Открыть в BENITIONS Открыть на ClinicalTrials.gov
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