CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 158 enrolled
Drug / intervention
Mifepristone +1 moredrug
Likely dose
Mifepristone 1200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05217758
NCT05217758Phase 2Completed

RESET-medication: Glucocorticoid Receptor (GR) Blockade As Diseasemodifying Treatment for Depression with Childhood Trauma

Amsterdam UMC, location VUmc·interventional·Posted Feb 1, 2022·Updated Dec 6, 2024

In Brief

A Phase 2 clinical trial evaluating Mifepristone and Placebo for Major Depressive Disorder and Childhood Trauma. Completed, enrolled 158 participants across 1 site.

Detailed Summary

Depression is a recurrent debilitating psychiatric disorder with a lifetime prevalence of 20%. Even though antidepressants and psychotherapy are often effective, a substantial proportion of patients does not respond to currently used evidence-based treatments. The heterogeneous nature of depressive symptoms is a major obstacle for the development of novel effective treatments, and targeted treatments for depression are currently lacking. The investigators propose a targeted disease-modifying treatment for the clinically distinct form of depression related to childhood trauma (CT, emotional/ physical/sexual abuse or neglect before the age of18). CT-related depression is critically different from non-CT depression: it emerges earlier in life with more severe and recurrent symptoms and less favorable responses to treatment. With an average 25% prevalence in depression, there is a large and unmet need for therapeutic strategies to treat depression in individuals with substantial CT. The GR is the major cortisol receptor in the brain and rodent studies have shown that GR blockade at adult age can reverse the effects of early-life adversity. Therefore, GR blockade is a potential novel treatment for CT-related depression but this has never been investigated. Based on the underlying stress neurobiology, the aim is to investigate whether the biological sequelae of excessive stress due to CT can be targeted by blocking the glucocorticoid receptor (GR) using the generic drug mifepristone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNetherlands

Timeline

Phase 2CompletedFinished
20222023202420252026
First PostedFeb 1, 2022
Enrollment StartDec 9, 2021
Primary CompletionAug 9, 2024
Study CompletionNov 12, 2024
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 4.4 years ago

Interventions

Mifepristonedrug

1200 mg/day, once daily, 7 days

Placebodrug

Placebo, once daily, 7 days