This study is a multicenter, open-label, single-arm Phase 2 clinical trial. Approximately 15 female participants with clinically diagnosed postpartum depression (PPD) will be included in this study. The participants will receive an individualized dosing regimen (IDR) with at least one and up to three doses of GH001 administered within a single day.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
GH001 is administered via inhalation
Amsterdam UMC
Amsterdam, Netherlands
Clerkenwell Health
London, United Kingdom
St. Pancras Clinical Research
London, United Kingdom
Sheffield Health and Social Care NHS Foundation
Sheffield, United Kingdom
The anti-depressive effects of GH001 evaluated by the change from baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) assessed at Day 7
The MADRS is a ten-item diagnostic questionnaire used to measure the severity of depressive episodes in patients with mood disorders. A higher MADRS score indicates more severe depression, and each item is scored from 0 to 6. The overall score ranges from 0 to 60
Time frame: From Baseline to Day 7
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.