Clinical trial

A Phase 2 Clinical Trial of GH001 in Patients With Postpartum Depression

Name
GH001-PPD-203
Description
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.
Trial arms
Trial start
2023-03-02
Estimated PCD
2023-12-01
Trial end
2023-12-01
Status
Recruiting
Phase
Early phase I
Treatment
GH001
GH001 is administered via inhalation
Arms:
GH001 Individualized Dosing Regimen
Other names:
5-Methoxy-N,N-Dimethyltryptamine, 5-MeO-DMT, Mebufotenin
Size
15
Primary endpoint
The anti-depressive effects of GH001 evaluated by the change from baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) assessed at Day 7
From Baseline to Day 7
Eligibility criteria
Inclusion Criteria: * Is female and in the age range between 18 and 45 years (inclusive) at screening. * Has a body mass index (BMI) in the range of 18.5 and 35 kg/m2 (inclusive) at screening. * Meets the trial criteria for PPD as assessed by a trial psychiatrist or registered clinical psychologist. Exclusion Criteria: * Has one or more first or second degree relatives with a current or prior diagnosis of bipolar disorder, psychotic disorder or other mood disorder (including MDD) with psychotic features. * Current pregnancy resulting in termination, still-birth, pre-term delivery (before week complete gestational week 37), need for intensive care therapy of mother or child, or adoption of child away from patient. * Has taken prohibited medication or prohibited dietary supplements within the specified timeframe prior to dosing. * Has previously experienced a significant adverse reaction to a hallucinogenic or psychedelic drug according to the investigator's judgment. * Has a clinically significant abnormality in physical examination, vital signs, ECG, or clinical laboratory parameters which renders the patient unsuitable for the trial according to the investigator's judgment. * Patient who has a positive pregnancy test at screening or on the pretest day, is pregnant, or plans to become pregnant during the course of the trial and up to 90 days after GH001 dosing.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 15, 'type': 'ESTIMATED'}}
Updated at
2023-11-02

1 organization

1 product

1 indication

Product
GH001