Last updated: July 4, 2023
Sponsor: University of Oxford
Overall Status: Active - Recruiting
Phase
1
Condition
Depression
Treatment
Ebselen
Placebo
Clinical Study ID
NCT05117710
276211
20/SC/0151
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Willing and able to give informed consent for participation in the study;
- Sufficiently fluent English to understand and complete the tasks;
- Registered with a General Practitioner (GP) and consents to GP being informed ofparticipation in the study;
- Participants need to meet a number of concurrent clinical criteria:
- Current criteria for Major Depressive Disorder as determined by the StructuredClinical Interview for Diagnostic and Statistical Manual-5 (SCID-5);
- Inadequate response to at least one adequate course of antidepressant therapy given ata therapeutic dose for at least four weeks in the current episode of depression.
- Minimum score on the 17-item Hamilton Depression Rating Scale (HAM-D) of at least 14;
- Currently taking a licensed antidepressant at a therapeutic dose for at least fourweeks
- Pre-menopausal women and male participants engaging in sex with a risk of pregnancymust agree to use a highly effective method of contraception from Screening Visituntil 30 days after receiving the study medication treatment. Acceptable methods ofcontraception include:
- Combined (estrogen- and progestogen-containing) hormonal contraception associatedwith inhibition of ovulation: oral, intravaginal or transdermal;
- Progestogen-only hormonal contraception associated with inhibition of ovulation:oral, injectable or implantable;
- Intrauterine device (IUD);
- Intrauterine hormone-releasing system (IUS);
- Bilateral tubal occlusion;
- Vasectomy (or vasectomised partner);
- Sexual abstinence. [Periodic abstinence (calendar, symptothermal, post-ovulationmethods), withdrawal (coitus interruptus), and spermicides only are notacceptable methods of contraception.]
- Male participants must not donate sperm.
- Participants taking non-prescription/prescription medication may still be entered intothe study, if, in the opinion of the Investigator, the medication received will notinterfere with the study procedures or compromise safety
- Willing to refrain from drinking alcohol for the duration of the study
Exclusion
Exclusion Criteria:
- History of /or current DSM-5 bipolar disorder, schizophrenia or emotionally unstablepersonality disorder;
- Participants who fulfil current criteria for other comorbid disorders may still beentered into the study, if, in the opinion of the Investigator, the psychiatricdiagnosis will not compromise safety or affect data quality;
- Participants who have failed to respond to standard pharmacological augmentationtreatments for depression (lithium and atypical antipsychotic drugs);
- Clinically significant risk of suicide;
- Participants undergoing or who have undergone electroconvulsive therapy for thetreatment of the current episode of depression;
- History of significant alcohol/substance misuse or dependence over the past 6 months;
- History of, or current general medical conditions that in the opinion of theInvestigator may interfere with the safety of the participant or the scientificintegrity of the study;
- Current pregnancy (as determined by urine pregnancy test taken during the ScreeningVisit and the Research Visit One), breastfeeding, or planning a pregnancy during thecourse of the study;
- Participants with Body Mass Index (BMI - kg/m2) outside the 18-36 range at ScreeningVisit;
- Participants with severe claustrophobia;
- Participants who are contraindicated for MRI;
- Previous participation in a study using the same, or similar, emotional processingtasks in the last three months;
- Previous participation in a study involving the use of an interventional medicationwithin the last three months;
- Participant with planned medical treatment within the study period that mightinterfere with the study procedures;
- Participant who is unlikely to comply with the clinical study protocol or isunsuitable for any other reason, in the opinion of the Investigator.
Study Design
Total Participants: 50
Treatment Group(s): 2
Primary Treatment: Ebselen
Phase: 1
Study Start date:
April 22, 2021
Estimated Completion Date:
May 31, 2024
Study Description
Connect with a study center
Neurosciences Building, Dept. Psychiatry, Warneford Hospital
Oxford, Oxfordshire OX37JX
United KingdomActive - Recruiting
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