Ebselen as an add-on Treatment in Hypo/Mania
Primary Purpose
Bipolar Disorder, Bipolar Disorder, Manic
Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Ebselen
Placebo oral capsule
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder
Eligibility Criteria
Inclusion Criteria:
- Participant is willing and able to give informed consent for participation in the trial.
- Male or Female, aged 18-70 years
- Diagnosed with bipolar disorder, screened using the Structured Clinical Interview for DSM-5 (SCID) to meet Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for Manic or Hypomanic Episode.
- Female participants of child bearing potential and male participants whose partner is of child bearing potential must be willing to ensure that they or their partner use effective contraception during the trial
- In the Investigator's opinion, is able and willing to comply with all trial requirements.
- Willing to allow clinical care team (including General Practitioner (GP)) to be made aware of trial participation.
- The Clinical team treating the patient are in agreement.
Exclusion Criteria:
- Female participant who is pregnant, lactating or planning pregnancy during the course of the trial.
- Known significant renal or hepatic impairment.
- Scheduled elective surgery or other procedures requiring general anaesthesia during the trial.
- Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
- Participants who have participated in another research trial involving an investigational product in the past 12 weeks.
- Clinically significant illicit substance or alcohol misuse where dependence criteria are satisfied.
- Taking lithium.
- Previous randomisation to this trial.
Sites / Locations
- Neurosciences Building, Dept. Psychiatry, Warneford Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Ebselen
Placebo
Arm Description
Three Ebselen capsules each containing 200mg taken orally twice a day for 3 weeks
Three Placebo capsules each containing 200mg taken orally twice a day for 3 weeks
Outcomes
Primary Outcome Measures
Change in Young Mania Rating Scale (YMRS)
Difference in the 11 item clinician-rated YMRS between groups.Total score 0-60.
Secondary Outcome Measures
Change in Clinical Global Impressions Bipolar (CGI-BP) mania scale
Improvement due to treatment between groups. Very much improved to very much worse.
Change in Altman Self Rating Mania Scale (ASRM)
Difference in the 5 item self-rated ASRM between groups.Total score 0-20.
Change in Hamilton Rating Scale for Depression (HAM-D)
Difference in the 17 item Clinician-rated HAM-D between groups. Total score 0-52.
Change in Quick Inventory of Depressive Symptomology-Self Rating 16 (QIDS-SR-16)
Difference in the 16 item self-rated QIDS-SR-16 between groups. Total score 0-42.
Change in Actigraphy
To compare the effect of ebselen versus placebo on motor behaviour and the sleep-wake cycle
Change in Leeds Sleep Evaluation Questionnaire (LSEQ)
Difference in the 4 self-rated sleep domains (10 visual analogue scales) between groups.
Levels of markers of inflammation in Plasma sample
To compare the effect of ebselen, versus placebo, on markers of inflammation including C-Reactive Protein and antibodies to common infectious agents such as human herpesviruses and Toxoplasma gondii
Ebselen levels in Plasma sample
To assess ebselen levels in plasma
Adverse Events reported
Self-rated Side Effects Questionnaire
Change in Concomitant medication recorded
To assess the overall use of concomitant medication during the trial period
Compliance assessment
capsule count and records checked
Full Information
NCT ID
NCT03013400
First Posted
December 9, 2016
Last Updated
September 5, 2019
Sponsor
University of Oxford
Collaborators
Stanley Medical Research Institute, Sound Pharmaceuticals, Incorporated
1. Study Identification
Unique Protocol Identification Number
NCT03013400
Brief Title
Ebselen as an add-on Treatment in Hypo/Mania
Official Title
A Randomised, Parallel Group, Double Blind, Placebo Controlled, Add on Clinical Trial to Investigate Whether the Lithium Mimetic, Ebselen, Can Reduce Symptoms of Hypomania and Mania in Bipolar Patients
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
October 1, 2017 (Actual)
Primary Completion Date
July 9, 2019 (Actual)
Study Completion Date
July 9, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oxford
Collaborators
Stanley Medical Research Institute, Sound Pharmaceuticals, Incorporated
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the effect of a 'lithium like' drug called ebselen (SP-1005) versus placebo as an 'add on' treatment to help stabilise hypo/manic symptoms in bipolar disorder. Half of the participants will receive ebselen and the other half placebo. The trial, will last a total of four weeks.
Detailed Description
Ebselen, a new drug for mania
Bipolar disorder, formerly known as manic depression, is a condition that affects mood, which can swing from one extreme to another.
Typically, there will be periods of:
Depression - very low mood and energy levels
Mania or hypomania (less severe) - very high mood and overactive energy levels
A drug called lithium, used to stabilise mood, is an important treatment for bipolar disorder but has a number of problematic side effects, is not well tolerated by patients and requires careful monitoring. To replace lithium with other, safer medicines would have clear advantages. The investigators are interested in an antioxidant medicine(substance that may prevent or delay cell damage) called ebselen which has been shown to work in a similar way as lithium and the investigators are investigating whether it might help improve recovery from manic episodes.
The present study aims to see whether ebselen, used as an 'add-on' treatment can help stabilise mood in patients experiencing high mood (hypo/mania). Sixty patients experiencing hypo/mania will be given in a randomised order (similar to tossing a coin) either ebselen or placebo (dummy) in addition to their usual medication for three weeks after which the add-on treatment will be stopped. A final follow up visit will take place one week after the study medication has been stopped. Participants can be in or outpatients and mood will be monitored with questionnaires and interviews. Activity will also be monitored with the use of an actiwatch (similar to a wrist watch) which will be worn continuously throughout the study. A single blood sample will be optional and occur after the first week of treatment to check plasma levels of ebselen and inflammatory markers. A positive outcome in this trial will be followed by longer term studies of ebselen in bipolar disorder.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Bipolar Disorder, Manic
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ebselen
Arm Type
Active Comparator
Arm Description
Three Ebselen capsules each containing 200mg taken orally twice a day for 3 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Three Placebo capsules each containing 200mg taken orally twice a day for 3 weeks
Intervention Type
Drug
Intervention Name(s)
Ebselen
Other Intervention Name(s)
SPI-1005, PZ-51, Ebselene, Ebselenum, Ebseleno, Harmokisane
Intervention Description
Ebselen is an opaque capsule containing 200 mg of ebselen is a selenium-based GPx mimic and IMPase inhibitor.
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Other Intervention Name(s)
Dummy
Intervention Description
Placebo is identical in appearance to the ebselen capsules
Primary Outcome Measure Information:
Title
Change in Young Mania Rating Scale (YMRS)
Description
Difference in the 11 item clinician-rated YMRS between groups.Total score 0-60.
Time Frame
Change between groups, every week, up to 4 weeks
Secondary Outcome Measure Information:
Title
Change in Clinical Global Impressions Bipolar (CGI-BP) mania scale
Description
Improvement due to treatment between groups. Very much improved to very much worse.
Time Frame
Change between groups, every week, up to 4 weeks
Title
Change in Altman Self Rating Mania Scale (ASRM)
Description
Difference in the 5 item self-rated ASRM between groups.Total score 0-20.
Time Frame
Change between groups, 3 x weekly, up to 4 weeks
Title
Change in Hamilton Rating Scale for Depression (HAM-D)
Description
Difference in the 17 item Clinician-rated HAM-D between groups. Total score 0-52.
Time Frame
Change between groups, every week, up to 4 weeks
Title
Change in Quick Inventory of Depressive Symptomology-Self Rating 16 (QIDS-SR-16)
Description
Difference in the 16 item self-rated QIDS-SR-16 between groups. Total score 0-42.
Time Frame
Change between groups, 3 x weekly, up to 4 weeks
Title
Change in Actigraphy
Description
To compare the effect of ebselen versus placebo on motor behaviour and the sleep-wake cycle
Time Frame
Change in activity between groups, each 24 hours, up to 4 weeks
Title
Change in Leeds Sleep Evaluation Questionnaire (LSEQ)
Description
Difference in the 4 self-rated sleep domains (10 visual analogue scales) between groups.
Time Frame
Change between groups, every week, up to 4 weeks
Title
Levels of markers of inflammation in Plasma sample
Description
To compare the effect of ebselen, versus placebo, on markers of inflammation including C-Reactive Protein and antibodies to common infectious agents such as human herpesviruses and Toxoplasma gondii
Time Frame
Once at week 1 visit
Title
Ebselen levels in Plasma sample
Description
To assess ebselen levels in plasma
Time Frame
Once at week 1 visit
Title
Adverse Events reported
Description
Self-rated Side Effects Questionnaire
Time Frame
Every week, up to 4 weeks
Title
Change in Concomitant medication recorded
Description
To assess the overall use of concomitant medication during the trial period
Time Frame
Change between groups, every week, up to 4 weeks
Title
Compliance assessment
Description
capsule count and records checked
Time Frame
Change between groups, every week, up to 3 weeks
Other Pre-specified Outcome Measures:
Title
Researcher and participant blinding questionnaire to determine treatment concealment
Description
Researcher and participant blinding questionnaire
Time Frame
Once, at week 4
Title
Participant and Researcher Randomisation Guess Visual Analogue Scale (VAS)
Description
To assess whether researchers and participants could guess the assigned randomised arm
Time Frame
Once, at week 4
Title
Public Participant Involvement (PPI) feedback questionnaire
Description
PPI questionnaire
Time Frame
Once, at week 4
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Participant is willing and able to give informed consent for participation in the trial.
Male or Female, aged 18-70 years
Diagnosed with bipolar disorder, screened using the Structured Clinical Interview for DSM-5 (SCID) to meet Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for Manic or Hypomanic Episode.
Female participants of child bearing potential and male participants whose partner is of child bearing potential must be willing to ensure that they or their partner use effective contraception during the trial
In the Investigator's opinion, is able and willing to comply with all trial requirements.
Willing to allow clinical care team (including General Practitioner (GP)) to be made aware of trial participation.
The Clinical team treating the patient are in agreement.
Exclusion Criteria:
Female participant who is pregnant, lactating or planning pregnancy during the course of the trial.
Known significant renal or hepatic impairment.
Scheduled elective surgery or other procedures requiring general anaesthesia during the trial.
Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
Participants who have participated in another research trial involving an investigational product in the past 12 weeks.
Clinically significant illicit substance or alcohol misuse where dependence criteria are satisfied.
Taking lithium.
Previous randomisation to this trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip J Cowen, MBBS, MD
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurosciences Building, Dept. Psychiatry, Warneford Hospital
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX37JX
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
27256357
Citation
Masaki C, Sharpley AL, Cooper CM, Godlewska BR, Singh N, Vasudevan SR, Harmer CJ, Churchill GC, Sharp T, Rogers RD, Cowen PJ. Effects of the potential lithium-mimetic, ebselen, on impulsivity and emotional processing. Psychopharmacology (Berl). 2016 Jul;233(14):2655-61. doi: 10.1007/s00213-016-4319-5. Epub 2016 Jun 2.
Results Reference
background
PubMed Identifier
26758281
Citation
Masaki C, Sharpley AL, Godlewska BR, Berrington A, Hashimoto T, Singh N, Vasudevan SR, Emir UE, Churchill GC, Cowen PJ. Effects of the potential lithium-mimetic, ebselen, on brain neurochemistry: a magnetic resonance spectroscopy study at 7 tesla. Psychopharmacology (Berl). 2016 Mar;233(6):1097-104. doi: 10.1007/s00213-015-4189-2. Epub 2016 Jan 12.
Results Reference
background
PubMed Identifier
26593266
Citation
Singh N, Sharpley AL, Emir UE, Masaki C, Herzallah MM, Gluck MA, Sharp T, Harmer CJ, Vasudevan SR, Cowen PJ, Churchill GC. Effect of the Putative Lithium Mimetic Ebselen on Brain Myo-Inositol, Sleep, and Emotional Processing in Humans. Neuropsychopharmacology. 2016 Jun;41(7):1768-78. doi: 10.1038/npp.2015.343. Epub 2015 Nov 23.
Results Reference
background
PubMed Identifier
23299882
Citation
Singh N, Halliday AC, Thomas JM, Kuznetsova OV, Baldwin R, Woon EC, Aley PK, Antoniadou I, Sharp T, Vasudevan SR, Churchill GC. A safe lithium mimetic for bipolar disorder. Nat Commun. 2013;4:1332. doi: 10.1038/ncomms2320.
Results Reference
background
PubMed Identifier
32909076
Citation
Sharpley AL, Williams C, Holder AA, Godlewska BR, Singh N, Shanyinde M, MacDonald O, Cowen PJ. A phase 2a randomised, double-blind, placebo-controlled, parallel-group, add-on clinical trial of ebselen (SPI-1005) as a novel treatment for mania or hypomania. Psychopharmacology (Berl). 2020 Dec;237(12):3773-3782. doi: 10.1007/s00213-020-05654-1. Epub 2020 Sep 9.
Results Reference
derived
PubMed Identifier
32483557
Citation
Garland M, Hryckowian AJ, Tholen M, Bender KO, Van Treuren WW, Loscher S, Sonnenburg JL, Bogyo M. The Clinical Drug Ebselen Attenuates Inflammation and Promotes Microbiome Recovery in Mice after Antibiotic Treatment for CDI. Cell Rep Med. 2020 Apr 21;1(1):100005. doi: 10.1016/j.xcrm.2020.100005.
Results Reference
derived
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Ebselen as an add-on Treatment in Hypo/Mania
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