GlyT-1 Inhibitor Treatment for Refractory Schizophrenia
Primary Purpose
Schizophrenia, Treatment Refractory
Status
Completed
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
GlyT-1 inhibitor-1
Placebo
Sponsored by

About this trial
This is an interventional treatment trial for Schizophrenia focused on measuring N-methyl-D-aspartate receptor, glycine transporter, schizophrenia
Eligibility Criteria
Inclusion Criteria:
- Fulfill the criteria of schizophrenia according to the Diagnostic and Statistic Manual, fourth edition (DSM-IV).
- Poor response of clozapine treatment: a 12-week treatment of clozapine without satisfactory response: a severity score of Clinical Global Impression Scale(CGI)>=4, a total score of Positive and Negative Syndrome Scale(PANSS)>= 60, and a Scale for the Assessment of Negative Symptoms(SANS)score of >=40. the doses of clozapine remain stable for at least 12 weeks prior to their enrollment in this proposed study,
- Agree to participate in the study and provide informed consent.
Exclusion Criteria:
- current substance abuse or history of substance dependence in the past 6 months
- use of depot antipsychotic in the past 6 months
- serious medical or neurological illness
- pregnancy
- inability to follow protocol.
Sites / Locations
- China Medical University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
GlyT-1 inhibitor-1
Arm Description
GlyT-1 inhibitor-1 4000 mg/day
Outcomes
Primary Outcome Measures
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
Secondary Outcome Measures
Neurocognitive Function
The neurocognitive functions will be assessed by:
Wisconsin Card Sorting Test (WCST)
Wechsler Memory Scale- logical memory
Neurocognitive function
The neurocognitive functions will be assessed by:
Wisconsin Card Sorting Test (WCST)
Wechsler Memory Scale- logical memory
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
The severity of psychiatric symptoms
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
Full Information
NCT ID
NCT01251055
First Posted
November 3, 2010
Last Updated
October 27, 2013
Sponsor
China Medical University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01251055
Brief Title
GlyT-1 Inhibitor Treatment for Refractory Schizophrenia
Official Title
GlyT-1 Inhibitor Treatment for Refractory Schizophrenia and Its Effects on NMDA Modulation
Study Type
Interventional
2. Study Status
Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
October 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
China Medical University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The etiology of schizophrenia remains unclear In recent one decade, hypofunction of N-methyl-D-aspartate (NMDA) receptor has been implicated in the pathophysiology of schizophrenia. Hence, enhancing NMDA neurotransmission was considered as a new approach for schizophrenia treatment.
To date, refractory schizophrenia (particularly clozapine-resistant) is still a difficult clinical issue. However, the effect of NMDA treatment in refractory schizophrenia is still unknown. Therefore, the primary goal of this study is to investigate the efficacy and safety of NMDA adjuvant therapy in refractory schizophrenia, and to identify the predictors for treatment response to NMDA enhancers.
Detailed Description
The etiology of schizophrenia remains unclear. In recent one decade, hypofunction of N-methyl-D-aspartate (NMDA) receptor has been implicated in the pathophysiology of schizophrenia. Hence, enhancing NMDA neurotransmission was considered as a new approach for schizophrenia treatment. To date, there have been a few pilot studies exploring the efficacy of NMDA enhancers as adjuvant therapy for schizophrenia, for instance, D-serine (an endogenous agonist of the NMDA-glycine site). They were not only well-tolerated but also synergistic in improving positive, negative and cognitive symptoms in those receiving typical and atypical antipsychotics (except clozapine).
Refractory schizophrenia (particularly clozapine-resistant) is still a difficult clinical issue at present. Previous studies revealed that add-on treatment of D-serine or other agonists of NMDA receptor failed to give significant benefits in such patients. The primary goal of this study is to investigate the efficacy and safety of glycine transporter(GlyT)-1 inhibitor adjuvant therapy in refractory schizophrenia, and to identify the predictors for treatment response to NMDA enhancers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Treatment Refractory
Keywords
N-methyl-D-aspartate receptor, glycine transporter, schizophrenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
GlyT-1 inhibitor-1
Arm Type
Experimental
Arm Description
GlyT-1 inhibitor-1 4000 mg/day
Intervention Type
Drug
Intervention Name(s)
GlyT-1 inhibitor-1
Intervention Description
GlyT-1 inhibitor-1(500) 4# BID
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
starch
Primary Outcome Measure Information:
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
Time Frame
baseline
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
Time Frame
2 weeks after the trial
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
Time Frame
4 weeks after the trial
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Positive and Negative Syndrome Scale(PANSS)
Assessment of Negative symptoms(SANS)
Global assessment of function(GAF)
Time Frame
6 weeks after the trial (The end of the trial)
Secondary Outcome Measure Information:
Title
Neurocognitive Function
Description
The neurocognitive functions will be assessed by:
Wisconsin Card Sorting Test (WCST)
Wechsler Memory Scale- logical memory
Time Frame
baseline
Title
Neurocognitive function
Description
The neurocognitive functions will be assessed by:
Wisconsin Card Sorting Test (WCST)
Wechsler Memory Scale- logical memory
Time Frame
6 weeks after the trial (The end of the trial)
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
Time Frame
baseline
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
Time Frame
2 weeks after the trial
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
Time Frame
4 weeks after the trial
Title
The severity of psychiatric symptoms
Description
The severity of psychiatric symptoms will be assessed by:
Clinical Global Impression(CGI)
Subscales of PANSS
Time Frame
6 weeks after the trial (the end of the trial)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Fulfill the criteria of schizophrenia according to the Diagnostic and Statistic Manual, fourth edition (DSM-IV).
Poor response of clozapine treatment: a 12-week treatment of clozapine without satisfactory response: a severity score of Clinical Global Impression Scale(CGI)>=4, a total score of Positive and Negative Syndrome Scale(PANSS)>= 60, and a Scale for the Assessment of Negative Symptoms(SANS)score of >=40. the doses of clozapine remain stable for at least 12 weeks prior to their enrollment in this proposed study,
Agree to participate in the study and provide informed consent.
Exclusion Criteria:
current substance abuse or history of substance dependence in the past 6 months
use of depot antipsychotic in the past 6 months
serious medical or neurological illness
pregnancy
inability to follow protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hsien-Yuan Lane, MD.PhD.
Organizational Affiliation
Department of Psychiatry, China Medical University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
ZIP/Postal Code
400
Country
Taiwan
12. IPD Sharing Statement
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GlyT-1 Inhibitor Treatment for Refractory Schizophrenia
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