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Safety and Effectiveness of D-serine in Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
D-serine
D-serine
D-serine
D-serine
Sponsored by
Nathan Kline Institute for Psychiatric Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Negative symptoms, NMDA, Glutamate, Glycine

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Structured Clinical Interview for DSM-III-R diagnosis of schizophrenia or schizoaffective disorder PANSS 3 factor negative symptom inclusion score greater than 20 prior to study entry PANSS total score between 60 and 110 Simpson-Angus Scale total score of 12 or less Calgary Depression Inventory total score of 10 and suicide score less than 2 No change in Clinical Global Impressions (CGI) Scale score prior to study entry Chlorpromazine (CPZ) equivalent of 1500 or less Willing to use an effective form of birth control throughout the study if sexually active Exclusion Criteria: High extrapyramidal symptom (EPS) levels Began, discontinued, or adjusted psychotropic medication within 2 weeks of study entry Taking investigational medication within 2 weeks of study entry Contraindication to study medication Serious or unstable medical illness Pregnant or breastfeeding Alcohol or drug abuse within 6 months of study entry Diagnosed with neurodegenerative disease or a seizure disorder History of a kidney impairment Currently taking clozapine Currently taking more than two antipsychotic medications Currently taking stimulants or cholinesterase inhibitors

Sites / Locations

  • Yale University School of Medicine
  • The Zucker Hillside Hospital
  • The Nathan S. Kline Institute for Psychiatric Research

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

D-serine 30 mg/kg

D-serine 60 mg/kg

D-serine 120 mg/kg

Arm Description

D-serine 30 mg/kg

D-serine 60 mg/kg

D-serine 120 mg/kg

Outcomes

Primary Outcome Measures

Renal Safety Measures
number of renal adverse events (serum and urinalysis)

Secondary Outcome Measures

Positive and Negative Symptoms Scale (PANSS)
Absolute Change in PANSS over four weeks (change between baseline and final measurements). The PANSS is a 30-item rating scale widely used in assessment of medication effects in schizophrenia. The PANSS ranges from 30-210, with lower scores showing less symptoms. Larger change is better.
Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Battery
Change over 4 weeks. The MATRICS is a scale measuring cognition, and reported as T-score, with 50 as the population average and every 10 points representing a change of 1 standard deviation from the population average. Higher scores represent an improvement

Full Information

First Posted
May 2, 2006
Last Updated
September 11, 2020
Sponsor
Nathan Kline Institute for Psychiatric Research
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00322023
Brief Title
Safety and Effectiveness of D-serine in Schizophrenia
Official Title
PK/PD Study of Escalating Dose D-serine as Adjunctive Treatment in Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nathan Kline Institute for Psychiatric Research
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will determine whether increasing D-serine within the body will improve negative symptoms and cognitive impairments in people with schizophrenia.
Detailed Description
Schizophrenia is a life-long brain disorder affecting approximately 1 percent of Americans each year. Schizophrenia can be extremely disabling, causing people to hear voices, experience paranoia or hallucinations, believe that others are controlling their thoughts, and even fail at maintaining a job or caring for themselves. Current medications help to relieve most of these symptoms, but not all. Some people with schizophrenia still suffer from negative symptoms, such as difficulty with talking, expressing emotions, and motivation; they may also suffer from cognitive impairments, such as decreased concentration and memory loss. D-serine, an amino acid found within the body, activates brain cell receptors that appear to play a role in learning and memory. This study will determine whether adding a D-serine solution to a stable antipsychotic medication regimen will decrease negative symptoms in people with schizophrenia. Participants in this open-label study will remain on their regular medication regimen for at least 2 weeks. During this time and before starting treatment, participants will be interviewed about their emotional problems, marital status, education, family background, employment history, and any drug or alcohol problems. Participants will also undergo a physical exam, an electrocardiogram (EKG), vital sign measurements, psychological tests, cognitive tasks, and an electroencephalogram (EEG). Participants will then begin 4 weeks of treatment with D-serine. In addition to participants' regular medication regimen, they will drink a D-serine powder mixed with water twice daily. Every 2 weeks, participants will undergo a physical exam and an interview about any changes in symptoms or emotional problems that they may be experiencing. Blood and urine samples will be taken throughout the study. After 4 weeks, participants will undergo an EKG, EEG, and the same psychological tests and cognitive tasks completed prior to treatment. A follow-up visit will occur 2 weeks post-treatment to monitor any changes in negative symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Negative symptoms, NMDA, Glutamate, Glycine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
D-serine 30 mg/kg
Arm Type
Experimental
Arm Description
D-serine 30 mg/kg
Arm Title
D-serine 60 mg/kg
Arm Type
Experimental
Arm Description
D-serine 60 mg/kg
Arm Title
D-serine 120 mg/kg
Arm Type
Experimental
Arm Description
D-serine 120 mg/kg
Intervention Type
Drug
Intervention Name(s)
D-serine
Intervention Description
D-serine at following dose levels: 30 mg/kg, 60 mg/kg, and 120 mg/kg. PK/PD studies done at day 1. Medication will be administered as powder dissolved in liquid given in two divided doses daily for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
D-serine
Intervention Type
Drug
Intervention Name(s)
D-serine
Intervention Type
Drug
Intervention Name(s)
D-serine
Primary Outcome Measure Information:
Title
Renal Safety Measures
Description
number of renal adverse events (serum and urinalysis)
Time Frame
Measured at Week 4
Secondary Outcome Measure Information:
Title
Positive and Negative Symptoms Scale (PANSS)
Description
Absolute Change in PANSS over four weeks (change between baseline and final measurements). The PANSS is a 30-item rating scale widely used in assessment of medication effects in schizophrenia. The PANSS ranges from 30-210, with lower scores showing less symptoms. Larger change is better.
Time Frame
Measured at Week 4
Title
Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Battery
Description
Change over 4 weeks. The MATRICS is a scale measuring cognition, and reported as T-score, with 50 as the population average and every 10 points representing a change of 1 standard deviation from the population average. Higher scores represent an improvement
Time Frame
Measured at Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Structured Clinical Interview for DSM-III-R diagnosis of schizophrenia or schizoaffective disorder PANSS 3 factor negative symptom inclusion score greater than 20 prior to study entry PANSS total score between 60 and 110 Simpson-Angus Scale total score of 12 or less Calgary Depression Inventory total score of 10 and suicide score less than 2 No change in Clinical Global Impressions (CGI) Scale score prior to study entry Chlorpromazine (CPZ) equivalent of 1500 or less Willing to use an effective form of birth control throughout the study if sexually active Exclusion Criteria: High extrapyramidal symptom (EPS) levels Began, discontinued, or adjusted psychotropic medication within 2 weeks of study entry Taking investigational medication within 2 weeks of study entry Contraindication to study medication Serious or unstable medical illness Pregnant or breastfeeding Alcohol or drug abuse within 6 months of study entry Diagnosed with neurodegenerative disease or a seizure disorder History of a kidney impairment Currently taking clozapine Currently taking more than two antipsychotic medications Currently taking stimulants or cholinesterase inhibitors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel C. Javitt, MD, PhD
Organizational Affiliation
Nathan Kline Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale University School of Medicine
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06512
Country
United States
Facility Name
The Zucker Hillside Hospital
City
Glen Oaks
State/Province
New York
ZIP/Postal Code
11004
Country
United States
Facility Name
The Nathan S. Kline Institute for Psychiatric Research
City
Orangeburg
State/Province
New York
ZIP/Postal Code
10962
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
28318835
Citation
Kantrowitz JT, Epstein ML, Lee M, Lehrfeld N, Nolan KA, Shope C, Petkova E, Silipo G, Javitt DC. Improvement in mismatch negativity generation during d-serine treatment in schizophrenia: Correlation with symptoms. Schizophr Res. 2018 Jan;191:70-79. doi: 10.1016/j.schres.2017.02.027. Epub 2017 Mar 18.
Results Reference
derived

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Safety and Effectiveness of D-serine in Schizophrenia

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