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Safety and Effectiveness of D-serine in Schizophrenia

PK/PD Study of Escalating Dose D-serine as Adjunctive Treatment in Schizophrenia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00322023
Enrollment
55
Registered
2006-05-04
Start date
2006-03-31
Completion date
2009-01-31
Last updated
2020-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia

Keywords

Negative symptoms, NMDA, Glutamate, Glycine

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.

Interventions

DRUGD-serine

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.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Nathan Kline Institute for Psychiatric Research
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Renal Safety MeasuresMeasured at Week 4number of renal adverse events (serum and urinalysis)

Secondary

MeasureTime frameDescription
Positive and Negative Symptoms Scale (PANSS)Measured at Week 4Absolute 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) BatteryMeasured at Week 4Change 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

Countries

United States

Participant flow

Recruitment details

Nathan Kline Institute, Yale University, Zucker Hillside

Participants by arm

ArmCount
D-serine 30 mg/kg12
D-serine 60 mg/kg21
D Serine 120 mg/kg22
Total55

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall Studyvarious026

Baseline characteristics

CharacteristicD-serine 30 mg/kgD-serine 60 mg/kgD Serine 120 mg/kgTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
12 Participants21 Participants22 Participants55 Participants
Age, Continuous41.7 years
STANDARD_DEVIATION 11.4
43.9 years
STANDARD_DEVIATION 9.4
43.2 years
STANDARD_DEVIATION 9.6
43 years
STANDARD_DEVIATION 10
Sex: Female, Male
Female
3 Participants4 Participants4 Participants11 Participants
Sex: Female, Male
Male
9 Participants17 Participants18 Participants44 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —
other
Total, other adverse events
0 / 120 / 192 / 16
serious
Total, serious adverse events
0 / 120 / 191 / 16

Outcome results

Primary

Renal Safety Measures

number of renal adverse events (serum and urinalysis)

Time frame: Measured at Week 4

Population: study completers

ArmMeasureValue (NUMBER)
D-serine 30 mg/kgRenal Safety Measures0 adverse events
D-serine 60 mg/kgRenal Safety Measures0 adverse events
D Serine 120 mg/kgRenal Safety Measures1 adverse events
Secondary

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

Time frame: Measured at Week 4

Population: study completers

ArmMeasureValue (MEAN)Dispersion
D-serine 30 mg/kgMeasurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Battery0.8 units on a scaleStandard Deviation 3
D-serine 60 mg/kgMeasurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Battery3.9 units on a scaleStandard Deviation 3.5
D Serine 120 mg/kgMeasurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Battery2.8 units on a scaleStandard Deviation 2.8
p-value: 0.39t-test, 2 sided
p-value: <0.001t-test, 2 sided
p-value: 0.01t-test, 2 sided
Secondary

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.

Time frame: Measured at Week 4

Population: Study completers

ArmMeasureValue (MEAN)Dispersion
D-serine 30 mg/kgPositive and Negative Symptoms Scale (PANSS)5.1 units on a scaleStandard Deviation 5.3
D-serine 60 mg/kgPositive and Negative Symptoms Scale (PANSS)4.4 units on a scaleStandard Deviation 8.9
D Serine 120 mg/kgPositive and Negative Symptoms Scale (PANSS)6.3 units on a scaleStandard Deviation 5.5
p-value: <0.0001t-test, 2 sided
p-value: <0.05t-test, 2 sided
p-value: <0.01t-test, 2 sided

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026