Phase 2
N=58
Oxytocin or Galantamine Versus Placebo for the Treatment of Negative Symptoms and Cognitive Impairments in Schizophrenia
Schizophrenia
Bottom Line
View on ClinicalTrials.gov: NCT01012167 ↗Enrolled (actual)
58
Serious AEs
1.7%
Results posted
Jun 2017
Primary outcome: Primary: Scale for the Assessment of Negative Symptoms (SANS) Total Score — 33.23; 36.63; 36.63; 30.07 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Oxytocin (Drug); Galantamine (Drug); Placebo-Oxytocin (Other); Placebo-Galantamine (Other)
- Age
- Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Maryland, Baltimore
- Primary completion
- Jul 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Scale for the Assessment of Negative Symptoms (SANS) Total Score |
33.23; 36.63; 36.63; 30.07; 35.22; 35.05 | — |
| PRIMARY Mean Z-Scores for Composite Cognitive Primary Outcome* by Treatment Group and Week |
0.23; -0.22; 0.21; 0.33; -0.05; 0.18 | — |
| SECONDARY Scale for the Assessment of Negative Symptoms (SANS) - Avolition |
2.94; 2.91; 2.44; 2.78; 2.73; 2.43 | — |
| SECONDARY Scale for the Assessment of Negative Symptoms (SANS) - Anhedonia |
2.42; 2.60; 2.66; 2.42; 2.59; 2.58 | — |
| SECONDARY Scale for the Assessment of Negative Symptoms (SANS) - Alogia |
0.60; 0.95; 0.99; 0.44; 0.89; 0.89 | — |
| SECONDARY Scale for the Assessment of Negative Symptoms (SANS) - Blunted Affect |
1.67; 1.96; 2.21; 1.32; 1.89; 2.05 | — |
| SECONDARY Brief Psychiatric Rating Scale (BPRS) - Total Score |
34.16; 30.35; 32.65; 34.00; 28.95; 31.75 | — |
| SECONDARY Brief Psychiatric Rating Scale (BPRS) - Psychosis Score |
9.34; 7.30; 8.18; 9.40; 7.21; 7.90 | — |
| SECONDARY Calgary Depression Scale (CDS) - Total Score |
2.37; 0.84; 1.59; 2.20; 1.05; 1.00 | — |
| SECONDARY Arizona Sexual Experience Questionnaire (ASEX) Female |
10.5; 21.2; 29.0; 13.5; 19.2; 30.0 | — |
| SECONDARY Arizona Sexual Experience Questionnaire (ASEX) Male |
16.5; 18.1; 20.8; 17.1; 20.2; 21.7 | — |
| SECONDARY Vital Signs - Diastolic Blood Pressure |
78.8; 76.6; 78.3; 78.4; 76.2; 75.5 | — |
| SECONDARY Vital Signs - Systolic Blood Pressure |
128.4; 123.4; 132.3; 126.1; 123.9; 127.4 | — |
| SECONDARY Vital Signs - Weight |
96.5; 96.2; 96.4; 97.8; 97.5; 97.9 | — |
| SECONDARY Vital Signs - Pulse |
81.2; 86.0; 85.2; 86.2; 91.6; 89.3 | — |
| SECONDARY Simpson-Angus Scale (SAS) |
80; 63.16; 78.95; 16.67; 10.53; 10.53 | — |
| SECONDARY Abnormal Involuntary Movement Scale (AIMS) |
86.67; 77.78; 76.47; 6.67; 16.67; 17.65 | — |
| SECONDARY Electrocardiogram (EKG) |
416.5; 419.0; 422.6; 415.7; 408.1; 423.8 | — |
| SECONDARY Barnes Akathisia Scale (BAS) - Global Score |
93.33; 100; 94.12; 6.67; 0; 5.88 | — |
| SECONDARY Blood Oxytocin Levels |
18.22; 13.76; 14.69; 17.22; 10.11; 13.21 | — |
| SECONDARY Laboratory Measures - ALT/SGPT |
22.87; 31.26; 27.40; 20.67; 28.90; 27.74 | — |
| SECONDARY Laboratory Measures - AST/SGOT |
19.87; 22.68; 22.50; 20.27; 21.45; 23.58 | — |
| SECONDARY Laboratory Measures - Alkaline Phosphatase |
83.47; 83.42; 86.40; 78.73; 82.50; 88.95 | — |
| SECONDARY Laboratory Measures - Calcium |
9.53; 9.36; 9.58; 9.57; 9.23; 9.54 | — |
| SECONDARY Laboratory Measures - Sodium |
138.53; 139.53; 137.30; 138.53; 139.15; 137.47 | — |
| SECONDARY Laboratory Measures - Potassium |
4.20; 4.14; 4.17; 4.07; 4.01; 4.16 | — |
| SECONDARY Laboratory Measures - Chloride |
100.60; 102.79; 100.15; 101.53; 102.90; 100.47 | — |
| SECONDARY Laboratory Measures - CO2 |
23.47; 22.42; 23.40; 23.27; 22.50; 22.83 | — |
| SECONDARY Laboratory Measures - Cholesterol |
159.18; 166.07; 179.60; 156.93; 162.93; 177.33 | — |
| SECONDARY Laboratory Measures - HDL |
44.09; 45.50; 41.14; 44.31; 43.64; 41.42 | — |
| SECONDARY Laboratory Measures - LDL |
90.36; 91.25; 105.79; 85.92; 92.29; 103.73 | — |
| SECONDARY Laboratory Measures - Triglycerides |
124.55; 155.20; 163.47; 124.79; 142.29; 162.17 | — |
| SECONDARY Laboratory Measures - VLDL |
24.73; 22.00; 33.17; 26.75; 23.62; 28.00 | — |
| SECONDARY Laboratory Measures - Glucose |
108.07; 98.61; 103.00; 99.67; 102.13; 112.31 | — |
| SECONDARY Laboratory Measures - Albumin |
4.39; 4.27; 4.35; 4.38; 4.23; 4.37 | — |
| SECONDARY Laboratory Measures - Globulin |
2.72; 2.81; 2.82; 2.58; 2.66; 2.78 | — |
| SECONDARY Laboratory Measures - A/G Ratio |
1.65; 1.58; 1.57; 1.71; 1.62; 1.60 | — |
| SECONDARY Laboratory Measures - Bilirubin |
0.45; 0.35; 0.40; 0.49; 0.39; 0.38 | — |
| SECONDARY Laboratory Measures - Protein |
7.10; 7.07; 7.17; 7.14; 6.92; 7.15 | — |
| SECONDARY Laboratory Measures - BUN |
12.80; 10.74; 11.95; 12.73; 11.55; 12.00 | — |
| SECONDARY Side Effect Checklist (SEC) - Abdominal Pain |
12.5; 5.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Anorexia |
18.8; 10.0; 15.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Bruising Easily |
0.0; 10.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Constipation |
0.0; 0.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Diarrhea |
18.8; 30.0; 5.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Dizziness |
18.8; 30.0; 5.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Dry Eye |
6.7; 0.0; 5.9 | — |
| SECONDARY Side Effect Checklist (SEC) - Dry Mouth |
18.8; 5.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Enuresis |
25.0; 5.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Excessive Tearing of the Eye |
6.7; 5.6; 5.9 | — |
| SECONDARY Side Effect Checklist (SEC) - Fever |
0.0; 5.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Headache |
12.5; 25.0; 15.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Hyperhydrosis |
0.0; 0.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Hypersalivation |
18.8; 15.0; 25.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Insomnia |
18.8; 10.0; 5.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Malaise |
18.8; 0.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Mucosal Ulceration |
6.3; 5.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Nasal Irritation |
33.3; 16.7; 23.5 | — |
| SECONDARY Side Effect Checklist (SEC) - Nausea |
18.8; 15.0; 5.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Rash |
12.5; 10.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Restlessness |
18.8; 10.0; 15.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Sedation |
12.5; 15.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Sore Throat |
6.3; 10.0; 5.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Stiffness |
6.3; 10.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Tinnitus |
0.0; 0.0; 10.5 | — |
| SECONDARY Side Effect Checklist (SEC) - Tremor |
6.3; 15.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Urticaria |
18.8; 15.0; 15.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Uterine Contractions |
0.0; 0.0; 0.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Vomiting |
12.5; 5.0; 10.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Weight Loss |
18.8; 5.0; 25.0 | — |
| SECONDARY Side Effect Checklist (SEC) - Wheezing |
13.3; 5.6; 11.8 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Composite Score |
25.9; 24.5; 28.2; 28.2; 26.2; 28.9 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Attention Vigilance |
36.9; 33.5; 37.2; 39.5; 34.5; 35.1 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Processing Speed |
33.5; 31.9; 34.0; 34.2; 35.4; 35.6 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Reasoning/Problem Solving |
39.7; 39.3; 41.4; 40.7; 42.9; 41.7 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Social Cognition |
31.7; 32.8; 30.4; 32.5; 29.6; 32.8 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Verbal Learning |
36.3; 33.4; 36.5; 38.7; 35.8; 36.4 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Visual Learning |
33.8; 37.2; 35.1; 36.2; 33.7; 34.2 | — |
| SECONDARY Neurocognitive Assessment Battery (MCCB) - Working Memory |
34.7; 33.7; 35.3; 34.8; 34.7; 38.1 | — |
| SECONDARY Positive and Negative Affect Schedule (PANAS) - Negative |
20.5; 18.2; 20.2; 18.8; 18.0; 18.9 | — |
| SECONDARY Positive and Negative Affect Schedule (PANAS) - Positive |
38.1; 37.0; 42.5; 38.5; 39.5; 40.8 | — |
| SECONDARY Reactions to Partner |
13.7; 14.4; 12.5; 13.7; 13.9; 12.5 | — |
| SECONDARY Willingness to Interact |
23.67; 23.18; 24.41; 24.47; 24.24; 25.00 | — |
Summary
The project is designed to address the following two primary aims:
1. To determine whether adjunctive oxytocin is superior to placebo for the treatment of persistent negative symptoms, as measured by the SANS total score, in people with schizophrenia.
2. To determine whether adjunctive Galantamine is superior to placebo for the treatment of cognitive impairments, as measured by improvement on a composite neurocognitive score in people with schizophrenia.
The investigators will also address the following secondary aims:
1. To determine whether people with schizophrenia treated with adjunctive oxytocin, compared to placebo, will show greater improvement on markers of negative symptom liability including: social affiliation, facial affect recognition, olfactory discrimination, initiation of smooth pursuit and latency of internally-driven saccades.
2. To determine whether people with schizophrenia treated with adjunctive Galantamine, compared to placebo, will show greater improvement on markers of cognitive impairment liability including: predictive pursuit, P50 sensory gating and visual-spatial working memory.
The investigators will address the following exploratory aims:
1. To determine whether changes in markers of negative symptom liability are correlated with changes in SANS total score.
2. To determine whether changes in markers of cognitive impairment liability are correlated with changes in the composite neurocognitive score.
3. To determine the response to oxytocin of all cognition domains assessed by the MATRICS battery, and to determine the response to Galantamine of all cognition domains assessed by the MATRICS, which are not included in the primary neurocognitive outcome score.
4. To determine whether there is a differential response of oxytocin and Galantamine on the SANS total score, composite neurocognitive score, and with the phenotypic measures of negative symptom and cognitive impairment liability.
5. To determine whether oxytocin and Galantamine are associated with:
* adverse effects on positive or depressive symptoms;
* adverse effects on motor symptoms;
* adverse effects on laboratory and EKG measures;
* increased occurrence of side effects;
* social interest that is independent of sexual desire.
Eligibility Criteria
Inclusion Criteria
- Any race
- Subjects will meet DSM-IV criteria for schizophrenia or schizoaffective disorder
- Judged clinically stable and will not exceed threshold levels of positive, depressive, and/or extrapyramidal symptoms
- The minimum level of negative symptoms will be defined as follows:
- Scale for the Assessment of Negative Symptoms (SANS) total score (minus the global items, and inappropriate affect, poverty of content of speech and attentional items) 20 or greater; OR
- SANS alogia global item score 3 or greater
- The maximum level of psychotic, depressive, and extrapyramidal symptoms at the beginning and end of leading in:
- Brief Psychiatric Rating Scale (BPRS) psychotic factor score (4-items) less or equal to 16
- BPRS Anxiety/Depression factor score (4-items) less than or equal to 14
- Simpson-Angus-Scale (SAS) total score (13-items) less than or equal to 10
- Subjects will be required to be on the same antipsychotic(s) for two months and on the same dose for the last month
Exclusion Criteria
- Participants with an organic brain disorder; mental retardation; or a medical condition, whose pathology or treatment could alter the presentation or treatment of schizophrenia or significantly increase the risk associated with the proposed treatment protocol
- Participants with intermittent alcohol or substance use will not be excluded unless they have met DSM-IV criteria for alcohol or substance abuse (other than nicotine) within the last month.
- Participants may be treated with one or more antipsychotics, except chlorpromazine, thioridazine, or mesoridazine. These latter antipsychotics are excluded because of the concern that their anticholinergic properties may interfere with the accurate assessment of galantamine efficacy.
- Participants may not be treated with anticholinergic medications or have clinically significant extrapyramidal symptoms. Additionally, subjects treated with glycopyrrolate will be accepted.
- Female participants may not be pregnant
- Female subjects may not be taking olanzapine at doses higher than 30 mg . Male subjects may not be taking olanzapine at doses higher than 40 mg.
Data sourced from ClinicalTrials.gov (NCT01012167). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.