Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Social Function
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | -2.43 |
| Placebo | -3.06 |
Trial · Interventional
CompletedPhase 2Results postedRegistry dataShort name OXY-R
United States, Canada
1 trial · 1 completed · 1 with posted results
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
We are studying an investigational drug called intranasal oxytocin (Syntocinon®). Syntocinon® has been approved by the U.S. Food and Drug Administration for use in helping women breastfeed, but it has not been approved for use in children with ASD. However, there is previous research conducted that has indicated that after administration of oxytocin, adults with ASD demonstrated improvements in social cognition, and reduced repetitive behaviours and anxiety. There is also early research to suggest that children may also benefit in these areas. The purpose of this study is to test if oxytocin works to help children and adolescents with ASD.
Experimental
Intranasal Oxytocin (Syntocinon)
The proposed dosing schedule is 0.4 IU/kg, taken twice daily, for a maximum of 24 IUs per dose
Placebo comparator
Placebo
The proposed dosing schedule is 0.4 IU/kg, taken twice daily, for a maximum of 24 IUs per dose
Outcomes the sponsor listed as primary.
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Social Function
Time frame · 12 and 24 weeks
This will be measured by a change in score on the Aberrant Behavior Checklist (ABC) - Social Withdrawal Subscale (0-48, where lower scores indicate improvement)
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Social Cognition
Time frame · 12 Weeks
This will be measured by a change in score the Revised Eyes Test (0- 28; where higher scores indicate better performance/improvement) Baseline to Week 12
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Social Cognition
Time frame · 12 Weeks
This will be measured by improvement on the Let's Face it! Skills Battery from Baseline to Week 12 Social Cognition (higher score=better outcome) a. Let's Face It Skills Battery; i. Matchmaker (0-100); ii. Faces (0-100); iii. Houses (0-100)
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Social Function
Time frame · 12 Weeks
This will be measured by improvement on the Behavioral Assessment System for Children (BASC-2) from Baseline to Week 12 Behavioral Assessment System for Children (higher score=positive response); i. \*Social Skills: age 6 to 11 (18-69); age 12 to 17 (21-70); ii. Functional Communication: age 6 to 11 (10-66); age 12 to 17 (10-64); iii. Withdrawal age 6-11 (21- 62) ; age 12-17 (14-42) \* only social subscales of BASC-2 reported
Number of Participant Considered Social Responders
Time frame · 12 Weeks
This will be measured by the Clinical Global Impressions - Improvement Scale - Social (CGI-I-Social) a) Clinical Global Impressions - Social Scale (1-7) (lower score=positive response). The results will be reported as the number of participants that were classified as a social responder (achieving a score of 1 or 2 on the scale).
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Repetitive Behaviors
Time frame · 12 Weeks
This will be measured by improvement on the Child Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) from Baseline to Week 12 -lower score= positive response (0-20)
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Repetitive Behaviors
Time frame · 12 Weeks
This will be measured by improvement on the Repetitive Behavior Scale (RBS-R)(0-129; where lower score= positive response) from Baseline to Week 12
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Anxiety
Time frame · 12 Weeks
This will be measured by the Child and Adolescent Symptom Inventory (CASI-4R) Generalized anxiety score (male (40-101); female (41-96) -where lower score= positive response) from Baseline to Week 12
Efficacy of Intranasal Oxytocin vs. Placebo on Measures of Quality of Life
Time frame · 12 Weeks
This will be measured by improvement on the Pediatric Quality of Life Inventory (PedsQL) (0-100, where higher scores indicate positive response) from Baseline to Week 12
Number of Participant Considered Overall Responders
Time frame · 12 Weeks
This will be measured by the Clinical Global Impressions - Improvement Scale - Global (CGI-I-Global) (1-7) (lower score=positive response). The results will be reported as the number of participants that were classified as an overall responder (achieving a score of 1 or 2 on the scale).
Safety and Tolerability of Intranasal Oxytocin in Children and Adolescents With ASD
Time frame · 12 Weeks
This will be measured by the Safety Monitoring Uniform Report Form (SMURF)
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | -2.43 |
| Placebo | -3.06 |
| Group | Value (score on a scale) |
|---|---|
| Intranasal Oxytocin | 0.14 |
| Placebo | -0.29 |
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | 4.50 |
| Placebo | 5.90 |
| Group | Value (score on a scale) |
|---|---|
| Intranasal Oxytocin | 1.40 |
| Placebo | 0.43 |
| Group | Value (Participants) |
|---|---|
| Intranasal Oxytocin | 6 |
| Placebo | 10 |
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | -2.77 |
| Placebo | -2.99 |
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | -6.74 |
| Placebo | -4.62 |
| Group | Value (units on a scale) |
|---|---|
| Intranasal Oxytocin | -4.45 |
| Placebo | -2.30 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| Intranasal Oxytocin (Syntocinon)The proposed dosing schedule is 0.4 IU/kg, taken twice daily, for a maximum of 24 IUs per dose Intranasal Oxytocin | 0 / 30 | 0 / 30 | 28 / 30 |
| PlaceboThe proposed dosing schedule is 0.4 IU/kg, taken twice daily, for a maximum of 24 IUs per dose Placebo | 0 / 30 | 0 / 30 | 25 / 30 |
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