Exploratory Study to Evaluate the Effect of SYN111 (Rufinamide) in Patients With Generalized Anxiety Disorder (GAD)
Primary Purpose
Generalized Anxiety Disorder
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
SYN111
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Generalized Anxiety Disorder focused on measuring GAD
Eligibility Criteria
Inclusion Criteria:
- Outpatient 18-65
- Meet Diagnostic and Statistical Manual,(DSM) IV criteria for GAD
- Have moderate to severe anxiety
- Sign IRB (Institutional Review Board) approved consent and can comply with visits and procedures
- Women of childbearing potential must use acceptable method of contraception
Exclusion Criteria:
- Have diagnosis of adjustment disorder or anxiety disorder Not otherwise specified (NOS)
- Have diagnosis of specific phobia
- Have diagnosis of antisocial personality disorder or other Axis II Disorder
- Have diagnosis of substance abuse disorder within 3 months of study entry
- Have diagnosis of major depressive disorder or panic disorder within 6 months of study entry
- Have diagnosis of PTSD, eating disorder substance dependence disorder within 12 months of study entry
- Have diagnosis anytime during lifetime of schizophrenia or other psychotic disorder, bipolar mood disorder, Obsessive-Compulsive Disorder (OCD), psychosurgery
- Require medication to treat GAD other than study medication
- Failed to show improvement with past treatment for GAD
- Excessively consume caffeine
- Are receiving treatment with prohibited medications
- Uncontrolled thyroid condition
- Positive urine drug screen
- Obese
- Clinically significant ECG finding
- Participating in other clinical trial
- Clinically significant out of range lab value
- Past exposure to rufinamide
- Pregnant or nursing females
Sites / Locations
- Carmen Research
- Midwest Clinical Research Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
SYN111
Placebo
Arm Description
500 mg 1 week, followed by 1000 mg for 7 weeks
0 mg tablets
Outcomes
Primary Outcome Measures
Change From Baseline in Hamilton Anxiety Scale (HAMA) - Total Score: Summary Statistics - Observed
The Hamilton Anxiety Scale is a 14-item test measuring the severity of anxiety symptoms. It provides measures of overall anxiety, psychic anxiety (mental agitation and psychological distress), and somatic anxiety (physical complaints related to anxiety). The interviewer then rated the individuals on a 5-point scale for each of the 14 items. Seven of the items specifically address psychic anxiety and the remaining 7 items address somatic anxiety. The total anxiety score ranges from 0 to 56. The 7 psychic anxiety items elicit a psychic anxiety score that ranges from 0 to 28. The remaining 7 items yield a somatic anxiety score that also ranges from 0 to 28. A score of 17 or less indicates mild anxiety severity. A score from 18 to 24 indicates mild to moderate anxiety severity, a score of 25 to 30 indicates a moderate to severe anxiety and lastly a score of 31-56 is very severe. HAM-A total score is the sum of items 1 - 14.
Change From Baseline in Hospital Anxiety and Depression Scale (HADS). Summary Statistics
The Hospital Anxiety and Depression Scale is a self screening questionnaire for depression and anxiety. It consists of 14 questions, seven for anxiety and seven for depression. The 14 statements are relevant to either generalized anxiety (7 statements) or 'depression' (again 7). Each question has 4 possible responses. Responses are scored on a scale from 3 to 0. The maximum score is therefore 21 for depression and 21 for anxiety. A score of 11 or higher indicates the probable presence of the mood disorder with a score of 8 to 10 being just suggestive of the presence of the respective state. The 2 subscales, anxiety and depression, have been found to be independent measures. In its current form the HADS is now divided into 4 ranges: normal (0-7), mild (8-10), moderate (11-15) and severe (16-21). Anxiety score = sum of items 1, 3, 5, 7, 9, 11, and 13. Depression score = sum of items 2, 4, 6, 8, 10, 12, and 14.
Change From Baseline in Montgomery-Asberg Depression Scale (MADRS) Summary Statistics.
The MADRS (Montgomery and Asberg 1979) is a clinician-rated instrument that measures the presence and severity of depression. This instrument consists of 10 items. Each item is rated on a defined step scale of 0 to 6 with anchors at 2-point intervals. The MADRS total score is the sum of the 10 items and ranges from 0 to 60. A high numeric rating shows a greater degree of symptom severity.
Change From Baseline in Clinical Global Impression Scale for Severity of Illness: (CGI-S)
Severity of illness is the first scale in the CGI. A rating is filled in by the investigator at the start of treatment based on a 0-7 point weighted scale. It goes from not assessed (0), to among the most extremely ill patients (7).
Change From Baseline Raskin Depression Scale.
It explores the extent to which an individual demonstrates depression on three sub-scales (rated 1-5): verbal self-report, behavior and secondary symptoms of depression. Scores range from 3-15, with higher scores indicating greater severity.
Change From Baseline in Covi Anxiety Scale (CAS) - Index Total Score: Summary Statistics Observed
The Covi Anxiety Scale is a simple 3 item scale for the assessment of severity of anxiety symptoms. The scale measures 3 dimensions: verbal report, behavior and somatic symptoms of anxiety. Each item scored on a scale of 1 - 5. (1)not at all, (2)somewhat, (3)moderately, (4) considerably, and (5)very much), hence the scale is a 5- to 15 point range. The three items are the patient's verbal report (feeling shaky, jittery, jumpy), observed behavior consistent with anxiety during the interview (e.g. appearing frightened, shaky, restless) and somatic complains (e.g., sweating, trembling, heart pounding).
COVI Rating Scale total score is the sum of items 1 - 3.
Secondary Outcome Measures
Full Information
NCT ID
NCT00595231
First Posted
January 7, 2008
Last Updated
February 11, 2019
Sponsor
Biotie Therapies Inc.
Collaborators
Syneos Health
1. Study Identification
Unique Protocol Identification Number
NCT00595231
Brief Title
Exploratory Study to Evaluate the Effect of SYN111 (Rufinamide) in Patients With Generalized Anxiety Disorder (GAD)
Official Title
A Multi-Center,Randomized, Double-Blind, Placebo-Controlled, Phase 2, Exploratory Study to Evaluate the Effect of Rufinamide on Anxiety in Patients With Moderate to Severe Generalized Anxiety Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
March 2008 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
October 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Biotie Therapies Inc.
Collaborators
Syneos Health
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A Multi-Centered Randomized, Double-Blind, Placebo-Controlled, Phase 2, Exploratory Study to Evaluate the Effect of Rufinamide on Anxiety in Patients with Moderate to Severe Generalized Anxiety Disorder.
Detailed Description
This was an exploratory study to evaluate the effect of 500 or 1000 mg per day for 8 weeks of Rufinamide compared to placebo on measures of anxiety in patients with Generalized Anxiety Disorder, and to determine tolerability of Rufinamide in this population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Generalized Anxiety Disorder
Keywords
GAD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
239 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SYN111
Arm Type
Experimental
Arm Description
500 mg 1 week, followed by 1000 mg for 7 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
0 mg tablets
Intervention Type
Drug
Intervention Name(s)
SYN111
Other Intervention Name(s)
Rufinamide
Intervention Description
500 mg for 1 week followed by 1000 mg for 7 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
0 mg tablets
Primary Outcome Measure Information:
Title
Change From Baseline in Hamilton Anxiety Scale (HAMA) - Total Score: Summary Statistics - Observed
Description
The Hamilton Anxiety Scale is a 14-item test measuring the severity of anxiety symptoms. It provides measures of overall anxiety, psychic anxiety (mental agitation and psychological distress), and somatic anxiety (physical complaints related to anxiety). The interviewer then rated the individuals on a 5-point scale for each of the 14 items. Seven of the items specifically address psychic anxiety and the remaining 7 items address somatic anxiety. The total anxiety score ranges from 0 to 56. The 7 psychic anxiety items elicit a psychic anxiety score that ranges from 0 to 28. The remaining 7 items yield a somatic anxiety score that also ranges from 0 to 28. A score of 17 or less indicates mild anxiety severity. A score from 18 to 24 indicates mild to moderate anxiety severity, a score of 25 to 30 indicates a moderate to severe anxiety and lastly a score of 31-56 is very severe. HAM-A total score is the sum of items 1 - 14.
Time Frame
8 Weeks
Title
Change From Baseline in Hospital Anxiety and Depression Scale (HADS). Summary Statistics
Description
The Hospital Anxiety and Depression Scale is a self screening questionnaire for depression and anxiety. It consists of 14 questions, seven for anxiety and seven for depression. The 14 statements are relevant to either generalized anxiety (7 statements) or 'depression' (again 7). Each question has 4 possible responses. Responses are scored on a scale from 3 to 0. The maximum score is therefore 21 for depression and 21 for anxiety. A score of 11 or higher indicates the probable presence of the mood disorder with a score of 8 to 10 being just suggestive of the presence of the respective state. The 2 subscales, anxiety and depression, have been found to be independent measures. In its current form the HADS is now divided into 4 ranges: normal (0-7), mild (8-10), moderate (11-15) and severe (16-21). Anxiety score = sum of items 1, 3, 5, 7, 9, 11, and 13. Depression score = sum of items 2, 4, 6, 8, 10, 12, and 14.
Time Frame
8 Weeks
Title
Change From Baseline in Montgomery-Asberg Depression Scale (MADRS) Summary Statistics.
Description
The MADRS (Montgomery and Asberg 1979) is a clinician-rated instrument that measures the presence and severity of depression. This instrument consists of 10 items. Each item is rated on a defined step scale of 0 to 6 with anchors at 2-point intervals. The MADRS total score is the sum of the 10 items and ranges from 0 to 60. A high numeric rating shows a greater degree of symptom severity.
Time Frame
8 Weeks
Title
Change From Baseline in Clinical Global Impression Scale for Severity of Illness: (CGI-S)
Description
Severity of illness is the first scale in the CGI. A rating is filled in by the investigator at the start of treatment based on a 0-7 point weighted scale. It goes from not assessed (0), to among the most extremely ill patients (7).
Time Frame
8 weeks
Title
Change From Baseline Raskin Depression Scale.
Description
It explores the extent to which an individual demonstrates depression on three sub-scales (rated 1-5): verbal self-report, behavior and secondary symptoms of depression. Scores range from 3-15, with higher scores indicating greater severity.
Time Frame
8 weeks
Title
Change From Baseline in Covi Anxiety Scale (CAS) - Index Total Score: Summary Statistics Observed
Description
The Covi Anxiety Scale is a simple 3 item scale for the assessment of severity of anxiety symptoms. The scale measures 3 dimensions: verbal report, behavior and somatic symptoms of anxiety. Each item scored on a scale of 1 - 5. (1)not at all, (2)somewhat, (3)moderately, (4) considerably, and (5)very much), hence the scale is a 5- to 15 point range. The three items are the patient's verbal report (feeling shaky, jittery, jumpy), observed behavior consistent with anxiety during the interview (e.g. appearing frightened, shaky, restless) and somatic complains (e.g., sweating, trembling, heart pounding).
COVI Rating Scale total score is the sum of items 1 - 3.
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Outpatient 18-65
Meet Diagnostic and Statistical Manual,(DSM) IV criteria for GAD
Have moderate to severe anxiety
Sign IRB (Institutional Review Board) approved consent and can comply with visits and procedures
Women of childbearing potential must use acceptable method of contraception
Exclusion Criteria:
Have diagnosis of adjustment disorder or anxiety disorder Not otherwise specified (NOS)
Have diagnosis of specific phobia
Have diagnosis of antisocial personality disorder or other Axis II Disorder
Have diagnosis of substance abuse disorder within 3 months of study entry
Have diagnosis of major depressive disorder or panic disorder within 6 months of study entry
Have diagnosis of PTSD, eating disorder substance dependence disorder within 12 months of study entry
Have diagnosis anytime during lifetime of schizophrenia or other psychotic disorder, bipolar mood disorder, Obsessive-Compulsive Disorder (OCD), psychosurgery
Require medication to treat GAD other than study medication
Failed to show improvement with past treatment for GAD
Excessively consume caffeine
Are receiving treatment with prohibited medications
Uncontrolled thyroid condition
Positive urine drug screen
Obese
Clinically significant ECG finding
Participating in other clinical trial
Clinically significant out of range lab value
Past exposure to rufinamide
Pregnant or nursing females
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christpher Kenney, MD
Organizational Affiliation
Biotie Therapies Inc.
Official's Role
Study Chair
Facility Information:
Facility Name
Carmen Research
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30080
Country
United States
Facility Name
Midwest Clinical Research Center
City
Dayton
State/Province
Ohio
ZIP/Postal Code
45408
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Exploratory Study to Evaluate the Effect of SYN111 (Rufinamide) in Patients With Generalized Anxiety Disorder (GAD)
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