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Atypical Antipsychotic
Cariprazine for Social Anxiety Disorder
Phase 4
Waitlist Available
Led By Michael R Liebowitz, MD
Research Sponsored by The Medical Research Network
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks or locf
Awards & highlights
Pivotal Trial
Drug Has Already Been Approved
Summary
This trial tests Vraylar® to see if it can help people with social anxiety disorder by balancing brain chemicals related to mood and anxiety. Current treatments are not effective for everyone and often have side effects, so new options are needed.
Eligible Conditions
- Social Anxiety Disorder
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks or locf
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks or locf
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in LSAS Score
Side effects data
From 2011 Phase 3 trial • 497 Patients • NCT0105866817%
Akathisia
11%
Headache
10%
Nausea
10%
Extrapyramidal disorder
10%
Insomnia
9%
Vomiting
9%
Restlessness
5%
Constipation
5%
Dizziness
4%
Dyspepsia
2%
Mania
2%
Diarrhoea
2%
Tremor
1%
Aggression
1%
Hospitalisation
1%
Bipolar disorder
1%
Endometrial cancer
1%
Pulmonary embolism
1%
Bipolar I disorder
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo
Cariprazine (3-6 mg/Day)
Cariprazine (6-12 mg/Day)
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: CariprazineExperimental Treatment1 Intervention
Cariprazine 1.5 to 3 mg per day
Group II: PlaceboPlacebo Group1 Intervention
Matching placebo
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cariprazine
2010
Completed Phase 3
~11050
Find a Location
Who is running the clinical trial?
The Medical Research NetworkLead Sponsor
5 Previous Clinical Trials
270 Total Patients Enrolled
AbbVieIndustry Sponsor
1,020 Previous Clinical Trials
520,051 Total Patients Enrolled
Michael R Liebowitz, MDPrincipal InvestigatorManaging Director
1 Previous Clinical Trials
30 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have taken certain medications called Monoamine Oxidase Inhibitors (MAOIs) within the past 14 days.You have a history of schizophrenia or bipolar disorder.You have a condition called body dysmorphic disorder that affects the way you see and think about your body.You have never had a seizure or a seizure disorder, except for one time when you were a child and had a fever.You have had electro-convulsive therapy (ECT) within the past 12 weeks.You should not be taking any other medications for mental health, such as gabapentin, pregabalin, antipsychotics, SSRIs, SNRIs, benzodiazepines, or other sleep aids, except for zolpidem (Ambien®) which can be taken occasionally for insomnia but not more than 3 times a week.You have a heart condition that is currently diagnosed or has been diagnosed in the past.You have had a problem with drugs or alcohol within the past 24 weeks.
Research Study Groups:
This trial has the following groups:- Group 1: Cariprazine
- Group 2: Placebo
Awards:
This trial has 2 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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