Intranasal PH94B for Management of the Symptoms of Generalized Social Phobia
NCT ID: NCT01217788
Last Updated: 2011-05-10
Study Results
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Basic Information
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COMPLETED
PHASE2
90 participants
INTERVENTIONAL
2008-02-29
2011-03-31
Brief Summary
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Detailed Description
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There are two subtypes of social phobia: (i) generalized (discrete), which is suffered by approximately 50% of social phobia patients and in which fear and avoidance extend to a wide range of social situations, and (ii) non-generalized, in which the patient fears only one or a few circumscribed situations. Speaking in front of large groups is by far the most prevalent of social fears (Lang and Stein, 2001).
Social phobia has a lifetime comorbidity rate of approximately 81% with other psychiatric disorders (particularly affective disorders, other anxiety disorders, and substance abuse disorders), as well as to being associated with increased nonpsychiatric medical difficulties. People with social phobia identify social impairment, inadequate social support, overall role impairment, specific impairment in education, work, and other activities, as well as interference in their efforts at self-improvement. Unfortunately, for these patients, there is a strong consensus that social phobia is one of the least commonly recognized and treated mental disorders
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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PH94B intranasal spray
PH94B intranasal spray
Comparison of PH94B single dose intranasal spray and Placebo single dose intranasal spray
Placebo intranasal spray
PH94B intranasal spray
Comparison of PH94B single dose intranasal spray and Placebo single dose intranasal spray
Interventions
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PH94B intranasal spray
Comparison of PH94B single dose intranasal spray and Placebo single dose intranasal spray
Eligibility Criteria
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Inclusion Criteria
* Liebowitz Social Anxiety Scale (LSAS) score greater than or equal to 60 at Screening.
* Score of 75 or greater on the SUD scale at one of the Performance Phase time points during either the Public Speaking or Social Interaction Challenge
* Written Informed Consent prior to commencing any study specific procedures.
* Women of child-bearing-potential must be able to commit to the consistent and correct use of an acceptable method of birth control throughout the study and have a negative serum pregnancy test result prior to study drug administration.
Exclusion Criteria
* Acute or chronic psychiatric disease which is the primary diagnosis (except Social Phobia) at the time of the study. Note that subjects with concurrent Generalized Anxiety Disorder (GAD) are allowed into the study provided this is not the primary diagnosis.
* Subjects with a history of psychiatric diseases such as schizophrenia, bipolar disorder, and psychosis are to be excluded.
* Presence of a clinical condition or disease, or use of a concomitant medication, that in the clinical judgment of the Investigator could place the patient at undue risk, interfere with study participation, or confound the results of the study.
* Use of substances of abuse within the year prior to study entry.
* Concomitant use of any over-the-counter, prescription product, or herbal preparation for treatment of the symptoms of social anxiety during the study and within 30 days prior to study entry and use of non-study anxiolytics such as benzodiazepines during the study and within 30 days prior to study entry.
18 Years
65 Years
ALL
No
Sponsors
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Pherin Pharmaceuticals, Inc.
INDUSTRY
Responsible Party
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The Medical Research Network LLC
Principal Investigators
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Michael L Liebowitz, M.D.
Role: PRINCIPAL_INVESTIGATOR
Medical Research Network
Locations
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Medical Research Network
New York, New York, United States
Countries
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References
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Liebowitz MR, Salman E, Nicolini H, Rosenthal N, Hanover R, Monti L. Effect of an acute intranasal aerosol dose of PH94B on social and performance anxiety in women with social anxiety disorder. Am J Psychiatry. 2014 Jun;171(6):675-82. doi: 10.1176/appi.ajp.2014.12101342.
Other Identifiers
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PH94B CL022
Identifier Type: -
Identifier Source: org_study_id
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