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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03095066
Other study ID # 17-AVP-786-205
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date May 30, 2017
Est. completion date August 31, 2022

Study information

Verified date September 2023
Source Otsuka Pharmaceutical Development & Commercialization, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a multicenter, randomized, placebo-controlled study to evaluate AVP-786 for the treatment of neurobehavioral disinhibition including aggression, agitation, and irritability in participants with traumatic brain injury (TBI).


Description:

Eligible participants for this study must have a diagnosis of neurobehavioral disinhibition including aggression, agitation, and irritability that persists after brain injury. This is a multicenter, randomized, placebo-controlled study, consisting of up to 12 weeks of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 168
Est. completion date August 31, 2022
Est. primary completion date August 22, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Participants with TBI - Participants with neurobehavioral disinhibition symptoms that are present after trauma or after recovery of consciousness - Score of =4 on the mCGI-S scale and the Agitation/Aggression or Irritability/Lability subscales of the Neuropsychiatric Inventory (NPI) scale at screening and baseline - Participants with a reliable caregiver Exclusion Criteria: - Participants with significant symptoms of a major depressive disorder - Participants with a history of or current clinical symptoms of schizophrenia, schizoaffective disorder, bipolar disorder, antisocial personality disorder, or borderline personality disorder

Study Design


Intervention

Drug:
Placebo
Administered as capsules
AVP-786-28
28 mg of d6-DM and 4.9 mg of Q
AVP-786-42.63
42.63 mg of d6-DM and 4.9 mg of Q

Locations

Country Name City State
United States Neurobehavioral Medicine Group #222 Bloomfield Hills Michigan
United States Bradenton Research Center, Inc Bradenton Florida
United States Valley Medical Research Centerville Ohio
United States Atrium Health - Carolinas Rehabilitation - Charlotte Site #166 Charlotte North Carolina
United States New Hope Clinical Research Site#194 Charlotte North Carolina
United States Cincinnati VA Medical Center Cincinnati Ohio
United States Mountain Mind Colorado Springs Colorado
United States WJB Dorn VA-Wm. Jennings Bryan Dorn VA Medical Center Columbia South Carolina
United States Healthcare Innovative Institute, LLC Site# 173 Coral Springs Florida
United States ATP Clinical Research Site#150 Costa Mesa California
United States Millennium Psychiatric Associates, LLC Creve Coeur Missouri
United States Connecticut Clinical Research Cromwell Connecticut
United States University of Texas Southwestern Medical Site#140 Dallas Texas
United States Mountain View Clinical Research, Inc. Site# 202 Denver Colorado
United States Design Neuroscience Center, PL Doral Florida
United States Science Connections, LLC Site#161 Doral Florida
United States Cedar Clinical Research #221 Draper Utah
United States Carolina Headache Institute Durham North Carolina
United States JFK Johnson Rehabilitation Institute Edison New Jersey
United States Hawaii Pacific Neuroscience Site#184 Honolulu Hawaii
United States Alphab Global Research Site#163 Jupiter Florida
United States Kaizen Brain Center #224 La Jolla California
United States Sunwise Clinical Research, LLC Site#216 Lafayette California
United States The University of Kentucky research foundation Lexington Kentucky
United States Torrance Clinical Research Institute Site#157 Lomita California
United States Tibor Rubin VA Medical Center, SCIRE Biomedical Research Institute Long Beach California
United States Medical Center of the Rockies Loveland Colorado
United States Meridien Research Maitland Florida
United States Allied Biomedical Research Institute, Inc. Site#151 Miami Florida
United States Premier Clinical Research Institute, Inc. Miami Florida
United States Project 4 Research Miami Florida
United States North Star Medical Research, LLC Site#154 Middleburg Heights Ohio
United States The NeuroCognitive Insititute Mount Arlington New Jersey
United States New York University School of Medicine Site #122 New York New York
United States Health Synergy Clinical Research Okeechobee Florida
United States IPS Research Site#196 Oklahoma City Oklahoma
United States Sharlin Health and Neurology Ozark Missouri
United States Asclepes Research Centers - Panorama City Site #208 Panorama City California
United States Absolute Clinical Research Site#207 Phoenix Arizona
United States University of Pittsburgh Pittsburgh Pennsylvania
United States The Neurology Group Pomona California
United States Baptist Health Richmond Kentucky
United States Virginia Commonwealth University #172 Richmond Virginia
United States Virginia Commonwealth University Site#172 Richmond Virginia
United States Clinical Research Professionals Saint Louis Missouri
United States Salem Research Institute Site# 138 Salem Virginia
United States Salisbury VAMC Salisbury North Carolina
United States Polytrauma Rehabilitation Center S. Texas VA Health Care System Site# 146 San Antonio Texas
United States Roskamp Institute Clinic, Inc. Sarasota Florida
United States Perseverance Research Center Site#152 Scottsdale Arizona
United States Sisu BHR Site#200 Springfield Massachusetts
United States Meridien Research Site# 108 Tampa Florida
United States USF Dept of Psychiatry and Behavioral Neurosciences Site# 214 Tampa Florida
United States Tuscaloosa Veterans Affairs Medical Center Tuscaloosa Alabama

Sponsors (1)

Lead Sponsor Collaborator
Otsuka Pharmaceutical Development & Commercialization, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline to Week 12 in the Composite of the Clinical Impression Severity Scores on the Neuropsychiatric Inventory Clinician Rating Scale (NPI-C) Subscales of Aggression, Agitation, and Irritability/Lability (NPI-C-3) The NPI-C can be used to rate the presence of neuropsychiatric symptoms across 14 domains. The scores for each item within an individual domain/subscale range from 0 to 3, with a higher score indicating increased severity. The NPI-C-3 is comprised of the aggression, agitation, and irritability/lability subscales. The scores for the three subscales are summed to create the total NPI-C-3 composite score, which ranges from 0 to 99, with a higher score indicating increased severity. Baseline; Week 12
Secondary Change from Baseline to Week 12 in Modified Clinical Global Impression of Change (mCGI-C) Raw Scores The mCGI-C will be used to assess the clinician's general impression of the participant's treatment response. The mCGI-C is a 7-point (1 to 7) modified version of the CGI-C scale. A higher score represents worsening of symptoms. Baseline; Week 12
Secondary Change from Baseline to Week 12 in NPI-C Rating Scale Subscales Scores for Aggression, Agitation, Irritability/Lability, and Disinhibition The NPI-C is used to rate the presence of neuropsychiatric symptoms across 14 domains. The scores for each item within an individual domain/subscale range from 0 to 3, with a higher score indicating increased severity. Baseline; Week 12
Secondary Change from Baseline to Week 12 in Modified Clinical Global Impression of Severity (mCGI-S) Scale Scores The mCGI-S will be used to assess the clinician's view of the participant's severity of aggression, agitation, and irritability symptoms. The mCGI-S is a 7-point (1 to 7) modified version of the CGI-S scale. In all cases, a higher score represents increased severity. Baseline; Week 12
Secondary Change from Baseline to Week 12 in Patient Global Impression of Severity (PGI-S) Scores The PGI-S is a single-question scale that specifically assesses the severity of symptoms of neurobehavioral disinhibition, including aggression, agitation, and irritability, on a 7-point scale : 1, normal, not at all ill; 2, borderline ill; 3, mildly ill; 4, moderately ill; 5, markedly ill; 6, severely ill; or 7, extremely ill. Baseline; Week 12
Secondary Change from Baseline to Week 12 in Patient Global Impression of Change (PGI-C) Raw Scores The PGI-C is a 7-point (1 to 7) scale used to assess the participant's assessment of treatment response. A higher score indicates worsening of the symptoms. Baseline; Week 12