Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions



Status:Completed
Conditions:Psychiatric
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:18 - 65
Updated:11/2/2017
Start Date:October 2014
End Date:May 2016

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A Phase 2, Double-Blind, Randomized, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TNX-102 SL Taken at Bedtime in Subjects With Military-Related PTSD and Related Conditions (Protocol No. TNX-CY-P201) -"AtEase STUDY"

This is a 12-week, multicenter, randomized, double-blind, placebo-controlled, fixed-dose,
parallel-group study that will investigate the efficacy and safety of two doses of TNX-102 SL
—a sublingual formulation of cyclobenzaprine. Following successful screening and
randomization, eligible subjects will return regularly to the study clinic for weekly or
biweekly visits for assessments of efficacy and safety.


Inclusion Criteria:

- Male or female between 18 and 65 years of age

- Diagnosed with current PTSD as defined by the Clinician-Administered PTSD Scale for
DSM-5 (CAPS-5),

- For patients with a qualifying Index trauma(s) resulting in PTSD that occurred during
military service, military contractor, Department of Homeland Security or law
enforcement

- Willing and able to withdraw and refrain from specific therapies (ask PI)

- Use medically acceptable form of contraception (female only)

- Signed informed consent

Exclusion Criteria:

- Significant traumatic brain injury

- Severe depression

- Bipolar and psychotic disorders

- Increase risk of suicide

- Significant clinical (cardiac, systemic infection, drug/alcohol abuse) or laboratory
abnormalities (including positivity for Hep B, Hep C, HIV)

- Unable to wash-out specific medications (ask PI)

- History of violent behavior within past 2 years, unrelated to work duties

- History of drug or alcohol abuse within past 6 months

- Positive illegal substance test

- Known hypersensitivity to cyclobenzaprine

- Others: seizure disorders, uncontrolled sleep apnea, BMI>40

- Participation in an investigational study in past 30 days

- In the process of litigating for compensation for a psychiatric disorder

- Females that are pregnant or breastfeeding
We found this trial at
23
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Imperial, California 92251
2490
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Imperial, CA
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7940 Floyd Curl Dr.
San Antonio, Texas 78229
210-949-0122
1763
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San Antonio, TX
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811 Juniper St NE
Atlanta, Georgia 30308
(404) 881-5800
Atlanta Center for Medical Research Welcome to the Atlanta Center for Medical Research, a leader...
932
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Atlanta, GA
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Bellevue, Washington 98007
2474
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Bellevue, WA
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Cedarhurst, New York 11516
181
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Cedarhurst, NY
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Chicago, Illinois 60640
847
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Chicago, IL
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Cincinnati, Ohio 45219
735
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Cincinnati, OH
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544
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Cleveland, OH
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Lake City, Florida 32025
1056
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Lake City, FL
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Las Vegas, Nevada 89102
2369
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Las Vegas, NV
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Leesburg, Florida 34748
1112
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Leesburg, FL
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1317
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Lincoln, NE
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National City, California 91950
2575
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National City, CA
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New Bedford, Massachusetts 02740
50
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New Bedford, MA
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Oceanside, California 92056
2566
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Oceanside, CA
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Oklahoma City, Oklahoma 73103
1489
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Oklahoma City, OK
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2578
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Orange, CA
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Orlando, Florida 32806
1115
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Orlando, FL
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Phoenix, Arizona 85032
2283
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Riverside, California 92506
2547
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Riverside, CA
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San Diego, California 92161
2576
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San Diego, CA
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Torrance, California 90502
2597
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Torrance, CA
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Tuscaloosa, Alabama 35404
1092
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Tuscaloosa, AL
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