Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
14,731
archived clinical trials in
Psychiatric

Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
North Charleston, SC
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
North Charleston, SC
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Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
Orem, UT
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
Orem, UT
Click here to add this to my saved trials
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
New York, NY
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
Fort Lauderdale, FL
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
Saint Louis, MO
Open-Label, Safety Study of Lofexidine
A Phase 3, Open-Label, Safety Study of Lofexidine
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Augmentation of Brief Habit Reversal Training With D-cycloserine or Placebo
Augmentation of Brief Habit Reversal Training With D-cycloserine or Placebo
Status: Enrolling
Updated:  10/24/2017
UCLA Semel Institute for Neuroscience and Human Behavior
mi
from
Los Angeles, CA
Augmentation of Brief Habit Reversal Training With D-cycloserine or Placebo
Augmentation of Brief Habit Reversal Training With D-cycloserine or Placebo
Status: Enrolling
Updated: 10/24/2017
UCLA Semel Institute for Neuroscience and Human Behavior
mi
from
Los Angeles, CA
Click here to add this to my saved trials
The Impact of Family Financial Support on Parental Mental Health
The Impact of Family Financial Support on Parental Mental Health
Status: Enrolling
Updated:  10/24/2017
LIFT-LA in Affiliation with UCLA
mi
from
Los Angeles, CA
The Impact of Family Financial Support on Parental Mental Health
The Impact of Family Financial Support on Parental Mental Health
Status: Enrolling
Updated: 10/24/2017
LIFT-LA in Affiliation with UCLA
mi
from
Los Angeles, CA
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Study to Evaluate the Exposures of Lofexidine and Its Major Metabolites in Subjects Seeking Buprenorphine Dose Reduction
A Phase 1 Study to Evaluate the Relative Exposures of Lofexidine and Its Major Metabolites in Subjects Seeking Buprenorphine Dose Reduction
Status: Enrolling
Updated:  10/24/2017
Clinical Research Facility
mi
from
Overland Park, KA
Study to Evaluate the Exposures of Lofexidine and Its Major Metabolites in Subjects Seeking Buprenorphine Dose Reduction
A Phase 1 Study to Evaluate the Relative Exposures of Lofexidine and Its Major Metabolites in Subjects Seeking Buprenorphine Dose Reduction
Status: Enrolling
Updated: 10/24/2017
Clinical Research Facility
mi
from
Overland Park, KA
Click here to add this to my saved trials
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Status: Enrolling
Updated:  10/24/2017
University of Missouri
mi
from
Columbia, MO
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Status: Enrolling
Updated: 10/24/2017
University of Missouri
mi
from
Columbia, MO
Click here to add this to my saved trials
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Status: Enrolling
Updated:  10/24/2017
University of Memphis
mi
from
Memphis, TN
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Improving Brief Alcohol Interventions With a Behavioral Economic Supplement
Status: Enrolling
Updated: 10/24/2017
University of Memphis
mi
from
Memphis, TN
Click here to add this to my saved trials
N-Acetyl Cysteine Plus Naltrexone in Methamphetamine Dependence
A Double-Blind Study of N-Acetyl Cysteine Plus Naltrexone in the Treatment of Methamphetamine Dependence
Status: Enrolling
Updated:  10/24/2017
University of Chicago
mi
from
Chicago, IL
N-Acetyl Cysteine Plus Naltrexone in Methamphetamine Dependence
A Double-Blind Study of N-Acetyl Cysteine Plus Naltrexone in the Treatment of Methamphetamine Dependence
Status: Enrolling
Updated: 10/24/2017
University of Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Chicago Social Drinking Project
Individual Differences After Consumption of Alcohol and Other Common Substances and Long-Term Follow-Up of Social Drinking, Young Adults
Status: Enrolling
Updated:  10/25/2017
Clinical Addictions Research Laboratory
mi
from
Chicago, IL
Chicago Social Drinking Project
Individual Differences After Consumption of Alcohol and Other Common Substances and Long-Term Follow-Up of Social Drinking, Young Adults
Status: Enrolling
Updated: 10/25/2017
Clinical Addictions Research Laboratory
mi
from
Chicago, IL
Click here to add this to my saved trials
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated:  10/25/2017
Directions for Mental Health
mi
from
Clearwater, FL
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated: 10/25/2017
Directions for Mental Health
mi
from
Clearwater, FL
Click here to add this to my saved trials
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated:  10/25/2017
Access Behavioral Health
mi
from
Pensacola, FL
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated: 10/25/2017
Access Behavioral Health
mi
from
Pensacola, FL
Click here to add this to my saved trials
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated:  10/25/2017
Henderson Behavioral Health
mi
from
Fort Lauderdale, FL
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated: 10/25/2017
Henderson Behavioral Health
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated:  10/25/2017
University of South Florida
mi
from
Saint Petersburg, FL
Computerized Cognitive Behavioral Therapy for Childhood Anxiety in Community Health Centers
Utilizing Health Information Technology to Improve Health Care Quality: Implementation of a Computerized Cognitive Behavioral Therapy Protocol for Childhood Anxiety
Status: Enrolling
Updated: 10/25/2017
University of South Florida
mi
from
Saint Petersburg, FL
Click here to add this to my saved trials
Early Nurse Detection and Management of Delirium
Early Nurse Detection of Delirium Superimposed on Dementia
Status: Enrolling
Updated:  10/25/2017
Mount Nittany Medical Center
mi
from
State College, PA
Early Nurse Detection and Management of Delirium
Early Nurse Detection of Delirium Superimposed on Dementia
Status: Enrolling
Updated: 10/25/2017
Mount Nittany Medical Center
mi
from
State College, PA
Click here to add this to my saved trials
Early Nurse Detection and Management of Delirium
Early Nurse Detection of Delirium Superimposed on Dementia
Status: Enrolling
Updated:  10/25/2017
Vanderbilt University Medical Center
mi
from
Nashville, TN
Early Nurse Detection and Management of Delirium
Early Nurse Detection of Delirium Superimposed on Dementia
Status: Enrolling
Updated: 10/25/2017
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Computer- Assisted Cognitive-Behavioral Treatment for Anxiety Disorders in Children With Autism Spectrum Disorders
Computer- Assisted Cognitive-Behavioral Treatment for Anxiety Disorders in Children With Autism Spectrum Disorders
Status: Enrolling
Updated:  10/25/2017
University of South Florida
mi
from
Saint Petersburg, FL
Computer- Assisted Cognitive-Behavioral Treatment for Anxiety Disorders in Children With Autism Spectrum Disorders
Computer- Assisted Cognitive-Behavioral Treatment for Anxiety Disorders in Children With Autism Spectrum Disorders
Status: Enrolling
Updated: 10/25/2017
University of South Florida
mi
from
Saint Petersburg, FL
Click here to add this to my saved trials
Exposure-Focused Family-Based CBT for Youth With ASD and Comorbid Anxiety
Exposure-Focused Family-Based CBT for Youth With ASD and Comorbid Anxiety
Status: Enrolling
Updated:  10/25/2017
Rothman Center for Neuropsychiatry
mi
from
Saint Petersburg, FL
Exposure-Focused Family-Based CBT for Youth With ASD and Comorbid Anxiety
Exposure-Focused Family-Based CBT for Youth With ASD and Comorbid Anxiety
Status: Enrolling
Updated: 10/25/2017
Rothman Center for Neuropsychiatry
mi
from
Saint Petersburg, FL
Click here to add this to my saved trials
Prevention of Phantom Limb Pain After Transtibial Amputation
Prevention of Phantom Limb Pain After Transtibial Amputation (PLATA) - Randomized, Double-blind, Controlled, Multi-center Trial Comparing Optimized Intravenous Pain Control vs Optimized Intravenous Pain Control Plus Nerve Block.
Status: Enrolling
Updated:  10/25/2017
Massachusetts General Hospital, Dept. of Anesthesiology, Perioperative and Pain Medicine
mi
from
Boston, MA
Prevention of Phantom Limb Pain After Transtibial Amputation
Prevention of Phantom Limb Pain After Transtibial Amputation (PLATA) - Randomized, Double-blind, Controlled, Multi-center Trial Comparing Optimized Intravenous Pain Control vs Optimized Intravenous Pain Control Plus Nerve Block.
Status: Enrolling
Updated: 10/25/2017
Massachusetts General Hospital, Dept. of Anesthesiology, Perioperative and Pain Medicine
mi
from
Boston, MA
Click here to add this to my saved trials
Prevention of Phantom Limb Pain After Transtibial Amputation
Prevention of Phantom Limb Pain After Transtibial Amputation (PLATA) - Randomized, Double-blind, Controlled, Multi-center Trial Comparing Optimized Intravenous Pain Control vs Optimized Intravenous Pain Control Plus Nerve Block.
Status: Enrolling
Updated:  10/25/2017
General Hospital Klagenfurt
mi
from
Klagenfurt,
Prevention of Phantom Limb Pain After Transtibial Amputation
Prevention of Phantom Limb Pain After Transtibial Amputation (PLATA) - Randomized, Double-blind, Controlled, Multi-center Trial Comparing Optimized Intravenous Pain Control vs Optimized Intravenous Pain Control Plus Nerve Block.
Status: Enrolling
Updated: 10/25/2017
General Hospital Klagenfurt
mi
from
Klagenfurt,
Click here to add this to my saved trials
Administration of Clomiphene: Short and Long Term Metabolism in an Anti-Doping Setting
Administration of Clomiphene: Short and Long Term Metabolism in an Anti-Doping Setting
Status: Enrolling
Updated:  10/25/2017
University of Utah Orthopaedic Center
mi
from
Salt Lake City, UT
Administration of Clomiphene: Short and Long Term Metabolism in an Anti-Doping Setting
Administration of Clomiphene: Short and Long Term Metabolism in an Anti-Doping Setting
Status: Enrolling
Updated: 10/25/2017
University of Utah Orthopaedic Center
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Posterior Vitreous Detachment (PVD) Assessment During Dual Retinal Vein Occlusion (RVO) Lucentis Evaluations
Posterior Vitreous Detachment (PVD) Assessment During Dual RVO Lucentis Evaluations (PADDLE Study)
Status: Enrolling
Updated:  10/26/2017
Barnes Retina Institute
mi
from
Saint Louis, MO
Posterior Vitreous Detachment (PVD) Assessment During Dual Retinal Vein Occlusion (RVO) Lucentis Evaluations
Posterior Vitreous Detachment (PVD) Assessment During Dual RVO Lucentis Evaluations (PADDLE Study)
Status: Enrolling
Updated: 10/26/2017
Barnes Retina Institute
mi
from
Saint Louis, MO
Click here to add this to my saved trials
Executive Functioning in TBI From Rehabilitation to Social Reintegration: COMPASS
Executive Functioning in TBI From Rehabilitation to Social Reintegration: COMPASS
Status: Enrolling
Updated:  10/26/2017
Washington DC VA Medical Center, Washington, DC
mi
from
Washington, D.C.,
Executive Functioning in TBI From Rehabilitation to Social Reintegration: COMPASS
Executive Functioning in TBI From Rehabilitation to Social Reintegration: COMPASS
Status: Enrolling
Updated: 10/26/2017
Washington DC VA Medical Center, Washington, DC
mi
from
Washington, D.C.,
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Tuscaloosa VA Medical Center
mi
from
Tuscaloosa, AL
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Tuscaloosa VA Medical Center
mi
from
Tuscaloosa, AL
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Noesis Pharma
mi
from
Phoenix, AZ
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Noesis Pharma
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Sun Valley Reserach Center
mi
from
Imperial, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Sun Valley Reserach Center
mi
from
Imperial, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Excell Research, Inc.
mi
from
Oceanside, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Excell Research, Inc.
mi
from
Oceanside, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Neuropsychiatric Research Center for Orange County
mi
from
Orange, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Neuropsychiatric Research Center for Orange County
mi
from
Orange, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
CITRIALS
mi
from
Riverside, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
CITRIALS
mi
from
Riverside, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Vetern Affairs, San Diego Health Care System
mi
from
San Diego, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Vetern Affairs, San Diego Health Care System
mi
from
San Diego, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Cns, Inc.
mi
from
Torrance, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Cns, Inc.
mi
from
Torrance, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Sarkis Clinical Trials
mi
from
Lake City, FL
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Sarkis Clinical Trials
mi
from
Lake City, FL
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Compass Research North, LLC
mi
from
Leesburg, FL
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Compass Research North, LLC
mi
from
Leesburg, FL
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Clinical Neuroscience Solutions, Inc
mi
from
Orlando, FL
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Clinical Neuroscience Solutions, Inc
mi
from
Orlando, FL
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Atlanta Center for Medical Research
mi
from
Atlanta, GA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Atlanta Center for Medical Research
mi
from
Atlanta, GA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Great Lakes Clinical Trials
mi
from
Chicago, IL
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Great Lakes Clinical Trials
mi
from
Chicago, IL
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Novex Clinical Research, LLC
mi
from
New Bedford, MA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Novex Clinical Research, LLC
mi
from
New Bedford, MA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Premier Psychiatric Research Instititute, Inc.
mi
from
Lincoln, NE
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Premier Psychiatric Research Instititute, Inc.
mi
from
Lincoln, NE
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Altea Research
mi
from
Las Vegas, NV
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Altea Research
mi
from
Las Vegas, NV
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
IPS Research Company
mi
from
Oklahoma City, OK
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
IPS Research Company
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Clinical Trials of Texas, Inc.
mi
from
San Antonio, TX
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Clinical Trials of Texas, Inc.
mi
from
San Antonio, TX
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Northwest Clinical Research Center
mi
from
Bellevue, WA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Northwest Clinical Research Center
mi
from
Bellevue, WA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
National City
mi
from
National City, CA
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
National City
mi
from
National City, CA
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Cedarhurst
mi
from
Cedarhurst, NY
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Cedarhurst
mi
from
Cedarhurst, NY
Click here to add this to my saved trials
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated:  10/26/2017
Investigator Site - Cincinnati
mi
from
Cincinnati, OH
Safety and Efficacy Study of TNX-102 SL in Subjects With Military-Related PTSD and Related Conditions
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"
Status: Enrolling
Updated: 10/26/2017
Investigator Site - Cincinnati
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Open Label Extension Safety and Efficacy Study of TNX-102 SL Tablets in Military Related PTSD and Related Conditions
A 12-Week, Open-Label, Multicenter, Extension Study To TNX-CY-P201 To Evaluate The Safety And Efficacy Of TNX-102 SL Taken Daily At Bedtime In Patients With Military-Related PTSD And Related Conditions
Status: Enrolling
Updated:  10/26/2017
Tuscaloosa VA Medical Center
mi
from
Tuscaloosa, AL
Open Label Extension Safety and Efficacy Study of TNX-102 SL Tablets in Military Related PTSD and Related Conditions
A 12-Week, Open-Label, Multicenter, Extension Study To TNX-CY-P201 To Evaluate The Safety And Efficacy Of TNX-102 SL Taken Daily At Bedtime In Patients With Military-Related PTSD And Related Conditions
Status: Enrolling
Updated: 10/26/2017
Tuscaloosa VA Medical Center
mi
from
Tuscaloosa, AL
Click here to add this to my saved trials
Open Label Extension Safety and Efficacy Study of TNX-102 SL Tablets in Military Related PTSD and Related Conditions
A 12-Week, Open-Label, Multicenter, Extension Study To TNX-CY-P201 To Evaluate The Safety And Efficacy Of TNX-102 SL Taken Daily At Bedtime In Patients With Military-Related PTSD And Related Conditions
Status: Enrolling
Updated:  10/26/2017
Noesis Pharma
mi
from
Phoenix, AZ
Open Label Extension Safety and Efficacy Study of TNX-102 SL Tablets in Military Related PTSD and Related Conditions
A 12-Week, Open-Label, Multicenter, Extension Study To TNX-CY-P201 To Evaluate The Safety And Efficacy Of TNX-102 SL Taken Daily At Bedtime In Patients With Military-Related PTSD And Related Conditions
Status: Enrolling
Updated: 10/26/2017
Noesis Pharma
mi
from
Phoenix, AZ
Click here to add this to my saved trials