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
33,560
archived clinical trials in
Neurology

Cebranopadol Efficacy and Safety in Diabetic Patients Suffering From Chronic Pain Caused by Damage to the Nerves
Efficacy, Safety and Tolerability of Multiple Doses of Oral Cebranopadol in Subjects With Moderate to Severe Chronic Pain Due to Diabetic Peripheral Neuropathy.
Status: Enrolling
Updated:  10/1/2014
1225
mi
from
New York, NY
Cebranopadol Efficacy and Safety in Diabetic Patients Suffering From Chronic Pain Caused by Damage to the Nerves
Efficacy, Safety and Tolerability of Multiple Doses of Oral Cebranopadol in Subjects With Moderate to Severe Chronic Pain Due to Diabetic Peripheral Neuropathy.
Status: Enrolling
Updated: 10/1/2014
US021
1225
mi
from
New York, NY
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Assess Safety, Bio-distribution, Dosimetry, and Optimize Imaging Protocol of GEH120714 (18F) Injection, in Healthy Volunteers and Participants With Relapsing and Remitting Multiple Sclerosis (rrMS)
A Phase 1, Open-label, Non-randomized Study to Assess Safety, Bio-distribution, and Radiation Dosimetry, and Optimize the Imaging Protocol of GEH120714 (18F) Injection, a Marker of Microglial Activation, in Healthy Volunteers and Participants With Relapsing and Remitting Multiple Sclerosis (rrMS)
Status: Enrolling
Updated:  10/7/2014
1252
mi
from
Princeton, NJ
Assess Safety, Bio-distribution, Dosimetry, and Optimize Imaging Protocol of GEH120714 (18F) Injection, in Healthy Volunteers and Participants With Relapsing and Remitting Multiple Sclerosis (rrMS)
A Phase 1, Open-label, Non-randomized Study to Assess Safety, Bio-distribution, and Radiation Dosimetry, and Optimize the Imaging Protocol of GEH120714 (18F) Injection, a Marker of Microglial Activation, in Healthy Volunteers and Participants With Relapsing and Remitting Multiple Sclerosis (rrMS)
Status: Enrolling
Updated: 10/7/2014
GE Healthcare
1252
mi
from
Princeton, NJ
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Consolidation & Interference in Multiple Sclerosis
Consolidation & Interference in Multiple Sclerosis
Status: Enrolling
Updated:  10/7/2014
mi
from
West Orange, NJ
Consolidation & Interference in Multiple Sclerosis
Consolidation & Interference in Multiple Sclerosis
Status: Enrolling
Updated: 10/7/2014
Kessler Foundation
mi
from
West Orange, NJ
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Crossover Comparison of MultiHance and Dotarem
Phase IV, Double Blind, Multi-Center, Randomized, Two-Arm Crossover Study to Compare 0.1 mmol/kg of MultiHance With 0.1 mmol/kg of Dotarem and 0.05 mmol/kg of MultiHance With 0.1 mmol/kg of Dotarem in Magnetic Resonance Imaging (MRI) of the Brain
Status: Enrolling
Updated:  10/9/2014
1397
mi
from
Corvallis, OR
Crossover Comparison of MultiHance and Dotarem
Phase IV, Double Blind, Multi-Center, Randomized, Two-Arm Crossover Study to Compare 0.1 mmol/kg of MultiHance With 0.1 mmol/kg of Dotarem and 0.05 mmol/kg of MultiHance With 0.1 mmol/kg of Dotarem in Magnetic Resonance Imaging (MRI) of the Brain
Status: Enrolling
Updated: 10/9/2014
Samaritan Health Services
1397
mi
from
Corvallis, OR
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Open Label Clinical Trial of Vitamin D in Children With Autism
Open Label Clinical Trial of Vitamin D Dosage Tolerability, and Effect on Behavioral Measures in Children With Autism
Status: Enrolling
Updated:  10/20/2014
1341
mi
from
San Francisco, CA
Open Label Clinical Trial of Vitamin D in Children With Autism
Open Label Clinical Trial of Vitamin D Dosage Tolerability, and Effect on Behavioral Measures in Children With Autism
Status: Enrolling
Updated: 10/20/2014
University of California at San Francisco
1341
mi
from
San Francisco, CA
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SENSE Theatre Intervention for Children With Autism Spectrum Disorder (ASD)
SENSE Theatre Research Program
Status: Enrolling
Updated:  10/27/2014
618
mi
from
Nashville, TN
SENSE Theatre Intervention for Children With Autism Spectrum Disorder (ASD)
SENSE Theatre Research Program
Status: Enrolling
Updated: 10/27/2014
Vanderbilt Kennedy Center
618
mi
from
Nashville, TN
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Study to Evaluate the Pharmacokinetic Profiles of BIIB017 (Peginterferon Beta-1a) and Rebif® (Interferon Beta-1a) in Healthy Volunteers
An Open-label Crossover Phase 1 Study to Evaluate the Pharmacokinetic Profiles of BIIB017 (Peginterferon Beta-1a) and Rebif® (Interferon Beta-1a) in Healthy Volunteers
Status: Enrolling
Updated:  11/6/2014
559
mi
from
Evansville, IN
Study to Evaluate the Pharmacokinetic Profiles of BIIB017 (Peginterferon Beta-1a) and Rebif® (Interferon Beta-1a) in Healthy Volunteers
An Open-label Crossover Phase 1 Study to Evaluate the Pharmacokinetic Profiles of BIIB017 (Peginterferon Beta-1a) and Rebif® (Interferon Beta-1a) in Healthy Volunteers
Status: Enrolling
Updated: 11/6/2014
Clinical Research Facility
559
mi
from
Evansville, IN
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Randomized Controlled Trial of Argatroban With Tissue Plasminogen Activator (tPA) for Acute Stroke
ARTSS-2: A Pilot, Phase 2b, Randomized, Multi-center Trial of Argatroban in Combination With Recombinant Tissue Plasminogen Activator for Acute Stroke
Status: Enrolling
Updated:  11/10/2014
563
mi
from
Houston, TX
Randomized Controlled Trial of Argatroban With Tissue Plasminogen Activator (tPA) for Acute Stroke
ARTSS-2: A Pilot, Phase 2b, Randomized, Multi-center Trial of Argatroban in Combination With Recombinant Tissue Plasminogen Activator for Acute Stroke
Status: Enrolling
Updated: 11/10/2014
University of Texas Health Science Center at Houston
563
mi
from
Houston, TX
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Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated:  11/13/2014
1127
mi
from
Washington,
Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated: 11/13/2014
Clinical Research Facility
1127
mi
from
Washington,
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Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated:  11/13/2014
510
mi
from
Normal, IL
Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated: 11/13/2014
Clinical Research Facility
510
mi
from
Normal, IL
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Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated:  11/13/2014
796
mi
from
Sylvania, OH
Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated: 11/13/2014
Clinical Research Facility
796
mi
from
Sylvania, OH
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Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated:  11/13/2014
1355
mi
from
Medford, OR
Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated: 11/13/2014
Clinical Research Facility
1355
mi
from
Medford, OR
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Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated:  11/13/2014
1201
mi
from
Spokane, WA
Grass Observational Study
An Observational Multi-Centre Field Study to Assess Symptom Scores and Allergy Medication Usage in Subjects With a History of Grass-Induced Rhinoconjunctivitis
Status: Enrolling
Updated: 11/13/2014
Clinical Research Facility
1201
mi
from
Spokane, WA
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Milnacipran in Autism and the Functional Locus Coeruleus and Noradrenergic Model of Autism
Milnacipran in Autism and the Functional Locus Coeruleus and Noradrenergic Model of Autism
Status: Enrolling
Updated:  11/19/2014
1294
mi
from
Bronx, NY
Milnacipran in Autism and the Functional Locus Coeruleus and Noradrenergic Model of Autism
Milnacipran in Autism and the Functional Locus Coeruleus and Noradrenergic Model of Autism
Status: Enrolling
Updated: 11/19/2014
Montefiore Medical Center, Albert Einstein College of Medicine
1294
mi
from
Bronx, NY
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Physical Activity in Multiple Sclerosis (MS): A Novel Approach to Study Outcomes
Physical Activity in Multiple Sclerosis (MS): A Novel Approach to Study Outcomes
Status: Enrolling
Updated:  11/20/2014
mi
from
West Orange, NJ
Physical Activity in Multiple Sclerosis (MS): A Novel Approach to Study Outcomes
Physical Activity in Multiple Sclerosis (MS): A Novel Approach to Study Outcomes
Status: Enrolling
Updated: 11/20/2014
Kessler Foundation
mi
from
West Orange, NJ
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Treating New Learning and Memory Deficits in Progressive Multiple Sclerosis (MS)
Treating New Learning and Memory Deficits in Progressive Multiple Sclerosis (MS)
Status: Enrolling
Updated:  11/21/2014
mi
from
West Orange, NJ
Treating New Learning and Memory Deficits in Progressive Multiple Sclerosis (MS)
Treating New Learning and Memory Deficits in Progressive Multiple Sclerosis (MS)
Status: Enrolling
Updated: 11/21/2014
Kessler Foundation
mi
from
West Orange, NJ
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Window to Hope-Evaluating a Psychological Treatment for Hopelessness Among Veterans With Traumatic Brain Injury
Window to Hope-Evaluating a Psychological Treatment for Hopelessness Among Veterans With Traumatic Brain Injury
Status: Enrolling
Updated:  11/24/2014
409
mi
from
Denver, CO
Window to Hope-Evaluating a Psychological Treatment for Hopelessness Among Veterans With Traumatic Brain Injury
Window to Hope-Evaluating a Psychological Treatment for Hopelessness Among Veterans With Traumatic Brain Injury
Status: Enrolling
Updated: 11/24/2014
VA Eastern Colorado Health Care System
409
mi
from
Denver, CO
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Trial Comparing Different Stimulation Paradigms in Patients Treated With Vagus Nerve Stimulation for Refractory Epilepsy
Prospective Randomized Trial Comparing Different Stimulation Paradigms in Patients Treated With Vagus Nerve Stimulation for Refractory Epilepsy
Status: Enrolling
Updated:  12/4/2014
1393
mi
from
Lebanon, NH
Trial Comparing Different Stimulation Paradigms in Patients Treated With Vagus Nerve Stimulation for Refractory Epilepsy
Prospective Randomized Trial Comparing Different Stimulation Paradigms in Patients Treated With Vagus Nerve Stimulation for Refractory Epilepsy
Status: Enrolling
Updated: 12/4/2014
Dartmouth Hitchcock Medical Center
1393
mi
from
Lebanon, NH
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Intraventricular Hemorrhage and Post Hemorrhagic Ventricular Dilation: Natural Course, Treatment, and Outcome
Intraventricular Hemorrhage and Post Hemorrhagic Ventricular Dilation: Natural Course, Treatment, and Outcome
Status: Enrolling
Updated:  12/4/2014
777
mi
from
Salt Lake City, UT
Intraventricular Hemorrhage and Post Hemorrhagic Ventricular Dilation: Natural Course, Treatment, and Outcome
Intraventricular Hemorrhage and Post Hemorrhagic Ventricular Dilation: Natural Course, Treatment, and Outcome
Status: Enrolling
Updated: 12/4/2014
University of Utah
777
mi
from
Salt Lake City, UT
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1274
mi
from
Carmichael, CA
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
Mercy Stroke Center
1274
mi
from
Carmichael, CA
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1288
mi
from
New York, NY
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
St Luke's - Roosevelt Hospital Center
1288
mi
from
New York, NY
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1383
mi
from
Portland, OR
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
Oregon Health and Science University
1383
mi
from
Portland, OR
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1063
mi
from
Charleston, SC
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
Medical college of South Carolina
1063
mi
from
Charleston, SC
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1049
mi
from
Charlottesville, VA
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
University of Virginia
1049
mi
from
Charlottesville, VA
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1181
mi
from
Norfolk, VA
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
Sentara Norfolk General Hospital
1181
mi
from
Norfolk, VA
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1166
mi
from
Los Angeles, CA
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
University of Southern California
1166
mi
from
Los Angeles, CA
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
1049
mi
from
Gainesville, FL
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
University of Florida
1049
mi
from
Gainesville, FL
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
411
mi
from
St. Louis, MO
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
Saint Louis University
411
mi
from
St. Louis, MO
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
349
mi
from
Dallas, TX
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
University of Texas Southwest Medical Center
349
mi
from
Dallas, TX
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HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated:  12/11/2014
572
mi
from
Houston, TX
HydroCoil Cerebral Aneurysm Treatment Trial
HydroCoil Cerebral Aneurysm Treatment Trial
Status: Enrolling
Updated: 12/11/2014
The Methodist Research Institute
572
mi
from
Houston, TX
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Effects of Protein Supplementation on Lean Body Mass Recovery From Extreme Military Training
Effect of Protein Supplementation on Lean Body Mass Recovery and Physiological Resilience Following Survive, Evade, Resist, Escape (SERE) School
Status: Enrolling
Updated:  12/17/2014
1152
mi
from
Camp Lejeune, NC
Effects of Protein Supplementation on Lean Body Mass Recovery From Extreme Military Training
Effect of Protein Supplementation on Lean Body Mass Recovery and Physiological Resilience Following Survive, Evade, Resist, Escape (SERE) School
Status: Enrolling
Updated: 12/17/2014
US Marine SERE School
1152
mi
from
Camp Lejeune, NC
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Real-world Outcomes on Tecfidera® (BG00012, Dimethyl Fumarate) Post-Tysabri® (BG00002, Natalizumab)
A Multicenter, Retrospective, Observational Study Evaluating Real-world Clinical Outcomes in Relapsing-remitting Multiple Sclerosis Patients Who Transition From Tysabri® (Natalizumab) to Tecfidera® (Dimethyl Fumarate)
Status: Enrolling
Updated:  12/18/2014
1290
mi
from
New York, NY
Real-world Outcomes on Tecfidera® (BG00012, Dimethyl Fumarate) Post-Tysabri® (BG00002, Natalizumab)
A Multicenter, Retrospective, Observational Study Evaluating Real-world Clinical Outcomes in Relapsing-remitting Multiple Sclerosis Patients Who Transition From Tysabri® (Natalizumab) to Tecfidera® (Dimethyl Fumarate)
Status: Enrolling
Updated: 12/18/2014
Clinical Research Facility
1290
mi
from
New York, NY
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Dose Optimization for Stroke Evaluation
Optimizing the Dose of Rehabilitation After Stroke.
Status: Enrolling
Updated:  12/22/2014
1166
mi
from
Los Angeles, CA
Dose Optimization for Stroke Evaluation
Optimizing the Dose of Rehabilitation After Stroke.
Status: Enrolling
Updated: 12/22/2014
University of Southern California Health Sciences Campus
1166
mi
from
Los Angeles, CA
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
372
mi
from
Little Rock, AR
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Woodland International Research Group, Inc.
372
mi
from
Little Rock, AR
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
386
mi
from
Colorado Springs, CO
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
MCB Clinical Research Centers
386
mi
from
Colorado Springs, CO
Click here to add this to my saved trials
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
1312
mi
from
Hialeah, FL
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Palm Springs Research Institute
1312
mi
from
Hialeah, FL
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
801
mi
from
Atlanta, GA
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Atlanta Center for Medical Research
801
mi
from
Atlanta, GA
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
805
mi
from
Decatur, GA
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
iResearch Atlanta LLC
805
mi
from
Decatur, GA
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
700
mi
from
New Orleans, LA
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Louisiana Research Associates, Inc.
700
mi
from
New Orleans, LA
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
1068
mi
from
Raleigh, NC
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Wake Research, LLC
1068
mi
from
Raleigh, NC
Click here to add this to my saved trials
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
153
mi
from
Oklahoma City, OK
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Cutting Edge Research Group
153
mi
from
Oklahoma City, OK
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
157
mi
from
Oklahoma City, OK
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
IPS Research Company
157
mi
from
Oklahoma City, OK
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
571
mi
from
San Antonio, TX
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Clinical Trials of Texas, Inc. (CTT)
571
mi
from
San Antonio, TX
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
561
mi
from
San Antonio, TX
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Road Runner Research
561
mi
from
San Antonio, TX
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Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated:  12/29/2014
764
mi
from
Orem, UT
Dasotraline SEP360-105 Pediatric PK/PD Study
A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Evaluation of Single Oral Doses of SEP-225289 in Subjects 6 to 17 Years of Age With Attention Deficit Hyperactivity Disorder
Status: Enrolling
Updated: 12/29/2014
Aspen Clinical Research, LLC
764
mi
from
Orem, UT
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Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCI)
Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCIMAG)
Status: Enrolling
Updated:  1/6/2015
1279
mi
from
Newark, NJ
Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCI)
Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCIMAG)
Status: Enrolling
Updated: 1/6/2015
Gaviota Clinic
1279
mi
from
Newark, NJ
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Physical Telerehabilitation in Veterans With Multiple Sclerosis
Physical Telerehabilitation in Veterans With Multiple Sclerosis
Status: Enrolling
Updated:  1/20/2015
1148
mi
from
Baltimore, MD
Physical Telerehabilitation in Veterans With Multiple Sclerosis
Physical Telerehabilitation in Veterans With Multiple Sclerosis
Status: Enrolling
Updated: 1/20/2015
University of Maryland
1148
mi
from
Baltimore, MD
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A Evaluation Of Biomarkers Associated With Sports Induced Concussions In College Student Athletes
A Prospective Evaluation Of Biomarkers Associated With Sports Induced Concussions In College Student Athletes
Status: Enrolling
Updated:  1/26/2015
1049
mi
from
Gainesville, FL
A Evaluation Of Biomarkers Associated With Sports Induced Concussions In College Student Athletes
A Prospective Evaluation Of Biomarkers Associated With Sports Induced Concussions In College Student Athletes
Status: Enrolling
Updated: 1/26/2015
University of Florida
1049
mi
from
Gainesville, FL
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Allopregnanolone for the Treatment of Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Clinical Trial of Allopregnanolone for the Treatment of Traumatic Brain Injury
Status: Enrolling
Updated:  2/2/2015
1166
mi
from
Los Angeles, CA
Allopregnanolone for the Treatment of Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Clinical Trial of Allopregnanolone for the Treatment of Traumatic Brain Injury
Status: Enrolling
Updated: 2/2/2015
University of Southern California
1166
mi
from
Los Angeles, CA
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Allopregnanolone for the Treatment of Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Clinical Trial of Allopregnanolone for the Treatment of Traumatic Brain Injury
Status: Enrolling
Updated:  2/2/2015
1283
mi
from
Sacramento, CA
Allopregnanolone for the Treatment of Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Clinical Trial of Allopregnanolone for the Treatment of Traumatic Brain Injury
Status: Enrolling
Updated: 2/2/2015
University of California, Davis Medical Center
1283
mi
from
Sacramento, CA
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