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
3,204
archived clinical trials in
Healthy Studies

Interactive Effects of IV Ethanol and IV Nicotine
A Laboratory Study on the Interactive Effects of IV Ethanol and IV Nicotine on Subjective Effects and Cognition
Status: Enrolling
Updated:  1/12/2018
West Haven VA Hospital
mi
from
West Haven, CT
Interactive Effects of IV Ethanol and IV Nicotine
A Laboratory Study on the Interactive Effects of IV Ethanol and IV Nicotine on Subjective Effects and Cognition
Status: Enrolling
Updated: 1/12/2018
West Haven VA Hospital
mi
from
West Haven, CT
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High-field Brain Magnetic Resonance Spectroscopy
Technical Developments for High-field Brain Magnetic Resonance Spectroscopy
Status: Enrolling
Updated:  1/12/2018
Center for Magnetic Resonance Research
mi
from
Minneapolis, MN
High-field Brain Magnetic Resonance Spectroscopy
Technical Developments for High-field Brain Magnetic Resonance Spectroscopy
Status: Enrolling
Updated: 1/12/2018
Center for Magnetic Resonance Research
mi
from
Minneapolis, MN
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Time Restricted Diet in Obese or Overweight Pre or Postmenopausal Participants
A Pilot Study of Time Restricted Diet in Obese/Overweight Pre &Amp; Postmenopausal Women
Status: Enrolling
Updated:  1/12/2018
Northwestern University
mi
from
Chicago, IL
Time Restricted Diet in Obese or Overweight Pre or Postmenopausal Participants
A Pilot Study of Time Restricted Diet in Obese/Overweight Pre &Amp; Postmenopausal Women
Status: Enrolling
Updated: 1/12/2018
Northwestern University
mi
from
Chicago, IL
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A Study to Evaluate the Safety of the Coadministration of ANS-6637 and Ethanol
A Phase 1b, Proof of Concept, Dose-Ranging Study to Evaluate the Safety of the Coadministration of Ascending Doses of ANS-6637 and Ethanol in Healthy Male Moderate Drinkers
Status: Enrolling
Updated:  1/12/2018
Vince and Associates
mi
from
Overland Park, KA
A Study to Evaluate the Safety of the Coadministration of ANS-6637 and Ethanol
A Phase 1b, Proof of Concept, Dose-Ranging Study to Evaluate the Safety of the Coadministration of Ascending Doses of ANS-6637 and Ethanol in Healthy Male Moderate Drinkers
Status: Enrolling
Updated: 1/12/2018
Vince and Associates
mi
from
Overland Park, KA
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GLASSIA Infusion Rate Study
A Phase 4 Double-Blind Study to Assess the Safety and Tolerability of Intravenous Administration of GLASSIA in Healthy Adult Volunteers
Status: Enrolling
Updated:  1/16/2018
Clinical Research Facility
mi
from
Overland Park, KA
GLASSIA Infusion Rate Study
A Phase 4 Double-Blind Study to Assess the Safety and Tolerability of Intravenous Administration of GLASSIA in Healthy Adult Volunteers
Status: Enrolling
Updated: 1/16/2018
Clinical Research Facility
mi
from
Overland Park, KA
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Effect of Oxytocin Nasal Sprays on Social Behavior in Social Anxiety Disorder
Effect of Oxytocin on Pro-Social Behavior in Social Anxiety Disorder
Status: Enrolling
Updated:  1/16/2018
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
Effect of Oxytocin Nasal Sprays on Social Behavior in Social Anxiety Disorder
Effect of Oxytocin on Pro-Social Behavior in Social Anxiety Disorder
Status: Enrolling
Updated: 1/16/2018
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
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Brain Computer Interface Control of a Robotic Device
Brain Computer Interface Control of a Robotic Device
Status: Enrolling
Updated:  1/16/2018
Nils Hasselmo Hall at the University of Minnesota - Twin Cities Campus
mi
from
Minneapolis, MN
Brain Computer Interface Control of a Robotic Device
Brain Computer Interface Control of a Robotic Device
Status: Enrolling
Updated: 1/16/2018
Nils Hasselmo Hall at the University of Minnesota - Twin Cities Campus
mi
from
Minneapolis, MN
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Heritability and Genetics of Fat Taste
Heritability and Genetics of Fat Taste
Status: Enrolling
Updated:  1/16/2018
Denver Museum of Nature & Science
mi
from
Denver, CO
Heritability and Genetics of Fat Taste
Heritability and Genetics of Fat Taste
Status: Enrolling
Updated: 1/16/2018
Denver Museum of Nature & Science
mi
from
Denver, CO
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A Study of Plasma-Derived Human Butyrylcholinesterase Administered Intramuscularly
A Phase 1, Randomized, Observer-Blinded, Single Dose, Placebo Controlled Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Plasma-Derived Human Butyrylcholinesterase (HuBChE) Administered Intramuscularly (IM)
Status: Enrolling
Updated:  1/16/2018
Quintiles Phase 1 Services
mi
from
Lenexa, KA
A Study of Plasma-Derived Human Butyrylcholinesterase Administered Intramuscularly
A Phase 1, Randomized, Observer-Blinded, Single Dose, Placebo Controlled Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Plasma-Derived Human Butyrylcholinesterase (HuBChE) Administered Intramuscularly (IM)
Status: Enrolling
Updated: 1/16/2018
Quintiles Phase 1 Services
mi
from
Lenexa, KA
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Treatment of Social Phobia
Treatment of Social Phobia: Mediators And Moderators
Status: Enrolling
Updated:  1/16/2018
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
Treatment of Social Phobia
Treatment of Social Phobia: Mediators And Moderators
Status: Enrolling
Updated: 1/16/2018
Center for Anxiety and Related Disorders, Boston University
mi
from
Boston, MA
Click here to add this to my saved trials
Emotion Regulation During RCT of CBT vs. MBSR for Social Anxiety Disorder
fMRI of Emotion Regulation During RCT of CBT vs. MBSR for Social Anxiety Disorder
Status: Enrolling
Updated:  1/16/2018
Stanford University
mi
from
Stanford, CA
Emotion Regulation During RCT of CBT vs. MBSR for Social Anxiety Disorder
fMRI of Emotion Regulation During RCT of CBT vs. MBSR for Social Anxiety Disorder
Status: Enrolling
Updated: 1/16/2018
Stanford University
mi
from
Stanford, CA
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A Study to Assess the Pharmacodynamic Effects of SAGE-217 in Healthy Adults Using an Insomnia Model
A Randomized, Double-Blind, Multiple Dose, 3-way Crossover, Exploratory Study to Assess the Pharmacodynamic Effects of SAGE-217 Capsules in Healthy Adults Using a 5-hour Phase Advance Model of Insomnia
Status: Enrolling
Updated:  1/17/2018
Sage Investigational Site
mi
from
New York, NY
A Study to Assess the Pharmacodynamic Effects of SAGE-217 in Healthy Adults Using an Insomnia Model
A Randomized, Double-Blind, Multiple Dose, 3-way Crossover, Exploratory Study to Assess the Pharmacodynamic Effects of SAGE-217 Capsules in Healthy Adults Using a 5-hour Phase Advance Model of Insomnia
Status: Enrolling
Updated: 1/17/2018
Sage Investigational Site
mi
from
New York, NY
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A Study of Lasmiditan When Given With Sumatriptan in Healthy Participants
A Randomized, Double-Blind, Four-Period, Crossover Study to Evaluate the Cardiovascular Effect of Single Oral Doses of Lasmiditan When Coadministered With Single Oral Doses of Sumatriptan in Healthy Subjects
Status: Enrolling
Updated:  1/17/2018
Covance-Daytona Beach
mi
from
Daytona Beach, FL
A Study of Lasmiditan When Given With Sumatriptan in Healthy Participants
A Randomized, Double-Blind, Four-Period, Crossover Study to Evaluate the Cardiovascular Effect of Single Oral Doses of Lasmiditan When Coadministered With Single Oral Doses of Sumatriptan in Healthy Subjects
Status: Enrolling
Updated: 1/17/2018
Covance-Daytona Beach
mi
from
Daytona Beach, FL
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An Investigational Study to Assess the Effect of a Light Meal and a High-Fat Meal on the Absorption of BMS-986205 in Healthy Participants
Randomized, Open-Label Study to Assess the Effect of a Light Meal and a High-Fat Meal on the Bioavailability of a Single 100-mg Dose of BMS-986205 Commercial Tablet in Healthy Participants
Status: Enrolling
Updated:  1/17/2018
PPD Austin Clinic
mi
from
Austin, TX
An Investigational Study to Assess the Effect of a Light Meal and a High-Fat Meal on the Absorption of BMS-986205 in Healthy Participants
Randomized, Open-Label Study to Assess the Effect of a Light Meal and a High-Fat Meal on the Bioavailability of a Single 100-mg Dose of BMS-986205 Commercial Tablet in Healthy Participants
Status: Enrolling
Updated: 1/17/2018
PPD Austin Clinic
mi
from
Austin, TX
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An Investigational Study to Assess the Effect of BMS-986177 on Aspirin in Healthy Participants
A Double-Blind, Randomized, Placebo-Controlled, Parallel Group Study to Evaluate the Effect of Coadministration of Multiple Doses of BMS-986177 on Aspirin in Healthy Participants
Status: Enrolling
Updated:  1/17/2018
PPD Austin Clinic
mi
from
Austin, TX
An Investigational Study to Assess the Effect of BMS-986177 on Aspirin in Healthy Participants
A Double-Blind, Randomized, Placebo-Controlled, Parallel Group Study to Evaluate the Effect of Coadministration of Multiple Doses of BMS-986177 on Aspirin in Healthy Participants
Status: Enrolling
Updated: 1/17/2018
PPD Austin Clinic
mi
from
Austin, TX
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Molecular MRI of the Fibrotic Heart
Molecular MRI of the Fibrotic Heart
Status: Enrolling
Updated:  1/18/2018
University of Kentucky Medical Center
mi
from
Lexington, KY
Molecular MRI of the Fibrotic Heart
Molecular MRI of the Fibrotic Heart
Status: Enrolling
Updated: 1/18/2018
University of Kentucky Medical Center
mi
from
Lexington, KY
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A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated:  1/18/2018
Clinical Research Facility
mi
from
Hartford, CT
A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated: 1/18/2018
Clinical Research Facility
mi
from
Hartford, CT
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A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated:  1/18/2018
Clinical Research Facility
mi
from
Boston, MA
A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated: 1/18/2018
Clinical Research Facility
mi
from
Boston, MA
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A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated:  1/18/2018
Clinical Research Facility
mi
from
Philadelphia, PA
A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated: 1/18/2018
Clinical Research Facility
mi
from
Philadelphia, PA
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A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated:  1/18/2018
Clinical Research Facility
mi
from
Dallas, TX
A Longitudinal, Observational Biomarker Study in Participants With Primary Sjogren's Syndrome
A Biomarker Study to Determine the Gene Expression Signatures of Salivary Gland and Blood in Subjects With Incident Primary Sjögren's Syndrome, Subjects With Sicca, and Healthy Volunteers
Status: Enrolling
Updated: 1/18/2018
Clinical Research Facility
mi
from
Dallas, TX
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Open Label Study Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions
Open Label, Single-center Study, Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions
Status: Enrolling
Updated:  1/19/2018
Baumann Cosmetic & Research Institute
mi
from
Miami, FL
Open Label Study Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions
Open Label, Single-center Study, Evaluating the Efficacy and Safety of JUVÉDERM VOLUMA™ XC for the Facial Temporal Regions
Status: Enrolling
Updated: 1/19/2018
Baumann Cosmetic & Research Institute
mi
from
Miami, FL
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PK Study in Adult Healthy Volunteers to Assess QD Dosing With the Selected Age-appropriate MR Formulations
A Phase 1, Randomized, Open Label, Partial Crossover Study To Evaluate The Pharmacokinetics And Safety Of Three Age-appropriate Modified Release Formulations And The Immediate Release Solution Of Tofacitinib In Healthy Adult Volunteers
Status: Enrolling
Updated:  1/20/2018
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
PK Study in Adult Healthy Volunteers to Assess QD Dosing With the Selected Age-appropriate MR Formulations
A Phase 1, Randomized, Open Label, Partial Crossover Study To Evaluate The Pharmacokinetics And Safety Of Three Age-appropriate Modified Release Formulations And The Immediate Release Solution Of Tofacitinib In Healthy Adult Volunteers
Status: Enrolling
Updated: 1/20/2018
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated:  1/22/2018
Mississippi Family Doctors
mi
from
Pearl, MS
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated: 1/22/2018
Mississippi Family Doctors
mi
from
Pearl, MS
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Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated:  1/22/2018
Carolina Medical Associates
mi
from
Charlotte, NC
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated: 1/22/2018
Carolina Medical Associates
mi
from
Charlotte, NC
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Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated:  1/22/2018
Logan General Hospital
mi
from
Logan, WV
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Toxicity and Safety Evaluation of an Omega-3 Fatty Acid and a Multivitamin and Antioxidant Nutritional Preparation
Status: Enrolling
Updated: 1/22/2018
Logan General Hospital
mi
from
Logan, WV
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Safety Study of Acellular Adipose Tissue for Soft Tissue Reconstruction
A Phase I Open-label Study Evaluating the Safety of Acellular Adipose Tissue (AAT), a Novel Soft Tissue Reconstruction Solution, in Healthy Volunteers
Status: Enrolling
Updated:  1/22/2018
Johns Hopkins University School of Medicine
mi
from
Baltimore, MD
Safety Study of Acellular Adipose Tissue for Soft Tissue Reconstruction
A Phase I Open-label Study Evaluating the Safety of Acellular Adipose Tissue (AAT), a Novel Soft Tissue Reconstruction Solution, in Healthy Volunteers
Status: Enrolling
Updated: 1/22/2018
Johns Hopkins University School of Medicine
mi
from
Baltimore, MD
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Safety Study of Mibefradil When Given Four Times a Day in Healthy Volunteers
A Study of the Pharmacokinetic and Safety Profile of QID Dosing of Mibefradil in Normal Human Volunteers
Status: Enrolling
Updated:  1/23/2018
Celerion
mi
from
Lincoln, NE
Safety Study of Mibefradil When Given Four Times a Day in Healthy Volunteers
A Study of the Pharmacokinetic and Safety Profile of QID Dosing of Mibefradil in Normal Human Volunteers
Status: Enrolling
Updated: 1/23/2018
Celerion
mi
from
Lincoln, NE
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Investigation on Safety, Tolerability and Pharmacokinetics of Single Doses of NNC0174-0833 in Normal Weight, Overweight to Obese But Otherwise Healthy Male Subjects
Investigation on Safety, Tolerability and Pharmacokinetics of Single Doses of NNC0174-0833 in Normal Weight, Overweight to Obese But Otherwise Healthy Male Subjects
Status: Enrolling
Updated:  1/23/2018
Novo Nordisk Investigational Site
mi
from
Overland Park, KA
Investigation on Safety, Tolerability and Pharmacokinetics of Single Doses of NNC0174-0833 in Normal Weight, Overweight to Obese But Otherwise Healthy Male Subjects
Investigation on Safety, Tolerability and Pharmacokinetics of Single Doses of NNC0174-0833 in Normal Weight, Overweight to Obese But Otherwise Healthy Male Subjects
Status: Enrolling
Updated: 1/23/2018
Novo Nordisk Investigational Site
mi
from
Overland Park, KA
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A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study to Assess the Recovery and Lifespan of Radiolabeled Autologous INTERCEPT Treated Apheresis Platelet Components Suspended in Nominal 35% Plasma and 65% InterSol Stored for 6 or 7 Days
Status: Enrolling
Updated:  1/24/2018
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study to Assess the Recovery and Lifespan of Radiolabeled Autologous INTERCEPT Treated Apheresis Platelet Components Suspended in Nominal 35% Plasma and 65% InterSol Stored for 6 or 7 Days
Status: Enrolling
Updated: 1/24/2018
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
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A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study to Assess the Recovery and Lifespan of Radiolabeled Autologous INTERCEPT Treated Apheresis Platelet Components Suspended in Nominal 35% Plasma and 65% InterSol Stored for 6 or 7 Days
Status: Enrolling
Updated:  1/24/2018
Hoxworth Blood Center
mi
from
Cincinnati, OH
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study to Assess the Recovery and Lifespan of Radiolabeled Autologous INTERCEPT Treated Apheresis Platelet Components Suspended in Nominal 35% Plasma and 65% InterSol Stored for 6 or 7 Days
Status: Enrolling
Updated: 1/24/2018
Hoxworth Blood Center
mi
from
Cincinnati, OH
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Study to Evaluate the Pharmacokinetics of a New Tablet Formulation of CPI-444 in Fed and Fasted Healthy Male and Female Subjects
A Phase 1, Open-label, Randomized, Single-dose, Three-way Crossover Study to Evaluate the Pharmacokinetics of a New Tablet Formulation of CPI-444 in Fed and Fasted Healthy Male and Female Subjects
Status: Enrolling
Updated:  1/24/2018
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
Study to Evaluate the Pharmacokinetics of a New Tablet Formulation of CPI-444 in Fed and Fasted Healthy Male and Female Subjects
A Phase 1, Open-label, Randomized, Single-dose, Three-way Crossover Study to Evaluate the Pharmacokinetics of a New Tablet Formulation of CPI-444 in Fed and Fasted Healthy Male and Female Subjects
Status: Enrolling
Updated: 1/24/2018
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
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Quantification of Human Adipogenesis
Quantification of Human Adipogenesis
Status: Enrolling
Updated:  1/25/2018
Brigham and Women's Hosp
mi
from
Boston, MA
Quantification of Human Adipogenesis
Quantification of Human Adipogenesis
Status: Enrolling
Updated: 1/25/2018
Brigham and Women's Hosp
mi
from
Boston, MA
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A Study of Lasmiditan in Healthy Participants When Co-administered With Topiramate
Safety, Tolerability, and Pharmacokinetics of Lasmiditan When Co-administered With Topiramate in Healthy Subjects
Status: Enrolling
Updated:  1/26/2018
Covance Madison CRU
mi
from
Madison, WI
A Study of Lasmiditan in Healthy Participants When Co-administered With Topiramate
Safety, Tolerability, and Pharmacokinetics of Lasmiditan When Co-administered With Topiramate in Healthy Subjects
Status: Enrolling
Updated: 1/26/2018
Covance Madison CRU
mi
from
Madison, WI
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Effects of Interrupting Sedentary Behavior on Metabolic and Cognitive Outcomes in Children
Effects of Interrupting Sedentary Behavior on Metabolic and Cognitive Outcomes in Children
Status: Enrolling
Updated:  1/30/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
Effects of Interrupting Sedentary Behavior on Metabolic and Cognitive Outcomes in Children
Effects of Interrupting Sedentary Behavior on Metabolic and Cognitive Outcomes in Children
Status: Enrolling
Updated: 1/30/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Study of Safety, Tolerability, and Pharmacokinetics of REGN3470-3471-3479 in Healthy Adult Volunteers
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study Investigating the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered REGN3470-3471-3479 in Healthy Adult Subjects
Status: Enrolling
Updated:  2/1/2018
Clinical Research Facility
mi
from
Evansville, IN
Study of Safety, Tolerability, and Pharmacokinetics of REGN3470-3471-3479 in Healthy Adult Volunteers
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study Investigating the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered REGN3470-3471-3479 in Healthy Adult Subjects
Status: Enrolling
Updated: 2/1/2018
Clinical Research Facility
mi
from
Evansville, IN
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Functional Effects of Botox on the Brain Using MRS and fMRI
Measuring the Functional Effects of Botox on the Brain Using MR Spectroscopy and fMRI
Status: Enrolling
Updated:  2/1/2018
University of California, Irvine
mi
from
Irvine, CA
Functional Effects of Botox on the Brain Using MRS and fMRI
Measuring the Functional Effects of Botox on the Brain Using MR Spectroscopy and fMRI
Status: Enrolling
Updated: 2/1/2018
University of California, Irvine
mi
from
Irvine, CA
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A Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adults
A Phase 1, First-in-human Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adult
Status: Enrolling
Updated:  2/2/2018
Clinical Research Facility
mi
from
Rockville, MD
A Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adults
A Phase 1, First-in-human Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adult
Status: Enrolling
Updated: 2/2/2018
Clinical Research Facility
mi
from
Rockville, MD
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AMD 3100 (Mozobil Plerixafor) to Mobilize Stem Cells for Donation
Peripheral Blood Hematopoietic Progenitor Cell Mobilization With AMD 3100 (Mozobil) in Healthy Volunteers Previously Mobilized With G-CSF
Status: Enrolling
Updated:  2/5/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
AMD 3100 (Mozobil Plerixafor) to Mobilize Stem Cells for Donation
Peripheral Blood Hematopoietic Progenitor Cell Mobilization With AMD 3100 (Mozobil) in Healthy Volunteers Previously Mobilized With G-CSF
Status: Enrolling
Updated: 2/5/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Pilot Study for Imaging of the Esophagus Using a Tethered Capsule OCT Endomicroscopy in the Primary Care Setting
Pilot Study for Imaging of the Esophagus Using a Tethered Capsule OCT Endomicroscopy in the Primary Care Setting
Status: Enrolling
Updated:  2/5/2018
Massachusetts General Hospital
mi
from
Boston, MA
Pilot Study for Imaging of the Esophagus Using a Tethered Capsule OCT Endomicroscopy in the Primary Care Setting
Pilot Study for Imaging of the Esophagus Using a Tethered Capsule OCT Endomicroscopy in the Primary Care Setting
Status: Enrolling
Updated: 2/5/2018
Massachusetts General Hospital
mi
from
Boston, MA
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Pilot Study for Imaging of the Esophagus Using Tethered Capsule OCT Endomicroscopy With Distal Scanning
Pilot Study for Imaging of the Esophagus Using Tethered Capsule OCT Endomicroscopy With Distal Scanning
Status: Enrolling
Updated:  2/5/2018
Massachusetts General Hospital
mi
from
Boston, MA
Pilot Study for Imaging of the Esophagus Using Tethered Capsule OCT Endomicroscopy With Distal Scanning
Pilot Study for Imaging of the Esophagus Using Tethered Capsule OCT Endomicroscopy With Distal Scanning
Status: Enrolling
Updated: 2/5/2018
Massachusetts General Hospital
mi
from
Boston, MA
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A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CC-90006 in Healthy Subjects
A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CC-90006 in Healthy Subjects
Status: Enrolling
Updated:  2/7/2018
PPD Phase 1 Unit
mi
from
Austin, TX
A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CC-90006 in Healthy Subjects
A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CC-90006 in Healthy Subjects
Status: Enrolling
Updated: 2/7/2018
PPD Phase 1 Unit
mi
from
Austin, TX
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Bioavailability Study of MGL-3196 Tablets Compared to Capsules
A Single Center, Open-Label, Single-Dose, Cross-over, Bioavailability Study of MGL-3196 Tablets Compared to Capsules in Healthy Subjects
Status: Enrolling
Updated:  2/9/2018
Celerion
mi
from
Tempe, AZ
Bioavailability Study of MGL-3196 Tablets Compared to Capsules
A Single Center, Open-Label, Single-Dose, Cross-over, Bioavailability Study of MGL-3196 Tablets Compared to Capsules in Healthy Subjects
Status: Enrolling
Updated: 2/9/2018
Celerion
mi
from
Tempe, AZ
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Glymphatic Kinetics In Healthy Adult Volunteers
Evaluation Of Brain Glymphatic Kinetics Following Intrathecal Administration Of Gadolinium In Healthy Adult Volunteers
Status: Enrolling
Updated:  2/9/2018
Weill-Cornell Medical College
mi
from
New York, NY
Glymphatic Kinetics In Healthy Adult Volunteers
Evaluation Of Brain Glymphatic Kinetics Following Intrathecal Administration Of Gadolinium In Healthy Adult Volunteers
Status: Enrolling
Updated: 2/9/2018
Weill-Cornell Medical College
mi
from
New York, NY
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Bioavailability of DFN-15 at 3 Different Doses vs. Comparator and to Determine Dose-proportionality of DFN-15 in Fasting Healthy Adults
Status: Enrolling
Updated:  2/10/2018
Clinical Research Facility
mi
from
Fargo, ND
Bioavailability of DFN-15 at 3 Different Doses vs. Comparator and to Determine Dose-proportionality of DFN-15 in Fasting Healthy Adults
Status: Enrolling
Updated: 2/10/2018
Clinical Research Facility
mi
from
Fargo, ND
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Effect of Nitrite on Exercise Physiology and Metabolism
Evaluation of Systemic Nitrite Infusion and Its Effect on Exercise Physiology and Metabolism
Status: Enrolling
Updated:  2/13/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
Effect of Nitrite on Exercise Physiology and Metabolism
Evaluation of Systemic Nitrite Infusion and Its Effect on Exercise Physiology and Metabolism
Status: Enrolling
Updated: 2/13/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Understanding the Influence of Pregnancy on Breast Milk
Mom2Baby Pilot: Understanding the Influence of Pregnancy on Breast Milk
Status: Enrolling
Updated:  2/14/2018
Pennington Biomedical Research Center
mi
from
Baton Rouge, LA
Understanding the Influence of Pregnancy on Breast Milk
Mom2Baby Pilot: Understanding the Influence of Pregnancy on Breast Milk
Status: Enrolling
Updated: 2/14/2018
Pennington Biomedical Research Center
mi
from
Baton Rouge, LA
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Immune Responses After Human Subject Challenge With Sand Fly Bites
Immune Responses After Human Subject Challenge With Sand Fly Bites: Exploratory Study for Selection of Potential Leishmania Vaccine Antigen Candidates
Status: Enrolling
Updated:  2/15/2018
Walter Reed National Military Medical Center
mi
from
Bethesda, MD
Immune Responses After Human Subject Challenge With Sand Fly Bites
Immune Responses After Human Subject Challenge With Sand Fly Bites: Exploratory Study for Selection of Potential Leishmania Vaccine Antigen Candidates
Status: Enrolling
Updated: 2/15/2018
Walter Reed National Military Medical Center
mi
from
Bethesda, MD
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Crossover Drug-Drug Interaction Study to Determine Effects of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
A Phase 1, Open-Label, Fixed-Sequence, Crossover Drug-Drug Interaction Study in Healthy Subjects to Determine the Effects of a Strong Inducer of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
Status: Enrolling
Updated:  2/21/2018
SeaView Reserch
mi
from
Miami, FL
Crossover Drug-Drug Interaction Study to Determine Effects of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
A Phase 1, Open-Label, Fixed-Sequence, Crossover Drug-Drug Interaction Study in Healthy Subjects to Determine the Effects of a Strong Inducer of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
Status: Enrolling
Updated: 2/21/2018
SeaView Reserch
mi
from
Miami, FL
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Mifepristone Drug-Drug Interaction Study With CYP3A Inhibitor
A Phase 1, Open-Label, Drug-Drug Interaction Study in Healthy Subjects to Determine the Effects of a Strong Inhibitor (Itraconazole) of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
Status: Enrolling
Updated:  2/21/2018
SeaView Research Inc.
mi
from
Miami, FL
Mifepristone Drug-Drug Interaction Study With CYP3A Inhibitor
A Phase 1, Open-Label, Drug-Drug Interaction Study in Healthy Subjects to Determine the Effects of a Strong Inhibitor (Itraconazole) of Cytochrome P450 3A on Exposure to Mifepristone and Its Metabolites
Status: Enrolling
Updated: 2/21/2018
SeaView Research Inc.
mi
from
Miami, FL
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Pharmacokinetic Drug Interactions of AEGR-733 on Lipid-lowering Agents
A Phase II, Fixed-sequenced, Open- Label, Research Study to Assess Pharmacokinetic Drug Interactions of AEGR-733 on Lipid-lowering Therapies in Healthy Volunteers
Status: Enrolling
Updated:  2/21/2018
Univ of Pennsylvania
mi
from
Philadelphia, PA
Pharmacokinetic Drug Interactions of AEGR-733 on Lipid-lowering Agents
A Phase II, Fixed-sequenced, Open- Label, Research Study to Assess Pharmacokinetic Drug Interactions of AEGR-733 on Lipid-lowering Therapies in Healthy Volunteers
Status: Enrolling
Updated: 2/21/2018
Univ of Pennsylvania
mi
from
Philadelphia, PA
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