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

PET Imaging of Brain Amyloid Using [11C]MeS-IMPY
PET Imaging of Brain Amyloid Using [11C]MeS-IMPY
Status: Enrolling
Updated:  10/5/2015
mi
from
Bethesda, MD
PET Imaging of Brain Amyloid Using [11C]MeS-IMPY
PET Imaging of Brain Amyloid Using [11C]MeS-IMPY
Status: Enrolling
Updated: 10/5/2015
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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A Drug-Drug Interaction Study To Investigate The Potential For Multiple Doses Of Palbociclib (PD-0332991) To Alter The Pharmacokinetics Of Oral Midazolam In Adult Healthy Women of Non-Childbearing Potential.
A Phase 1 Randomized, Open-Label, 2-Sequence, 2-Period Crossover Study Of The Effect Of Multiple Doses Of PD-0332991 On Midazolam Pharmacokinetics In Healthy Women of Non-Childbearing Potential
Status: Enrolling
Updated:  10/6/2015
mi
from
South Miami, FL
A Drug-Drug Interaction Study To Investigate The Potential For Multiple Doses Of Palbociclib (PD-0332991) To Alter The Pharmacokinetics Of Oral Midazolam In Adult Healthy Women of Non-Childbearing Potential.
A Phase 1 Randomized, Open-Label, 2-Sequence, 2-Period Crossover Study Of The Effect Of Multiple Doses Of PD-0332991 On Midazolam Pharmacokinetics In Healthy Women of Non-Childbearing Potential
Status: Enrolling
Updated: 10/6/2015
Pfizer Investigational Site
mi
from
South Miami, FL
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A Study To Determine If Coadministration Of Tamoxifen Alters The Extent Or Rate Of Palbociclib (PD-0332991) Absorption Or Elimination In Healthy Male Volunteers
A Phase 1 Open-Label Fixed-Sequence Two-Period Crossover Study Of The Effect Of Multiple Doses Of Tamoxifen On PD-0332991 Pharmacokinetics In Healthy Male Volunteers
Status: Enrolling
Updated:  10/6/2015
mi
from
New Haven, CT
A Study To Determine If Coadministration Of Tamoxifen Alters The Extent Or Rate Of Palbociclib (PD-0332991) Absorption Or Elimination In Healthy Male Volunteers
A Phase 1 Open-Label Fixed-Sequence Two-Period Crossover Study Of The Effect Of Multiple Doses Of Tamoxifen On PD-0332991 Pharmacokinetics In Healthy Male Volunteers
Status: Enrolling
Updated: 10/6/2015
Pfizer Investigational Site
mi
from
New Haven, CT
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Drug Interaction Study To Investigate The Potential Effect Of Proton Pump Inhibitor On The Pharmacokinetics Of Palbociclib (PD-0332991)
A Phase 1, Open-Label Fixed-Sequence 2-Period Crossover Study Of Palbociclib In Healthy Subjects To Investigate The Potential Effect Of Antacid Treatment On The Pharmacokinetics Of A Single Oral Dose Administered Under Fasted Conditions
Status: Enrolling
Updated:  10/6/2015
mi
from
South Miami, FL
Drug Interaction Study To Investigate The Potential Effect Of Proton Pump Inhibitor On The Pharmacokinetics Of Palbociclib (PD-0332991)
A Phase 1, Open-Label Fixed-Sequence 2-Period Crossover Study Of Palbociclib In Healthy Subjects To Investigate The Potential Effect Of Antacid Treatment On The Pharmacokinetics Of A Single Oral Dose Administered Under Fasted Conditions
Status: Enrolling
Updated: 10/6/2015
Pfizer Investigational Site
mi
from
South Miami, FL
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Effect of Pharmacist Initiated Recommendations On Prescribing For Participants In the Senior MEDS Personalized Medication Review
Participant Characteristics, Medication Utilization, and the Effects of Pharmacist Initiated Recommendations On the Prescribing For Participants In the Senior MEDS Personalized Medication Review for Adults Age 55 and Older
Status: Enrolling
Updated:  10/6/2015
mi
from
Madison, WI
Effect of Pharmacist Initiated Recommendations On Prescribing For Participants In the Senior MEDS Personalized Medication Review
Participant Characteristics, Medication Utilization, and the Effects of Pharmacist Initiated Recommendations On the Prescribing For Participants In the Senior MEDS Personalized Medication Review for Adults Age 55 and Older
Status: Enrolling
Updated: 10/6/2015
University of Wisconsin
mi
from
Madison, WI
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Myogenic and Osteogenic Responses to eXercise and Ibuprofen
COX Inhibition & Musculoskeletal Responses to Exercise
Status: Enrolling
Updated:  10/7/2015
mi
from
Aurora, CO
Myogenic and Osteogenic Responses to eXercise and Ibuprofen
COX Inhibition & Musculoskeletal Responses to Exercise
Status: Enrolling
Updated: 10/7/2015
University of Colorado Denver
mi
from
Aurora, CO
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Drug Interaction Study of MGL-3196 With Rosuvastatin and Simvastatin
A Single Center, Open-label, Drug Interaction Study of MGL-3196 With Rosuvastatin and Simvastatin in Healthy Subjects
Status: Enrolling
Updated:  10/7/2015
mi
from
Tempe, AZ
Drug Interaction Study of MGL-3196 With Rosuvastatin and Simvastatin
A Single Center, Open-label, Drug Interaction Study of MGL-3196 With Rosuvastatin and Simvastatin in Healthy Subjects
Status: Enrolling
Updated: 10/7/2015
Celerion
mi
from
Tempe, AZ
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Radiolabeled Study of AG-221 in Healthy Male Subjects.
A Phase 1, Open-Label, Two-Part Study to Evaluate the Metabolism, Excretion, and Absolute Bioavailability of AG-221 in Healthy Adult Male Subjects
Status: Enrolling
Updated:  10/9/2015
mi
from
Madison, WI
Radiolabeled Study of AG-221 in Healthy Male Subjects.
A Phase 1, Open-Label, Two-Part Study to Evaluate the Metabolism, Excretion, and Absolute Bioavailability of AG-221 in Healthy Adult Male Subjects
Status: Enrolling
Updated: 10/9/2015
Covance Clinical Research Unit
mi
from
Madison, WI
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mi
from
Los Angeles, CA
LAC-USC Medical Center GCRC
mi
from
Los Angeles, CA
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Collection of Anatomical and Reference Data for Development of a Novel Non-Invasive Lung Hydration Status Technology
Collection of Anatomical and Reference Data for Development of a Novel Non-Invasive Lung Hydration Status Technology
Status: Enrolling
Updated:  10/13/2015
mi
from
Carlsbad, CA
Collection of Anatomical and Reference Data for Development of a Novel Non-Invasive Lung Hydration Status Technology
Collection of Anatomical and Reference Data for Development of a Novel Non-Invasive Lung Hydration Status Technology
Status: Enrolling
Updated: 10/13/2015
Intersection Medical Inc.
mi
from
Carlsbad, CA
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Circulatory Levels of Irisin in Response to Chronic Resistance Training
Circulatory Levels of Irisin in Response to Chronic Resistance Training
Status: Enrolling
Updated:  10/19/2015
mi
from
Lubbock, TX
Circulatory Levels of Irisin in Response to Chronic Resistance Training
Circulatory Levels of Irisin in Response to Chronic Resistance Training
Status: Enrolling
Updated: 10/19/2015
Exercise and Sport Sciences Building
mi
from
Lubbock, TX
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Circulatory Levels of Irisin in Response to Acute Resistance Training
Circulatory Levels of Irisin in Response to Acute Resistance Training
Status: Enrolling
Updated:  10/19/2015
mi
from
Lubbock, TX
Circulatory Levels of Irisin in Response to Acute Resistance Training
Circulatory Levels of Irisin in Response to Acute Resistance Training
Status: Enrolling
Updated: 10/19/2015
Exercise and Sport Sciences Building
mi
from
Lubbock, TX
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To Determine the Fasting Bioequivalence of Reformulated OXY Tablets Manufactured at Two Different Facilities
A Randomized, Open-Label, Single-Dose, Two-Way Crossover Study in Healthy Subjects to Determine the Fasting Bioequivalence of Oxycodone Tamper Resistant (OTR) 80-mg Tablets Manufactured at the Totowa, NJ Facility to Oxycodone Tamper Resistant (OTR) 80-mg Tablets Manufactured at the Wilson, NC Facility
Status: Enrolling
Updated:  10/19/2015
mi
from
Honolulu, HI
To Determine the Fasting Bioequivalence of Reformulated OXY Tablets Manufactured at Two Different Facilities
A Randomized, Open-Label, Single-Dose, Two-Way Crossover Study in Healthy Subjects to Determine the Fasting Bioequivalence of Oxycodone Tamper Resistant (OTR) 80-mg Tablets Manufactured at the Totowa, NJ Facility to Oxycodone Tamper Resistant (OTR) 80-mg Tablets Manufactured at the Wilson, NC Facility
Status: Enrolling
Updated: 10/19/2015
Covance Clinical Research Unit Honolulu
mi
from
Honolulu, HI
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Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment
A Phase I, Open-Label, Parallel-Group, Multiple-Dose Study to Determine the Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment and in Healthy Control Volunteers
Status: Enrolling
Updated:  10/20/2015
mi
from
Miami, FL
Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment
A Phase I, Open-Label, Parallel-Group, Multiple-Dose Study to Determine the Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment and in Healthy Control Volunteers
Status: Enrolling
Updated: 10/20/2015
University of Miami
mi
from
Miami, FL
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Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment
A Phase I, Open-Label, Parallel-Group, Multiple-Dose Study to Determine the Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment and in Healthy Control Volunteers
Status: Enrolling
Updated:  10/20/2015
mi
from
Orlando, FL
Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment
A Phase I, Open-Label, Parallel-Group, Multiple-Dose Study to Determine the Pharmacokinetics of Favipiravir in Volunteers With Hepatic Impairment and in Healthy Control Volunteers
Status: Enrolling
Updated: 10/20/2015
Orlando Clinical Research Center
mi
from
Orlando, FL
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The Effect of Rifapentine on Raltegravir
The Effect of Rifapentine on Plasma Concentrations of Raltegravir
Status: Enrolling
Updated:  10/21/2015
mi
from
San Antonio, TX
The Effect of Rifapentine on Raltegravir
The Effect of Rifapentine on Plasma Concentrations of Raltegravir
Status: Enrolling
Updated: 10/21/2015
Audie L Murphy Veterans Administration Hospital
mi
from
San Antonio, TX
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The Effect of Rifapentine on Raltegravir
The Effect of Rifapentine on Plasma Concentrations of Raltegravir
Status: Enrolling
Updated:  10/21/2015
mi
from
San Antonio, TX
The Effect of Rifapentine on Raltegravir
The Effect of Rifapentine on Plasma Concentrations of Raltegravir
Status: Enrolling
Updated: 10/21/2015
University of Texas Health Science Center
mi
from
San Antonio, TX
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Frequency of Aerobic/Resistance Training in Older Women
Frequency of Aerobic/Resistance Training in Older Women
Status: Enrolling
Updated:  10/26/2015
UAB
mi
from
Birmingham, AL
Frequency of Aerobic/Resistance Training in Older Women
Frequency of Aerobic/Resistance Training in Older Women
Status: Enrolling
Updated: 10/26/2015
UAB
mi
from
Birmingham, AL
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Bioavailability and Effect of Food on TAK-385 Tablet Formulations in Healthy Participants
A Phase 1, Open-Label, Randomized, Three-Way Crossover Study Evaluating the Relative Bioavailability and Effect of Food on TAK-385 Tablet Formulations in Healthy Subjects
Status: Enrolling
Updated:  10/26/2015
mi
from
Tempe, AZ
Bioavailability and Effect of Food on TAK-385 Tablet Formulations in Healthy Participants
A Phase 1, Open-Label, Randomized, Three-Way Crossover Study Evaluating the Relative Bioavailability and Effect of Food on TAK-385 Tablet Formulations in Healthy Subjects
Status: Enrolling
Updated: 10/26/2015
Clinical Research Facility
mi
from
Tempe, AZ
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A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated:  10/27/2015
mi
from
New Haven, CT
A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated: 10/27/2015
Anylan Center
mi
from
New Haven, CT
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A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated:  10/27/2015
mi
from
New Haven, CT
A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated: 10/27/2015
New Haven Clinical Research Unit
mi
from
New Haven, CT
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A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated:  10/27/2015
mi
from
New Haven, CT
A Study Testing A Radioactive Compound Given Through A Vein With And Without The Non-Radioactive Compound, Given By Mouth, To Characterize Tissue Distribution Using Positron Emission Tomography Scanning
A Phase 1, Open-label, 3-period, Randomized, Partially Fixed Sequence, 2-way Crossover Study With A Microdose Of [11c]Pf-06427878 Administered With And Without Two Non-radioactive Doses Of Pf-06427878 To Characterize Tissue Distribution Using Positron Emission Tomography In Healthy Adult Male Subjects
Status: Enrolling
Updated: 10/27/2015
Yale University School of Medicine
mi
from
New Haven, CT
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Evaluation of 18F-FP-DTBZ Pancreatic PET Scanning as a Tool to Measure Beta Cell Mass
Scan Re-Scan Pancreatic Beta Cell Imaging Using PET Imaging and 18F-FP-DTBZ
Status: Enrolling
Updated:  10/27/2015
mi
from
New York, NY
Evaluation of 18F-FP-DTBZ Pancreatic PET Scanning as a Tool to Measure Beta Cell Mass
Scan Re-Scan Pancreatic Beta Cell Imaging Using PET Imaging and 18F-FP-DTBZ
Status: Enrolling
Updated: 10/27/2015
Naomi Berrie Diabetes Center
mi
from
New York, NY
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Safety & Health Improvement: Enhancing Law Enforcement Departments
Safety & Health Improvement: Enhancing Law Enforcement Departments
Status: Enrolling
Updated:  10/28/2015
mi
from
Portland, OR
Safety & Health Improvement: Enhancing Law Enforcement Departments
Safety & Health Improvement: Enhancing Law Enforcement Departments
Status: Enrolling
Updated: 10/28/2015
Oregon Health and Science University
mi
from
Portland, OR
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Health Protection & Promotion for Oregon Correctional Officers
Health Protection & Promotion for Oregon Correctional Officers
Status: Enrolling
Updated:  10/28/2015
mi
from
Portland, OR
Health Protection & Promotion for Oregon Correctional Officers
Health Protection & Promotion for Oregon Correctional Officers
Status: Enrolling
Updated: 10/28/2015
Oregon Health and Science University
mi
from
Portland, OR
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Improvement in Memory With Plasticity-Based Adaptive Cognitive Training (IMPACT)
Improvement in Memory With Plasticity-Based Adaptive Cognitive Training (IMPACT)
Status: Enrolling
Updated:  10/29/2015
mi
from
San Francisco, CA
Improvement in Memory With Plasticity-Based Adaptive Cognitive Training (IMPACT)
Improvement in Memory With Plasticity-Based Adaptive Cognitive Training (IMPACT)
Status: Enrolling
Updated: 10/29/2015
Posit Science Corporation
mi
from
San Francisco, CA
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Computer-Based Training for Cognitive Enhancement: Classroom Study
Computer-Based Training for Cognitive Enhancement: Classroom Study
Status: Enrolling
Updated:  10/29/2015
mi
from
San Francisco, CA
Computer-Based Training for Cognitive Enhancement: Classroom Study
Computer-Based Training for Cognitive Enhancement: Classroom Study
Status: Enrolling
Updated: 10/29/2015
Posit Science Corporation
mi
from
San Francisco, CA
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Computer-Based Training for Cognitive Enhancement: In Home Study
Computer-Based Training for Cognitive Enhancement: In Home Study
Status: Enrolling
Updated:  10/29/2015
mi
from
San Francisco, CA
Computer-Based Training for Cognitive Enhancement: In Home Study
Computer-Based Training for Cognitive Enhancement: In Home Study
Status: Enrolling
Updated: 10/29/2015
Posit Science Corporation
mi
from
San Francisco, CA
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Evaluation of Biomarker Expression in Diabetic and Healthy Subjects Over a One Year Period
An Observational Study Evaluating Biomarker Expression in Diabetic and Healthy Subjects Over a One Year Period
Status: Enrolling
Updated:  10/29/2015
mi
from
Princeton, NJ
Evaluation of Biomarker Expression in Diabetic and Healthy Subjects Over a One Year Period
An Observational Study Evaluating Biomarker Expression in Diabetic and Healthy Subjects Over a One Year Period
Status: Enrolling
Updated: 10/29/2015
Novo Nordisk Clinical Trial Call Center
mi
from
Princeton, NJ
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Evaluation of the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of E2609 in Healthy Subjects
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of E2609 in Healthy Subjects
Status: Enrolling
Updated:  11/2/2015
mi
from
Orlando, FL
Evaluation of the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of E2609 in Healthy Subjects
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of E2609 in Healthy Subjects
Status: Enrolling
Updated: 11/2/2015
Compass Research Phase 1, LLC
mi
from
Orlando, FL
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A Two-Part Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006 in Healthy Japanese and White Subjects
A Two-Part, Randomized, Double-Blind, Placebo-Controlled, Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006 in Healthy Japanese and White Subjects
Status: Enrolling
Updated:  11/2/2015
mi
from
Glendale, CA
A Two-Part Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006 in Healthy Japanese and White Subjects
A Two-Part, Randomized, Double-Blind, Placebo-Controlled, Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006 in Healthy Japanese and White Subjects
Status: Enrolling
Updated: 11/2/2015
Clinical Research Facility
mi
from
Glendale, CA
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mi
from
Madison, WI
Covance Clinical Research Unit
mi
from
Madison, WI
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Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2609 in Healthy Adult Male Japanese and White Subjects
A Randomized, Double-Blind, Placebo-Controlled, Single Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2609 in Healthy Adult Male Japanese and White Subjects
Status: Enrolling
Updated:  11/2/2015
mi
from
Glendale, CA
Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2609 in Healthy Adult Male Japanese and White Subjects
A Randomized, Double-Blind, Placebo-Controlled, Single Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2609 in Healthy Adult Male Japanese and White Subjects
Status: Enrolling
Updated: 11/2/2015
Clinical Research Facility
mi
from
Glendale, CA
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A Study to Evaluate the Effects of E2609 on QTc Interval in Healthy Subjects
A Randomized, Double-Blind, Placebo and Active-Controlled, Single-Dose, 4-Treatment Crossover Study to Evaluate the Effects of E2609 on QTc Interval in Healthy Subjects
Status: Enrolling
Updated:  11/2/2015
mi
from
San Antonio, TX
A Study to Evaluate the Effects of E2609 on QTc Interval in Healthy Subjects
A Randomized, Double-Blind, Placebo and Active-Controlled, Single-Dose, 4-Treatment Crossover Study to Evaluate the Effects of E2609 on QTc Interval in Healthy Subjects
Status: Enrolling
Updated: 11/2/2015
Clinical Research Facility
mi
from
San Antonio, TX
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Drug-Drug Interaction Potential of Orbactiv (Oritavancin) Co-Administered With Warfarin in Healthy Subjects
An Open-Label Study to Assess the Drug-Drug Interaction Potential of a Single 1200 mg IV Dose of Orbactiv (Oritavancin) Co-Administered With Warfarin in Healthy Subjects.
Status: Enrolling
Updated:  11/2/2015
mi
from
West Bend, WI
Drug-Drug Interaction Potential of Orbactiv (Oritavancin) Co-Administered With Warfarin in Healthy Subjects
An Open-Label Study to Assess the Drug-Drug Interaction Potential of a Single 1200 mg IV Dose of Orbactiv (Oritavancin) Co-Administered With Warfarin in Healthy Subjects.
Status: Enrolling
Updated: 11/2/2015
Spaulding Clinical
mi
from
West Bend, WI
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mi
from
Austin, TX
PPD Development
mi
from
Austin, TX
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MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated:  11/4/2015
mi
from
Nashville, TN
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated: 11/4/2015
VA - TN Valley Healthcare System
mi
from
Nashville, TN
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MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated:  11/4/2015
mi
from
Salt Lake City, UT
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated: 11/4/2015
Salt Lake City VA
mi
from
Salt Lake City, UT
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MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated:  11/4/2015
mi
from
Seattle, WA
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
MIND-ICU Study: Delirium and Dementia in Veterans Surviving ICU Care
Status: Enrolling
Updated: 11/4/2015
Puget Sound VA
mi
from
Seattle, WA
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LMA Cuff Pressure and LMA-induced Complications
Using the Natural Recoil of the Inflating Syringe as a Safety Valve to Limit LMA Cuff Pressure and Decrease LMA-Induced Complications
Status: Enrolling
Updated:  11/5/2015
mi
from
Gainesville, FL
LMA Cuff Pressure and LMA-induced Complications
Using the Natural Recoil of the Inflating Syringe as a Safety Valve to Limit LMA Cuff Pressure and Decrease LMA-Induced Complications
Status: Enrolling
Updated: 11/5/2015
University of Florida College of Medicine
mi
from
Gainesville, FL
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LMA Cuff Pressure and LMA-induced Complications
Using the Natural Recoil of the Inflating Syringe as a Safety Valve to Limit LMA Cuff Pressure and Decrease LMA-Induced Complications
Status: Enrolling
Updated:  11/5/2015
mi
from
Jacksonville, FL
LMA Cuff Pressure and LMA-induced Complications
Using the Natural Recoil of the Inflating Syringe as a Safety Valve to Limit LMA Cuff Pressure and Decrease LMA-Induced Complications
Status: Enrolling
Updated: 11/5/2015
Mayo Clinic
mi
from
Jacksonville, FL
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A Study of the Abuse Liability Potential of ALKS 5461 in Healthy, Non-Dependent, Recreational Opioid Users
A Phase 1, Single-Dose, Double-Blind, Placebo-and Active-Controlled, Randomized, 6-way Crossover Human Abuse Liability Evaluation of ALKS 5461
Status: Enrolling
Updated:  11/9/2015
mi
from
Overland Park, KA
A Study of the Abuse Liability Potential of ALKS 5461 in Healthy, Non-Dependent, Recreational Opioid Users
A Phase 1, Single-Dose, Double-Blind, Placebo-and Active-Controlled, Randomized, 6-way Crossover Human Abuse Liability Evaluation of ALKS 5461
Status: Enrolling
Updated: 11/9/2015
Alkermes Study Site
mi
from
Overland Park, KA
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A Water Consumption Study of ALKS 5461 in Healthy Volunteers
A Phase 1 Study to Evaluate the Impact of Water Consumption on the Pharmacokinetics of Sublingually Administered ALKS 5461
Status: Enrolling
Updated:  11/9/2015
mi
from
Overland Park, KA
A Water Consumption Study of ALKS 5461 in Healthy Volunteers
A Phase 1 Study to Evaluate the Impact of Water Consumption on the Pharmacokinetics of Sublingually Administered ALKS 5461
Status: Enrolling
Updated: 11/9/2015
Alkermes Study Site
mi
from
Overland Park, KA
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A Drug-drug Interaction Study of ALKS 5461 in Healthy Volunteers
A Phase 1 Study to Evaluate the Impact of CYP3A4 Induction on the Single Dose Pharmacokinetics of ALKS 5461
Status: Enrolling
Updated:  11/9/2015
mi
from
Overland Park, KA
A Drug-drug Interaction Study of ALKS 5461 in Healthy Volunteers
A Phase 1 Study to Evaluate the Impact of CYP3A4 Induction on the Single Dose Pharmacokinetics of ALKS 5461
Status: Enrolling
Updated: 11/9/2015
Alkermes Study Site
mi
from
Overland Park, KA
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Intralumenal Effects on Cholesterol Absorption/Synthesis
Intralumenal Effects on Cholesterol Absorption/Synthesis
Status: Enrolling
Updated:  11/10/2015
mi
from
Cincinnati, OH
Intralumenal Effects on Cholesterol Absorption/Synthesis
Intralumenal Effects on Cholesterol Absorption/Synthesis
Status: Enrolling
Updated: 11/10/2015
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
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Effect of Teduglutide on Gastric Emptying in Healthy Subjects
A Randomized, Double-Blind, Placebo-Controlled, Multiple Dosing, Parallel Group Study to Assess the Effects of Teduglutide (ALX-0600) on Gastric Emptying in Healthy Subjects
Status: Enrolling
Updated:  11/10/2015
mi
from
San Antonio, TX
Effect of Teduglutide on Gastric Emptying in Healthy Subjects
A Randomized, Double-Blind, Placebo-Controlled, Multiple Dosing, Parallel Group Study to Assess the Effects of Teduglutide (ALX-0600) on Gastric Emptying in Healthy Subjects
Status: Enrolling
Updated: 11/10/2015
Cetero Clinical Research
mi
from
San Antonio, TX
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Reliability and Validity of Online Cognitive Assessments
Reliability and Validity of Online Cognitive Assessments
Status: Enrolling
Updated:  11/11/2015
mi
from
San Francisco, CA
Reliability and Validity of Online Cognitive Assessments
Reliability and Validity of Online Cognitive Assessments
Status: Enrolling
Updated: 11/11/2015
Lumos Labs, Inc.
mi
from
San Francisco, CA
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Evaluation of the Mechanism of Action of Platelet Rich Fibrin Matrix (PRFM) in Producing Skin Volume Augmentation
Evaluation of the Mechanism of Action of Platelet Rich Fibrin Matrix (PRFM) in Producing Skin Volume Augmentation
Status: Enrolling
Updated:  11/11/2015
mi
from
New York, NY
Evaluation of the Mechanism of Action of Platelet Rich Fibrin Matrix (PRFM) in Producing Skin Volume Augmentation
Evaluation of the Mechanism of Action of Platelet Rich Fibrin Matrix (PRFM) in Producing Skin Volume Augmentation
Status: Enrolling
Updated: 11/11/2015
The NY Eye & Ear Infirmary
mi
from
New York, NY
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