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

A Comparison of Various Combinations of BiDil Capsules and BiDil Tablets in Healthy Human Volunteers
A Four-arm, Single Dose, Two-Period, Pharmacokinetic Study of BiDil SR and IR Capsules and Commercial BiDil Tablets
Status: Enrolling
Updated:  8/4/2015
Frontage Cinical Services
mi
from
Hackensack, NJ
A Comparison of Various Combinations of BiDil Capsules and BiDil Tablets in Healthy Human Volunteers
A Four-arm, Single Dose, Two-Period, Pharmacokinetic Study of BiDil SR and IR Capsules and Commercial BiDil Tablets
Status: Enrolling
Updated: 8/4/2015
Frontage Cinical Services
mi
from
Hackensack, NJ
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Oral Bioequivalence Study of PL 3100 and Naproxen in Healthy Adults
"A Single-Dose Crossover Oral Bioequivalence Study of PL 3100 and Naproxen in Healthy Adult Volunteers in the Fasted State"
Status: Enrolling
Updated:  8/6/2015
Houston Institute for Clinical Research
mi
from
Houston, TX
Oral Bioequivalence Study of PL 3100 and Naproxen in Healthy Adults
"A Single-Dose Crossover Oral Bioequivalence Study of PL 3100 and Naproxen in Healthy Adult Volunteers in the Fasted State"
Status: Enrolling
Updated: 8/6/2015
Houston Institute for Clinical Research
mi
from
Houston, TX
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Skin Safety Study to Evaluate the Sensitizing Potential in Healthy Volunteers
A Phase 1, Randomized, Evaluator Blinded, Controlled Study to Evaluate the Sensitizing Potential of M518101 in Healthy Volunteers Using a Repeat Insult Patch Test Design
Status: Enrolling
Updated:  8/7/2015
TKL research
mi
from
Fair Lawn, NJ
Skin Safety Study to Evaluate the Sensitizing Potential in Healthy Volunteers
A Phase 1, Randomized, Evaluator Blinded, Controlled Study to Evaluate the Sensitizing Potential of M518101 in Healthy Volunteers Using a Repeat Insult Patch Test Design
Status: Enrolling
Updated: 8/7/2015
TKL research
mi
from
Fair Lawn, NJ
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Long-term Behavior Change - 1
Behavior Change: Reinforcement Schedule Effects
Status: Enrolling
Updated:  8/11/2015
Friends Research Institute
mi
from
Los Angeles, CA
Long-term Behavior Change - 1
Behavior Change: Reinforcement Schedule Effects
Status: Enrolling
Updated: 8/11/2015
Friends Research Institute
mi
from
Los Angeles, CA
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Long-term Behavior Change - 1
Behavior Change: Reinforcement Schedule Effects
Status: Enrolling
Updated:  8/11/2015
Friends Research Institute
mi
from
Rancho Cucamonga, CA
Long-term Behavior Change - 1
Behavior Change: Reinforcement Schedule Effects
Status: Enrolling
Updated: 8/11/2015
Friends Research Institute
mi
from
Rancho Cucamonga, CA
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Phenytoin as a Neuroprotective Agent Against Corticosteroid-induced Functional Imaging Changes
Phenytoin as a Neuroprotective Agent Against Corticosteroid-induced Functional Imaging Changes
Status: Enrolling
Updated:  8/12/2015
UT Southwestern Medical Center of Dallas/Parkland Memorial Hospital
mi
from
Dallas, TX
Phenytoin as a Neuroprotective Agent Against Corticosteroid-induced Functional Imaging Changes
Phenytoin as a Neuroprotective Agent Against Corticosteroid-induced Functional Imaging Changes
Status: Enrolling
Updated: 8/12/2015
UT Southwestern Medical Center of Dallas/Parkland Memorial Hospital
mi
from
Dallas, TX
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Food Effect and Bioavailability of Deflazacort Formulations in Healthy Volunteers
A Single-Dose, Single-Center, Randomized, Five Period Crossover Study Comparing Food Effect and Bioavailability of Deflazacort Formulations in Healthy Volunteers
Status: Enrolling
Updated:  8/12/2015
ICON Early Phase Services
mi
from
San Antonio, TX
Food Effect and Bioavailability of Deflazacort Formulations in Healthy Volunteers
A Single-Dose, Single-Center, Randomized, Five Period Crossover Study Comparing Food Effect and Bioavailability of Deflazacort Formulations in Healthy Volunteers
Status: Enrolling
Updated: 8/12/2015
ICON Early Phase Services
mi
from
San Antonio, TX
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An Study to Evaluate the Effects of Fluconazole on the Pharmacokinetics (PK) of Sativex® in Healthy Subjects With Cannabis Experience.
An Open-Label, Randomized, Single-Dose, Two-Sequence, Two-Treatment, Four-Period, Crossover Study to Evaluate the Effects of Fluconazole on the Pharmacokinetics (PK) of Sativex® in Healthy Subjects With Cannabis Experience.
Status: Enrolling
Updated:  8/13/2015
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
An Study to Evaluate the Effects of Fluconazole on the Pharmacokinetics (PK) of Sativex® in Healthy Subjects With Cannabis Experience.
An Open-Label, Randomized, Single-Dose, Two-Sequence, Two-Treatment, Four-Period, Crossover Study to Evaluate the Effects of Fluconazole on the Pharmacokinetics (PK) of Sativex® in Healthy Subjects With Cannabis Experience.
Status: Enrolling
Updated: 8/13/2015
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
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Physical Activity Intervention in Preschool Children
Physical Activity Intervention in Preschool Children
Status: Enrolling
Updated:  8/13/2015
Hamline University
mi
from
St. Paul, MN
Physical Activity Intervention in Preschool Children
Physical Activity Intervention in Preschool Children
Status: Enrolling
Updated: 8/13/2015
Hamline University
mi
from
St. Paul, MN
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Comparative Effects of Aspirin and NHP-544C
Comparative Effects of Rapid-Release Aspirin and NHP-544C on Basal and Bradykinin Stimulated Prostacyclin Production
Status: Enrolling
Updated:  8/17/2015
Vanderbilt University Medical Center
mi
from
Nashville, TN
Comparative Effects of Aspirin and NHP-544C
Comparative Effects of Rapid-Release Aspirin and NHP-544C on Basal and Bradykinin Stimulated Prostacyclin Production
Status: Enrolling
Updated: 8/17/2015
Vanderbilt University Medical Center
mi
from
Nashville, TN
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Effect of UV Exposure on the PD of Multiple Doses of CC-90001 and Pilot Food Effect Study
A Two-Part, Phase 1 Study to Evaluate Pharmacokinetics and Pharmacodynamics of Multiple Dose CC-90001 and to Evaluate the Effects of Food and Formulation on Pharmacokinetics of Single Dose CC-90001 in Healthy Subjects
Status: Enrolling
Updated:  8/17/2015
TKL research
mi
from
Fair Lawn, NJ
Effect of UV Exposure on the PD of Multiple Doses of CC-90001 and Pilot Food Effect Study
A Two-Part, Phase 1 Study to Evaluate Pharmacokinetics and Pharmacodynamics of Multiple Dose CC-90001 and to Evaluate the Effects of Food and Formulation on Pharmacokinetics of Single Dose CC-90001 in Healthy Subjects
Status: Enrolling
Updated: 8/17/2015
TKL research
mi
from
Fair Lawn, NJ
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Effect of UV Exposure on the PD of Multiple Doses of CC-90001 and Pilot Food Effect Study
A Two-Part, Phase 1 Study to Evaluate Pharmacokinetics and Pharmacodynamics of Multiple Dose CC-90001 and to Evaluate the Effects of Food and Formulation on Pharmacokinetics of Single Dose CC-90001 in Healthy Subjects
Status: Enrolling
Updated:  8/17/2015
Covance-Daytona Beach
mi
from
Daytona Beach, FL
Effect of UV Exposure on the PD of Multiple Doses of CC-90001 and Pilot Food Effect Study
A Two-Part, Phase 1 Study to Evaluate Pharmacokinetics and Pharmacodynamics of Multiple Dose CC-90001 and to Evaluate the Effects of Food and Formulation on Pharmacokinetics of Single Dose CC-90001 in Healthy Subjects
Status: Enrolling
Updated: 8/17/2015
Covance-Daytona Beach
mi
from
Daytona Beach, FL
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Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
Status: Enrolling
Updated:  8/18/2015
Rollins School of Public Health, Emory University
mi
from
Atlanta, GA
Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
Status: Enrolling
Updated: 8/18/2015
Rollins School of Public Health, Emory University
mi
from
Atlanta, GA
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Optical Coherence Tomography (OCT) Normative Data Collection Study
Multi-center Study for Normal Database of Optic Nerve Head, Retinal Nerve Fiber Layer, and Macula Parameters With the Heidelberg Spectralis OCT, Study 3
Status: Enrolling
Updated:  8/19/2015
New York Eye & Ear Infirmary
mi
from
New York, NY
Optical Coherence Tomography (OCT) Normative Data Collection Study
Multi-center Study for Normal Database of Optic Nerve Head, Retinal Nerve Fiber Layer, and Macula Parameters With the Heidelberg Spectralis OCT, Study 3
Status: Enrolling
Updated: 8/19/2015
New York Eye & Ear Infirmary
mi
from
New York, NY
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TMS Measures of Plasticity and Excitatory/Inhibitory Ratio as Biomarkers: R-baclofen Effects in Normal Volunteers
Transcranial Magnetic Stimulation (TMS) Measures of Plasticity and Excitatory/Inhibitory Ratio as Biomarkers for R-baclofen Effects in Normal Volunteers
Status: Enrolling
Updated:  8/20/2015
Berenson-Allen Center for Noninvansive Brain Stimulation Beth Israel Deaconess Medical Center
mi
from
Boston, MA
TMS Measures of Plasticity and Excitatory/Inhibitory Ratio as Biomarkers: R-baclofen Effects in Normal Volunteers
Transcranial Magnetic Stimulation (TMS) Measures of Plasticity and Excitatory/Inhibitory Ratio as Biomarkers for R-baclofen Effects in Normal Volunteers
Status: Enrolling
Updated: 8/20/2015
Berenson-Allen Center for Noninvansive Brain Stimulation Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Investigations Regarding B-cell Subsets in Humans
Investigations Regarding B-cell Subsets in Humans
Status: Enrolling
Updated:  8/24/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
Investigations Regarding B-cell Subsets in Humans
Investigations Regarding B-cell Subsets in Humans
Status: Enrolling
Updated: 8/24/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
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ObseRvation of PeripHEral rEtinal Morphology in Normals
ObseRvation of PeripHEral rEtinal Morphology in Normals
Status: Enrolling
Updated:  8/24/2015
Medical Center Ophthalmology Associates
mi
from
San Antonio, TX
ObseRvation of PeripHEral rEtinal Morphology in Normals
ObseRvation of PeripHEral rEtinal Morphology in Normals
Status: Enrolling
Updated: 8/24/2015
Medical Center Ophthalmology Associates
mi
from
San Antonio, TX
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Pharmacokinetics And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers
Open Label, Single Dose, Randomized, Crossover Study To Evaluate The Pharmacokinetics And Relative Bioavailability Of Oxycodone Following Oral Administration Of 40 Mg Doses Of PF 00345439 Taken Whole Under Fed Conditions And After Chewing Under Fasted Conditions In Healthy Volunteers
Status: Enrolling
Updated:  8/28/2015
Pfizer Investigational Site
mi
from
New Haven, CT
Pharmacokinetics And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers
Open Label, Single Dose, Randomized, Crossover Study To Evaluate The Pharmacokinetics And Relative Bioavailability Of Oxycodone Following Oral Administration Of 40 Mg Doses Of PF 00345439 Taken Whole Under Fed Conditions And After Chewing Under Fasted Conditions In Healthy Volunteers
Status: Enrolling
Updated: 8/28/2015
Pfizer Investigational Site
mi
from
New Haven, CT
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Food Effect And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers
An Open-label, Single-dose, Randomized, Three-way Crossover Study to Estimate the Effects of Food on Oxycodone Pharmacokinetics Following Oral 40 Mg Doses of PF-00345439 Formulation K and to Estimate Its Relative Bioavailability of Oxycodone Compared to PF-003454390 Formulation X in the Fasted State in Healthy Volunteers
Status: Enrolling
Updated:  8/28/2015
Pfizer Investigational Site
mi
from
Baltimore, MD
Food Effect And Relative Bioavailability Study Of Oxycodone in Healthy Volunteers
An Open-label, Single-dose, Randomized, Three-way Crossover Study to Estimate the Effects of Food on Oxycodone Pharmacokinetics Following Oral 40 Mg Doses of PF-00345439 Formulation K and to Estimate Its Relative Bioavailability of Oxycodone Compared to PF-003454390 Formulation X in the Fasted State in Healthy Volunteers
Status: Enrolling
Updated: 8/28/2015
Pfizer Investigational Site
mi
from
Baltimore, MD
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Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated:  8/31/2015
DaVita Research
mi
from
Denver, CO
Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated: 8/31/2015
DaVita Research
mi
from
Denver, CO
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Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated:  8/31/2015
Clinical Pharmacology of Miami
mi
from
Miami, FL
Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated: 8/31/2015
Clinical Pharmacology of Miami
mi
from
Miami, FL
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Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated:  8/31/2015
DaVita Clinical Research
mi
from
Minneapolis, MN
Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.
A Phase 1 Open Label, 2 Part, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole
Status: Enrolling
Updated: 8/31/2015
DaVita Clinical Research
mi
from
Minneapolis, MN
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Cognitive Effects of Transcranial Direct Current Stimulation in Older Adults
Cognitive Effects of Transcranial Direct Current Stimulation in Older Adults
Status: Enrolling
Updated:  8/31/2015
Department of Neurology
mi
from
Baltimore, MD
Cognitive Effects of Transcranial Direct Current Stimulation in Older Adults
Cognitive Effects of Transcranial Direct Current Stimulation in Older Adults
Status: Enrolling
Updated: 8/31/2015
Department of Neurology
mi
from
Baltimore, MD
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Study of the Pharmacokinetics of Isavuconazole in Healthy Non-Elderly and Elderly Male and Female Subjects
A Phase 1, Open Label, Parallel Group, Single Dose Study to Evaluate the Pharmacokinetics of Isavuconazole in Healthy Non-Elderly and Elderly Male and Female Subjects
Status: Enrolling
Updated:  8/31/2015
Parexel International
mi
from
Glendale, CA
Study of the Pharmacokinetics of Isavuconazole in Healthy Non-Elderly and Elderly Male and Female Subjects
A Phase 1, Open Label, Parallel Group, Single Dose Study to Evaluate the Pharmacokinetics of Isavuconazole in Healthy Non-Elderly and Elderly Male and Female Subjects
Status: Enrolling
Updated: 8/31/2015
Parexel International
mi
from
Glendale, CA
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A Study to Assess Pharmacokinetic Interaction of Multiple Dose Ketoconazole on Single Dose YM178 Oral Controlled Absorption System (OCAS) in Healthy Adult Volunteers
A Phase 1, Open-Label, Two-Period, One-Sequence Crossover Study to Assess Pharmacokinetic Interaction of Multiple Dose Ketoconazole on Single Dose YM178 Oral Controlled Absorption System (OCAS) in Healthy Male and Female Adult Volunteers
Status: Enrolling
Updated:  8/31/2015
MDS Pharma Services (US) Inc.
mi
from
Lincoln, NE
A Study to Assess Pharmacokinetic Interaction of Multiple Dose Ketoconazole on Single Dose YM178 Oral Controlled Absorption System (OCAS) in Healthy Adult Volunteers
A Phase 1, Open-Label, Two-Period, One-Sequence Crossover Study to Assess Pharmacokinetic Interaction of Multiple Dose Ketoconazole on Single Dose YM178 Oral Controlled Absorption System (OCAS) in Healthy Male and Female Adult Volunteers
Status: Enrolling
Updated: 8/31/2015
MDS Pharma Services (US) Inc.
mi
from
Lincoln, NE
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Drug Interaction Study of Isavuconazole and Digoxin
A Phase 1, Open-Label, Sequential Study of the Effect of Multiple Doses of Isavuconazole on the Pharmacokinetics of a Single Dose of Digoxin in Healthy Adult Subjects
Status: Enrolling
Updated:  8/31/2015
Parexel International
mi
from
Baltimore, MD
Drug Interaction Study of Isavuconazole and Digoxin
A Phase 1, Open-Label, Sequential Study of the Effect of Multiple Doses of Isavuconazole on the Pharmacokinetics of a Single Dose of Digoxin in Healthy Adult Subjects
Status: Enrolling
Updated: 8/31/2015
Parexel International
mi
from
Baltimore, MD
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Drug Interaction Study of Multiple Doses of Isavuconazole and a Single Dose of Bupropion
A Phase 1, Open-Label Study to Evaluate the Effect of Multiple Doses of Isavuconazole on the Pharmacokinetics of a Single Dose of Bupropion
Status: Enrolling
Updated:  8/31/2015
Clinical Pharmacology of Miami
mi
from
Miami, FL
Drug Interaction Study of Multiple Doses of Isavuconazole and a Single Dose of Bupropion
A Phase 1, Open-Label Study to Evaluate the Effect of Multiple Doses of Isavuconazole on the Pharmacokinetics of a Single Dose of Bupropion
Status: Enrolling
Updated: 8/31/2015
Clinical Pharmacology of Miami
mi
from
Miami, FL
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A Phase I Study to Compare 3 Different Strengths of an Extended Release Formulation of ASP015K to an Immediate Release Formulation of ASP015K
A Phase 1, Open-Label, Randomized, Parallel Dose Group Study to Compare the Pharmacokinetic Profiles of Three Different Strengths of ASP015K Extended Release Formulation With ASP015K Immediate Release Formulation and to Evaluate Food Effect on Extended Release Strengths in Healthy Volunteers
Status: Enrolling
Updated:  8/31/2015
Parexel International
mi
from
Baltimore, MD
A Phase I Study to Compare 3 Different Strengths of an Extended Release Formulation of ASP015K to an Immediate Release Formulation of ASP015K
A Phase 1, Open-Label, Randomized, Parallel Dose Group Study to Compare the Pharmacokinetic Profiles of Three Different Strengths of ASP015K Extended Release Formulation With ASP015K Immediate Release Formulation and to Evaluate Food Effect on Extended Release Strengths in Healthy Volunteers
Status: Enrolling
Updated: 8/31/2015
Parexel International
mi
from
Baltimore, MD
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The Effect of Dietary Strawberry Supplementation on Older Adults
The Effect of Dietary Strawberry Supplementation on Older Adults
Status: Enrolling
Updated:  9/1/2015
Jean Meyer USDA Human Nutrition Research Center on Aging at Tufts University
mi
from
Boston, MA
The Effect of Dietary Strawberry Supplementation on Older Adults
The Effect of Dietary Strawberry Supplementation on Older Adults
Status: Enrolling
Updated: 9/1/2015
Jean Meyer USDA Human Nutrition Research Center on Aging at Tufts University
mi
from
Boston, MA
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Dress for Success: Can Just Dressing for the Gym Help Going to the Gym?
Dress for Success: Can Just Dressing for the Gym Help Going to the Gym?
Status: Enrolling
Updated:  9/2/2015
Univ of Pennsylvania
mi
from
Philadelphia, PA
Dress for Success: Can Just Dressing for the Gym Help Going to the Gym?
Dress for Success: Can Just Dressing for the Gym Help Going to the Gym?
Status: Enrolling
Updated: 9/2/2015
Univ of Pennsylvania
mi
from
Philadelphia, PA
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Genotype and Phenotype Registry: Enrollment of Normal Control Subjects for Current and Future Research
TAP0307: Enrollment of Normal Control Subjects for Current and Future Research
Status: Enrolling
Updated:  9/9/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
Genotype and Phenotype Registry: Enrollment of Normal Control Subjects for Current and Future Research
TAP0307: Enrollment of Normal Control Subjects for Current and Future Research
Status: Enrolling
Updated: 9/9/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
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The Effects of Breakfast on Brain Function
The Effects of Breakfast on Cognitive Functioning
Status: Enrolling
Updated:  9/9/2015
Arkansas Children's Nutrition Center
mi
from
Little Rock, AR
The Effects of Breakfast on Brain Function
The Effects of Breakfast on Cognitive Functioning
Status: Enrolling
Updated: 9/9/2015
Arkansas Children's Nutrition Center
mi
from
Little Rock, AR
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A Study of Three Modified-Release Formulations of RO4917523 in Healthy Volunteers
A Single-center, Open Label, Randomized Cross-over Study to Compare 3 Modified-release Formulations With Different Release Profiles of RO4917523 Along With a Reference Intravenous Microdose Infusion
Status: Enrolling
Updated:  9/9/2015
Clinical Research Facility
mi
from
Marlton, NJ
A Study of Three Modified-Release Formulations of RO4917523 in Healthy Volunteers
A Single-center, Open Label, Randomized Cross-over Study to Compare 3 Modified-release Formulations With Different Release Profiles of RO4917523 Along With a Reference Intravenous Microdose Infusion
Status: Enrolling
Updated: 9/9/2015
Clinical Research Facility
mi
from
Marlton, NJ
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Meals and Grazing Study
Meals and Grazing Study
Status: Enrolling
Updated:  9/10/2015
Fred Hutchinson Cancer Research Center
mi
from
Seattle, WA
Meals and Grazing Study
Meals and Grazing Study
Status: Enrolling
Updated: 9/10/2015
Fred Hutchinson Cancer Research Center
mi
from
Seattle, WA
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PEP005 Gel - Evaluation of Local Tolerability After Exposure to Ingenol Mebutate Gel Followed by Hand Washing in Healthy Subjects
PEP005 Gel - Evaluation of Local Tolerability After Exposure to Ingenol Mebutate 0.05% and 0.015% Gel Followed by Hand Washing in Healthy Subjects.
Status: Enrolling
Updated:  9/11/2015
TKL Research
mi
from
Paramus, NJ
PEP005 Gel - Evaluation of Local Tolerability After Exposure to Ingenol Mebutate Gel Followed by Hand Washing in Healthy Subjects
PEP005 Gel - Evaluation of Local Tolerability After Exposure to Ingenol Mebutate 0.05% and 0.015% Gel Followed by Hand Washing in Healthy Subjects.
Status: Enrolling
Updated: 9/11/2015
TKL Research
mi
from
Paramus, NJ
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Pharmacokinetic Study Comparing Nicotine Delivery From E-cigarettes and a Conventional Cigarette in Healthy Subjects
A Pharmacokinetic Study to Compare Nicotine Delivery From e Cigarettes and a Conventional Cigarette in Healthy Subjects During a Brief Period of ad Libitum Use
Status: Enrolling
Updated:  9/14/2015
Los Angeles Clinical Trials
mi
from
Burbank, CA
Pharmacokinetic Study Comparing Nicotine Delivery From E-cigarettes and a Conventional Cigarette in Healthy Subjects
A Pharmacokinetic Study to Compare Nicotine Delivery From e Cigarettes and a Conventional Cigarette in Healthy Subjects During a Brief Period of ad Libitum Use
Status: Enrolling
Updated: 9/14/2015
Los Angeles Clinical Trials
mi
from
Burbank, CA
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BioGene Bank Cohort Study for Approved Research Requests
The BioGene Bank Cohort Study is a Collection of Human Blood Samples (DNA and Plasma) Along With De-identified (Coded) Health Information, Questionnaire Responses on Environment and History of Family Disease to be Used for Research
Status: Enrolling
Updated:  9/14/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
BioGene Bank Cohort Study for Approved Research Requests
The BioGene Bank Cohort Study is a Collection of Human Blood Samples (DNA and Plasma) Along With De-identified (Coded) Health Information, Questionnaire Responses on Environment and History of Family Disease to be Used for Research
Status: Enrolling
Updated: 9/14/2015
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
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Web-Based Delivery of MOVE! to Veterans With Serious Mental Illness (SMI)
Web-Based Delivery of MOVE! to Veterans With Serious Mental Illness
Status: Enrolling
Updated:  9/15/2015
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
mi
from
West Los Angeles, CA
Web-Based Delivery of MOVE! to Veterans With Serious Mental Illness (SMI)
Web-Based Delivery of MOVE! to Veterans With Serious Mental Illness
Status: Enrolling
Updated: 9/15/2015
VA Greater Los Angeles Healthcare System, West Los Angeles, CA
mi
from
West Los Angeles, CA
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Non-invasive Ocular Surface Measurements Before and After Interventions
Non-invasive Ocular Surface Measurements Before and After Interventions
Status: Enrolling
Updated:  9/17/2015
The Flaum Eye Institute-University of Rochester
mi
from
Rochester, NY
Non-invasive Ocular Surface Measurements Before and After Interventions
Non-invasive Ocular Surface Measurements Before and After Interventions
Status: Enrolling
Updated: 9/17/2015
The Flaum Eye Institute-University of Rochester
mi
from
Rochester, NY
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Test-retest Reproducibility of [11C]PHNO PET Using the Constant Infusion Paradigm
Test-retest Reproducibility of [11C]PHNO PET Using the Constant Infusion
Status: Enrolling
Updated:  9/17/2015
Yale University
mi
from
New Haven, CT
Test-retest Reproducibility of [11C]PHNO PET Using the Constant Infusion Paradigm
Test-retest Reproducibility of [11C]PHNO PET Using the Constant Infusion
Status: Enrolling
Updated: 9/17/2015
Yale University
mi
from
New Haven, CT
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A Study of [14c]-Samidorphan (Also Known as ALKS 33) in Healthy, Male Volunteers
A Single-Center, Open-Label Study to Evaluate the Absorption, Metabolism, and Excretion of Single Doses of [14c]-Samidorphan in Healthy Male Subjects
Status: Enrolling
Updated:  9/17/2015
Alkermes Study Site
mi
from
Austin, TX
A Study of [14c]-Samidorphan (Also Known as ALKS 33) in Healthy, Male Volunteers
A Single-Center, Open-Label Study to Evaluate the Absorption, Metabolism, and Excretion of Single Doses of [14c]-Samidorphan in Healthy Male Subjects
Status: Enrolling
Updated: 9/17/2015
Alkermes Study Site
mi
from
Austin, TX
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Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Birmingham, AL
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Birmingham, AL
Click here to add this to my saved trials
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Los Angeles, CA
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Bradenton, FL
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Bradenton, FL
Click here to add this to my saved trials
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Metairie, LA
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Metairie, LA
Click here to add this to my saved trials
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
White Plains, NY
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
White Plains, NY
Click here to add this to my saved trials
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Cincinnati, OH
Safety Study of ATX-101 for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
A Multicenter, Double-blind, Placebo-controlled Safety Study of ATX-101 (Deoxycholic Acid Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area in Subjects 65 to 75 Years of Age
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
To Evaluate the Effect of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers
A Phase 1, Single-center, Fixed-sequence, Open Label Study to Evaluate the Effect of Oral Repeated Doses of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Overland Park, KA
To Evaluate the Effect of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers
A Phase 1, Single-center, Fixed-sequence, Open Label Study to Evaluate the Effect of Oral Repeated Doses of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Overland Park, KA
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To Assess the Effect of AZD1722 on the Pharmacokinetics of Cefadroxil in Healthy Volunteers
A Phase 1, Single-center, Randomized, 2-Way Cross-over, Open-label Study to Evaluate the Effect of Oral Repeated Doses of AZD1722 on the Pharmacokinetics of Oral Cefadroxil in Healthy Volunteers
Status: Enrolling
Updated:  9/18/2015
Clinical Research Facility
mi
from
Overland Park, KA
To Assess the Effect of AZD1722 on the Pharmacokinetics of Cefadroxil in Healthy Volunteers
A Phase 1, Single-center, Randomized, 2-Way Cross-over, Open-label Study to Evaluate the Effect of Oral Repeated Doses of AZD1722 on the Pharmacokinetics of Oral Cefadroxil in Healthy Volunteers
Status: Enrolling
Updated: 9/18/2015
Clinical Research Facility
mi
from
Overland Park, KA
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Effect of Daily Low Dose Aspirin on Exhaled Inflammatory Mediators in Normal Subjects
Effect of Daily Low Dose Aspirin on Exhaled Inflammatory Mediators in Normal Subjects
Status: Enrolling
Updated:  9/21/2015
Asthma Research Center, Brigham and Women's Hospital
mi
from
Boston, MA
Effect of Daily Low Dose Aspirin on Exhaled Inflammatory Mediators in Normal Subjects
Effect of Daily Low Dose Aspirin on Exhaled Inflammatory Mediators in Normal Subjects
Status: Enrolling
Updated: 9/21/2015
Asthma Research Center, Brigham and Women's Hospital
mi
from
Boston, MA
Click here to add this to my saved trials