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 Bioavailability Study of MIV-711 Oral Formulations in Healthy Volunteers
A Single-Center, Randomised, 4-Period, Phase 1 Study to Evaluate the Pharmacokinetics, Safety and Tolerability, and Effect of Food on Pharmacokinetics Following Single Doses of MIV-711 Capsule and Tablet Formulations in Healthy Volunteers
Status: Enrolling
Updated:  2/21/2018
Celerion
mi
from
Lincoln, NE
A Bioavailability Study of MIV-711 Oral Formulations in Healthy Volunteers
A Single-Center, Randomised, 4-Period, Phase 1 Study to Evaluate the Pharmacokinetics, Safety and Tolerability, and Effect of Food on Pharmacokinetics Following Single Doses of MIV-711 Capsule and Tablet Formulations in Healthy Volunteers
Status: Enrolling
Updated: 2/21/2018
Celerion
mi
from
Lincoln, NE
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Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
Status: Enrolling
Updated:  2/22/2018
Mohs, Dermatologic and Laser Surgery
mi
from
Miami, FL
Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
Topical Imiquimod in Conjunction With Nd:YAG Laser for Tattoo Removal
Status: Enrolling
Updated: 2/22/2018
Mohs, Dermatologic and Laser Surgery
mi
from
Miami, FL
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Lofexidine Pharmacokinetics in the Presence of Paroxetine in Healthy Volunteers
Lofexidine Pharmacokinetics in the Presence of Paroxetine, a Strong CYP2D6 Inhibitor, in Healthy Volunteers
Status: Enrolling
Updated:  2/22/2018
Worldwide Clinical Trials
mi
from
San Antonio, TX
Lofexidine Pharmacokinetics in the Presence of Paroxetine in Healthy Volunteers
Lofexidine Pharmacokinetics in the Presence of Paroxetine, a Strong CYP2D6 Inhibitor, in Healthy Volunteers
Status: Enrolling
Updated: 2/22/2018
Worldwide Clinical Trials
mi
from
San Antonio, TX
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Lofexidine Food Effect Study in Healthy Volunteers
A Single-Dose, Open-Label, Randomized, Two-Way Crossover Food Effect Study of Lofexidine 400 μg (2 x 200 μg) Tablets
Status: Enrolling
Updated:  2/22/2018
Worldwide Clinical Trials
mi
from
San Antonio, TX
Lofexidine Food Effect Study in Healthy Volunteers
A Single-Dose, Open-Label, Randomized, Two-Way Crossover Food Effect Study of Lofexidine 400 μg (2 x 200 μg) Tablets
Status: Enrolling
Updated: 2/22/2018
Worldwide Clinical Trials
mi
from
San Antonio, TX
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A Study to Assess the Absorption of a Single Dose of BMS-986205 in Healthy Volunteers When Administered as a Crushed Tablet Orally or Crushed Tablet Suspension Via Nasogastric Tube, as Compared to a Tablet
Randomized, Open-Label Study to Assess the Relative Bioavailability of a Single 100-mg Dose of BMS-986205 in Healthy Participants When Administered as a Crushed Tablet Orally or Crushed Tablet Suspension Via Nasogastric Tube Compared to an Intact Tablet of Similar Dose
Status: Enrolling
Updated:  2/22/2018
PPD Austin Clinic
mi
from
Austin, TX
A Study to Assess the Absorption of a Single Dose of BMS-986205 in Healthy Volunteers When Administered as a Crushed Tablet Orally or Crushed Tablet Suspension Via Nasogastric Tube, as Compared to a Tablet
Randomized, Open-Label Study to Assess the Relative Bioavailability of a Single 100-mg Dose of BMS-986205 in Healthy Participants When Administered as a Crushed Tablet Orally or Crushed Tablet Suspension Via Nasogastric Tube Compared to an Intact Tablet of Similar Dose
Status: Enrolling
Updated: 2/22/2018
PPD Austin Clinic
mi
from
Austin, TX
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Accuracy of Oxygen Saturation (SpO2) Noninvasive Pulse Oximeter Sensor (RD Disposable) Under Motion Conditions
Status: Enrolling
Updated:  2/23/2018
Masimo Corporation
mi
from
Irvine, CA
Accuracy of Oxygen Saturation (SpO2) Noninvasive Pulse Oximeter Sensor (RD Disposable) Under Motion Conditions
Status: Enrolling
Updated: 2/23/2018
Masimo Corporation
mi
from
Irvine, CA
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Resistant Maltodextrin Supplementation: Gastrointestinal Health
Resistant Maltodextrin Supplementation and the Effect on Fecal Bifidobacteria, Bowel Function, Dietary Intake and Quality of Life
Status: Enrolling
Updated:  2/28/2018
University of Florida
mi
from
Gainesville, FL
Resistant Maltodextrin Supplementation: Gastrointestinal Health
Resistant Maltodextrin Supplementation and the Effect on Fecal Bifidobacteria, Bowel Function, Dietary Intake and Quality of Life
Status: Enrolling
Updated: 2/28/2018
University of Florida
mi
from
Gainesville, FL
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Evaluating the Plasma, Epithelial Lining, and Alveolar Macrophage Concentrations of Intravenous Carbavance™ (RPX2014/RPX7009) in Healthy Adult Subjects
A Phase 1, Randomized, Open-Label, Trial Evaluating the Plasma, Epithelial Lining Fluid, and Alveolar Macrophage Concentrations of Intravenous Carbavance™ (RPX2014/RPX7009) in Healthy Adult Subjects
Status: Enrolling
Updated:  3/1/2018
Pulmonary Associates, PA
mi
from
Phoenix, AZ
Evaluating the Plasma, Epithelial Lining, and Alveolar Macrophage Concentrations of Intravenous Carbavance™ (RPX2014/RPX7009) in Healthy Adult Subjects
A Phase 1, Randomized, Open-Label, Trial Evaluating the Plasma, Epithelial Lining Fluid, and Alveolar Macrophage Concentrations of Intravenous Carbavance™ (RPX2014/RPX7009) in Healthy Adult Subjects
Status: Enrolling
Updated: 3/1/2018
Pulmonary Associates, PA
mi
from
Phoenix, AZ
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Dose-Response of Gonadal Steroids and Bone Turnover in Men
Dose-Response of Gonadal Steroids and Bone Turnover in Men
Status: Enrolling
Updated:  3/2/2018
Massachusetts General Hospital
mi
from
Boston, MA
Dose-Response of Gonadal Steroids and Bone Turnover in Men
Dose-Response of Gonadal Steroids and Bone Turnover in Men
Status: Enrolling
Updated: 3/2/2018
Massachusetts General Hospital
mi
from
Boston, MA
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A Study to Investigate Safety, Tolerability, and Pharmacokinetics of DSTA4637S in Healthy Volunteers
A PHASE I, RANDOMIZED, DOUBLE-BLIND,PLACEBO-CONTROLLED, SINGLE-ASCENDING DOSE STUDY TO INVESTIGATE THE SAFETY,TOLERABILITY, AND PHARMACOKINETICS OF DSTA4637S IN HEALTHY VOLUNTEERS
Status: Enrolling
Updated:  3/2/2018
PRA International Clinical Pharmacology Center (EDS US Clinic)
mi
from
Lenexa, KA
A Study to Investigate Safety, Tolerability, and Pharmacokinetics of DSTA4637S in Healthy Volunteers
A PHASE I, RANDOMIZED, DOUBLE-BLIND,PLACEBO-CONTROLLED, SINGLE-ASCENDING DOSE STUDY TO INVESTIGATE THE SAFETY,TOLERABILITY, AND PHARMACOKINETICS OF DSTA4637S IN HEALTHY VOLUNTEERS
Status: Enrolling
Updated: 3/2/2018
PRA International Clinical Pharmacology Center (EDS US Clinic)
mi
from
Lenexa, KA
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A Study of LY3323795 in Healthy Participants
Single-Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3323795 in Healthy Subjects
Status: Enrolling
Updated:  3/5/2018
California Clinical Trials Medical Group
mi
from
Glendale, CA
A Study of LY3323795 in Healthy Participants
Single-Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3323795 in Healthy Subjects
Status: Enrolling
Updated: 3/5/2018
California Clinical Trials Medical Group
mi
from
Glendale, CA
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Phase 0 Study of [18F]MNI-968 as a Marker for D1 Receptor in Healthy Subjects
An Open Label, Brain Positron Emission Tomography, Phase 0 Study of [18F]MNI-968 as a Marker for D1 Receptor in Healthy Subjects
Status: Enrolling
Updated:  3/5/2018
Molecular Neuroimaging, LLC
mi
from
New Haven, CT
Phase 0 Study of [18F]MNI-968 as a Marker for D1 Receptor in Healthy Subjects
An Open Label, Brain Positron Emission Tomography, Phase 0 Study of [18F]MNI-968 as a Marker for D1 Receptor in Healthy Subjects
Status: Enrolling
Updated: 3/5/2018
Molecular Neuroimaging, LLC
mi
from
New Haven, CT
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Assessment of the Biodistribution and Safety of [18F]MNI-968 in Healthy Subjects
Assessment of the Biodistribution and Safety of [18F]MNI-968 (Aka PF-06730110) in Healthy Subjects
Status: Enrolling
Updated:  3/5/2018
Molecular Neuroimaging, LLC
mi
from
New Haven, CT
Assessment of the Biodistribution and Safety of [18F]MNI-968 in Healthy Subjects
Assessment of the Biodistribution and Safety of [18F]MNI-968 (Aka PF-06730110) in Healthy Subjects
Status: Enrolling
Updated: 3/5/2018
Molecular Neuroimaging, LLC
mi
from
New Haven, CT
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A Study of Multiple Doses of Lasmiditan in Healthy Participants
Multiple-Ascending Dose, Safety, Tolerability, Pharmacokinetic, and Drug-Drug Interaction Study of Lasmiditan
Status: Enrolling
Updated:  3/5/2018
Covance-Daytona Beach
mi
from
Daytona Beach, FL
A Study of Multiple Doses of Lasmiditan in Healthy Participants
Multiple-Ascending Dose, Safety, Tolerability, Pharmacokinetic, and Drug-Drug Interaction Study of Lasmiditan
Status: Enrolling
Updated: 3/5/2018
Covance-Daytona Beach
mi
from
Daytona Beach, FL
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"Beverage Hydration Index" of Commercial Therapeutic Beverages
Beverage Hydration Index of Three Commercial Oral Rehydration Therapy ORT Beverages
Status: Enrolling
Updated:  3/5/2018
Sonoma State Univrsity
mi
from
Rohnert Park, CA
"Beverage Hydration Index" of Commercial Therapeutic Beverages
Beverage Hydration Index of Three Commercial Oral Rehydration Therapy ORT Beverages
Status: Enrolling
Updated: 3/5/2018
Sonoma State Univrsity
mi
from
Rohnert Park, CA
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The Efficacy of Claritin in Healthy Subjects
The Efficacy of Claritin in Healthy Subjects
Status: Enrolling
Updated:  3/9/2018
University of Chicago
mi
from
Chicago, IL
The Efficacy of Claritin in Healthy Subjects
The Efficacy of Claritin in Healthy Subjects
Status: Enrolling
Updated: 3/9/2018
University of Chicago
mi
from
Chicago, IL
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Effect of Aspirin on Gut Microbiome
Pilot Trial to Examine the Effect of Aspirin on the Gut Microbiome
Status: Enrolling
Updated:  3/12/2018
Epidemiology Clinical Research Center
mi
from
Minneapolis, MN
Effect of Aspirin on Gut Microbiome
Pilot Trial to Examine the Effect of Aspirin on the Gut Microbiome
Status: Enrolling
Updated: 3/12/2018
Epidemiology Clinical Research Center
mi
from
Minneapolis, MN
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Single Ascending Dose to Study the Safety, Tolerability, PK and PD Effects of AEF0117
A Phase 1, Single Center, Double-blind, Placebo-controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Effects of Single Oral Doses of AEF0117 in Healthy Male and Female Subjects
Status: Enrolling
Updated:  3/12/2018
Biotrial Inc.
mi
from
Newark, NJ
Single Ascending Dose to Study the Safety, Tolerability, PK and PD Effects of AEF0117
A Phase 1, Single Center, Double-blind, Placebo-controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Effects of Single Oral Doses of AEF0117 in Healthy Male and Female Subjects
Status: Enrolling
Updated: 3/12/2018
Biotrial Inc.
mi
from
Newark, NJ
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Effects of THC on Emotional Memory Retrieval
The Effects of Δ⁹-Tetrahydrocannabinol on the Retrieval of Emotional Memories
Status: Enrolling
Updated:  3/13/2018
University of Chicago
mi
from
Chicago, IL
Effects of THC on Emotional Memory Retrieval
The Effects of Δ⁹-Tetrahydrocannabinol on the Retrieval of Emotional Memories
Status: Enrolling
Updated: 3/13/2018
University of Chicago
mi
from
Chicago, IL
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Proton Pump Inhibitors and Dysbiosis in Cirrhosis
Status: Enrolling
Updated:  3/14/2018
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
Proton Pump Inhibitors and Dysbiosis in Cirrhosis
Status: Enrolling
Updated: 3/14/2018
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
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Vitamin D and Muscle Metabolic Function
Vitamin D Contribution to Muscle Metabolic Function in Aged Adults
Status: Enrolling
Updated:  3/14/2018
University of Kentucky
mi
from
Lexington, KY
Vitamin D and Muscle Metabolic Function
Vitamin D Contribution to Muscle Metabolic Function in Aged Adults
Status: Enrolling
Updated: 3/14/2018
University of Kentucky
mi
from
Lexington, KY
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A Bioavailability Crossover Study of Two Formulations of Lamotrigine Extended Release Tablets in Healthy Subjects
A Randomized, 2-Sequence, 2-Treatment, 4-Period, Open-Label, Single Dose, Fully Replicated Comparative Bioavailability Crossover Study of Two Formulations of Lamotrigine Extended Release Tablets in Healthy Subjects Under Fed Conditions
Status: Enrolling
Updated:  3/14/2018
Vince and Associates Clinical Research
mi
from
Overland Park, KA
A Bioavailability Crossover Study of Two Formulations of Lamotrigine Extended Release Tablets in Healthy Subjects
A Randomized, 2-Sequence, 2-Treatment, 4-Period, Open-Label, Single Dose, Fully Replicated Comparative Bioavailability Crossover Study of Two Formulations of Lamotrigine Extended Release Tablets in Healthy Subjects Under Fed Conditions
Status: Enrolling
Updated: 3/14/2018
Vince and Associates Clinical Research
mi
from
Overland Park, KA
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A Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-56136379 in Healthy Japanese Adult Participants
A Double-blind, Placebo-controlled, Randomized, Phase 1, Single Ascending Dose Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-56136379 in Healthy Japanese Adult Subjects
Status: Enrolling
Updated:  3/14/2018
Clinical Research Facility
mi
from
Glendale, CA
A Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-56136379 in Healthy Japanese Adult Participants
A Double-blind, Placebo-controlled, Randomized, Phase 1, Single Ascending Dose Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-56136379 in Healthy Japanese Adult Subjects
Status: Enrolling
Updated: 3/14/2018
Clinical Research Facility
mi
from
Glendale, CA
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A 21-Day Study to Evaluate the Skin Irritation Potential of CCP-020 (Diacerein 1%) Topical Ointment in Healthy Subjects Using a Cumulative Irritant Patch Test Design
A 21-Day, Randomized, Controlled Study to Evaluate the Skin Irritation Potential of CCP-020 (Diacerein 1%) Topical Ointment in Healthy Subjects Using a Cumulative Irritant Patch Test Design
Status: Enrolling
Updated:  3/14/2018
TKL research
mi
from
Fair Lawn, NJ
A 21-Day Study to Evaluate the Skin Irritation Potential of CCP-020 (Diacerein 1%) Topical Ointment in Healthy Subjects Using a Cumulative Irritant Patch Test Design
A 21-Day, Randomized, Controlled Study to Evaluate the Skin Irritation Potential of CCP-020 (Diacerein 1%) Topical Ointment in Healthy Subjects Using a Cumulative Irritant Patch Test Design
Status: Enrolling
Updated: 3/14/2018
TKL research
mi
from
Fair Lawn, NJ
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Absorption and Metabolic Profiles of a Sugar-based Beverage
Absorption Profile of a Sugar-based Beverage on Inflammatory Mechanism by Timing of Beverage Consumption Relative to Meal Intake.
Status: Enrolling
Updated:  3/15/2018
Clinical Nutrition Research Center
mi
from
Chicago, IL
Absorption and Metabolic Profiles of a Sugar-based Beverage
Absorption Profile of a Sugar-based Beverage on Inflammatory Mechanism by Timing of Beverage Consumption Relative to Meal Intake.
Status: Enrolling
Updated: 3/15/2018
Clinical Nutrition Research Center
mi
from
Chicago, IL
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Placebo-Controlled Single Dose Study to Evaluate Safety and Pharmacokinetics of SXC-2023 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Food Effect of SXC-2023 When Administered Orally to Healthy Adult Subjects
Status: Enrolling
Updated:  3/15/2018
Celerion
mi
from
Tempe, AZ
Placebo-Controlled Single Dose Study to Evaluate Safety and Pharmacokinetics of SXC-2023 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Food Effect of SXC-2023 When Administered Orally to Healthy Adult Subjects
Status: Enrolling
Updated: 3/15/2018
Celerion
mi
from
Tempe, AZ
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Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Status: Enrolling
Updated:  3/16/2018
SNBL Clinical Pharmacology Center
mi
from
Baltimore, MD
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Status: Enrolling
Updated: 3/16/2018
SNBL Clinical Pharmacology Center
mi
from
Baltimore, MD
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Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Status: Enrolling
Updated:  3/16/2018
Frontage Clinical Services
mi
from
Hackensack, NJ
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Blood Collection In Healthy Adult Volunteers To Obtain Serum For Use In Serum Bactericidal Activity Assay Development
Status: Enrolling
Updated: 3/16/2018
Frontage Clinical Services
mi
from
Hackensack, NJ
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Human Brain Antioxidants During Oxidative Stress
Noninvasive Antioxidant Quantification in the Human Brain Under Oxidative Stress
Status: Enrolling
Updated:  3/20/2018
Univ of Minnesota
mi
from
Minneapolis, MN
Human Brain Antioxidants During Oxidative Stress
Noninvasive Antioxidant Quantification in the Human Brain Under Oxidative Stress
Status: Enrolling
Updated: 3/20/2018
Univ of Minnesota
mi
from
Minneapolis, MN
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Human Brain Antioxidants During Oxidative Stress
Noninvasive Antioxidant Quantification in the Human Brain Under Oxidative Stress
Status: Enrolling
Updated:  3/20/2018
Univ of Minnesota
mi
from
Minneapolis, MN
Human Brain Antioxidants During Oxidative Stress
Noninvasive Antioxidant Quantification in the Human Brain Under Oxidative Stress
Status: Enrolling
Updated: 3/20/2018
Univ of Minnesota
mi
from
Minneapolis, MN
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Progesterone Amplifies Estrogen-stimulated Growth Hormone Secretion in Older Women
Progesterone Amplifies Estrogen-stimulated Growth Hormone Secretion in Older Women
Status: Enrolling
Updated:  3/20/2018
Mayo Clinic Rochester
mi
from
Rochester, MN
Progesterone Amplifies Estrogen-stimulated Growth Hormone Secretion in Older Women
Progesterone Amplifies Estrogen-stimulated Growth Hormone Secretion in Older Women
Status: Enrolling
Updated: 3/20/2018
Mayo Clinic Rochester
mi
from
Rochester, MN
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Study of Methodologies to Measure Blood Flow and Oxygenation in Adults With Sickle Cell Disease
A Study of Methodologies to Measure Blood Flow and Oxygenation as Potential Biomarkers in Adults With Sickle Cell Disease
Status: Enrolling
Updated:  3/20/2018
Clinical Research Facility
mi
from
Detroit, MI
Study of Methodologies to Measure Blood Flow and Oxygenation in Adults With Sickle Cell Disease
A Study of Methodologies to Measure Blood Flow and Oxygenation as Potential Biomarkers in Adults With Sickle Cell Disease
Status: Enrolling
Updated: 3/20/2018
Clinical Research Facility
mi
from
Detroit, MI
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Evaluation of Jarro-Dophilus EPS® Probiotic Formulations
Evaluation of Jarro-Dophilus EPS® Probiotic Formulations on Probiotic Survival, Fecal Microbiota, Gastrointestinal Function and General Wellness in Healthy Adults: a Randomized, Double-blind, Dose-response Study
Status: Enrolling
Updated:  3/21/2018
Food Science and Human Nutrition Department, University of Florida
mi
from
Gainesville, FL
Evaluation of Jarro-Dophilus EPS® Probiotic Formulations
Evaluation of Jarro-Dophilus EPS® Probiotic Formulations on Probiotic Survival, Fecal Microbiota, Gastrointestinal Function and General Wellness in Healthy Adults: a Randomized, Double-blind, Dose-response Study
Status: Enrolling
Updated: 3/21/2018
Food Science and Human Nutrition Department, University of Florida
mi
from
Gainesville, FL
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Bioequivalence Study of Fentanyl Transdermal System (JNJ-35685-AAA-G021) Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Participants
An Open-Label, Randomized, Single Application, Two-Period Crossover, Pivotal Bioequivalence Study to Evaluate the Bioequivalence of Fentanyl Transdermal System (JNJ-35685-AAA-G021) Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Subjects
Status: Enrolling
Updated:  3/26/2018
Clinical Research Facility
mi
from
Cypress, CA
Bioequivalence Study of Fentanyl Transdermal System (JNJ-35685-AAA-G021) Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Participants
An Open-Label, Randomized, Single Application, Two-Period Crossover, Pivotal Bioequivalence Study to Evaluate the Bioequivalence of Fentanyl Transdermal System (JNJ-35685-AAA-G021) Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Subjects
Status: Enrolling
Updated: 3/26/2018
Clinical Research Facility
mi
from
Cypress, CA
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Comparative Pharmacokinetics and Food-Effect Bioavailability of Lubiprostone Sprinkle in Healthy Volunteers
Comparative Pharmacokinetics and Food-Effect Bioavailability of a Sprinkle Formulation of Lubiprostone After Oral Administration in Healthy Volunteers
Status: Enrolling
Updated:  3/26/2018
ICON
mi
from
San Antonio, TX
Comparative Pharmacokinetics and Food-Effect Bioavailability of Lubiprostone Sprinkle in Healthy Volunteers
Comparative Pharmacokinetics and Food-Effect Bioavailability of a Sprinkle Formulation of Lubiprostone After Oral Administration in Healthy Volunteers
Status: Enrolling
Updated: 3/26/2018
ICON
mi
from
San Antonio, TX
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Psychophysical Correlates of Pain Reduction by Topical Analgesic Compounds
Psychophysical Correlates of Pain Reduction by Topical Analgesic Compounds
Status: Enrolling
Updated:  3/27/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
Psychophysical Correlates of Pain Reduction by Topical Analgesic Compounds
Psychophysical Correlates of Pain Reduction by Topical Analgesic Compounds
Status: Enrolling
Updated: 3/27/2018
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Central Venous Catheter Insertion Train the Trainer
Dissemination of a Simulation-based Mastery Learning Curriculum for Central Venous Catheter Insertion at Veterans Affairs Hospitals: A Quantitative Study
Status: Enrolling
Updated:  3/27/2018
Northwestern University
mi
from
Chicago, IL
Central Venous Catheter Insertion Train the Trainer
Dissemination of a Simulation-based Mastery Learning Curriculum for Central Venous Catheter Insertion at Veterans Affairs Hospitals: A Quantitative Study
Status: Enrolling
Updated: 3/27/2018
Northwestern University
mi
from
Chicago, IL
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
San Diego Blood Bank
mi
from
San Diego, CA
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
San Diego Blood Bank
mi
from
San Diego, CA
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
Bonfils Blood Center
mi
from
Denver, CO
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
Bonfils Blood Center
mi
from
Denver, CO
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
Indiana Blood Center
mi
from
Indianapolis, IN
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
Indiana Blood Center
mi
from
Indianapolis, IN
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
Memorial Blood Centers
mi
from
Minneapolis, MN
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
Memorial Blood Centers
mi
from
Minneapolis, MN
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
Community Blood Center of Greater Kansas
mi
from
Kansas City, MO
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
Community Blood Center of Greater Kansas
mi
from
Kansas City, MO
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
Hoxworth Blood Center
mi
from
Cincinnati, OH
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
Hoxworth Blood Center
mi
from
Cincinnati, OH
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Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated:  3/27/2018
The Blood Center of Wisconsin
mi
from
Milwaukee, WI
Evaluation of Trima Version 7.0 Platelets in 100% Plasma
Evaluation of the Performance of Trima Accel® Version 7.0 Software Enhancements for the Collection of Platelets Stored in 100% Plasma
Status: Enrolling
Updated: 3/27/2018
The Blood Center of Wisconsin
mi
from
Milwaukee, WI
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Study of TAK-071 in Healthy Participants and Participants With Mild Cognitive Impairment/Mild Alzheimer Disease and Relative Bioavailability (BA) and Food Effect of TAK-071 in Healthy Participants
A Phase 1 Safety, Tolerability, and Pharmacokinetic Study of Escalating Single and Multiple Oral Doses of TAK-071 in Healthy Subjects and Subjects With Mild Cognitive Impairment/Mild Alzheimer Disease and Relative Bioavailability and Food Effect of TAK-071 in Healthy Subjects
Status: Enrolling
Updated:  3/27/2018
Clinical Research Facility
mi
from
Glendale, CA
Study of TAK-071 in Healthy Participants and Participants With Mild Cognitive Impairment/Mild Alzheimer Disease and Relative Bioavailability (BA) and Food Effect of TAK-071 in Healthy Participants
A Phase 1 Safety, Tolerability, and Pharmacokinetic Study of Escalating Single and Multiple Oral Doses of TAK-071 in Healthy Subjects and Subjects With Mild Cognitive Impairment/Mild Alzheimer Disease and Relative Bioavailability and Food Effect of TAK-071 in Healthy Subjects
Status: Enrolling
Updated: 3/27/2018
Clinical Research Facility
mi
from
Glendale, CA
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TAK-071 Scopolamine-Induced Cognitive Impairment Study
A Randomized, Double-Blind, Sponsor Unblinded, Placebo-Controlled, 5-Period Crossover, Phase 1b Study To Evaluate The Effects Of Single Oral Administration of TAK-071 On Scopolamine-Induced Cognitive Impairment In Healthy Subjects
Status: Enrolling
Updated:  3/27/2018
Clinical Research Facility
mi
from
Glendale, CA
TAK-071 Scopolamine-Induced Cognitive Impairment Study
A Randomized, Double-Blind, Sponsor Unblinded, Placebo-Controlled, 5-Period Crossover, Phase 1b Study To Evaluate The Effects Of Single Oral Administration of TAK-071 On Scopolamine-Induced Cognitive Impairment In Healthy Subjects
Status: Enrolling
Updated: 3/27/2018
Clinical Research Facility
mi
from
Glendale, CA
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The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function and Wellness in Older Women
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function, Wellness and the Potential Mitigating Effects of a Multi-strain Probiotic, Prebiotic, and Synbiotic: a Randomized, Double-blinded Crossover Study in Older Women.
Status: Enrolling
Updated:  3/28/2018
UF Food Science and Human Nutrition Department
mi
from
Gainesville, FL
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function and Wellness in Older Women
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function, Wellness and the Potential Mitigating Effects of a Multi-strain Probiotic, Prebiotic, and Synbiotic: a Randomized, Double-blinded Crossover Study in Older Women.
Status: Enrolling
Updated: 3/28/2018
UF Food Science and Human Nutrition Department
mi
from
Gainesville, FL
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The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function and Wellness in Older Women
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function, Wellness and the Potential Mitigating Effects of a Multi-strain Probiotic, Prebiotic, and Synbiotic: a Randomized, Double-blinded Crossover Study in Older Women.
Status: Enrolling
Updated:  3/28/2018
UF/IFAS Extension Office Marion County
mi
from
Ocala, FL
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function and Wellness in Older Women
The Effects of a High Protein Diet on Microbiota, Gastrointestinal Function, Wellness and the Potential Mitigating Effects of a Multi-strain Probiotic, Prebiotic, and Synbiotic: a Randomized, Double-blinded Crossover Study in Older Women.
Status: Enrolling
Updated: 3/28/2018
UF/IFAS Extension Office Marion County
mi
from
Ocala, FL
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Study to Assess the Bioequivalence of Ibrutinib 560- Milligram (mg) Tablet to Four 140 -mg IMBRUVICA Capsules
A Single-Dose, Open-Label, Randomized, Replicate Crossover Study in Healthy Adult Subjects to Assess the Bioequivalence of an Ibrutinib 560-mg Tablet Compared to the Four IMBRUVICA 140 mg Capsules
Status: Enrolling
Updated:  3/28/2018
Clinical Research Facility
mi
from
Tempe, AZ
Study to Assess the Bioequivalence of Ibrutinib 560- Milligram (mg) Tablet to Four 140 -mg IMBRUVICA Capsules
A Single-Dose, Open-Label, Randomized, Replicate Crossover Study in Healthy Adult Subjects to Assess the Bioequivalence of an Ibrutinib 560-mg Tablet Compared to the Four IMBRUVICA 140 mg Capsules
Status: Enrolling
Updated: 3/28/2018
Clinical Research Facility
mi
from
Tempe, AZ
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Effect of a Multivitamin/Multimineral/Phytochemical Dietary Supplement on Indices of Human Health
Effect of a Multivitamin/Multimineral/Phytochemical Dietary Supplement on Gene Expression, Epigenetics and Nutritional Status in Healthy Adults
Status: Enrolling
Updated:  3/28/2018
USANA Health Sciences
mi
from
Salt Lake City, UT
Effect of a Multivitamin/Multimineral/Phytochemical Dietary Supplement on Indices of Human Health
Effect of a Multivitamin/Multimineral/Phytochemical Dietary Supplement on Gene Expression, Epigenetics and Nutritional Status in Healthy Adults
Status: Enrolling
Updated: 3/28/2018
USANA Health Sciences
mi
from
Salt Lake City, UT
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