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

Feeding Tolerance Evaluation
Feeding Tolerance Evaluation
Status: Enrolling
Updated:  5/11/2016
Tanner Clinic
mi
from
Layton, UT
Feeding Tolerance Evaluation
Feeding Tolerance Evaluation
Status: Enrolling
Updated: 5/11/2016
Tanner Clinic
mi
from
Layton, UT
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Relationship Between Potassium Level in Venous Blood Samples Drawn and Heel Sticks In Infants and Newborns
In Infants and Newborns, is There a Relation Between the Potassium Level in Blood Samples Drawn From a Vein and Those Drawn From a Heel Stick?
Status: Enrolling
Updated:  5/12/2016
Memorial Hermann Hospital
mi
from
Houston, TX
Relationship Between Potassium Level in Venous Blood Samples Drawn and Heel Sticks In Infants and Newborns
In Infants and Newborns, is There a Relation Between the Potassium Level in Blood Samples Drawn From a Vein and Those Drawn From a Heel Stick?
Status: Enrolling
Updated: 5/12/2016
Memorial Hermann Hospital
mi
from
Houston, TX
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Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated:  5/17/2016
University of Michigan
mi
from
Ann Arbor, MI
Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated: 5/17/2016
University of Michigan
mi
from
Ann Arbor, MI
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Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated:  5/17/2016
The Mayo Clinic
mi
from
Rochester, MN
Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated: 5/17/2016
The Mayo Clinic
mi
from
Rochester, MN
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Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated:  5/17/2016
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Glaucoma Biomarkers
Aqueous Humor Dynamic Components That Determine Intraocular Pressure Variance
Status: Enrolling
Updated: 5/17/2016
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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A Food-Drug Interaction Study of Serum Urate After Oral Inosine
A Phase 1, Open-label, Randomized, Two-period, Two-treatment, Crossover Study to Evaluate the Effects of Food on the Pharmacokinetics of Urate After a Single Dose of Inosine in Healthy Male Subjects
Status: Enrolling
Updated:  5/17/2016
Covance Clinical Research Unit Inc.
mi
from
Evansville, IN
A Food-Drug Interaction Study of Serum Urate After Oral Inosine
A Phase 1, Open-label, Randomized, Two-period, Two-treatment, Crossover Study to Evaluate the Effects of Food on the Pharmacokinetics of Urate After a Single Dose of Inosine in Healthy Male Subjects
Status: Enrolling
Updated: 5/17/2016
Covance Clinical Research Unit Inc.
mi
from
Evansville, IN
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Evaluation of Salt Sensitivity in Young Adults
Evaluation of Salt Sensitivity in Young Adults
Status: Enrolling
Updated:  5/18/2016
NYU Langone Medical Center
mi
from
New York, NY
Evaluation of Salt Sensitivity in Young Adults
Evaluation of Salt Sensitivity in Young Adults
Status: Enrolling
Updated: 5/18/2016
NYU Langone Medical Center
mi
from
New York, NY
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Effect of Renal Impairment on the Pharmacokinetics, and Safety of Megestrol Acetate Concentrated Suspension
An Open-Label, Single-Dose Study to Assess the Effect of Renal Impairment on the Pharmacokinetic Characteristics, Safety, and Tolerability of Megestrol Acetate
Status: Enrolling
Updated:  5/18/2016
SFBC International
mi
from
Miami, FL
Effect of Renal Impairment on the Pharmacokinetics, and Safety of Megestrol Acetate Concentrated Suspension
An Open-Label, Single-Dose Study to Assess the Effect of Renal Impairment on the Pharmacokinetic Characteristics, Safety, and Tolerability of Megestrol Acetate
Status: Enrolling
Updated: 5/18/2016
SFBC International
mi
from
Miami, FL
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At-home Auditory Training Clinical Trial
At-home Auditory Training Clinical Trial
Status: Enrolling
Updated:  5/19/2016
IU Department of Speech & Hearing Sciences
mi
from
Bloomington, IN
At-home Auditory Training Clinical Trial
At-home Auditory Training Clinical Trial
Status: Enrolling
Updated: 5/19/2016
IU Department of Speech & Hearing Sciences
mi
from
Bloomington, IN
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Effect of Nalbuphine and Naloxone on Experimentally Induced Skin Sensitivity
Effect of Kappa Opioid Agonist-Antagonists in the Heat/Capsaicin Sensitization Model
Status: Enrolling
Updated:  5/19/2016
University of California
mi
from
San Francisco, CA
Effect of Nalbuphine and Naloxone on Experimentally Induced Skin Sensitivity
Effect of Kappa Opioid Agonist-Antagonists in the Heat/Capsaicin Sensitization Model
Status: Enrolling
Updated: 5/19/2016
University of California
mi
from
San Francisco, CA
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A Study of the Effects of Posaconazole on RO5424802 Pharmacokinetics in Healthy Volunteers
An Open-Label, Three-Period, Fixed Sequence Study to Investigate the Effect of Multiple Oral Doses of Posaconazole, a Potent Cytochrome P450 3A Inhibitor, on the Single Dose Pharmacokinetics of RO5424802 in Healthy Subjects
Status: Enrolling
Updated:  6/1/2016
Clinical Research Facility
mi
from
Austin, TX
A Study of the Effects of Posaconazole on RO5424802 Pharmacokinetics in Healthy Volunteers
An Open-Label, Three-Period, Fixed Sequence Study to Investigate the Effect of Multiple Oral Doses of Posaconazole, a Potent Cytochrome P450 3A Inhibitor, on the Single Dose Pharmacokinetics of RO5424802 in Healthy Subjects
Status: Enrolling
Updated: 6/1/2016
Clinical Research Facility
mi
from
Austin, TX
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A Study of the Effect of Multiple Doses of Rifampin on the Single Dose Pharmacokinetics of RO5424802
An Open-Label, Three-Period, Fixed Sequence Study to Investigate the Effect of Multiple Oral Doses of Rifampin, a Potent Cytochrome P450 3A Inducer, on the Single Dose Pharmacokinetics of RO5424802 in Healthy Subjects
Status: Enrolling
Updated:  6/1/2016
Clinical Research Facility
mi
from
Austin, TX
A Study of the Effect of Multiple Doses of Rifampin on the Single Dose Pharmacokinetics of RO5424802
An Open-Label, Three-Period, Fixed Sequence Study to Investigate the Effect of Multiple Oral Doses of Rifampin, a Potent Cytochrome P450 3A Inducer, on the Single Dose Pharmacokinetics of RO5424802 in Healthy Subjects
Status: Enrolling
Updated: 6/1/2016
Clinical Research Facility
mi
from
Austin, TX
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A Study Investigating the Effect of Food and Esomeprazole on the Single Oral Dose Pharmacokinetics of RO5424802 in Healthy Volunteers.
AN OPEN-LABEL, TWO GROUP STUDY TO INVESTIGATE THE EFFECT OF FOOD (GROUP 1) AND ESOMEPRAZOLE (GROUP 2) ON THE SINGLE ORAL DOSE PHARMACOKINETICS OF RO5424802 IN HEALTHY SUBJECTS
Status: Enrolling
Updated:  6/1/2016
Clinical Research Facility
mi
from
Austin, TX
A Study Investigating the Effect of Food and Esomeprazole on the Single Oral Dose Pharmacokinetics of RO5424802 in Healthy Volunteers.
AN OPEN-LABEL, TWO GROUP STUDY TO INVESTIGATE THE EFFECT OF FOOD (GROUP 1) AND ESOMEPRAZOLE (GROUP 2) ON THE SINGLE ORAL DOSE PHARMACOKINETICS OF RO5424802 IN HEALTHY SUBJECTS
Status: Enrolling
Updated: 6/1/2016
Clinical Research Facility
mi
from
Austin, TX
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A Cross-over Study Examining the Bioequivalence of 3 Test Formulations to a Reference Formulation of Alectinib (RO5424802) in Healthy Volunteers
A Randomized, Open-Label, Single Dose, Cross-Over Study to Investigate the Bioequivalence of Three RO5424802 Test Formulations Versus a Reference Formulation Following Oral Administration in Healthy Subjects
Status: Enrolling
Updated:  6/1/2016
Clinical Research Facility
mi
from
Austin, TX
A Cross-over Study Examining the Bioequivalence of 3 Test Formulations to a Reference Formulation of Alectinib (RO5424802) in Healthy Volunteers
A Randomized, Open-Label, Single Dose, Cross-Over Study to Investigate the Bioequivalence of Three RO5424802 Test Formulations Versus a Reference Formulation Following Oral Administration in Healthy Subjects
Status: Enrolling
Updated: 6/1/2016
Clinical Research Facility
mi
from
Austin, TX
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Evaluation of PK of AC1204 v Caprylic Triglyceride Oil Incl Food Effect on Ketone Body Production
A Phase 1, Pilot, Single-Dose, 3-Way Crossover Study to Evaluate the Pharmacokinetic of AC-1204 Versus Caprylic Triglyceride Oil Including the Effect of Food on Ketone Body Production
Status: Enrolling
Updated:  6/1/2016
Celerion
mi
from
Tempe, AZ
Evaluation of PK of AC1204 v Caprylic Triglyceride Oil Incl Food Effect on Ketone Body Production
A Phase 1, Pilot, Single-Dose, 3-Way Crossover Study to Evaluate the Pharmacokinetic of AC-1204 Versus Caprylic Triglyceride Oil Including the Effect of Food on Ketone Body Production
Status: Enrolling
Updated: 6/1/2016
Celerion
mi
from
Tempe, AZ
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Study to Assess the Safety, Tolerability, and Pharmacokinetics of BIIB061 in Healthy Adult Volunteers
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB061 in Healthy Adult Volunteers
Status: Enrolling
Updated:  6/14/2016
Clinical Research Facility
mi
from
Madison, WI
Study to Assess the Safety, Tolerability, and Pharmacokinetics of BIIB061 in Healthy Adult Volunteers
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB061 in Healthy Adult Volunteers
Status: Enrolling
Updated: 6/14/2016
Clinical Research Facility
mi
from
Madison, WI
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A Study of LY3200327 in Healthy Participants
A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3200327 in Healthy Subjects
Status: Enrolling
Updated:  6/15/2016
Parexel International/ California Clinical Trials
mi
from
Glendale, CA
A Study of LY3200327 in Healthy Participants
A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3200327 in Healthy Subjects
Status: Enrolling
Updated: 6/15/2016
Parexel International/ California Clinical Trials
mi
from
Glendale, CA
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A Pharmacokinetic Study of [14C]-GDC-0810 After Single Oral Administration in Healthy Female Participants
Status: Enrolling
Updated:  6/15/2016
Clinical Research Facility
mi
from
Madison, WI
A Pharmacokinetic Study of [14C]-GDC-0810 After Single Oral Administration in Healthy Female Participants
Status: Enrolling
Updated: 6/15/2016
Clinical Research Facility
mi
from
Madison, WI
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Multi-cycle Prolon Diet
Effect of a Periodic Fasting-mimicking Diet on Risk Factors for Metabolic Syndrome and Age-related Diseases
Status: Enrolling
Updated:  6/16/2016
Davis School of Gerontology
mi
from
Los Angeles, CA
Multi-cycle Prolon Diet
Effect of a Periodic Fasting-mimicking Diet on Risk Factors for Metabolic Syndrome and Age-related Diseases
Status: Enrolling
Updated: 6/16/2016
Davis School of Gerontology
mi
from
Los Angeles, CA
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In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
Status: Enrolling
Updated:  6/16/2016
Hoxworth Blood Center
mi
from
Cincinnati, OH
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
Status: Enrolling
Updated: 6/16/2016
Hoxworth Blood Center
mi
from
Cincinnati, OH
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In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
Status: Enrolling
Updated:  6/16/2016
The Blood Center of Wisconsin
mi
from
Milwaukee, WI
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
In-Vitro Study of Platelets Collected on Trima Accel System and Stored in InterSol Solution
Status: Enrolling
Updated: 6/16/2016
The Blood Center of Wisconsin
mi
from
Milwaukee, WI
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Trima Accel® System Post Count Algorithm Study
A Multicenter Study to Evaluate Modified Postcount Algorithm Software on the Trima Accel® System in Volunteer Blood Donors
Status: Enrolling
Updated:  6/16/2016
San Diego Blood Bank
mi
from
San Diego, CA
Trima Accel® System Post Count Algorithm Study
A Multicenter Study to Evaluate Modified Postcount Algorithm Software on the Trima Accel® System in Volunteer Blood Donors
Status: Enrolling
Updated: 6/16/2016
San Diego Blood Bank
mi
from
San Diego, CA
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Trima Accel® System Post Count Algorithm Study
A Multicenter Study to Evaluate Modified Postcount Algorithm Software on the Trima Accel® System in Volunteer Blood Donors
Status: Enrolling
Updated:  6/16/2016
Bonfils Blood Center
mi
from
Denver, CO
Trima Accel® System Post Count Algorithm Study
A Multicenter Study to Evaluate Modified Postcount Algorithm Software on the Trima Accel® System in Volunteer Blood Donors
Status: Enrolling
Updated: 6/16/2016
Bonfils Blood Center
mi
from
Denver, CO
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Drug-Interaction Study to Evaluate the Effect of Rifampin, a Potent CYP3A4 Inducer, on the Systemic Exposure of Pacritinib in Healthy Subjects
A Phase 1, Open-Label, Drug-Interaction Study to Evaluate the Effect of Rifampin, a Potent CYP3A4 Inducer, on the Systemic Exposure of Pacritinib in Healthy Subjects
Status: Enrolling
Updated:  6/20/2016
Covance Clinical Research Unit, Inc.
mi
from
Daytona Beach, FL
Drug-Interaction Study to Evaluate the Effect of Rifampin, a Potent CYP3A4 Inducer, on the Systemic Exposure of Pacritinib in Healthy Subjects
A Phase 1, Open-Label, Drug-Interaction Study to Evaluate the Effect of Rifampin, a Potent CYP3A4 Inducer, on the Systemic Exposure of Pacritinib in Healthy Subjects
Status: Enrolling
Updated: 6/20/2016
Covance Clinical Research Unit, Inc.
mi
from
Daytona Beach, FL
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Effect of a Proton Pump Inhibitor on Gleevec® in Healthy Volunteers
Effect of a Proton Pump Inhibitor (Omeprazole, Prilosec®) on Imatinib Mesylate (Gleevec®) Pharmacokinetics in Healthy Volunteers (CSTI571BUS258)
Status: Enrolling
Updated:  6/21/2016
University of Pittsburgh Cancer Institute / Clinical and Translational Research Center (Hillman Cancer Center and Montefiore University Hospital locations)
mi
from
Pittsburgh, PA
Effect of a Proton Pump Inhibitor on Gleevec® in Healthy Volunteers
Effect of a Proton Pump Inhibitor (Omeprazole, Prilosec®) on Imatinib Mesylate (Gleevec®) Pharmacokinetics in Healthy Volunteers (CSTI571BUS258)
Status: Enrolling
Updated: 6/21/2016
University of Pittsburgh Cancer Institute / Clinical and Translational Research Center (Hillman Cancer Center and Montefiore University Hospital locations)
mi
from
Pittsburgh, PA
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Effect of Antacids on Gleevec® in Healthy Volunteers
Effect of Antacids (Mg-Al-based) on Imatinib Mesylate (Gleevec®) Pharmacokinetics in Healthy Volunteers (CSTI571BUS257)
Status: Enrolling
Updated:  6/21/2016
University of Pittsburgh Cancer Institute / Clinical and Translational Research Center (Hillman Cancer Center and Montefiore University Hospital locations)
mi
from
Pittsburgh, PA
Effect of Antacids on Gleevec® in Healthy Volunteers
Effect of Antacids (Mg-Al-based) on Imatinib Mesylate (Gleevec®) Pharmacokinetics in Healthy Volunteers (CSTI571BUS257)
Status: Enrolling
Updated: 6/21/2016
University of Pittsburgh Cancer Institute / Clinical and Translational Research Center (Hillman Cancer Center and Montefiore University Hospital locations)
mi
from
Pittsburgh, PA
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A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated:  6/27/2016
Arcadia MRI & Imaging Center
mi
from
Arcadia, CA
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated: 6/27/2016
Arcadia MRI & Imaging Center
mi
from
Arcadia, CA
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A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated:  6/27/2016
California Clinical Trials Medical Group
mi
from
Glendale, CA
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated: 6/27/2016
California Clinical Trials Medical Group
mi
from
Glendale, CA
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A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated:  6/27/2016
California Clinical Trials Medical Group
mi
from
Glendale, CA
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated: 6/27/2016
California Clinical Trials Medical Group
mi
from
Glendale, CA
Click here to add this to my saved trials
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated:  6/27/2016
Glendale Adventist Medical Center
mi
from
Glendale, CA
A Study To Examine Safety, Pharmacokinetics, And Pharmacodynamic Of Pf 06412562 In Healthy Males
A Randomized,Subject And Investigator Blind, Sponsor Open Placebo Controlled, Parallel Phase 1b Study To Examine The Safety, Pharmacokinetics, And Pharmacodynamic Effects Of Pf‑06412562 On Cognitive And Reward/Motivation Domains In Healthy Male Volunteers Selected By Cognitive Phenotype
Status: Enrolling
Updated: 6/27/2016
Glendale Adventist Medical Center
mi
from
Glendale, CA
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A Study to Evaluate the Adherence of 2 Strengths of Newly Manufactured Samples and Aged Samples of a New Formulation (JNJ-35685-AAA-G016 and JNJ-35685-AAA-G021) of Fentanyl Transdermal System Compared With Duragesic Fentanyl Transdermal Patch in Healthy Participants
A Randomized, Partially-blinded, Two-arm, Single-application, 3-way Crossover Study to Evaluate the Adherence of 2 Strengths of Newly Manufactured Samples and Aged Samples of a New Formulation (JNJ-35685-AAA-G016 and JNJ-35685-AAA-G021) of Fentanyl Transdermal System Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Subjects
Status: Enrolling
Updated:  6/27/2016
Clinical Research Facility
mi
from
Cypress, CA
A Study to Evaluate the Adherence of 2 Strengths of Newly Manufactured Samples and Aged Samples of a New Formulation (JNJ-35685-AAA-G016 and JNJ-35685-AAA-G021) of Fentanyl Transdermal System Compared With Duragesic Fentanyl Transdermal Patch in Healthy Participants
A Randomized, Partially-blinded, Two-arm, Single-application, 3-way Crossover Study to Evaluate the Adherence of 2 Strengths of Newly Manufactured Samples and Aged Samples of a New Formulation (JNJ-35685-AAA-G016 and JNJ-35685-AAA-G021) of Fentanyl Transdermal System Compared With DURAGESIC Fentanyl Transdermal Patch in Healthy Subjects
Status: Enrolling
Updated: 6/27/2016
Clinical Research Facility
mi
from
Cypress, CA
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A Study to Investigate Whether Pharmacokinetic and Pharmacodynamic Interactions Exist Between Metformin and Canagliflozin (JNJ-28431754) in Healthy Volunteers
An Open-Label, Fixed Sequence, Single and Multiple Dose Study in Male and Female Subjects to Investigate the Potential for Pharmacokinetic and Pharmacodynamic Interaction Between Metformin and JNJ-28431754
Status: Enrolling
Updated:  6/28/2016
Clinical Research Facility
mi
from
Neptune, NJ
A Study to Investigate Whether Pharmacokinetic and Pharmacodynamic Interactions Exist Between Metformin and Canagliflozin (JNJ-28431754) in Healthy Volunteers
An Open-Label, Fixed Sequence, Single and Multiple Dose Study in Male and Female Subjects to Investigate the Potential for Pharmacokinetic and Pharmacodynamic Interaction Between Metformin and JNJ-28431754
Status: Enrolling
Updated: 6/28/2016
Clinical Research Facility
mi
from
Neptune, NJ
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A Study to Assess Electrocardiogram Results in Healthy Volunteers Receiving Canagliflozin (JNJ-28431754)
A Randomized, Double-Blind, Double-Dummy, Placebo- and Positive-Controlled, Four-Way Crossover Study Evaluating ECG Intervals in Healthy Adults Receiving a Single, Oral Dose of JNJ-28431754 at Therapeutic and Supra-Therapeutic Doses
Status: Enrolling
Updated:  6/28/2016
Clinical Research Facility
mi
from
Tempe, AZ
A Study to Assess Electrocardiogram Results in Healthy Volunteers Receiving Canagliflozin (JNJ-28431754)
A Randomized, Double-Blind, Double-Dummy, Placebo- and Positive-Controlled, Four-Way Crossover Study Evaluating ECG Intervals in Healthy Adults Receiving a Single, Oral Dose of JNJ-28431754 at Therapeutic and Supra-Therapeutic Doses
Status: Enrolling
Updated: 6/28/2016
Clinical Research Facility
mi
from
Tempe, AZ
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SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects
A Double-blinded, Randomized, Placebo-controlled, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TD-1473 in Healthy Subjects
Status: Enrolling
Updated:  6/29/2016
Celerion
mi
from
Lincoln, NE
SAD and MAD Study to Evaluate Safety, Tolerability, and Pharmacokinetics (PK) of TD-1473 in Healthy Subjects
A Double-blinded, Randomized, Placebo-controlled, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TD-1473 in Healthy Subjects
Status: Enrolling
Updated: 6/29/2016
Celerion
mi
from
Lincoln, NE
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Open-Label Phase 1 Study of Aerosolized Amikacin and Fosfomycin in Healthy Volunteers
An Open-Label Phase 1 Study of Aerosolized Amikacin and Fosfomycin Delivered Via the PARI Investigational eFlow Nebulizer System or the PARI LC Sprint Nebulizer in Healthy Volunteers
Status: Enrolling
Updated:  7/8/2016
DaVita Clinical Research
mi
from
Minneapolis, MN
Open-Label Phase 1 Study of Aerosolized Amikacin and Fosfomycin in Healthy Volunteers
An Open-Label Phase 1 Study of Aerosolized Amikacin and Fosfomycin Delivered Via the PARI Investigational eFlow Nebulizer System or the PARI LC Sprint Nebulizer in Healthy Volunteers
Status: Enrolling
Updated: 7/8/2016
DaVita Clinical Research
mi
from
Minneapolis, MN
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Ketamine Infusion for Social Anxiety Disorder
Ketamine Infusion for Social Anxiety Disorder
Status: Enrolling
Updated:  7/11/2016
Connecticut Mental Health Center
mi
from
New Haven, CT
Ketamine Infusion for Social Anxiety Disorder
Ketamine Infusion for Social Anxiety Disorder
Status: Enrolling
Updated: 7/11/2016
Connecticut Mental Health Center
mi
from
New Haven, CT
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A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated:  7/11/2016
Clinical Research Facility
mi
from
San Diego, CA
A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated: 7/11/2016
Clinical Research Facility
mi
from
San Diego, CA
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A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated:  7/11/2016
Clinical Research Facility
mi
from
Mishawaka, IN
A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated: 7/11/2016
Clinical Research Facility
mi
from
Mishawaka, IN
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A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated:  7/11/2016
Clinical Research Facility
mi
from
Rockville, MD
A Study to Evaluate the Immunogenicity, Safety and Tolerability of Ad26.ZEBOV and MVA‐BN‐Filo in Healthy Adult Participants
A Phase 3, Randomized, Double‐Blind, Placebo‐Controlled Study to Evaluate the Immunogenicity, Safety and Tolerability of a Heterologous Prime‐Boost Regimen Using Three Different Batches of Ad26.ZEBOV and a Single Batch of MVA‐BN®‐Filo in Healthy Adult Subjects
Status: Enrolling
Updated: 7/11/2016
Clinical Research Facility
mi
from
Rockville, MD
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A Study of LY3039478 in Healthy Participants
A Single Ascending Dose Study for the Evaluation of the Effects of LY3039478 on the QT/Corrected QT Interval in Healthy Subjects and Pilot Relative Bioavailability
Status: Enrolling
Updated:  7/11/2016
Covance, Inc.
mi
from
Daytona Beach, FL
A Study of LY3039478 in Healthy Participants
A Single Ascending Dose Study for the Evaluation of the Effects of LY3039478 on the QT/Corrected QT Interval in Healthy Subjects and Pilot Relative Bioavailability
Status: Enrolling
Updated: 7/11/2016
Covance, Inc.
mi
from
Daytona Beach, FL
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Drug Interaction Study Between AVP-923 and Itraconazole and Between AVP-786 and Itraconazole in Healthy Adult Subejcts
A Phase 1, Single-center, Randomized, Double-blind, Double-dummy, Drug Interaction Study Between AVP-923 and Itraconazole, and Between AVP-786 and Itraconazole in Healthy Adult Subjects
Status: Enrolling
Updated:  7/13/2016
Vince and Associates Clinical Research
mi
from
Overland Park, KA
Drug Interaction Study Between AVP-923 and Itraconazole and Between AVP-786 and Itraconazole in Healthy Adult Subejcts
A Phase 1, Single-center, Randomized, Double-blind, Double-dummy, Drug Interaction Study Between AVP-923 and Itraconazole, and Between AVP-786 and Itraconazole in Healthy Adult Subjects
Status: Enrolling
Updated: 7/13/2016
Vince and Associates Clinical Research
mi
from
Overland Park, KA
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Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated:  7/13/2016
Sall Research Center
mi
from
Artesia, CA
Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated: 7/13/2016
Sall Research Center
mi
from
Artesia, CA
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Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated:  7/13/2016
Lugene Eye Institute
mi
from
Glendale, CA
Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated: 7/13/2016
Lugene Eye Institute
mi
from
Glendale, CA
Click here to add this to my saved trials
Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated:  7/13/2016
Montebello Medical Center, Inc.
mi
from
Montebello, CA
Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With Dry Eye
Status: Enrolling
Updated: 7/13/2016
Montebello Medical Center, Inc.
mi
from
Montebello, CA
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Phase 1 TAK-915 Single-Dose Positron Emission Tomography (PET) Occupancy Study
A Phase 1, Open-Label, Positron Emission Tomography Study With [18F]MNI-794 to Determine Phosphodiesterase 2A Brain Enzyme Occupancy of TAK-915 After Single-Dose Oral Administration in Healthy Subjects
Status: Enrolling
Updated:  7/19/2016
Clinical Research Facility
mi
from
New Haven, CT
Phase 1 TAK-915 Single-Dose Positron Emission Tomography (PET) Occupancy Study
A Phase 1, Open-Label, Positron Emission Tomography Study With [18F]MNI-794 to Determine Phosphodiesterase 2A Brain Enzyme Occupancy of TAK-915 After Single-Dose Oral Administration in Healthy Subjects
Status: Enrolling
Updated: 7/19/2016
Clinical Research Facility
mi
from
New Haven, CT
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A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated:  7/25/2016
Collaborative Neuroscience Network, Inc.
mi
from
Long Beach, CA
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated: 7/25/2016
Collaborative Neuroscience Network, Inc.
mi
from
Long Beach, CA
Click here to add this to my saved trials
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated:  7/25/2016
Broward Research Group
mi
from
Hollywood, FL
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated: 7/25/2016
Broward Research Group
mi
from
Hollywood, FL
Click here to add this to my saved trials
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated:  7/25/2016
Miami Research Associates
mi
from
South Miami, FL
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated: 7/25/2016
Miami Research Associates
mi
from
South Miami, FL
Click here to add this to my saved trials
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated:  7/25/2016
Jasper Clinic, Inc.
mi
from
Kalamazoo, MI
A Study To Evaluate The Difference In iPad-Based Cognitive Video Game (Akili Interactive's Project: EVO) Performance In Amyloid-Positive Versus Amyloid-Negative Healthy Elderly Volunteers
A Randomized, Double Blind, Placebo Controlled Trial To Study Difference In Cognitive Learning Associated With Repeated Self-administration Of Remote Computer Tablet-based Application Assessing Dual-task Performance Based On Amyloid Status In Healthy Elderly Volunteers
Status: Enrolling
Updated: 7/25/2016
Jasper Clinic, Inc.
mi
from
Kalamazoo, MI
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Preparing Older Veterans With Serious and Chronic Illness for Decision Making
Preparing Older Veterans With Serious and Chronic Illness for Decision Making
Status: Enrolling
Updated:  7/26/2016
San Francisco VA Medical Center, San Francisco, CA
mi
from
San Francisco, CA
Preparing Older Veterans With Serious and Chronic Illness for Decision Making
Preparing Older Veterans With Serious and Chronic Illness for Decision Making
Status: Enrolling
Updated: 7/26/2016
San Francisco VA Medical Center, San Francisco, CA
mi
from
San Francisco, CA
Click here to add this to my saved trials