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

Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Status: Enrolling
Updated:  3/30/2016
Northern California Research Center
mi
from
Oakland, CA
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Status: Enrolling
Updated: 3/30/2016
Northern California Research Center
mi
from
Oakland, CA
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Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Status: Enrolling
Updated:  3/30/2016
South Bay Research Center
mi
from
Torrance, CA
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Validity of an Online Neurocognitive Test Battery, the Brain Performance Test (BPT), in Normal Healthy Adults
Status: Enrolling
Updated: 3/30/2016
South Bay Research Center
mi
from
Torrance, CA
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Normative Data of Brain Network Activation in Adolescents and Young Adults
Establishment of Normative Data of Brain Network Activation (BNA) Using Evoked Response Potentials in Adolescents and Young Adults
Status: Enrolling
Updated:  3/31/2016
Vince and Associates Clinical Research
mi
from
Overland Park, KA
Normative Data of Brain Network Activation in Adolescents and Young Adults
Establishment of Normative Data of Brain Network Activation (BNA) Using Evoked Response Potentials in Adolescents and Young Adults
Status: Enrolling
Updated: 3/31/2016
Vince and Associates Clinical Research
mi
from
Overland Park, KA
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Normative Data of Brain Network Activation
Establishment of Normative Data of Brain Network Activation Analysis (BNA) Using Evoked Response Potentials, in Adolescents and Young Adults
Status: Enrolling
Updated:  3/31/2016
Electrical Geodesics, Inc.
mi
from
Eugene, OR
Normative Data of Brain Network Activation
Establishment of Normative Data of Brain Network Activation Analysis (BNA) Using Evoked Response Potentials, in Adolescents and Young Adults
Status: Enrolling
Updated: 3/31/2016
Electrical Geodesics, Inc.
mi
from
Eugene, OR
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Single-Dose, Crossover Study To Compare Bioavailability Of Two Formulations Under Fed And Fasted Conditions
An Open-Label, Randomized, 2-Cohort, Single-Dose, Crossover Study Of 40 Mg Doses Of Pf-00345439 To Evaluate The Bioequivalence Of Modified Formulation K Vs. Original Formulation X Under Intermediate-Fat Fed Conditions And To Estimate Relative Bioavailability Under Fasting Conditions In Healthy Volunteers
Status: Enrolling
Updated:  3/31/2016
Pfizer Investigational Site
mi
from
St. Paul, MN
Single-Dose, Crossover Study To Compare Bioavailability Of Two Formulations Under Fed And Fasted Conditions
An Open-Label, Randomized, 2-Cohort, Single-Dose, Crossover Study Of 40 Mg Doses Of Pf-00345439 To Evaluate The Bioequivalence Of Modified Formulation K Vs. Original Formulation X Under Intermediate-Fat Fed Conditions And To Estimate Relative Bioavailability Under Fasting Conditions In Healthy Volunteers
Status: Enrolling
Updated: 3/31/2016
Pfizer Investigational Site
mi
from
St. Paul, MN
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Effects of Ethanol on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open Label, Single Dose, Randomized, Two Way Crossover Study to Estimate Oxycodone Relative Bioavailability in Healthy Volunteers Following Administration of PF 00345439 Formulation K 40 Mg Under Fasting Conditions With 40% Ethanol Compared With Water
Status: Enrolling
Updated:  3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
Effects of Ethanol on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open Label, Single Dose, Randomized, Two Way Crossover Study to Estimate Oxycodone Relative Bioavailability in Healthy Volunteers Following Administration of PF 00345439 Formulation K 40 Mg Under Fasting Conditions With 40% Ethanol Compared With Water
Status: Enrolling
Updated: 3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
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Effects of Ethanol on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open Label, Single Dose, Randomized, Two Way Crossover Study to Estimate Oxycodone Relative Bioavailability in Healthy Volunteers Following Administration of PF 00345439 Formulation K 40 Mg Under Fasting Conditions With 40% Ethanol Compared With Water
Status: Enrolling
Updated:  3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
Effects of Ethanol on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open Label, Single Dose, Randomized, Two Way Crossover Study to Estimate Oxycodone Relative Bioavailability in Healthy Volunteers Following Administration of PF 00345439 Formulation K 40 Mg Under Fasting Conditions With 40% Ethanol Compared With Water
Status: Enrolling
Updated: 3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
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Oral Liposomal Glutathione Supplementation in Healthy Subjects
Pilot Study of Oral Liposomal Glutathione Supplementation on Levels of Glutathione in Blood and Biomarkers of Oxidative Stress and Immune Function in Healthy Adults
Status: Enrolling
Updated:  3/31/2016
MS Hershey Medical Center
mi
from
Hershey, PA
Oral Liposomal Glutathione Supplementation in Healthy Subjects
Pilot Study of Oral Liposomal Glutathione Supplementation on Levels of Glutathione in Blood and Biomarkers of Oxidative Stress and Immune Function in Healthy Adults
Status: Enrolling
Updated: 3/31/2016
MS Hershey Medical Center
mi
from
Hershey, PA
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Dose Proportionality Study Of PF-00345439 Formulation Under Fed Conditions
An Open-label, Randomized, Single-dose, Three-way Crossover Study to Evaluate the Dose Proportionality of 5 Mg, 20 Mg and 40 Mg of PF-00345439 Formulation K Under Intermediate-fat Fed Conditions in Healthy Volunteers
Status: Enrolling
Updated:  3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
Dose Proportionality Study Of PF-00345439 Formulation Under Fed Conditions
An Open-label, Randomized, Single-dose, Three-way Crossover Study to Evaluate the Dose Proportionality of 5 Mg, 20 Mg and 40 Mg of PF-00345439 Formulation K Under Intermediate-fat Fed Conditions in Healthy Volunteers
Status: Enrolling
Updated: 3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
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Effects of Food on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open-Label, Randomized, 2-Cohort, Single-Dose, Crossover Study To Estimate The Effects Of Food On Oxycodone Pharmacokinetics Following Oral Administration Of 40 Mg Doses Of Pf 00345439 Formulation K Taken Whole Or After Chewing In Healthy Volunteers
Status: Enrolling
Updated:  3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
Effects of Food on Oxycodone Pharmacokinetics in Healthy Volunteers
An Open-Label, Randomized, 2-Cohort, Single-Dose, Crossover Study To Estimate The Effects Of Food On Oxycodone Pharmacokinetics Following Oral Administration Of 40 Mg Doses Of Pf 00345439 Formulation K Taken Whole Or After Chewing In Healthy Volunteers
Status: Enrolling
Updated: 3/31/2016
Pfizer Investigational Site
mi
from
Overland Park, KA
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A Study to Investigate the Safety, Tolerability, and Pharmacokinetics (PK) of Oseltamivir and Its Carboxylate Metabolite, RO0640802 in Healthy Volunteers
A Multiple-Center, Randomized, Double-blind, Multiple-Dose, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO0640796 (Oseltamivir) and Its Carboxylate Metabolite, RO0640802, Following Intravenous Administrations in Healthy Subjects
Status: Enrolling
Updated:  4/2/2016
Clinical Research Facility
mi
from
Little Rock, AR
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics (PK) of Oseltamivir and Its Carboxylate Metabolite, RO0640802 in Healthy Volunteers
A Multiple-Center, Randomized, Double-blind, Multiple-Dose, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO0640796 (Oseltamivir) and Its Carboxylate Metabolite, RO0640802, Following Intravenous Administrations in Healthy Subjects
Status: Enrolling
Updated: 4/2/2016
Clinical Research Facility
mi
from
Little Rock, AR
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A Study to Investigate the Safety, Tolerability, and Pharmacokinetics (PK) of Oseltamivir and Its Carboxylate Metabolite, RO0640802 in Healthy Volunteers
A Multiple-Center, Randomized, Double-blind, Multiple-Dose, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO0640796 (Oseltamivir) and Its Carboxylate Metabolite, RO0640802, Following Intravenous Administrations in Healthy Subjects
Status: Enrolling
Updated:  4/2/2016
Clinical Research Facility
mi
from
Austin, TX
A Study to Investigate the Safety, Tolerability, and Pharmacokinetics (PK) of Oseltamivir and Its Carboxylate Metabolite, RO0640802 in Healthy Volunteers
A Multiple-Center, Randomized, Double-blind, Multiple-Dose, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, and Pharmacokinetics of RO0640796 (Oseltamivir) and Its Carboxylate Metabolite, RO0640802, Following Intravenous Administrations in Healthy Subjects
Status: Enrolling
Updated: 4/2/2016
Clinical Research Facility
mi
from
Austin, TX
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Using a Sheathed Speculum to Visualize and Access the Cervix in Women With Excessive Vaginal Tissue
Using a Sheathed Speculum to Visualize and Access the Cervix in Women With Excessive Vaginal Tissue
Status: Enrolling
Updated:  4/4/2016
USF South Tampa Center for Advanced Healthcare
mi
from
Tampa, FL
Using a Sheathed Speculum to Visualize and Access the Cervix in Women With Excessive Vaginal Tissue
Using a Sheathed Speculum to Visualize and Access the Cervix in Women With Excessive Vaginal Tissue
Status: Enrolling
Updated: 4/4/2016
USF South Tampa Center for Advanced Healthcare
mi
from
Tampa, FL
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A Study of LY3154207 on Sleep in Healthy Male Participants
An Evaluation of the Impact of Single Doses of LY3154207 on Sleep Latency in Sleep-Deprived Healthy Subjects
Status: Enrolling
Updated:  4/4/2016
Parexel Early Phase Unit at Glendale
mi
from
Glendale, CA
A Study of LY3154207 on Sleep in Healthy Male Participants
An Evaluation of the Impact of Single Doses of LY3154207 on Sleep Latency in Sleep-Deprived Healthy Subjects
Status: Enrolling
Updated: 4/4/2016
Parexel Early Phase Unit at Glendale
mi
from
Glendale, CA
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A Study of AZD3293 (LY3314814) in Healthy Participants
A Bioequivalence and Food Effect Study in Healthy Subjects Administered 2 Different Tablet Formulations of AZD3293
Status: Enrolling
Updated:  4/4/2016
Covance Clinical Research Inc
mi
from
Evansville, IN
A Study of AZD3293 (LY3314814) in Healthy Participants
A Bioequivalence and Food Effect Study in Healthy Subjects Administered 2 Different Tablet Formulations of AZD3293
Status: Enrolling
Updated: 4/4/2016
Covance Clinical Research Inc
mi
from
Evansville, IN
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Study to Determine the Sensitizing Potential of PEP005 Topical Gel in Healthy Volunteers Using a Repeat Insult Patch Test Design
A Randomized, Controlled Study to Evaluate the Sensitizing Potential of PEP005 Topical Gel (0.01% Concentration) in Healthy Volunteers Using a Repeat Insult Patch Test Design
Status: Enrolling
Updated:  4/4/2016
TKL Research
mi
from
Paramus, NJ
Study to Determine the Sensitizing Potential of PEP005 Topical Gel in Healthy Volunteers Using a Repeat Insult Patch Test Design
A Randomized, Controlled Study to Evaluate the Sensitizing Potential of PEP005 Topical Gel (0.01% Concentration) in Healthy Volunteers Using a Repeat Insult Patch Test Design
Status: Enrolling
Updated: 4/4/2016
TKL Research
mi
from
Paramus, NJ
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Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Galeterone
An Open-Label, Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Galeterone in Healthy Male Subjects After Oral Administration
Status: Enrolling
Updated:  4/5/2016
Celerion
mi
from
Lincoln, NE
Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Galeterone
An Open-Label, Single-Dose Study to Assess the Absorption, Metabolism, Excretion, and Mass Balance of Radiolabeled Galeterone in Healthy Male Subjects After Oral Administration
Status: Enrolling
Updated: 4/5/2016
Celerion
mi
from
Lincoln, NE
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Sonographic Features of Normal Soft Tissues of the Feet
Sonographic Features of Normal Soft Tissues of the Feet
Status: Enrolling
Updated:  4/6/2016
University of Michigan Medical Center
mi
from
Ann Arbor, MI
Sonographic Features of Normal Soft Tissues of the Feet
Sonographic Features of Normal Soft Tissues of the Feet
Status: Enrolling
Updated: 4/6/2016
University of Michigan Medical Center
mi
from
Ann Arbor, MI
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A Study to Evaluate Safety, Acceptability, Pharmacokinetics, and ex Vivo Pharmacodynamics of TMC278 Long Acting Formulation in HIV-1 Seronegative Participants
Phase 1 Open Label Safety, Acceptability, Pharmacokinetic and ex Vivo Pharmacodynamic Study of TMC278 Long Acting (LA) Administered Intramuscularly to HIV-1 Seronegative Individuals
Status: Enrolling
Updated:  4/6/2016
Clinical Research Facility
mi
from
Pittsburgh, PA
A Study to Evaluate Safety, Acceptability, Pharmacokinetics, and ex Vivo Pharmacodynamics of TMC278 Long Acting Formulation in HIV-1 Seronegative Participants
Phase 1 Open Label Safety, Acceptability, Pharmacokinetic and ex Vivo Pharmacodynamic Study of TMC278 Long Acting (LA) Administered Intramuscularly to HIV-1 Seronegative Individuals
Status: Enrolling
Updated: 4/6/2016
Clinical Research Facility
mi
from
Pittsburgh, PA
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A Study to Assess the Levels of CAZ-AVI and Metronidazole in the Blood When Given Together and Separately
A Phase I, Open-Label, 3-way Crossover, Pharmacokinetic and Drug-Drug Interaction Study of Ceftazidime Avibactam (CAZ-AVI) and Metronidazole When Administered Alone and in Combination in Healthy Subjects
Status: Enrolling
Updated:  4/7/2016
Clinical Research Facility
mi
from
Overland Park, KA
A Study to Assess the Levels of CAZ-AVI and Metronidazole in the Blood When Given Together and Separately
A Phase I, Open-Label, 3-way Crossover, Pharmacokinetic and Drug-Drug Interaction Study of Ceftazidime Avibactam (CAZ-AVI) and Metronidazole When Administered Alone and in Combination in Healthy Subjects
Status: Enrolling
Updated: 4/7/2016
Clinical Research Facility
mi
from
Overland Park, KA
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Phase 1, Febuxostat XR Bioavailability Study
A Phase 1, Randomized, Open-Label, Single-Dose, 4-Way Crossover Study to Assess the Relative Bioavailability of Four 80 mg Febuxostat XR Formulations
Status: Enrolling
Updated:  4/11/2016
Clinical Research Facility
mi
from
Austin, TX
Phase 1, Febuxostat XR Bioavailability Study
A Phase 1, Randomized, Open-Label, Single-Dose, 4-Way Crossover Study to Assess the Relative Bioavailability of Four 80 mg Febuxostat XR Formulations
Status: Enrolling
Updated: 4/11/2016
Clinical Research Facility
mi
from
Austin, TX
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A Study to Characterize the Elimination of Guselkumab Glycoform Variants in Healthy Participants
Phase 1, Open-label, Single-dose Study to Characterize the Elimination of Guselkumab Glycoform Variants in Healthy Subjects
Status: Enrolling
Updated:  4/11/2016
Clinical Research Facility
mi
from
Tempe, AZ
A Study to Characterize the Elimination of Guselkumab Glycoform Variants in Healthy Participants
Phase 1, Open-label, Single-dose Study to Characterize the Elimination of Guselkumab Glycoform Variants in Healthy Subjects
Status: Enrolling
Updated: 4/11/2016
Clinical Research Facility
mi
from
Tempe, AZ
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Multiphase Activity Promotion Study
A Social-Cognitive Smartphone Application for Improving Physical Activity in Adults
Status: Enrolling
Updated:  4/11/2016
University of Illinois at Urbana-Champaign
mi
from
Urbana, IL
Multiphase Activity Promotion Study
A Social-Cognitive Smartphone Application for Improving Physical Activity in Adults
Status: Enrolling
Updated: 4/11/2016
University of Illinois at Urbana-Champaign
mi
from
Urbana, IL
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THE EFFECT OF CYP3A5 GENOTYPE ON THE PHARMACOKINETICS OF MARAVIROC
A Phase 1, Open-label, Parallel-group Study To Assess The Effect Of Cyp3a5 Genotype On The Pharmacokinetics Of Maraviroc And Cyp3a5-derived Metabolites With And Without Darunavir/Cobicistat In African-american And Caucasian Healthy Volunteers
Status: Enrolling
Updated:  4/11/2016
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
THE EFFECT OF CYP3A5 GENOTYPE ON THE PHARMACOKINETICS OF MARAVIROC
A Phase 1, Open-label, Parallel-group Study To Assess The Effect Of Cyp3a5 Genotype On The Pharmacokinetics Of Maraviroc And Cyp3a5-derived Metabolites With And Without Darunavir/Cobicistat In African-american And Caucasian Healthy Volunteers
Status: Enrolling
Updated: 4/11/2016
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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A Single-Dose Study of an Investigational Capsule Formulation of 2 mg/0.5 mg Buprenorphine/Naloxone
A Single-Dose, 1-Period, 1-Treatment Pilot Study of an Investigational Capsule Formulation of 2 mg/.05 mg Buprenorphine/Naloxone Under Fasting Conditions
Status: Enrolling
Updated:  4/11/2016
CEDRA Clinical Research, LLC
mi
from
Austin, TX
A Single-Dose Study of an Investigational Capsule Formulation of 2 mg/0.5 mg Buprenorphine/Naloxone
A Single-Dose, 1-Period, 1-Treatment Pilot Study of an Investigational Capsule Formulation of 2 mg/.05 mg Buprenorphine/Naloxone Under Fasting Conditions
Status: Enrolling
Updated: 4/11/2016
CEDRA Clinical Research, LLC
mi
from
Austin, TX
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A Phase 1, Randomized, Double-Blind, Placebo-Controlled Escalating Single Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ND-L02-s0201 Injection in Normal Healthy Subjects
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Escalating Single Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ND-L02-s0201 Injection, a Vitamin A-Coupled Lipid Nanoparticle Containing siRNA Against HSP47, in Healthy Normal Subjects
Status: Enrolling
Updated:  4/12/2016
Quintiles Phase One Services
mi
from
Overland Park, KA
A Phase 1, Randomized, Double-Blind, Placebo-Controlled Escalating Single Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ND-L02-s0201 Injection in Normal Healthy Subjects
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Escalating Single Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ND-L02-s0201 Injection, a Vitamin A-Coupled Lipid Nanoparticle Containing siRNA Against HSP47, in Healthy Normal Subjects
Status: Enrolling
Updated: 4/12/2016
Quintiles Phase One Services
mi
from
Overland Park, KA
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Clinical Evaluation of the Carestream PRO 3543 and PRO 3543C Digital Detectors
Clinical Evaluation of the Carestream PRO 3543 and PRO 3543C Digital Detectors
Status: Enrolling
Updated:  4/14/2016
University of Rochester
mi
from
Rochester, NY
Clinical Evaluation of the Carestream PRO 3543 and PRO 3543C Digital Detectors
Clinical Evaluation of the Carestream PRO 3543 and PRO 3543C Digital Detectors
Status: Enrolling
Updated: 4/14/2016
University of Rochester
mi
from
Rochester, NY
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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAP311 in Healthy Subjects and Dyslipidemic Patients
A First-in-human Randomized, Double-blind, Placebo-controlled, 4-part Study to Assess Safety, Tolerability, Pharmacokinetics (Including Open Label Study of Food Effect and Interaction With Simvastatin) and Pharmacodynamics of Interwoven Single- and Multiple-ascending Doses of TAP311 in Healthy Subjects and Dyslipidemic Patients.
Status: Enrolling
Updated:  4/15/2016
Novartis Investigative Site
mi
from
Miramar, FL
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAP311 in Healthy Subjects and Dyslipidemic Patients
A First-in-human Randomized, Double-blind, Placebo-controlled, 4-part Study to Assess Safety, Tolerability, Pharmacokinetics (Including Open Label Study of Food Effect and Interaction With Simvastatin) and Pharmacodynamics of Interwoven Single- and Multiple-ascending Doses of TAP311 in Healthy Subjects and Dyslipidemic Patients.
Status: Enrolling
Updated: 4/15/2016
Novartis Investigative Site
mi
from
Miramar, FL
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Clinical Evaluation of DRX Plus 3543 and DRX Plus 3543C Digital Detectors
Clinical Evaluation of DRX Plus 3543 and DRX Plus 3543C Digital Detectors
Status: Enrolling
Updated:  4/15/2016
University of Rochester
mi
from
Rochester, NY
Clinical Evaluation of DRX Plus 3543 and DRX Plus 3543C Digital Detectors
Clinical Evaluation of DRX Plus 3543 and DRX Plus 3543C Digital Detectors
Status: Enrolling
Updated: 4/15/2016
University of Rochester
mi
from
Rochester, NY
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Single Dose Study of PF-05230907 in Healthy Japanese Subjects
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo-controlled, Single Ascending Dose Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of An Intravenous Bolus Infusion Pf-05230907 In Healthy Japanese Subjects
Status: Enrolling
Updated:  4/20/2016
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
Single Dose Study of PF-05230907 in Healthy Japanese Subjects
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo-controlled, Single Ascending Dose Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of An Intravenous Bolus Infusion Pf-05230907 In Healthy Japanese Subjects
Status: Enrolling
Updated: 4/20/2016
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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Lipidomics Screening of Celecoxib in ex Vivo Human Whole Blood Assay - Part B
A Randomized, Double-blinded, Placebo-controlled Study Investigating the Pharmacological Response to Celecoxib Using ex Vivo Human Whole-blood Assay (hWBA) and Broad-spectrum Lipidomics Analysis
Status: Enrolling
Updated:  4/21/2016
Clinical and Translational Research Center (CTRC); Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
Lipidomics Screening of Celecoxib in ex Vivo Human Whole Blood Assay - Part B
A Randomized, Double-blinded, Placebo-controlled Study Investigating the Pharmacological Response to Celecoxib Using ex Vivo Human Whole-blood Assay (hWBA) and Broad-spectrum Lipidomics Analysis
Status: Enrolling
Updated: 4/21/2016
Clinical and Translational Research Center (CTRC); Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
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Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime
Phase I Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime Administered as Single IV Doses in Healthy Human Volunteers
Status: Enrolling
Updated:  5/2/2016
Quintiles, Inc.
mi
from
Overland Park, KA
Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime
Phase I Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime Administered as Single IV Doses in Healthy Human Volunteers
Status: Enrolling
Updated: 5/2/2016
Quintiles, Inc.
mi
from
Overland Park, KA
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Exploratory Pharmacokinetic and Bioavailability Study of 2 Capsule Formulations of Torezolid Phosphate
An Open-Label, Randomized, Single-Dose, 2-Treatment, 2-Sequence, Crossover, Exploratory Pharmacokinetic and Bioavailability Study of 2 Capsule Formulations of TR-701 (Torezolid Phosphate) in Normal Healthy Adults
Status: Enrolling
Updated:  5/2/2016
Covance Clinical Research Unit
mi
from
Austin, TX
Exploratory Pharmacokinetic and Bioavailability Study of 2 Capsule Formulations of Torezolid Phosphate
An Open-Label, Randomized, Single-Dose, 2-Treatment, 2-Sequence, Crossover, Exploratory Pharmacokinetic and Bioavailability Study of 2 Capsule Formulations of TR-701 (Torezolid Phosphate) in Normal Healthy Adults
Status: Enrolling
Updated: 5/2/2016
Covance Clinical Research Unit
mi
from
Austin, TX
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A Phase 1 TR-701 FA Study of Blood Pressure Response Post Tyramine Challenge
A Phase 1, Blinded, Placebo-Controlled, Crossover TR-701 FA Study of Blood Pressure Response Post-Tyramine Challenge
Status: Enrolling
Updated:  5/2/2016
Trius Investigator Site 001
mi
from
Evansville, IN
A Phase 1 TR-701 FA Study of Blood Pressure Response Post Tyramine Challenge
A Phase 1, Blinded, Placebo-Controlled, Crossover TR-701 FA Study of Blood Pressure Response Post-Tyramine Challenge
Status: Enrolling
Updated: 5/2/2016
Trius Investigator Site 001
mi
from
Evansville, IN
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A Drug Interaction Study in Healthy Participants to Assess the Effect of Rifampin on the Pharmacokinetics of JNJ-42847922
An Open-Label Drug Interaction Study to Assess the Pharmacokinetics of JNJ-42847922 When Administered Alone and in Combination With Rifampin in Healthy Male and Female Subjects
Status: Enrolling
Updated:  5/4/2016
Clinical Research Facility
mi
from
Overland Park, KA
A Drug Interaction Study in Healthy Participants to Assess the Effect of Rifampin on the Pharmacokinetics of JNJ-42847922
An Open-Label Drug Interaction Study to Assess the Pharmacokinetics of JNJ-42847922 When Administered Alone and in Combination With Rifampin in Healthy Male and Female Subjects
Status: Enrolling
Updated: 5/4/2016
Clinical Research Facility
mi
from
Overland Park, KA
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A Study to Evaluate of Itraconazole on the Pharmacokinetics of Cobimetinib in Healthy Volunteers
A Phase 1, Open-Label Study to Evaluate the Effect of Itraconazole on the Pharmacokinetics of Cobimetinib in Healthy Subjects
Status: Enrolling
Updated:  5/4/2016
Clinical Research Facility
mi
from
Dallas, TX
A Study to Evaluate of Itraconazole on the Pharmacokinetics of Cobimetinib in Healthy Volunteers
A Phase 1, Open-Label Study to Evaluate the Effect of Itraconazole on the Pharmacokinetics of Cobimetinib in Healthy Subjects
Status: Enrolling
Updated: 5/4/2016
Clinical Research Facility
mi
from
Dallas, TX
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Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Total Skin and Beauty Dermatology Center
mi
from
Birmingham, AL
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Total Skin and Beauty Dermatology Center
mi
from
Birmingham, AL
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Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
The Clinical Testing Center of Beverly Hills
mi
from
Beverly Hills, CA
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
The Clinical Testing Center of Beverly Hills
mi
from
Beverly Hills, CA
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Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Mokusiga, Inc
mi
from
Beverly Hills, CA
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Mokusiga, Inc
mi
from
Beverly Hills, CA
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Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Plastic & Reconstructive Surgery
mi
from
San Francisco, CA
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Plastic & Reconstructive Surgery
mi
from
San Francisco, CA
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Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Dermatology Institute of DuPage Medical Group in Naperville
mi
from
Naperville, IL
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Dermatology Institute of DuPage Medical Group in Naperville
mi
from
Naperville, IL
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Skin Care Physicians
mi
from
Chestnut Hill, MA
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Skin Care Physicians
mi
from
Chestnut Hill, MA
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Minnesota Clinical Study Center
mi
from
Fridley, MN
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Minnesota Clinical Study Center
mi
from
Fridley, MN
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Body Aesthetic Research Center
mi
from
St Louis, MO
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Body Aesthetic Research Center
mi
from
St Louis, MO
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Skin Specialists, PC
mi
from
Omaha, NE
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Skin Specialists, PC
mi
from
Omaha, NE
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Research Across America
mi
from
Plano, TX
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Research Across America
mi
from
Plano, TX
Click here to add this to my saved trials
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated:  5/5/2016
Mei-Heng Tan
mi
from
Sydney,
Long Term Follow-up Study on Safety and Maintenance of Efficacy of ATX-101
Long-term Follow-up Study of Subjects Who Completed Kythera-sponsored Trials of ATX-101 (Sodium Deoxycholate Injection) for the Reduction of Localized Subcutaneous Fat in the Submental Area
Status: Enrolling
Updated: 5/5/2016
Mei-Heng Tan
mi
from
Sydney,
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Propofol's Hypnotic and Memory Effects
CNS Targets of Propofol's Hypnotic and Memory Effects
Status: Enrolling
Updated:  5/5/2016
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
Propofol's Hypnotic and Memory Effects
CNS Targets of Propofol's Hypnotic and Memory Effects
Status: Enrolling
Updated: 5/5/2016
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
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To Evaluate the Safety, Tolerability and to Compare the Pharmacokinetic Profile of ATX-101
Phase 1, Open-Label, Crossover, Safety and Pharmacokinetic Study of ATX-101 (Sodium Deoxycholate Injection) Following Subcutaneous Injections in the Submental and Abdominal Areas
Status: Enrolling
Updated:  5/5/2016
Cetero Research
mi
from
Fargo, ND
To Evaluate the Safety, Tolerability and to Compare the Pharmacokinetic Profile of ATX-101
Phase 1, Open-Label, Crossover, Safety and Pharmacokinetic Study of ATX-101 (Sodium Deoxycholate Injection) Following Subcutaneous Injections in the Submental and Abdominal Areas
Status: Enrolling
Updated: 5/5/2016
Cetero Research
mi
from
Fargo, ND
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Feeding Tolerance Evaluation
Feeding Tolerance Evaluation
Status: Enrolling
Updated:  5/11/2016
Pedia Research LLC
mi
from
Owensboro, KY
Feeding Tolerance Evaluation
Feeding Tolerance Evaluation
Status: Enrolling
Updated: 5/11/2016
Pedia Research LLC
mi
from
Owensboro, KY
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