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

Social Adaptation in Long Term Survivors of Blood and Marrow Transplantation
Social Adaptation in Long Term Survivors of Blood and Marrow Transplantation
Status: Enrolling
Updated:  11/29/2017
Stanford University School of Medicine
mi
from
Stanford, CA
Social Adaptation in Long Term Survivors of Blood and Marrow Transplantation
Social Adaptation in Long Term Survivors of Blood and Marrow Transplantation
Status: Enrolling
Updated: 11/29/2017
Stanford University School of Medicine
mi
from
Stanford, CA
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Insulin Modulation of fMRI Connectivity in Healthy Adults
Insulin Modulation of fMRI Connectivity and Food Reward
Status: Enrolling
Updated:  11/30/2017
Western Psychiatric Institute and Clinic
mi
from
Pittsburgh, PA
Insulin Modulation of fMRI Connectivity in Healthy Adults
Insulin Modulation of fMRI Connectivity and Food Reward
Status: Enrolling
Updated: 11/30/2017
Western Psychiatric Institute and Clinic
mi
from
Pittsburgh, PA
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A Study of Lasmiditan and Propranolol in Healthy Participants
Effect of Lasmiditan on Heart Rate and Blood Pressure in Healthy Subjects Receiving Oral Doses of Propranolol
Status: Enrolling
Updated:  12/4/2017
Covance-Daytona Beach
mi
from
Daytona Beach, FL
A Study of Lasmiditan and Propranolol in Healthy Participants
Effect of Lasmiditan on Heart Rate and Blood Pressure in Healthy Subjects Receiving Oral Doses of Propranolol
Status: Enrolling
Updated: 12/4/2017
Covance-Daytona Beach
mi
from
Daytona Beach, FL
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Denver Garden Environment and Microbiome Study Disease
A Pilot Randomized Controlled Trial of Gardening as an Intervention to Reduce Risk of Cancer and Heart
Status: Enrolling
Updated:  12/4/2017
University of Colorado, Boulder
mi
from
Boulder, CO
Denver Garden Environment and Microbiome Study Disease
A Pilot Randomized Controlled Trial of Gardening as an Intervention to Reduce Risk of Cancer and Heart
Status: Enrolling
Updated: 12/4/2017
University of Colorado, Boulder
mi
from
Boulder, CO
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Assess the Effect of Zolpidem, Silenor & Placebo on Arousability, Ataxia/Balance & Cognition in Healthy Volunteers
Phase IV 4 Way Crossover Study to Assess and Compare the Effect of a Single Nighttime Administration of Zolpidem, Silenor and Placebo on Arousability, Ataxia/Balance and Cognitive Performance in Healthy Volunteers.
Status: Enrolling
Updated:  12/6/2017
Henry Ford Hospital Sleep Disorders & Research Center
mi
from
Novi, MI
Assess the Effect of Zolpidem, Silenor & Placebo on Arousability, Ataxia/Balance & Cognition in Healthy Volunteers
Phase IV 4 Way Crossover Study to Assess and Compare the Effect of a Single Nighttime Administration of Zolpidem, Silenor and Placebo on Arousability, Ataxia/Balance and Cognitive Performance in Healthy Volunteers.
Status: Enrolling
Updated: 12/6/2017
Henry Ford Hospital Sleep Disorders & Research Center
mi
from
Novi, MI
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XmAb5871 Bioavailability Study
Pharmacokinetics and Relative Bioavailability of XmAb®5871 Administered Either Intravenously or Subcutaneously
Status: Enrolling
Updated:  12/6/2017
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
XmAb5871 Bioavailability Study
Pharmacokinetics and Relative Bioavailability of XmAb®5871 Administered Either Intravenously or Subcutaneously
Status: Enrolling
Updated: 12/6/2017
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
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Safety and Tolerability of PF-06818883 in Healthy Subjects
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo-controlled, Single-ascending Dose Study To Evaluate The Safety, Tolerability And Pharmacokinetics Of Pf-06818883 Following Single Intravenous Administration In Healthy Subjects
Status: Enrolling
Updated:  12/7/2017
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
Safety and Tolerability of PF-06818883 in Healthy Subjects
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo-controlled, Single-ascending Dose Study To Evaluate The Safety, Tolerability And Pharmacokinetics Of Pf-06818883 Following Single Intravenous Administration In Healthy Subjects
Status: Enrolling
Updated: 12/7/2017
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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LAAM-HAART PET Imaging
Efavirenz and Ritonavir Influence on Human Brain Levo-acetylmethadol (LAAM) Disposition Assessed Using PET Imaging
Status: Enrolling
Updated:  12/11/2017
Washington University School of Medicine
mi
from
Saint Louis, MO
LAAM-HAART PET Imaging
Efavirenz and Ritonavir Influence on Human Brain Levo-acetylmethadol (LAAM) Disposition Assessed Using PET Imaging
Status: Enrolling
Updated: 12/11/2017
Washington University School of Medicine
mi
from
Saint Louis, MO
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Evaluation of the Safety and Immunogenicity of Autologous Thrombosomes® in Healthy Human Subjects; A Microdose Escalation Study (Cohorts 1 - 4) and Repeat Microdose Immunogenicity Study (Cohort 5)
Evaluation of the Safety and Immunogenicity of Autologous Thrombosomes® in Healthy Human Subjects; A Microdose Escalation Study (Cohorts 1 - 4) and Repeat Microdose Immunogenicity Study (Cohort 5)
Status: Enrolling
Updated:  12/11/2017
Bloodworks Northwest
mi
from
Seattle, WA
Evaluation of the Safety and Immunogenicity of Autologous Thrombosomes® in Healthy Human Subjects; A Microdose Escalation Study (Cohorts 1 - 4) and Repeat Microdose Immunogenicity Study (Cohort 5)
Evaluation of the Safety and Immunogenicity of Autologous Thrombosomes® in Healthy Human Subjects; A Microdose Escalation Study (Cohorts 1 - 4) and Repeat Microdose Immunogenicity Study (Cohort 5)
Status: Enrolling
Updated: 12/11/2017
Bloodworks Northwest
mi
from
Seattle, WA
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Physical Therapists - Recommending EnhanceFitness to Expand Reach
Promoting Healthy Aging by Scaling Up What Works
Status: Enrolling
Updated:  12/11/2017
Health Promotion Research Center
mi
from
Seattle, WA
Physical Therapists - Recommending EnhanceFitness to Expand Reach
Promoting Healthy Aging by Scaling Up What Works
Status: Enrolling
Updated: 12/11/2017
Health Promotion Research Center
mi
from
Seattle, WA
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The Effectiveness of Piano Therapy vs. Piano Listening on Manual Dexterity in the Elderly
Active Versus Passive Piano Intervention for Dexterity in Older Adults: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/13/2017
Shanango on the Green
mi
from
New Wilmington, PA
The Effectiveness of Piano Therapy vs. Piano Listening on Manual Dexterity in the Elderly
Active Versus Passive Piano Intervention for Dexterity in Older Adults: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/13/2017
Shanango on the Green
mi
from
New Wilmington, PA
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Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation Retreat
Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation
Status: Enrolling
Updated:  12/14/2017
Thomas Jefferson University
mi
from
Philadelphia, PA
Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation Retreat
Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation
Status: Enrolling
Updated: 12/14/2017
Thomas Jefferson University
mi
from
Philadelphia, PA
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Effects of Infant Formula Composition on Infant Feeding Behaviors
Effects of Infant Formula Composition on Infant Feeding Behaviors
Status: Enrolling
Updated:  12/14/2017
Monell Chemical Senses Center
mi
from
Philadelphia, PA
Effects of Infant Formula Composition on Infant Feeding Behaviors
Effects of Infant Formula Composition on Infant Feeding Behaviors
Status: Enrolling
Updated: 12/14/2017
Monell Chemical Senses Center
mi
from
Philadelphia, PA
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The Molecular Basis for a Broad Range of Phenotypes Related to hTAS2R38
The Molecular Basis for a Broad Range of Phenotypes Related to hTAS2R38
Status: Enrolling
Updated:  12/14/2017
Monell Chemical Senses Center
mi
from
Philadelphia, PA
The Molecular Basis for a Broad Range of Phenotypes Related to hTAS2R38
The Molecular Basis for a Broad Range of Phenotypes Related to hTAS2R38
Status: Enrolling
Updated: 12/14/2017
Monell Chemical Senses Center
mi
from
Philadelphia, PA
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Radiolabeled Study to Determine the Mass Balance of [14C] MGL-3196
An Open-Label, Single-Radiolabeled Dose, Non-Randomized Study to Determine the Mass Balance of [14C] MGL-3196
Status: Enrolling
Updated:  12/15/2017
Worldwide Clinical Trials Early Phase Services
mi
from
San Antonio, TX
Radiolabeled Study to Determine the Mass Balance of [14C] MGL-3196
An Open-Label, Single-Radiolabeled Dose, Non-Randomized Study to Determine the Mass Balance of [14C] MGL-3196
Status: Enrolling
Updated: 12/15/2017
Worldwide Clinical Trials Early Phase Services
mi
from
San Antonio, TX
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Effect of Pioglitazone and Exenatide on Body Weight and Beta Cell Function
Effect of Pioglitazone With and Without Exenatide on Body Weight, Fat Topography, Beta Cell Function, and Glycemic Control in Type 2 Diabetic Patients
Status: Enrolling
Updated:  12/18/2017
Barter Research Center, ALM VA Hospital
mi
from
San Antonio, TX
Effect of Pioglitazone and Exenatide on Body Weight and Beta Cell Function
Effect of Pioglitazone With and Without Exenatide on Body Weight, Fat Topography, Beta Cell Function, and Glycemic Control in Type 2 Diabetic Patients
Status: Enrolling
Updated: 12/18/2017
Barter Research Center, ALM VA Hospital
mi
from
San Antonio, TX
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Study to Investigate the Food Effect and Oral Bioavailability of Tablet Formulations Relative to Suspension Formulation of JNJ-54416076 in Healthy Participants
An Exploratory Open-Label, Single Dose, Randomized, Three-Way Crossover Study In Healthy Subjects to Investigate the Food Effect and Oral Bioavailability of Tablet Formulations Relative to Suspension Formulation of JNJ-54416076
Status: Enrolling
Updated:  12/18/2017
Clinical Research Facility
mi
from
Tempe, AZ
Study to Investigate the Food Effect and Oral Bioavailability of Tablet Formulations Relative to Suspension Formulation of JNJ-54416076 in Healthy Participants
An Exploratory Open-Label, Single Dose, Randomized, Three-Way Crossover Study In Healthy Subjects to Investigate the Food Effect and Oral Bioavailability of Tablet Formulations Relative to Suspension Formulation of JNJ-54416076
Status: Enrolling
Updated: 12/18/2017
Clinical Research Facility
mi
from
Tempe, AZ
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Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial
A Randomized, Open-label, Parallel-group, Single Subcutaneous Dose, Relative Bioavailability Study of the Pharmacokinetics of Lulizumab (BMS-931699) From Prefilled Syringe (Process A) Compared to Drug in Vial (Process A) in Healthy Participants
Status: Enrolling
Updated:  12/18/2017
Qps-Mra, Llc
mi
from
South Miami, FL
Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial
A Randomized, Open-label, Parallel-group, Single Subcutaneous Dose, Relative Bioavailability Study of the Pharmacokinetics of Lulizumab (BMS-931699) From Prefilled Syringe (Process A) Compared to Drug in Vial (Process A) in Healthy Participants
Status: Enrolling
Updated: 12/18/2017
Qps-Mra, Llc
mi
from
South Miami, FL
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Healthy Combine Study
Short-Term Effects of Nicotinamide and Lanthanum Carbonate on Phosphorus Homeostasis in Healthy Volunteers
Status: Enrolling
Updated:  12/20/2017
Center for Translational Metabolism and Health (CTMH), Northwestern University
mi
from
Chicago, IL
Healthy Combine Study
Short-Term Effects of Nicotinamide and Lanthanum Carbonate on Phosphorus Homeostasis in Healthy Volunteers
Status: Enrolling
Updated: 12/20/2017
Center for Translational Metabolism and Health (CTMH), Northwestern University
mi
from
Chicago, IL
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Evansville, IN
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Evansville, IN
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Dallas, TX
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Dallas, TX
Click here to add this to my saved trials
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Oviedo, FL
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Oviedo, FL
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Farmington Hills, MI
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Farmington Hills, MI
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Spokane, WA
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Spokane, WA
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Hallandale Beach, FL
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Hallandale Beach, FL
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Durham, NC
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Durham, NC
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Cleveland, OH
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Cleveland, OH
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Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Washington,
Single-Ascending Dose Study of BIIB054 in Healthy Participants and Early Parkinson's Disease
A Phase 1 Randomized, Double-Blinded, Placebo-Controlled Single-Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of BIIB054 in Healthy Subjects and Subjects With Early Parkinson's Disease
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Washington,
Click here to add this to my saved trials
Study to Assess the Relative Bioavailability of Fixed-Dose Combination (FDC) Tablet (Simeprevir, Odalasvir and AL-335) Compared With Single Agents Administered Together, and to Assess the Effect of Multiple-Dose Lansoprazole or Omeprazole on Single-Dose Pharmacokinetics of SMV, ODV, and AL-335 (FDC)
Phase 1, Open-label, Partially Randomized, Parallel-group Study in Healthy Adult Subjects to Assess the Relative Bioavailability of Single-dose Simeprevir (SMV), Odalasvir (ODV), and AL-335 Administered as a Fixed-dose Combination (FDC) Compared With the Single Agents Administered Together, and to Assess the Effect of Multiple-dose Lansoprazole or Omeprazole on the Single-dose Pharmacokinetics of SMV, ODV, and AL-335 Administered as an FDC
Status: Enrolling
Updated:  12/21/2017
Celerion
mi
from
Tempe, AZ
Study to Assess the Relative Bioavailability of Fixed-Dose Combination (FDC) Tablet (Simeprevir, Odalasvir and AL-335) Compared With Single Agents Administered Together, and to Assess the Effect of Multiple-Dose Lansoprazole or Omeprazole on Single-Dose Pharmacokinetics of SMV, ODV, and AL-335 (FDC)
Phase 1, Open-label, Partially Randomized, Parallel-group Study in Healthy Adult Subjects to Assess the Relative Bioavailability of Single-dose Simeprevir (SMV), Odalasvir (ODV), and AL-335 Administered as a Fixed-dose Combination (FDC) Compared With the Single Agents Administered Together, and to Assess the Effect of Multiple-dose Lansoprazole or Omeprazole on the Single-dose Pharmacokinetics of SMV, ODV, and AL-335 Administered as an FDC
Status: Enrolling
Updated: 12/21/2017
Celerion
mi
from
Tempe, AZ
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A Study of Two Different Formulations of LY3074828 in Healthy Participants
Relative Bioavailability of LY3074828 Solution Formulation in Pre-Filled Syringes Compared to Lyophilized Formulation After Single Subcutaneous Administration
Status: Enrolling
Updated:  12/21/2017
Covance, Inc.
mi
from
Dallas, TX
A Study of Two Different Formulations of LY3074828 in Healthy Participants
Relative Bioavailability of LY3074828 Solution Formulation in Pre-Filled Syringes Compared to Lyophilized Formulation After Single Subcutaneous Administration
Status: Enrolling
Updated: 12/21/2017
Covance, Inc.
mi
from
Dallas, TX
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Trial to Evaluate the PK Profile of Glepaglutide (ZP1848) After a Single IV and After Multiple SC Injections in Healthy Subjects
A Phase 1, Open-Label, Partially Randomized, 3-Part, Parallel Group Trial to Evaluate the Pharmacokinetic Profile of Glepaglutide (ZP1848) After a Single Intravenous Injection and After Multiple Subcutaneous Injections in Healthy Subjects
Status: Enrolling
Updated:  12/21/2017
Covance CRU
mi
from
Dallas, TX
Trial to Evaluate the PK Profile of Glepaglutide (ZP1848) After a Single IV and After Multiple SC Injections in Healthy Subjects
A Phase 1, Open-Label, Partially Randomized, 3-Part, Parallel Group Trial to Evaluate the Pharmacokinetic Profile of Glepaglutide (ZP1848) After a Single Intravenous Injection and After Multiple Subcutaneous Injections in Healthy Subjects
Status: Enrolling
Updated: 12/21/2017
Covance CRU
mi
from
Dallas, TX
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AG200-15 Transdermal Contraceptive Delivery System (TCDS) of Levonorgestrel and Ethinyl Estradiol
An Open-Label Study to Evaluate Pharmacokinetic Profile of Agile TCDS AG200-15 and to Compare Exposure to Ethinyl Estradiol to Oral Contraceptive (Orthocyclen®) in Healthy Female Volunteers
Status: Enrolling
Updated:  12/21/2017
Clinical Research Facility
mi
from
Miami, FL
AG200-15 Transdermal Contraceptive Delivery System (TCDS) of Levonorgestrel and Ethinyl Estradiol
An Open-Label Study to Evaluate Pharmacokinetic Profile of Agile TCDS AG200-15 and to Compare Exposure to Ethinyl Estradiol to Oral Contraceptive (Orthocyclen®) in Healthy Female Volunteers
Status: Enrolling
Updated: 12/21/2017
Clinical Research Facility
mi
from
Miami, FL
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The Impact of Reward-induced Dopamine Release on Functional Connectivity: a Combined PET/fMRI Study
The Impact of Reward-induced Dopamine Release on Functional Connectivity: a Combined PET/fMRI Study
Status: Enrolling
Updated:  12/28/2017
Health Sciences Center
mi
from
Stony Brook, NY
The Impact of Reward-induced Dopamine Release on Functional Connectivity: a Combined PET/fMRI Study
The Impact of Reward-induced Dopamine Release on Functional Connectivity: a Combined PET/fMRI Study
Status: Enrolling
Updated: 12/28/2017
Health Sciences Center
mi
from
Stony Brook, NY
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The Safety and Efficacy of Recombinant Human Prolactin
Phase 2 Study of Recombinant Human Prolactin Efficacy and Safety
Status: Enrolling
Updated:  12/31/2017
Corrine Welt
mi
from
Boston, MA
The Safety and Efficacy of Recombinant Human Prolactin
Phase 2 Study of Recombinant Human Prolactin Efficacy and Safety
Status: Enrolling
Updated: 12/31/2017
Corrine Welt
mi
from
Boston, MA
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Study the Impact of the CommunityRx Program on Health, Self-care and Cost
Evaluating CommunityRx, a Self-Care Innovation for Older Adults, Using Agent-Based Modeling: Collecting and Analyzing Data to Build the Agent Based Model
Status: Enrolling
Updated:  1/2/2018
University of Chicago Medicine - Adult Emergency Department and Primary Care Group clinic
mi
from
Chicago, IL
Study the Impact of the CommunityRx Program on Health, Self-care and Cost
Evaluating CommunityRx, a Self-Care Innovation for Older Adults, Using Agent-Based Modeling: Collecting and Analyzing Data to Build the Agent Based Model
Status: Enrolling
Updated: 1/2/2018
University of Chicago Medicine - Adult Emergency Department and Primary Care Group clinic
mi
from
Chicago, IL
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Osteoclast Inhibition and Bone Formation
Effects of Age and Osteoclast Inhibition on Bone Formation
Status: Enrolling
Updated:  1/3/2018
Mayo Clinic Rochester
mi
from
Rochester, MN
Osteoclast Inhibition and Bone Formation
Effects of Age and Osteoclast Inhibition on Bone Formation
Status: Enrolling
Updated: 1/3/2018
Mayo Clinic Rochester
mi
from
Rochester, MN
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Cognitive and Functional Connectivity Effects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer's Disease
Cognitive and Functional Connectivity Effects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer's Disease
Status: Enrolling
Updated:  1/3/2018
Research Imaging Institute, The University of Texas Health Science Center at San Antonio
mi
from
San Antonio, TX
Cognitive and Functional Connectivity Effects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer's Disease
Cognitive and Functional Connectivity Effects of Methylene Blue in Healthy Aging, Mild Cognitive Impairment and Alzheimer's Disease
Status: Enrolling
Updated: 1/3/2018
Research Imaging Institute, The University of Texas Health Science Center at San Antonio
mi
from
San Antonio, TX
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"Fermented Dairy Beverage on Inflammation/Immune Function in Stressful Exercise"
"Effects of Two Doses of Fermented Dairy Beverage on Inflammation/Immune Function in Healthy Adults Undergoing Stressful Exercise; Compared to a Placebo Beverage"
Status: Enrolling
Updated:  1/3/2018
QPS Bio-Kinetic Clinical Applications
mi
from
Springfield, MO
"Fermented Dairy Beverage on Inflammation/Immune Function in Stressful Exercise"
"Effects of Two Doses of Fermented Dairy Beverage on Inflammation/Immune Function in Healthy Adults Undergoing Stressful Exercise; Compared to a Placebo Beverage"
Status: Enrolling
Updated: 1/3/2018
QPS Bio-Kinetic Clinical Applications
mi
from
Springfield, MO
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Pharmacokinetic (PK) and Safety Study of Plasma-derived Human Butyrylcholinesterase Administered Intravenously
A Phase 1, Randomized, Observer-blinded, Single Dose, Placebo Controlled Dosage-Escalation Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Plasma-Derived Human Butyrylcholinesterase (HuBChE) Administered Intravenously (IV)
Status: Enrolling
Updated:  1/4/2018
Quintiles Phase 1 Services
mi
from
Lenexa, KA
Pharmacokinetic (PK) and Safety Study of Plasma-derived Human Butyrylcholinesterase Administered Intravenously
A Phase 1, Randomized, Observer-blinded, Single Dose, Placebo Controlled Dosage-Escalation Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Plasma-Derived Human Butyrylcholinesterase (HuBChE) Administered Intravenously (IV)
Status: Enrolling
Updated: 1/4/2018
Quintiles Phase 1 Services
mi
from
Lenexa, KA
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Behavioral Differences in Effortful Control
Behavioral Differences in Effortful Control
Status: Enrolling
Updated:  1/5/2018
Rachel Upjohn Building, East Medical Campus
mi
from
Ann Arbor, MI
Behavioral Differences in Effortful Control
Behavioral Differences in Effortful Control
Status: Enrolling
Updated: 1/5/2018
Rachel Upjohn Building, East Medical Campus
mi
from
Ann Arbor, MI
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The Dose-Response Effects of Lean Beef in a Mediterranean-Style Dietary Pattern on Cardiovascular Disease Risk Factors
Status: Enrolling
Updated:  1/5/2018
USDA-ARS, Beltsville Human Nutrition Research Center
mi
from
Beltsville, MD
The Dose-Response Effects of Lean Beef in a Mediterranean-Style Dietary Pattern on Cardiovascular Disease Risk Factors
Status: Enrolling
Updated: 1/5/2018
USDA-ARS, Beltsville Human Nutrition Research Center
mi
from
Beltsville, MD
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The Dose-Response Effects of Lean Beef in a Mediterranean-Style Dietary Pattern on Cardiovascular Disease Risk Factors
Status: Enrolling
Updated:  1/5/2018
Penn State University
mi
from
University Park, PA
The Dose-Response Effects of Lean Beef in a Mediterranean-Style Dietary Pattern on Cardiovascular Disease Risk Factors
Status: Enrolling
Updated: 1/5/2018
Penn State University
mi
from
University Park, PA
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Quantitative Heat Loss With Laminar Air Flow
Status: Enrolling
Updated:  1/5/2018
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Quantitative Heat Loss With Laminar Air Flow
Status: Enrolling
Updated: 1/5/2018
Cleveland Clinic Foundation
mi
from
Cleveland, OH
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Breastfeeding Self-Management for Nipple and Breast Pain
Promoting Self-Management of Breast and Nipple Pain in Breastfeeding Women
Status: Enrolling
Updated:  1/5/2018
UConn Health
mi
from
Farmington, CT
Breastfeeding Self-Management for Nipple and Breast Pain
Promoting Self-Management of Breast and Nipple Pain in Breastfeeding Women
Status: Enrolling
Updated: 1/5/2018
UConn Health
mi
from
Farmington, CT
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Breastfeeding Self-Management for Nipple and Breast Pain
Promoting Self-Management of Breast and Nipple Pain in Breastfeeding Women
Status: Enrolling
Updated:  1/5/2018
Manchester Memorial Hospital
mi
from
Manchester, CT
Breastfeeding Self-Management for Nipple and Breast Pain
Promoting Self-Management of Breast and Nipple Pain in Breastfeeding Women
Status: Enrolling
Updated: 1/5/2018
Manchester Memorial Hospital
mi
from
Manchester, CT
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Biomarkers in Post-Menopausal Women Receiving Flaxseed
A Pilot Study of the Flaxseed Effects on Hormones and Lignans: Role of Race, Genes, and Gut Microbiome
Status: Enrolling
Updated:  1/8/2018
Roswell Park Cancer Institute
mi
from
Buffalo, NY
Biomarkers in Post-Menopausal Women Receiving Flaxseed
A Pilot Study of the Flaxseed Effects on Hormones and Lignans: Role of Race, Genes, and Gut Microbiome
Status: Enrolling
Updated: 1/8/2018
Roswell Park Cancer Institute
mi
from
Buffalo, NY
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Japanese Bridging Study of Ivosidenib (AG-120) in Healthy Subjects
A Phase 1, Single-Dose, Open-Label Trial to Evaluate the Pharmacokinetics and Safety of AG-120 in Healthy Male Japanese Subjects Relative to Healthy Male Caucasian Subjects
Status: Enrolling
Updated:  1/9/2018
West Coast Clinical Trial (WCCT)
mi
from
Cypress, CA
Japanese Bridging Study of Ivosidenib (AG-120) in Healthy Subjects
A Phase 1, Single-Dose, Open-Label Trial to Evaluate the Pharmacokinetics and Safety of AG-120 in Healthy Male Japanese Subjects Relative to Healthy Male Caucasian Subjects
Status: Enrolling
Updated: 1/9/2018
West Coast Clinical Trial (WCCT)
mi
from
Cypress, CA
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Study to Evaluate the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations in Healthy Adults
A Phase 1, Randomized, Open-Label, Two-Period Crossover Study Evaluating the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations After Single-Dose Administration in Healthy Adults
Status: Enrolling
Updated:  1/10/2018
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
Study to Evaluate the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations in Healthy Adults
A Phase 1, Randomized, Open-Label, Two-Period Crossover Study Evaluating the Relative Bioavailability and Safety of the AG-348 Tablet and Capsule Formulations After Single-Dose Administration in Healthy Adults
Status: Enrolling
Updated: 1/10/2018
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
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Brain-Computer Interface and Mind-Body Awareness Training
Brain-Computer Interface and Mind-Body Awareness Training
Status: Enrolling
Updated:  1/11/2018
Nils Hasselmo Hall at the University of Minnesota - Twin Cities Campus
mi
from
Minneapolis, MN
Brain-Computer Interface and Mind-Body Awareness Training
Brain-Computer Interface and Mind-Body Awareness Training
Status: Enrolling
Updated: 1/11/2018
Nils Hasselmo Hall at the University of Minnesota - Twin Cities Campus
mi
from
Minneapolis, MN
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Absorption, Metabolism and Excretion of [14C]-Lasmiditan - Single Oral Dose Administration
A Phase 1 Study to Investigate the Absorption, Metabolism, and Excretion of [14C]-Lasmiditan Following Single Oral Dose Administration in Healthy Male and Female Subjects
Status: Enrolling
Updated:  1/11/2018
Covance Clinical Research Unit
mi
from
Madison, WI
Absorption, Metabolism and Excretion of [14C]-Lasmiditan - Single Oral Dose Administration
A Phase 1 Study to Investigate the Absorption, Metabolism, and Excretion of [14C]-Lasmiditan Following Single Oral Dose Administration in Healthy Male and Female Subjects
Status: Enrolling
Updated: 1/11/2018
Covance Clinical Research Unit
mi
from
Madison, WI
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