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

What's Hopping? Cricket Protein and Human Gut Microbiota
What's Hopping? Edible Cricket (Gryllodes Sigillatus) Consumption and Gut Microbiota in Healthy Adults, a Double-blind, Randomized Crossover Trial
Status: Enrolling
Updated:  12/31/1969
mi
from
Fort Collins, CO
What's Hopping? Cricket Protein and Human Gut Microbiota
What's Hopping? Edible Cricket (Gryllodes Sigillatus) Consumption and Gut Microbiota in Healthy Adults, a Double-blind, Randomized Crossover Trial
Status: Enrolling
Updated: 12/31/1969
Colorado State University
mi
from
Fort Collins, CO
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In Vivo Assessment of Glutamine Utilization by Bone Marrow Plasma Cells
In Vivo Assessment of Glutamine Utilization by Bone Marrow Plasma Cells in Healthy Subjects Using Stable Isotope Resolved Metabolomics: A Pilot Study
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, MN
In Vivo Assessment of Glutamine Utilization by Bone Marrow Plasma Cells
In Vivo Assessment of Glutamine Utilization by Bone Marrow Plasma Cells in Healthy Subjects Using Stable Isotope Resolved Metabolomics: A Pilot Study
Status: Enrolling
Updated: 12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
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Effects of Aprepitant on Satiation, Gastric Volume, Gastric Accommodation and Gastric Emptying
A Single-Center, Placebo-Controlled, Double-Blind Study to Evaluate the Effects of Aprepitant on Satiation, Gastric Volume, Gastric Accommodation and Gastric Emptying in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, MN
Effects of Aprepitant on Satiation, Gastric Volume, Gastric Accommodation and Gastric Emptying
A Single-Center, Placebo-Controlled, Double-Blind Study to Evaluate the Effects of Aprepitant on Satiation, Gastric Volume, Gastric Accommodation and Gastric Emptying in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
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Impact of a Smartphone Application on Postpartum Weight Loss and Breastfeeding Rates Among Low-income, Urban Women
Impact of a Novel Smartphone Application on Postpartum Weight Loss and Breastfeeding Rates Among Low-income, Urban Women
Status: Enrolling
Updated:  12/31/1969
mi
from
Saint Louis, MO
Impact of a Smartphone Application on Postpartum Weight Loss and Breastfeeding Rates Among Low-income, Urban Women
Impact of a Novel Smartphone Application on Postpartum Weight Loss and Breastfeeding Rates Among Low-income, Urban Women
Status: Enrolling
Updated: 12/31/1969
Center for Outpatient Health
mi
from
Saint Louis, MO
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Safety and Effectiveness of BPL HRIG With Active Rabies Vaccine in Healthy Subjects
A Prospective, Randomized, Double-Blind Parallel-group, Non-inferiority Phase II/III Study of the Safety and Effectiveness of BPL HRIG With Co Administration of Active Rabies Vaccine in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Saint Paul, MN
Safety and Effectiveness of BPL HRIG With Active Rabies Vaccine in Healthy Subjects
A Prospective, Randomized, Double-Blind Parallel-group, Non-inferiority Phase II/III Study of the Safety and Effectiveness of BPL HRIG With Co Administration of Active Rabies Vaccine in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Prism Research Inc.
mi
from
Saint Paul, MN
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Safety and Effectiveness of BPL HRIG With Active Rabies Vaccine in Healthy Subjects
A Prospective, Randomized, Double-Blind Parallel-group, Non-inferiority Phase II/III Study of the Safety and Effectiveness of BPL HRIG With Co Administration of Active Rabies Vaccine in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Raleigh, NC
Safety and Effectiveness of BPL HRIG With Active Rabies Vaccine in Healthy Subjects
A Prospective, Randomized, Double-Blind Parallel-group, Non-inferiority Phase II/III Study of the Safety and Effectiveness of BPL HRIG With Co Administration of Active Rabies Vaccine in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Wake Research Associates, LLC
mi
from
Raleigh, NC
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Breakfast and Metabolism in Men
The Effect of Breakfast on Energy Metabolism, Appetite, and Food Intake in Men
Status: Enrolling
Updated:  12/31/1969
mi
from
Fayetteville, AR
Breakfast and Metabolism in Men
The Effect of Breakfast on Energy Metabolism, Appetite, and Food Intake in Men
Status: Enrolling
Updated: 12/31/1969
University of Arkansas
mi
from
Fayetteville, AR
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Mapping the Human HIV Chronobiome
Mapping the Human HIV Chronobiome
Status: Enrolling
Updated:  12/31/1969
mi
from
Philadelphia, PA
Mapping the Human HIV Chronobiome
Mapping the Human HIV Chronobiome
Status: Enrolling
Updated: 12/31/1969
Institute for Translational Medicine and Therapeutics (ITMAT), University of Pennsylvania School of Medicine
mi
from
Philadelphia, PA
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Blue Island, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Center Blue Island
mi
from
Blue Island, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago Heights, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Aunt Martha's Pediatric Health & Wellness Center
mi
from
Chicago Heights, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Chicago Department of Public Health WIC Centers (Greater Lawn Health Center, Friend Family Health Center, Westside Health Partnership)
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Mile Square Health Center (Main, Englewood, Cicero, South Shore, Back of the Yards)
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
University of Illinois at Chicago Outpatient Care Center
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Aunt Martha's Southeast Side Community Health Center
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Vida Pediatrics
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Centers (Diversey, Irving Park)
mi
from
Chicago, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Harvey, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Center Harvey
mi
from
Harvey, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Maywood, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Center Maywood
mi
from
Maywood, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Oak Park, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Oak Park
mi
from
Oak Park, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
South Holland, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
Aunt Martha's South Holland Community Health Center
mi
from
South Holland, IL
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Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated:  12/31/1969
mi
from
Summit, IL
Coordinated Oral Health Promotion (CO-OP) Chicago
Coordinated Oral Health Promotion (CO-OP) Chicago
Status: Enrolling
Updated: 12/31/1969
CEDA WIC Summit
mi
from
Summit, IL
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A Phase 1 AVB-S6-500 Safety and Tolerability Study
A Single-blind, Randomized, Placebo-controlled, Phase 1, Single Ascending-dose and Repeat-dose, Safety and Tolerability Study of Intravenous AVB-S6-500 in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Orlando, FL
A Phase 1 AVB-S6-500 Safety and Tolerability Study
A Single-blind, Randomized, Placebo-controlled, Phase 1, Single Ascending-dose and Repeat-dose, Safety and Tolerability Study of Intravenous AVB-S6-500 in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Orlando Clinical Research Center
mi
from
Orlando, FL
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Modulation of Episodic Memory Using Theta Burst Stimulation (TBS)
Modulation of Episodic Memory Using Theta Burst Stimulation (TBS)
Status: Enrolling
Updated:  12/31/1969
mi
from
Durham, NC
Modulation of Episodic Memory Using Theta Burst Stimulation (TBS)
Modulation of Episodic Memory Using Theta Burst Stimulation (TBS)
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
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A Study of Lasmiditan in Healthy Elderly Participants
A Study to Investigate the Cardiovascular Effects of Lasmiditan in Healthy Elderly Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Daytona Beach, FL
A Study of Lasmiditan in Healthy Elderly Participants
A Study to Investigate the Cardiovascular Effects of Lasmiditan in Healthy Elderly Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Daytona Beach, FL
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A Study of Lasmiditan in Healthy Elderly Participants
A Study to Investigate the Cardiovascular Effects of Lasmiditan in Healthy Elderly Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Madison, WI
A Study of Lasmiditan in Healthy Elderly Participants
A Study to Investigate the Cardiovascular Effects of Lasmiditan in Healthy Elderly Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Madison, WI
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Bioavailability Study of K0706 in Healthy Subjects
A Randomized, Open Label, Four Period, Four Sequence, Single Dose, Crossover Study to Evaluate Relative Bioavailability of K0706 24 mg Tablet Formulation Relative to 24 mg Capsule Formulation Under Fasted Conditions and to Evaluate the Food Effect for Tablet Formulation in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Las Vegas, NV
Bioavailability Study of K0706 in Healthy Subjects
A Randomized, Open Label, Four Period, Four Sequence, Single Dose, Crossover Study to Evaluate Relative Bioavailability of K0706 24 mg Tablet Formulation Relative to 24 mg Capsule Formulation Under Fasted Conditions and to Evaluate the Food Effect for Tablet Formulation in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
SPARC Site 1
mi
from
Las Vegas, NV
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Study of Lanadelumab in Healthy Japanese and Matched Caucasian Adult Subjects
A Phase 1, Open-label Study to Evaluate the Pharmacokinetics, Safety and Tolerability, and Pharmacodynamics of a Single Dose of Lanadelumab Administered Subcutaneously in Healthy Adult Japanese Subjects and Matched Healthy Adult Caucasian Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Cypress, CA
Study of Lanadelumab in Healthy Japanese and Matched Caucasian Adult Subjects
A Phase 1, Open-label Study to Evaluate the Pharmacokinetics, Safety and Tolerability, and Pharmacodynamics of a Single Dose of Lanadelumab Administered Subcutaneously in Healthy Adult Japanese Subjects and Matched Healthy Adult Caucasian Subjects
Status: Enrolling
Updated: 12/31/1969
Wcct Global, Llc
mi
from
Cypress, CA
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Extremity Manipulation Impact on Postural Sway Characteristics
Assessment of Balance Changes After Extremity Manipulation Therapy
Status: Enrolling
Updated:  12/31/1969
mi
from
Dallas, TX
Extremity Manipulation Impact on Postural Sway Characteristics
Assessment of Balance Changes After Extremity Manipulation Therapy
Status: Enrolling
Updated: 12/31/1969
Parker University
mi
from
Dallas, TX
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Study of AC0058TA in Healthy Male and Female Subjects
A Phase 1, Randomized Double-Blind, Placebo-Controlled, Single- and Multiple-Dose, Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of AC0058TA in Healthy Male and Female Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Dallas, TX
Study of AC0058TA in Healthy Male and Female Subjects
A Phase 1, Randomized Double-Blind, Placebo-Controlled, Single- and Multiple-Dose, Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of AC0058TA in Healthy Male and Female Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Development Services
mi
from
Dallas, TX
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Glycemic Index of Table Grape Varietals
Investigation of the Glycemic Index of Table Grape Varietals
Status: Enrolling
Updated:  12/31/1969
mi
from
Davis, CA
Glycemic Index of Table Grape Varietals
Investigation of the Glycemic Index of Table Grape Varietals
Status: Enrolling
Updated: 12/31/1969
University of California Davis (Academic Surge, Ragle Human Nutrition Research Facility)
mi
from
Davis, CA
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A Study Comparing The Effects Of Epoetin Hospira Single-Dose Vial (SDV) And Multi-Dose Vial (MDV) When Administered Subcutaneously To Normal Healthy Subjects
A Phase 1, Open-label, Randomized, Single Dose, Crossover Study Evaluating The Pharmacokinetics Of Epoetin Following Administration Of Epoetin Hospira Multiple Dose Vial (Mdv) Product Compared To Epoetin Hospira Single Dose Vial (Sdv) Product As Subcutaneous Injection To Normal Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
New Haven, CT
A Study Comparing The Effects Of Epoetin Hospira Single-Dose Vial (SDV) And Multi-Dose Vial (MDV) When Administered Subcutaneously To Normal Healthy Subjects
A Phase 1, Open-label, Randomized, Single Dose, Crossover Study Evaluating The Pharmacokinetics Of Epoetin Following Administration Of Epoetin Hospira Multiple Dose Vial (Mdv) Product Compared To Epoetin Hospira Single Dose Vial (Sdv) Product As Subcutaneous Injection To Normal Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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Effect of Whey Protein Hydrolysate on Human Muscle Protein Synthesis
Effect of Whey Protein Hydrolysate on Human Muscle Protein Synthesis
Status: Enrolling
Updated:  12/31/1969
mi
from
Galveston, TX
Effect of Whey Protein Hydrolysate on Human Muscle Protein Synthesis
Effect of Whey Protein Hydrolysate on Human Muscle Protein Synthesis
Status: Enrolling
Updated: 12/31/1969
Utmb
mi
from
Galveston, TX
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Diagnosing Natriuretic Peptide Deficiency
Diagnosing Natriuretic Peptide Deficiency: A Pilot Study
Status: Enrolling
Updated:  12/31/1969
mi
from
Nashville, TN
Diagnosing Natriuretic Peptide Deficiency
Diagnosing Natriuretic Peptide Deficiency: A Pilot Study
Status: Enrolling
Updated: 12/31/1969
Vanderbilt University Medical Center
mi
from
Nashville, TN
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Personalized Dietary Program and Markers of Wellness
A Clinical Trial to Evaluate the Effects of Proprietary Personalized Dietary Programs on Markers of Health and Wellness, Body Composition, and Quality of Life
Status: Enrolling
Updated:  12/31/1969
mi
from
Camden, NJ
Personalized Dietary Program and Markers of Wellness
A Clinical Trial to Evaluate the Effects of Proprietary Personalized Dietary Programs on Markers of Health and Wellness, Body Composition, and Quality of Life
Status: Enrolling
Updated: 12/31/1969
Campbell Soup Company
mi
from
Camden, NJ
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Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated:  12/31/1969
mi
from
Los Angeles, CA
Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated: 12/31/1969
University of Southern California
mi
from
Los Angeles, CA
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Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, NY
Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated: 12/31/1969
University of Rochester Medical Center Wilmot Cancer Institute
mi
from
Rochester, NY
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Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated: 12/31/1969
UT MD Anderson Cancer Center
mi
from
Houston, TX
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Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Harvest of CTCs From MBC Patients Using the Parsortix™ PC1 System
Harvest of Circulating Tumor Cells (CTCs) From Patients With Metastatic Breast Cancer (MBC) Using the Parsortix™ PC1 System
Status: Enrolling
Updated: 12/31/1969
Northwestern University
mi
from
Chicago, IL
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A Two-Part Phase 1 Study to Investigate the Safety and Tolerability of Supratherapeutic Dose of Zanubrutinib and Effect of Zanubrutinib on Cardiac Repolarization in Healthy Subjects
A Two-Part Study Consisting of a Randomized, Placebo-Controlled, Single Dose Safety and Tolerability Study (Part A) Evaluating a Supratherapeutic Dose of Zanubrutinib Followed by a Randomized, Placebo- and Positive-Controlled, Crossover Study (Part B) to Evaluate the Effect of Zanubrutinib on Cardiac Repolarization in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
mi
from
Secaucus, NJ
A Two-Part Phase 1 Study to Investigate the Safety and Tolerability of Supratherapeutic Dose of Zanubrutinib and Effect of Zanubrutinib on Cardiac Repolarization in Healthy Subjects
A Two-Part Study Consisting of a Randomized, Placebo-Controlled, Single Dose Safety and Tolerability Study (Part A) Evaluating a Supratherapeutic Dose of Zanubrutinib Followed by a Randomized, Placebo- and Positive-Controlled, Crossover Study (Part B) to Evaluate the Effect of Zanubrutinib on Cardiac Repolarization in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Frontage Clinical Services Inc.
mi
from
Secaucus, NJ
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A Study to Evaluate the Relative Oral Bioavailability of Seltorexant (JNJ-42847922) After Administration of 3 Different Formulations in Healthy Participants Under Fasted and Semi-fasted Conditions
A Randomized, Open-label, Single-dose, 6-Period, 8-Sequence Crossover Study to Evaluate the Relative Oral Bioavailability of Seltorexant (JNJ-42847922) After Administration of 3 Different Formulations in Healthy Subjects Under Fasted and Semi-fasted Conditions
Status: Enrolling
Updated:  12/31/1969
mi
from
Salt Lake City, UT
A Study to Evaluate the Relative Oral Bioavailability of Seltorexant (JNJ-42847922) After Administration of 3 Different Formulations in Healthy Participants Under Fasted and Semi-fasted Conditions
A Randomized, Open-label, Single-dose, 6-Period, 8-Sequence Crossover Study to Evaluate the Relative Oral Bioavailability of Seltorexant (JNJ-42847922) After Administration of 3 Different Formulations in Healthy Subjects Under Fasted and Semi-fasted Conditions
Status: Enrolling
Updated: 12/31/1969
PRAHS
mi
from
Salt Lake City, UT
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Relacorilant Food Effect Study in Healthy Subjects
A Phase 1, Open-label, Single-dose, Randomized, Crossover Study in Healthy Subjects of the Effects of Co-administration With Food on Exposure, and to Determine the Within-subject Variability in Exposure, to Relacorilant and Its Metabolites
Status: Enrolling
Updated:  12/31/1969
mi
from
Tempe, AZ
Relacorilant Food Effect Study in Healthy Subjects
A Phase 1, Open-label, Single-dose, Randomized, Crossover Study in Healthy Subjects of the Effects of Co-administration With Food on Exposure, and to Determine the Within-subject Variability in Exposure, to Relacorilant and Its Metabolites
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Tempe, AZ
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Multiple Ascending Dose to Study the Safety, Tolerability, PK and PD Effects of AEF0117
A Phase 1, Single Center, Double-blind, Placebo-Controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Effects of Multiple Oral Doses of AEF0117 in Healthy Male and Female Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Newark, NJ
Multiple Ascending Dose to Study the Safety, Tolerability, PK and PD Effects of AEF0117
A Phase 1, Single Center, Double-blind, Placebo-Controlled, Dose Escalating Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Effects of Multiple Oral Doses of AEF0117 in Healthy Male and Female Subjects
Status: Enrolling
Updated: 12/31/1969
Biotrial Inc.
mi
from
Newark, NJ
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Fiber Effects on Glycemic Index
Verifying Fibers Meet Regulatory Definitions for Nutrition Facts Labeling: A Randomized, Controlled Trial Evaluating Polydextrose in Dry Form
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Fiber Effects on Glycemic Index
Verifying Fibers Meet Regulatory Definitions for Nutrition Facts Labeling: A Randomized, Controlled Trial Evaluating Polydextrose in Dry Form
Status: Enrolling
Updated: 12/31/1969
Clinical Nutrition Research Center
mi
from
Chicago, IL
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Scopolamine Patch Pharmacokinetics in Healthy Adults
Absolute Bioavailability/Pharmacokinetic and Residual Drug Analysis of the Transderm Scōp System in Healthy Adults
Status: Enrolling
Updated:  12/31/1969
mi
from
Iowa City, IA
Scopolamine Patch Pharmacokinetics in Healthy Adults
Absolute Bioavailability/Pharmacokinetic and Residual Drug Analysis of the Transderm Scōp System in Healthy Adults
Status: Enrolling
Updated: 12/31/1969
University of Iowa
mi
from
Iowa City, IA
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Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain
Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain of Patients With Probable Alzheimer's Disease or Progressive Supranuclear Palsy Compared With Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
mi
from
New Haven, CT
Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain
Phase 0 Evaluation of [18F]MNI-958 as a Potential PET Radioligand for Imaging Tau Protein in the Brain of Patients With Probable Alzheimer's Disease or Progressive Supranuclear Palsy Compared With Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Molecular Neuroimaging, LLC
mi
from
New Haven, CT
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Racial Differences in the Natriuretic Peptide Response to Glucose Challenge
A Study of Racial Differences in Natriuretic Peptides Response to Glucose Challenge
Status: Enrolling
Updated:  12/31/1969
mi
from
Birmingham, AL
Racial Differences in the Natriuretic Peptide Response to Glucose Challenge
A Study of Racial Differences in Natriuretic Peptides Response to Glucose Challenge
Status: Enrolling
Updated: 12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Pubic Hair and the Urinary and Vaginal Microbiome
Effects of Pubic Hair Grooming on Urinary and Vaginal Microbiome
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Pubic Hair and the Urinary and Vaginal Microbiome
Effects of Pubic Hair Grooming on Urinary and Vaginal Microbiome
Status: Enrolling
Updated: 12/31/1969
Northwestern University
mi
from
Chicago, IL
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Study Evaluating the Effects of Food, Cytochrome P450 Inhibition and Induction on the Pharmacokinetics of CC-122
A Phase 1, Open-Label, 4-Part Study to Evaluate the Effect of Food, Cytochrome P 450 Inhibition and Induction on the Pharmacokinetics of CC 122 in Healthy Adult Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
Study Evaluating the Effects of Food, Cytochrome P450 Inhibition and Induction on the Pharmacokinetics of CC-122
A Phase 1, Open-Label, 4-Part Study to Evaluate the Effect of Food, Cytochrome P 450 Inhibition and Induction on the Pharmacokinetics of CC 122 in Healthy Adult Subjects
Status: Enrolling
Updated: 12/31/1969
PPD, Phase 1 Clinic
mi
from
Austin, TX
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Single-dose Study of [14C]PF-05221304 Metabolism and Excretion in Healthy Adult Male Subjects
A Phase 1, Open Label, Single-period, Non-randomized Study To Evaluate The Pharmacokinetics, Excretion, Mass Balance, And Metabolism Of [14c]Pf-05221304 Administered Orally To Healthy Adult Male Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Madison, WI
Single-dose Study of [14C]PF-05221304 Metabolism and Excretion in Healthy Adult Male Subjects
A Phase 1, Open Label, Single-period, Non-randomized Study To Evaluate The Pharmacokinetics, Excretion, Mass Balance, And Metabolism Of [14c]Pf-05221304 Administered Orally To Healthy Adult Male Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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Effect of Kale Consumption on Human Xenobiotic Metabolizing Enzymes
Effect of Kale Consumption on Human Xenobiotic Metabolizing Enzymes
Status: Enrolling
Updated:  12/31/1969
mi
from
Beltsville, MD
Effect of Kale Consumption on Human Xenobiotic Metabolizing Enzymes
Effect of Kale Consumption on Human Xenobiotic Metabolizing Enzymes
Status: Enrolling
Updated: 12/31/1969
USDA-ARS, Beltsville Human Nutrition Research Center
mi
from
Beltsville, MD
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