Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
3,204
archived clinical trials in
Healthy Studies

A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated:  12/31/1969
Clinical Pharmacology of Miami (CPMI)
mi
from
Miami, FL
A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated: 12/31/1969
Clinical Pharmacology of Miami (CPMI)
mi
from
Miami, FL
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A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated:  12/31/1969
Orlando Clinical Research Center (OCRC)
mi
from
Orlando, FL
A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated: 12/31/1969
Orlando Clinical Research Center (OCRC)
mi
from
Orlando, FL
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A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated:  12/31/1969
Indiana University - Digestive and Liver Diseases
mi
from
Indianapolis, IN
A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated: 12/31/1969
Indiana University - Digestive and Liver Diseases
mi
from
Indianapolis, IN
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A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated:  12/31/1969
DaVita Clinical Research
mi
from
Minneapolis, MN
A Study of Abemaciclib in Participants With Varying Degrees of Liver Impairment
A Single-Dose Pharmacokinetic Study of Abemaciclib (LY2835219) in Subjects With Varying Degrees of Hepatic Impairment
Status: Enrolling
Updated: 12/31/1969
DaVita Clinical Research
mi
from
Minneapolis, MN
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PK and Safety Study of AG-221 in Healthy Male Japanese Subjects and Healthy Male Caucasian Subjects
A Phase 1, Single Ascending Dose, Open-label Study to Evaluate the Pharmacokinetics and Safety of AG-221 in Healthy Male Japanese Subjects Relative to Healthy Male Caucasian Subjects
Status: Enrolling
Updated:  12/31/1969
Parexel International
mi
from
Glendale, CA
PK and Safety Study of AG-221 in Healthy Male Japanese Subjects and Healthy Male Caucasian Subjects
A Phase 1, Single Ascending Dose, Open-label Study to Evaluate the Pharmacokinetics and Safety of AG-221 in Healthy Male Japanese Subjects Relative to Healthy Male Caucasian Subjects
Status: Enrolling
Updated: 12/31/1969
Parexel International
mi
from
Glendale, CA
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Zinc Lozenges and Their Effect on Postoperative Sore Throat Syndrome
Zinc Lozenges and Their Effect on Postoperative Sore Throat Syndrome: A Randomized, Double-blinded, Placebo-controlled Prospective Study
Status: Enrolling
Updated:  12/31/1969
University of Vermont Medical Center
mi
from
Burlington, VT
Zinc Lozenges and Their Effect on Postoperative Sore Throat Syndrome
Zinc Lozenges and Their Effect on Postoperative Sore Throat Syndrome: A Randomized, Double-blinded, Placebo-controlled Prospective Study
Status: Enrolling
Updated: 12/31/1969
University of Vermont Medical Center
mi
from
Burlington, VT
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A Drug-Drug Interaction Study of Lanabecestat (LY3314814) in Healthy Participants
A Study to Characterize LY3314814 Pharmacokinetics as a Function of Dosing Duration and to Determine the Effect of LY3314814 on the Pharmacokinetics of CYP3A Substrates in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance, Inc.
mi
from
Daytona Beach, FL
A Drug-Drug Interaction Study of Lanabecestat (LY3314814) in Healthy Participants
A Study to Characterize LY3314814 Pharmacokinetics as a Function of Dosing Duration and to Determine the Effect of LY3314814 on the Pharmacokinetics of CYP3A Substrates in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance, Inc.
mi
from
Daytona Beach, FL
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A Drug-Drug Interaction Study of Lanabecestat (LY3314814) in Healthy Participants
A Study to Characterize LY3314814 Pharmacokinetics as a Function of Dosing Duration and to Determine the Effect of LY3314814 on the Pharmacokinetics of CYP3A Substrates in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance, Inc.
mi
from
Dallas, TX
A Drug-Drug Interaction Study of Lanabecestat (LY3314814) in Healthy Participants
A Study to Characterize LY3314814 Pharmacokinetics as a Function of Dosing Duration and to Determine the Effect of LY3314814 on the Pharmacokinetics of CYP3A Substrates in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance, Inc.
mi
from
Dallas, TX
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Acute Effect of Exercise on Vascular Function
Acute Effect of Exercise on Vascular Function
Status: Enrolling
Updated:  12/31/1969
Integrative Cardiovascular Physiology Laboratory
mi
from
Gainesville, FL
Acute Effect of Exercise on Vascular Function
Acute Effect of Exercise on Vascular Function
Status: Enrolling
Updated: 12/31/1969
Integrative Cardiovascular Physiology Laboratory
mi
from
Gainesville, FL
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Relative Bioavailability of Two Formulations of AKB-6548 and the Food Effect of a New Tablet in Healthy Adult Subjects
A Randomized, Open-Label, Single-Dose, Three-Period Crossover Study in Healthy Adults to Assess the Relative Bioavailability of Test and Reference Formulations of AKB-6548 Tablets and to Evaluate the Effect of Food on the Bioavailability of AKB-6548
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kalamazoo, MI
Relative Bioavailability of Two Formulations of AKB-6548 and the Food Effect of a New Tablet in Healthy Adult Subjects
A Randomized, Open-Label, Single-Dose, Three-Period Crossover Study in Healthy Adults to Assess the Relative Bioavailability of Test and Reference Formulations of AKB-6548 Tablets and to Evaluate the Effect of Food on the Bioavailability of AKB-6548
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kalamazoo, MI
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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Ascending Single- and Multiple-Doses of TAK-020 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Sequential-Panel, Ascending Single- and Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAK-020 in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Glendale, CA
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Ascending Single- and Multiple-Doses of TAK-020 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Sequential-Panel, Ascending Single- and Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAK-020 in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Glendale, CA
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Total Energy Expenditure and Fat Oxidation in 2 Year Old Children
Total Energy Expenditure and Fat Oxidation in 2 Year Old Children
Status: Enrolling
Updated:  12/31/1969
Arkansas Children's Nutrition Center
mi
from
Little Rock, AR
Total Energy Expenditure and Fat Oxidation in 2 Year Old Children
Total Energy Expenditure and Fat Oxidation in 2 Year Old Children
Status: Enrolling
Updated: 12/31/1969
Arkansas Children's Nutrition Center
mi
from
Little Rock, AR
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A Study to Evaluate the Effect of SYN-004 on the PK of IV Ceftriaxone in Adults With a Functioning Ileostomy
A Phase 1b/2a, Randomized, Multi-center, Open-label, Fixed-sequence Study to Evaluate the Effect of Oral SYN-004 on the Pharmacokinetics of Intravenous Ceftriaxone in Healthy Adult Subjects With a Functioning Ileostomy
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Columbus, OH
A Study to Evaluate the Effect of SYN-004 on the PK of IV Ceftriaxone in Adults With a Functioning Ileostomy
A Phase 1b/2a, Randomized, Multi-center, Open-label, Fixed-sequence Study to Evaluate the Effect of Oral SYN-004 on the Pharmacokinetics of Intravenous Ceftriaxone in Healthy Adult Subjects With a Functioning Ileostomy
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Columbus, OH
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A Study to Evaluate the Effect of SYN-004 on the PK of IV Ceftriaxone in Adults With a Functioning Ileostomy
A Phase 1b/2a, Randomized, Multi-center, Open-label, Fixed-sequence Study to Evaluate the Effect of Oral SYN-004 on the Pharmacokinetics of Intravenous Ceftriaxone in Healthy Adult Subjects With a Functioning Ileostomy
Status: Enrolling
Updated:  12/31/1969
mi
from
Edmonton,
A Study to Evaluate the Effect of SYN-004 on the PK of IV Ceftriaxone in Adults With a Functioning Ileostomy
A Phase 1b/2a, Randomized, Multi-center, Open-label, Fixed-sequence Study to Evaluate the Effect of Oral SYN-004 on the Pharmacokinetics of Intravenous Ceftriaxone in Healthy Adult Subjects With a Functioning Ileostomy
Status: Enrolling
Updated: 12/31/1969
mi
from
Edmonton,
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Metformin in Longevity Study (MILES).
Metformin in Longevity Study (MILES).
Status: Enrolling
Updated:  12/31/1969
Einstein College of Medicine of Yeshiva University
mi
from
Bronx, NY
Metformin in Longevity Study (MILES).
Metformin in Longevity Study (MILES).
Status: Enrolling
Updated: 12/31/1969
Einstein College of Medicine of Yeshiva University
mi
from
Bronx, NY
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Supporting Baby Behavior Through Pediatric Offices
Supporting Baby Behavior Through Pediatric Offices
Status: Enrolling
Updated:  12/31/1969
University of California Davis
mi
from
Davis, CA
Supporting Baby Behavior Through Pediatric Offices
Supporting Baby Behavior Through Pediatric Offices
Status: Enrolling
Updated: 12/31/1969
University of California Davis
mi
from
Davis, CA
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Intra-epidermal Stimulation (IES) of Small Nerve Fibers (A-delta Fibers)
Intra-epidermal Stimulation (IES) of Small Nerve Fibers (A-delta Fibers)
Status: Enrolling
Updated:  12/31/1969
Univ of Minnesota
mi
from
Minneapolis, MN
Intra-epidermal Stimulation (IES) of Small Nerve Fibers (A-delta Fibers)
Intra-epidermal Stimulation (IES) of Small Nerve Fibers (A-delta Fibers)
Status: Enrolling
Updated: 12/31/1969
Univ of Minnesota
mi
from
Minneapolis, MN
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Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Men
A Randomized, Two Center, Double-Blind Trial to Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Healthy Men
Status: Enrolling
Updated:  12/31/1969
LA Biomedical Research Institute
mi
from
Torrance, CA
Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Men
A Randomized, Two Center, Double-Blind Trial to Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Healthy Men
Status: Enrolling
Updated: 12/31/1969
LA Biomedical Research Institute
mi
from
Torrance, CA
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Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Men
A Randomized, Two Center, Double-Blind Trial to Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Healthy Men
Status: Enrolling
Updated:  12/31/1969
Univ of Washington
mi
from
Seattle, WA
Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Men
A Randomized, Two Center, Double-Blind Trial to Evaluate the Pharmacokinetics and Gonadotropin Suppression of Nestorone®-Testosterone (NES/T) Combination Gel in Healthy Men
Status: Enrolling
Updated: 12/31/1969
Univ of Washington
mi
from
Seattle, WA
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Safety, Tolerability and Pharmacokinetics of PF-05251749
A Phase 1, Randomized, Double Blind, Placebo Controlled Study To Investigate The Safety, Tolerability, Pharmacokinetics And Relative Bioavailability Of Single Escalating Oral Doses Of Pf-05251749 In Healthy Adult Subjects
Status: Enrolling
Updated:  12/31/1969
New Haven Clinical Research Unit
mi
from
New Haven, CT
Safety, Tolerability and Pharmacokinetics of PF-05251749
A Phase 1, Randomized, Double Blind, Placebo Controlled Study To Investigate The Safety, Tolerability, Pharmacokinetics And Relative Bioavailability Of Single Escalating Oral Doses Of Pf-05251749 In Healthy Adult Subjects
Status: Enrolling
Updated: 12/31/1969
New Haven Clinical Research Unit
mi
from
New Haven, CT
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Pilot Study to Image the Esophagus Using a SECM Tethered Endoscopic Capsule
Pilot Study for Imaging of Barrett's Esophagus Using an Spectrally Encoded Confocal Microscopy Tethered Endoscopic Capsule
Status: Enrolling
Updated:  12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
Pilot Study to Image the Esophagus Using a SECM Tethered Endoscopic Capsule
Pilot Study for Imaging of Barrett's Esophagus Using an Spectrally Encoded Confocal Microscopy Tethered Endoscopic Capsule
Status: Enrolling
Updated: 12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
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PET Imaging Study to Evaluate the mGlu5r Occupancy Following ADX48621 (Dipraglurant) Administration
An Open Label PET Imaging Study to Evaluate the mGlu5 Receptor Occupancy Following ADX48621 (Dipraglurant) Administration
Status: Enrolling
Updated:  12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
PET Imaging Study to Evaluate the mGlu5r Occupancy Following ADX48621 (Dipraglurant) Administration
An Open Label PET Imaging Study to Evaluate the mGlu5 Receptor Occupancy Following ADX48621 (Dipraglurant) Administration
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Hospital
mi
from
Baltimore, MD
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RDEA3170 Tablet and Capsule Bioavailability Study
A Phase 1, Randomized, Open-Label, Study in Healthy Adult Male Subjects to Assess the Relative Bioavailability and Food Effect of Various Formulations of RDEA3170
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Austin, TX
RDEA3170 Tablet and Capsule Bioavailability Study
A Phase 1, Randomized, Open-Label, Study in Healthy Adult Male Subjects to Assess the Relative Bioavailability and Food Effect of Various Formulations of RDEA3170
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Austin, TX
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Study of PF614 Compared to OxyContin® in Healthy Volunteers
A Phase 1, Single-Center, Dose-Escalation Study to Determine the Safety and Pharmacokinetics of a Single Oral Dose of PF614 in Healthy Subjects Compared to OxyContin®
Status: Enrolling
Updated:  12/31/1969
PRA Health Sciences - Early Development Services
mi
from
Lenexa, KA
Study of PF614 Compared to OxyContin® in Healthy Volunteers
A Phase 1, Single-Center, Dose-Escalation Study to Determine the Safety and Pharmacokinetics of a Single Oral Dose of PF614 in Healthy Subjects Compared to OxyContin®
Status: Enrolling
Updated: 12/31/1969
PRA Health Sciences - Early Development Services
mi
from
Lenexa, KA
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Expandability of Aging Adipose Tissue
Aging Subcutaneous Adipose Tissue Response to Overfeeding
Status: Enrolling
Updated:  12/31/1969
Univeristy of Colorado Anschutz Medical Campus
mi
from
Aurora, CO
Expandability of Aging Adipose Tissue
Aging Subcutaneous Adipose Tissue Response to Overfeeding
Status: Enrolling
Updated: 12/31/1969
Univeristy of Colorado Anschutz Medical Campus
mi
from
Aurora, CO
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Sleep, Circadian Rhythm & Skin Health
Sleep, Circadian Rhythm & Skin Health
Status: Enrolling
Updated:  12/31/1969
University Hospitals of Cleveland Medical Center
mi
from
Cleveland, OH
Sleep, Circadian Rhythm & Skin Health
Sleep, Circadian Rhythm & Skin Health
Status: Enrolling
Updated: 12/31/1969
University Hospitals of Cleveland Medical Center
mi
from
Cleveland, OH
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Infant Microbiota and Probiotic Intake Study
Infant Supplementation With Probiotic Bifidobacterium Longum Subsp. Infantis Study
Status: Enrolling
Updated:  12/31/1969
University of California, Davis Medical Center
mi
from
Sacramento, CA
Infant Microbiota and Probiotic Intake Study
Infant Supplementation With Probiotic Bifidobacterium Longum Subsp. Infantis Study
Status: Enrolling
Updated: 12/31/1969
University of California, Davis Medical Center
mi
from
Sacramento, CA
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Behavioral Research of Environment and Air Pollution Through Education
Behavioral Research of Environment and Air Pollution Through Education (BREATHE Study)
Status: Enrolling
Updated:  12/31/1969
University of California at San Francisco
mi
from
San Francisco, CA
Behavioral Research of Environment and Air Pollution Through Education
Behavioral Research of Environment and Air Pollution Through Education (BREATHE Study)
Status: Enrolling
Updated: 12/31/1969
University of California at San Francisco
mi
from
San Francisco, CA
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Study to Assess the Relative Potency of Multiple Oral Doses of LUM001 and SHP626 in Overweight and Obese Adults as Assessed by Fecal Bile Acid Excretion
A Randomized, Blinded, Placebo-controlled, Phase 1 Study to Assess the Relative Potency of Multiple Oral Doses of LUM001 and SHP626 in Overweight and Obese Adult Subjects, as Assessed by Fecal Bile Acid Excretion
Status: Enrolling
Updated:  12/31/1969
New Orleans Center for Clinical Research
mi
from
Knoxville, TN
Study to Assess the Relative Potency of Multiple Oral Doses of LUM001 and SHP626 in Overweight and Obese Adults as Assessed by Fecal Bile Acid Excretion
A Randomized, Blinded, Placebo-controlled, Phase 1 Study to Assess the Relative Potency of Multiple Oral Doses of LUM001 and SHP626 in Overweight and Obese Adult Subjects, as Assessed by Fecal Bile Acid Excretion
Status: Enrolling
Updated: 12/31/1969
New Orleans Center for Clinical Research
mi
from
Knoxville, TN
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A Study of Abemaciclib (LY2835219) in Healthy Participants With and Without Food
The Effect of Food on the Pharmacokinetics of the Proposed Commercial Formulation of Abemaciclib in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit, Inc.
mi
from
Daytona Beach, FL
A Study of Abemaciclib (LY2835219) in Healthy Participants With and Without Food
The Effect of Food on the Pharmacokinetics of the Proposed Commercial Formulation of Abemaciclib in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit, Inc.
mi
from
Daytona Beach, FL
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A Study of Abemaciclib (LY2835219) in Healthy Participants With and Without Food
The Effect of Food on the Pharmacokinetics of the Proposed Commercial Formulation of Abemaciclib in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
A Study of Abemaciclib (LY2835219) in Healthy Participants With and Without Food
The Effect of Food on the Pharmacokinetics of the Proposed Commercial Formulation of Abemaciclib in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit, Inc.
mi
from
Dallas, TX
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The Effect of Bikram Yoga on Arterial Stiffness and Endothelial Function in Middle-Aged Adults
Bikram Yoga and Vascular Health
Status: Enrolling
Updated:  12/31/1969
Cardiovascular Aging Research Laboratory
mi
from
Austin, TX
The Effect of Bikram Yoga on Arterial Stiffness and Endothelial Function in Middle-Aged Adults
Bikram Yoga and Vascular Health
Status: Enrolling
Updated: 12/31/1969
Cardiovascular Aging Research Laboratory
mi
from
Austin, TX
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Brain Changes With Game Training in Aging
Brain Changes With Game Training in Aging
Status: Enrolling
Updated:  12/31/1969
University of Wisconsin-Madison
mi
from
Madison, WI
Brain Changes With Game Training in Aging
Brain Changes With Game Training in Aging
Status: Enrolling
Updated: 12/31/1969
University of Wisconsin-Madison
mi
from
Madison, WI
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Dietary Supplementation to Increase Serum Choline Levels
Dietary Supplementation to Increase Serum Choline Levels
Status: Enrolling
Updated:  12/31/1969
University of Colorado Anschutz Medical Campus
mi
from
Aurora, CO
Dietary Supplementation to Increase Serum Choline Levels
Dietary Supplementation to Increase Serum Choline Levels
Status: Enrolling
Updated: 12/31/1969
University of Colorado Anschutz Medical Campus
mi
from
Aurora, CO
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Phase 1, TAK-915-1001, Single-Rising Dose, Multiple-Rising Dose, Drug-Drug Interaction, Relative Bioavailability, Food Effect, and Effect on Elderly Participants Study
A Phase 1 Safety, Tolerability, Pharmacokinetic, Placebo-Controlled and Open-Label Study of Escalating Single and Multiple Oral Doses, Drug-Drug Interaction, Relative Bioavailability, Food Effect, and Effect on Elderly Subjects of TAK-915 in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Austin, TX
Phase 1, TAK-915-1001, Single-Rising Dose, Multiple-Rising Dose, Drug-Drug Interaction, Relative Bioavailability, Food Effect, and Effect on Elderly Participants Study
A Phase 1 Safety, Tolerability, Pharmacokinetic, Placebo-Controlled and Open-Label Study of Escalating Single and Multiple Oral Doses, Drug-Drug Interaction, Relative Bioavailability, Food Effect, and Effect on Elderly Subjects of TAK-915 in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Austin, TX
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The UNCODE Study: Unravelling the Neural Contributors Of Dynapenia in Elders
Neural Mechanisms of Dynapenia
Status: Enrolling
Updated:  12/31/1969
Ohio Musculoskeletal and Neurological Institute (OMNI) at Ohio University
mi
from
Athens, OH
The UNCODE Study: Unravelling the Neural Contributors Of Dynapenia in Elders
Neural Mechanisms of Dynapenia
Status: Enrolling
Updated: 12/31/1969
Ohio Musculoskeletal and Neurological Institute (OMNI) at Ohio University
mi
from
Athens, OH
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First-In-Human Study Of Single And Multiple Ascending Doses Of PF-06751979
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo Controlled First-in-human Trial To Evaluate The Safety,Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-06751979 After Oral Administration Of Single And Multiple Ascending Doses To Healthy Adult And Elderly Subjects
Status: Enrolling
Updated:  12/31/1969
California Clinical Trials Medical Group
mi
from
Glendale, CA
First-In-Human Study Of Single And Multiple Ascending Doses Of PF-06751979
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo Controlled First-in-human Trial To Evaluate The Safety,Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-06751979 After Oral Administration Of Single And Multiple Ascending Doses To Healthy Adult And Elderly Subjects
Status: Enrolling
Updated: 12/31/1969
California Clinical Trials Medical Group
mi
from
Glendale, CA
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First-In-Human Study Of Single And Multiple Ascending Doses Of PF-06751979
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo Controlled First-in-human Trial To Evaluate The Safety,Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-06751979 After Oral Administration Of Single And Multiple Ascending Doses To Healthy Adult And Elderly Subjects
Status: Enrolling
Updated:  12/31/1969
Glendale Adventist Medical Center
mi
from
Glendale, CA
First-In-Human Study Of Single And Multiple Ascending Doses Of PF-06751979
A Phase 1, Randomized, Double-blind, Sponsor-open, Placebo Controlled First-in-human Trial To Evaluate The Safety,Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-06751979 After Oral Administration Of Single And Multiple Ascending Doses To Healthy Adult And Elderly Subjects
Status: Enrolling
Updated: 12/31/1969
Glendale Adventist Medical Center
mi
from
Glendale, CA
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Resveratrol and Exercise to Treat Functional Limitations in Late Life
Resveratrol and Exercise to Treat Functional Limitations in Late Life
Status: Enrolling
Updated:  12/31/1969
UAB Center for Exercise Medicine
mi
from
Birmingham, AL
Resveratrol and Exercise to Treat Functional Limitations in Late Life
Resveratrol and Exercise to Treat Functional Limitations in Late Life
Status: Enrolling
Updated: 12/31/1969
UAB Center for Exercise Medicine
mi
from
Birmingham, AL
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Relative Bioavailability of Two Different Milk Thistle Formulations
Relative Bioavailability of Two Different Milk Thistle Formulations: A Single Dose Randomized Crossover Pharmacokinetic Study
Status: Enrolling
Updated:  12/31/1969
Uf Ctsi Crc
mi
from
Gainesville, FL
Relative Bioavailability of Two Different Milk Thistle Formulations
Relative Bioavailability of Two Different Milk Thistle Formulations: A Single Dose Randomized Crossover Pharmacokinetic Study
Status: Enrolling
Updated: 12/31/1969
Uf Ctsi Crc
mi
from
Gainesville, FL
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Semi-Recumbent Vibration Therapy in Older Adults
Semi-Recumbent Vibration Therapy in Older Adults
Status: Enrolling
Updated:  12/31/1969
Jewish Home and Care Center
mi
from
Milwaukee, WI
Semi-Recumbent Vibration Therapy in Older Adults
Semi-Recumbent Vibration Therapy in Older Adults
Status: Enrolling
Updated: 12/31/1969
Jewish Home and Care Center
mi
from
Milwaukee, WI
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The Lake Nona Life Project
A Community Epidemiology Study Evaluating the Factors Influencing Overall Health and Wellness
Status: Enrolling
Updated:  12/31/1969
Lake Nona Institute
mi
from
Orlando, FL
The Lake Nona Life Project
A Community Epidemiology Study Evaluating the Factors Influencing Overall Health and Wellness
Status: Enrolling
Updated: 12/31/1969
Lake Nona Institute
mi
from
Orlando, FL
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A Drug Interaction Study of Lanabecestat (LY3314814) and Warfarin in Healthy Participants
Effect of LY3314814 on the Pharmacokinetics of Warfarin in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Inc
mi
from
Evansville, IN
A Drug Interaction Study of Lanabecestat (LY3314814) and Warfarin in Healthy Participants
Effect of LY3314814 on the Pharmacokinetics of Warfarin in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Evansville, IN
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mesa, AZ
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mesa, AZ
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Hollywood, FL
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Hollywood, FL
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Leesburg, FL
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Leesburg, FL
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Miami, FL
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Miami, FL
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Meridian, ID
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Meridian, ID
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Wichita, KA
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Wichita, KA
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A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bardstown, KY
A Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Randomized, Double-blind, Placebo-controlled, Multicenter Phase 2 Study in Healthy Adults to Evaluate the Safety and Immunogenicity of Different Doses of JNJ-63871860
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bardstown, KY
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