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

Study to Assess the Pharmacokinetic Drug-Drug Interactions of Lemborexant When Coadministered With an Oral Contraceptive, Famotidine, or Fluconazole in Healthy Subjects
A 3-Part, Open-label Study to Assess the Pharmacokinetic Drug-Drug Interactions of Lemborexant When Coadministered With an Oral Contraceptive, Famotidine, or Fluconazole in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Worldwide Clinical Trials
mi
from
San Antonio, TX
Study to Assess the Pharmacokinetic Drug-Drug Interactions of Lemborexant When Coadministered With an Oral Contraceptive, Famotidine, or Fluconazole in Healthy Subjects
A 3-Part, Open-label Study to Assess the Pharmacokinetic Drug-Drug Interactions of Lemborexant When Coadministered With an Oral Contraceptive, Famotidine, or Fluconazole in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Worldwide Clinical Trials
mi
from
San Antonio, TX
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The Role of CD4+ Memory Phenotype, Memory, and Effector T Cells in Vaccination and Infection
The Role of CD4+ Memory Phenotype, Memory, and Effector T Cells in Vaccination and Infection Adaptive Immune Responses and Repertoire in Influenza Vaccination and Infection
Status: Enrolling
Updated:  12/31/1969
Stanford University
mi
from
Stanford, CA
The Role of CD4+ Memory Phenotype, Memory, and Effector T Cells in Vaccination and Infection
The Role of CD4+ Memory Phenotype, Memory, and Effector T Cells in Vaccination and Infection Adaptive Immune Responses and Repertoire in Influenza Vaccination and Infection
Status: Enrolling
Updated: 12/31/1969
Stanford University
mi
from
Stanford, CA
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A Study of LY3074828 in Healthy Participants
A Safety, Tolerability, and Pharmacokinetic Study of 1- and 2-mL Injections of LY3074828 Solution Using Investigational Pre-filled Syringes and Investigational Autoinjectors in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance, Inc.
mi
from
Dallas, TX
A Study of LY3074828 in Healthy Participants
A Safety, Tolerability, and Pharmacokinetic Study of 1- and 2-mL Injections of LY3074828 Solution Using Investigational Pre-filled Syringes and Investigational Autoinjectors in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance, Inc.
mi
from
Dallas, TX
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Study in Healthy Subjects to Determine the Effect of Relacorilant on Exposure to Probe Substrates for Cytochrome P450s
A Phase 1, Open-Label, Single-Sequence Crossover Study in Healthy Subjects to Determine the Effect of Relacorilant on Exposure to Probe Substrates for Cytochrome P450s 3A4, 2C8, 2C9, 2C19, and 2D6
Status: Enrolling
Updated:  12/31/1969
Celerion
mi
from
Tempe, AZ
Study in Healthy Subjects to Determine the Effect of Relacorilant on Exposure to Probe Substrates for Cytochrome P450s
A Phase 1, Open-Label, Single-Sequence Crossover Study in Healthy Subjects to Determine the Effect of Relacorilant on Exposure to Probe Substrates for Cytochrome P450s 3A4, 2C8, 2C9, 2C19, and 2D6
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Tempe, AZ
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Yellow Fever Immune Response at Single Cell Resolution
Single Cell Transcriptomics for Characterizing the Human Immune Response to Yellow Fever Vaccination
Status: Enrolling
Updated:  12/31/1969
Rockefeller University
mi
from
New York, NY
Yellow Fever Immune Response at Single Cell Resolution
Single Cell Transcriptomics for Characterizing the Human Immune Response to Yellow Fever Vaccination
Status: Enrolling
Updated: 12/31/1969
Rockefeller University
mi
from
New York, NY
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Berry Components and Blood Sugar & Fat Metabolism
Berry Components and Blood Sugar & Fat Metabolism
Status: Enrolling
Updated:  12/31/1969
USDA-ARS, Beltsville Human Nutrition Research Center
mi
from
Beltsville, MD
Berry Components and Blood Sugar & Fat Metabolism
Berry Components and Blood Sugar & Fat Metabolism
Status: Enrolling
Updated: 12/31/1969
USDA-ARS, Beltsville Human Nutrition Research Center
mi
from
Beltsville, MD
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Nitrate Supplementation and Muscle Blood Flow
Nitric Oxide Bioavailability and Dynamics of Blood Flow and Vasodilation With Age
Status: Enrolling
Updated:  12/31/1969
Medical Education Building
mi
from
Iowa City, IA
Nitrate Supplementation and Muscle Blood Flow
Nitric Oxide Bioavailability and Dynamics of Blood Flow and Vasodilation With Age
Status: Enrolling
Updated: 12/31/1969
Medical Education Building
mi
from
Iowa City, IA
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A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Inc
mi
from
Daytona Beach, FL
A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Daytona Beach, FL
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A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Covance, Inc.
mi
from
Dallas, TX
A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Covance, Inc.
mi
from
Dallas, TX
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A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Inc
mi
from
Madison, WI
A Study of Lasmiditan on Simulated Driving Performance in Healthy Participants
A Phase I, Randomized, Subject- and Investigator-Blind, Placebo-Controlled, 4-Period Cross-Over Study Assessing the Duration of Effect of Lasmiditan on Simulated Driving Performance in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Madison, WI
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Brief Shame Intervention Study
The Development and Evaluation of a Brief Shame Intervention Module: Proof of Concept in Social Anxiety Disorder
Status: Enrolling
Updated:  12/31/1969
Anxiety Cognition and Emotion Laboratory
mi
from
Oxford, OH
Brief Shame Intervention Study
The Development and Evaluation of a Brief Shame Intervention Module: Proof of Concept in Social Anxiety Disorder
Status: Enrolling
Updated: 12/31/1969
Anxiety Cognition and Emotion Laboratory
mi
from
Oxford, OH
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Pulmonary Associates, PA
mi
from
Phoenix, AZ
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Pulmonary Associates, PA
mi
from
Phoenix, AZ
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Pacific Research Network
mi
from
San Diego, CA
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Pacific Research Network
mi
from
San Diego, CA
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
PAB Clinical Research
mi
from
Brandon, FL
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
PAB Clinical Research
mi
from
Brandon, FL
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Research Centers of America
mi
from
Hollywood, FL
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Research Centers of America
mi
from
Hollywood, FL
Click here to add this to my saved trials
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Neurotrials Research, Inc.
mi
from
Atlanta, GA
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Neurotrials Research, Inc.
mi
from
Atlanta, GA
Click here to add this to my saved trials
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
The Center for Sleep and Wake Disorders
mi
from
Chevy Chase, MD
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
The Center for Sleep and Wake Disorders
mi
from
Chevy Chase, MD
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Clinilabs Drug Development
mi
from
New York, NY
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Clinilabs Drug Development
mi
from
New York, NY
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
CTI Clinical Research Center
mi
from
Cincinnati, OH
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
CTI Clinical Research Center
mi
from
Cincinnati, OH
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
PACT
mi
from
Glendale, AZ
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
PACT
mi
from
Glendale, AZ
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Advarra
mi
from
Columbia, MD
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Advarra
mi
from
Columbia, MD
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Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated:  12/31/1969
Community Research
mi
from
Cincinnati, OH
Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Evaluate the Respiratory Safety of Lemborexant in Adult and Elderly Healthy Subjects and Adult and Elderly Subjects With Mild Obstructive Sleep Apnea
Status: Enrolling
Updated: 12/31/1969
Community Research
mi
from
Cincinnati, OH
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Assessment of the Biodistribution and Safety of [18F]MNI-958 in Healthy Subjects
Assessment of the Biodistribution and Safety of [18F]MNI-958 in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Invicro
mi
from
New Haven, CT
Assessment of the Biodistribution and Safety of [18F]MNI-958 in Healthy Subjects
Assessment of the Biodistribution and Safety of [18F]MNI-958 in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Invicro
mi
from
New Haven, CT
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A 4-Day Study to Evaluate Phototoxicity of CCP-020 (Diacerein 1%) in Healthy Subjects
A 4 Day, Randomized Study to Evaluate the Potential of CCP-020 (Diacerein 1%) Topical Ointment to Induce a Phototoxicity Skin Reaction in Healthy Subjects, Using a Controlled Photopatch Test
Status: Enrolling
Updated:  12/31/1969
TKL research
mi
from
Fair Lawn, NJ
A 4-Day Study to Evaluate Phototoxicity of CCP-020 (Diacerein 1%) in Healthy Subjects
A 4 Day, Randomized Study to Evaluate the Potential of CCP-020 (Diacerein 1%) Topical Ointment to Induce a Phototoxicity Skin Reaction in Healthy Subjects, Using a Controlled Photopatch Test
Status: Enrolling
Updated: 12/31/1969
TKL research
mi
from
Fair Lawn, NJ
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A 6-Week Study to Evaluate Photoallergic Skin Reaction of CCP-020 (Diacerein 1%) in Healthy Subjects
A 6-Week, Randomized Study to Evaluate the Potential of CCP-020 (Diacerein 1%) Topical Ointment to Induce a Photoallergic Skin Reaction in Healthy Subjects, Using a Controlled Photopatch Test Design
Status: Enrolling
Updated:  12/31/1969
TKL research
mi
from
Fair Lawn, NJ
A 6-Week Study to Evaluate Photoallergic Skin Reaction of CCP-020 (Diacerein 1%) in Healthy Subjects
A 6-Week, Randomized Study to Evaluate the Potential of CCP-020 (Diacerein 1%) Topical Ointment to Induce a Photoallergic Skin Reaction in Healthy Subjects, Using a Controlled Photopatch Test Design
Status: Enrolling
Updated: 12/31/1969
TKL research
mi
from
Fair Lawn, NJ
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ID-Cap System Under Direct Observation
Clinical Performance of the ID-Cap System, an Ingestion Event Marker, in the Clinical Setting as an Aid to Measure Medication Adherence
Status: Enrolling
Updated:  12/31/1969
Quotient Sciences
mi
from
Jacksonville, FL
ID-Cap System Under Direct Observation
Clinical Performance of the ID-Cap System, an Ingestion Event Marker, in the Clinical Setting as an Aid to Measure Medication Adherence
Status: Enrolling
Updated: 12/31/1969
Quotient Sciences
mi
from
Jacksonville, FL
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A Study to Evaluate the Pharmacokinetics (PK), Safety and Tolerability of TAK-788 Followed by Evaluation of the Effects of a Low-Fat Meal on TAK-788 PK and Evaluation of Relative Bioavailability of TAK-788 Capsules in Healthy Participants
Phase 1, Randomized, Double-blind, Placebo-Controlled, Single Rising Dose Study to Evaluate Pharmacokinetics, Safety, and Tolerability of TAK-788 Followed by Open-Label, Crossover Evaluation of the Effects of a Low-Fat Meal on TAK-788 Pharmacokinetics and Evaluation of Relative Bioavailability of TAK-788 Capsules in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
PRA Health Sciences
mi
from
Salt Lake City, UT
A Study to Evaluate the Pharmacokinetics (PK), Safety and Tolerability of TAK-788 Followed by Evaluation of the Effects of a Low-Fat Meal on TAK-788 PK and Evaluation of Relative Bioavailability of TAK-788 Capsules in Healthy Participants
Phase 1, Randomized, Double-blind, Placebo-Controlled, Single Rising Dose Study to Evaluate Pharmacokinetics, Safety, and Tolerability of TAK-788 Followed by Open-Label, Crossover Evaluation of the Effects of a Low-Fat Meal on TAK-788 Pharmacokinetics and Evaluation of Relative Bioavailability of TAK-788 Capsules in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
PRA Health Sciences
mi
from
Salt Lake City, UT
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Pediatric Microbiome Study With Children Now Approximately 8-10 Years Old.
The Evolution of the Skin Microbiome of Children Approximately Ages 8-10 Years of Age
Status: Enrolling
Updated:  12/31/1969
Consumer Experience Center
mi
from
Skillman, NJ
Pediatric Microbiome Study With Children Now Approximately 8-10 Years Old.
The Evolution of the Skin Microbiome of Children Approximately Ages 8-10 Years of Age
Status: Enrolling
Updated: 12/31/1969
Consumer Experience Center
mi
from
Skillman, NJ
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Project Options - The ABC Method
Efficacy of a Behavioral Intervention to Reduce Skin Cancer Risk Among Patients
Status: Enrolling
Updated:  12/31/1969
Penn State Health Milton S. Hershey Medical Center
mi
from
Hershey, PA
Project Options - The ABC Method
Efficacy of a Behavioral Intervention to Reduce Skin Cancer Risk Among Patients
Status: Enrolling
Updated: 12/31/1969
Penn State Health Milton S. Hershey Medical Center
mi
from
Hershey, PA
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Pain Modulatory Profiles in Massage for Healthy Participants
Pain Modulatory Profiles in Massage for Healthy Participants
Status: Enrolling
Updated:  12/31/1969
UF Health
mi
from
Gainesville, FL
Pain Modulatory Profiles in Massage for Healthy Participants
Pain Modulatory Profiles in Massage for Healthy Participants
Status: Enrolling
Updated: 12/31/1969
UF Health
mi
from
Gainesville, FL
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Study to Evaluate the Safety, Tolerability, PK, and PD of PB2452 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MEDI2452 (PB2452) With and Without Ticagrelor Pretreatment in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
PPD
mi
from
Austin, TX
Study to Evaluate the Safety, Tolerability, PK, and PD of PB2452 in Healthy Volunteers
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MEDI2452 (PB2452) With and Without Ticagrelor Pretreatment in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
PPD
mi
from
Austin, TX
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A Single Dose Crossover Study In Healthy Subjects To Evaluate Different Formulations Of PF-06882961
A Phase 1, Open-label Study In Healthy Subjects To Evaluate The Pharmacokinetics Of Pf-06882961 Following Single Oral Administration Of Immediate Release Tablets And An Immediate Release Oral Solution In The Fed State, And Controlled Release Tablets In The Fed And Fasted States
Status: Enrolling
Updated:  12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
A Single Dose Crossover Study In Healthy Subjects To Evaluate Different Formulations Of PF-06882961
A Phase 1, Open-label Study In Healthy Subjects To Evaluate The Pharmacokinetics Of Pf-06882961 Following Single Oral Administration Of Immediate Release Tablets And An Immediate Release Oral Solution In The Fed State, And Controlled Release Tablets In The Fed And Fasted States
Status: Enrolling
Updated: 12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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Safety and Pharmacokinetics (PK) of a Polyurethane Tenofovir Disoproxil Fumarate (TDF) Vaginal Ring (TDF IVR-002)
Phase 1 Safety and Pharmacokinetic Study of a Polyurethane Tenofovir Disoproxil Fumarate Vaginal Ring in Sexually Active Women (TDF IVR-002)
Status: Enrolling
Updated:  12/31/1969
Albert Einstein College of Medicine
mi
from
Bronx, NY
Safety and Pharmacokinetics (PK) of a Polyurethane Tenofovir Disoproxil Fumarate (TDF) Vaginal Ring (TDF IVR-002)
Phase 1 Safety and Pharmacokinetic Study of a Polyurethane Tenofovir Disoproxil Fumarate Vaginal Ring in Sexually Active Women (TDF IVR-002)
Status: Enrolling
Updated: 12/31/1969
Albert Einstein College of Medicine
mi
from
Bronx, NY
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Safety and Pharmacokinetics (PK) of a Polyurethane Tenofovir Disoproxil Fumarate (TDF) Vaginal Ring (TDF IVR-002)
Phase 1 Safety and Pharmacokinetic Study of a Polyurethane Tenofovir Disoproxil Fumarate Vaginal Ring in Sexually Active Women (TDF IVR-002)
Status: Enrolling
Updated:  12/31/1969
Kenya Medical Research Institute, Partners in Prevention, University of Nairobi
mi
from
Nairobi,
Safety and Pharmacokinetics (PK) of a Polyurethane Tenofovir Disoproxil Fumarate (TDF) Vaginal Ring (TDF IVR-002)
Phase 1 Safety and Pharmacokinetic Study of a Polyurethane Tenofovir Disoproxil Fumarate Vaginal Ring in Sexually Active Women (TDF IVR-002)
Status: Enrolling
Updated: 12/31/1969
Kenya Medical Research Institute, Partners in Prevention, University of Nairobi
mi
from
Nairobi,
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Study to Compare Kowa OCT Bi-μ and the Optovue iVue 100
Pilot Comparative Study of the Kowa OCT Bi-μ and the Optovue iVue 100
Status: Enrolling
Updated:  12/31/1969
Andover Eye Associates
mi
from
Andover, MA
Study to Compare Kowa OCT Bi-μ and the Optovue iVue 100
Pilot Comparative Study of the Kowa OCT Bi-μ and the Optovue iVue 100
Status: Enrolling
Updated: 12/31/1969
Andover Eye Associates
mi
from
Andover, MA
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A Trial to Evaluate the Effect of Itraconazole (ITZ), a CYP3A4 Inhibitor, on the Pharmacokinetics of Praliciguat (IW-1973) in Healthy Volunteers
An Open-label, 2-Period, Fixed-sequence, Phase 1 Study in Healthy Volunteers to Evaluate the Effect of Itraconazole, a Potent CYP3A Inhibitor, on the Pharmacokinetics of IW-1973
Status: Enrolling
Updated:  12/31/1969
IQVIA
mi
from
Overland Park, KA
A Trial to Evaluate the Effect of Itraconazole (ITZ), a CYP3A4 Inhibitor, on the Pharmacokinetics of Praliciguat (IW-1973) in Healthy Volunteers
An Open-label, 2-Period, Fixed-sequence, Phase 1 Study in Healthy Volunteers to Evaluate the Effect of Itraconazole, a Potent CYP3A Inhibitor, on the Pharmacokinetics of IW-1973
Status: Enrolling
Updated: 12/31/1969
IQVIA
mi
from
Overland Park, KA
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A Study to Assess the Absorption of Apixaban (BMS-562247) Sprinkle Capsules Compared With Tablets in Healthy Volunteers
Relative Bioavailability of Apixaban (BMS-562247) 0.1 mg Sprinkle Capsules Compared With 0.5 mg Tablets in Healthy Participants
Status: Enrolling
Updated:  12/31/1969
PPD Austin Clinic
mi
from
Austin, TX
A Study to Assess the Absorption of Apixaban (BMS-562247) Sprinkle Capsules Compared With Tablets in Healthy Volunteers
Relative Bioavailability of Apixaban (BMS-562247) 0.1 mg Sprinkle Capsules Compared With 0.5 mg Tablets in Healthy Participants
Status: Enrolling
Updated: 12/31/1969
PPD Austin Clinic
mi
from
Austin, TX
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Preventing Avoidable Admissions Among Assisted Living Elders
Preventing Avoidable Admissions Among Assisted Living Elders (PA4LE)
Status: Enrolling
Updated:  12/31/1969
St. Luke's Home
mi
from
Tucson, AZ
Preventing Avoidable Admissions Among Assisted Living Elders
Preventing Avoidable Admissions Among Assisted Living Elders (PA4LE)
Status: Enrolling
Updated: 12/31/1969
St. Luke's Home
mi
from
Tucson, AZ
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Pharmacokinetic Study Evaluating Staccato® Alprazolam 1 mg Inhaler in Smokers Versus Non-Smokers
A Phase 1 Open-Label, Non-Randomized, Single-Dose, Pharmacokinetic Study Evaluating Staccato® Alprazolam 1 mg Inhaler in Smoker Versus Non-Smoker Healthy Adult Volunteers
Status: Enrolling
Updated:  12/31/1969
Clinilabs Research Unit
mi
from
Eatontown, NJ
Pharmacokinetic Study Evaluating Staccato® Alprazolam 1 mg Inhaler in Smokers Versus Non-Smokers
A Phase 1 Open-Label, Non-Randomized, Single-Dose, Pharmacokinetic Study Evaluating Staccato® Alprazolam 1 mg Inhaler in Smoker Versus Non-Smoker Healthy Adult Volunteers
Status: Enrolling
Updated: 12/31/1969
Clinilabs Research Unit
mi
from
Eatontown, NJ
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A Study to Compare the Oral Bioavailability of Single Doses of Three Vapendavir Drug Formulations in Healthy Volunteers
A Randomized, Single-Center, Open-Label, Three-Period, Six-Sequence, Crossover, Comparative Study to Compare the Oral Bioavailability of Single Doses of Three Vapendavir Drug Product Formulations in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Aviragen Investigational Site
mi
from
Saint Paul, MN
A Study to Compare the Oral Bioavailability of Single Doses of Three Vapendavir Drug Formulations in Healthy Volunteers
A Randomized, Single-Center, Open-Label, Three-Period, Six-Sequence, Crossover, Comparative Study to Compare the Oral Bioavailability of Single Doses of Three Vapendavir Drug Product Formulations in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Aviragen Investigational Site
mi
from
Saint Paul, MN
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The Cellular Pharmacology of F-TAF in Dried Blood Spots
The Cellular Pharmacology of F-TAF in Dried Blood Spots
Status: Enrolling
Updated:  12/31/1969
University of Colorado- Anschutz Campus
mi
from
Aurora, CO
The Cellular Pharmacology of F-TAF in Dried Blood Spots
The Cellular Pharmacology of F-TAF in Dried Blood Spots
Status: Enrolling
Updated: 12/31/1969
University of Colorado- Anschutz Campus
mi
from
Aurora, CO
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The Effect of Dairy on Bone Mass and Body Composition in 4th-8th Grade Boys and Girls
Influence of Dairy on Bone Accrual and Bone Size and Fat and Lean Mass in Early Pubertal Overweight vs. Healthy-weight Boys and Girls
Status: Enrolling
Updated:  12/31/1969
Indiana University School of Medicine
mi
from
Indianapolis, IN
The Effect of Dairy on Bone Mass and Body Composition in 4th-8th Grade Boys and Girls
Influence of Dairy on Bone Accrual and Bone Size and Fat and Lean Mass in Early Pubertal Overweight vs. Healthy-weight Boys and Girls
Status: Enrolling
Updated: 12/31/1969
Indiana University School of Medicine
mi
from
Indianapolis, IN
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The Effect of Dairy on Bone Mass and Body Composition in 4th-8th Grade Boys and Girls
Influence of Dairy on Bone Accrual and Bone Size and Fat and Lean Mass in Early Pubertal Overweight vs. Healthy-weight Boys and Girls
Status: Enrolling
Updated:  12/31/1969
Purdue University
mi
from
West Lafayette, IN
The Effect of Dairy on Bone Mass and Body Composition in 4th-8th Grade Boys and Girls
Influence of Dairy on Bone Accrual and Bone Size and Fat and Lean Mass in Early Pubertal Overweight vs. Healthy-weight Boys and Girls
Status: Enrolling
Updated: 12/31/1969
Purdue University
mi
from
West Lafayette, IN
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Behavioral CVD Prevention Using Informatics
Behavioral Cardiovascular Disease Prevention Using Informatics
Status: Enrolling
Updated:  12/31/1969
Boston Med Ctr
mi
from
Boston, MA
Behavioral CVD Prevention Using Informatics
Behavioral Cardiovascular Disease Prevention Using Informatics
Status: Enrolling
Updated: 12/31/1969
Boston Med Ctr
mi
from
Boston, MA
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A Study to Evaluate the Mass Balance of 14C-Napabucasin in Healthy Adult Male Subjects
A Phase I, Open Label, Single Dose Study to Evaluate the Mass Balance of 14C-Napabucasin in Healthy Adult Male Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
A Study to Evaluate the Mass Balance of 14C-Napabucasin in Healthy Adult Male Subjects
A Phase I, Open Label, Single Dose Study to Evaluate the Mass Balance of 14C-Napabucasin in Healthy Adult Male Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Status: Enrolling
Updated:  12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Status: Enrolling
Updated: 12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
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Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Status: Enrolling
Updated:  12/31/1969
UC Davis
mi
from
Davis, CA
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Absorption, Metabolism and Excretion of Apigenin and Apigenin Glycosides
Status: Enrolling
Updated: 12/31/1969
UC Davis
mi
from
Davis, CA
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Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Status: Enrolling
Updated:  12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Status: Enrolling
Updated: 12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
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Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Status: Enrolling
Updated:  12/31/1969
UC Davis
mi
from
Davis, CA
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Flavanol Absorption, Metabolism and Excretion From Fruit-based Drinks and Other Food Matrixes
Status: Enrolling
Updated: 12/31/1969
UC Davis
mi
from
Davis, CA
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Food Matrix Effect on Flavanol Absorption, Metabolism and Excretion: Methylxanthines
Food Matrix Effect on Flavanol Absorption, Metabolism and Excretion: Methylxanthines
Status: Enrolling
Updated:  12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
Food Matrix Effect on Flavanol Absorption, Metabolism and Excretion: Methylxanthines
Food Matrix Effect on Flavanol Absorption, Metabolism and Excretion: Methylxanthines
Status: Enrolling
Updated: 12/31/1969
Ragle Human Nutrition Research Center, Department of Nutrition at UC Davis
mi
from
Davis, CA
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