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 to Investigate the Effect of RO7049389 on the Pharmacokinetics of Pitavastatin in Healthy Volunteers
An Open-Label, Fixed Sequence, Two-Period Study to Investigate the Effect of RO7049389 on the Pharmacokinetics of Pitavastatin in Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Covance Research Unit - Daytona
mi
from
Daytona Beach, FL
A Study to Investigate the Effect of RO7049389 on the Pharmacokinetics of Pitavastatin in Healthy Volunteers
An Open-Label, Fixed Sequence, Two-Period Study to Investigate the Effect of RO7049389 on the Pharmacokinetics of Pitavastatin in Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Covance Research Unit - Daytona
mi
from
Daytona Beach, FL
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Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
An Open-label Study to Evaluate the Absorption, Metabolism, and Excretion of Orally Administered [14C]-TR-701 in Healthy Adult Male Subjects
Status: Enrolling
Updated:  12/31/1969
Trius Investigator Site 001
mi
from
Madison, WI
Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
An Open-label Study to Evaluate the Absorption, Metabolism, and Excretion of Orally Administered [14C]-TR-701 in Healthy Adult Male Subjects
Status: Enrolling
Updated: 12/31/1969
Trius Investigator Site 001
mi
from
Madison, WI
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A Study to Evaluate the Relative Bioavailability (BA) and Effect of Food on TAK-831 Tablet Formulations in Healthy Participants
A Phase 1, Open-Label, Randomized, Single Dose, 5-Period, 5-Treatment Study to Evaluate the Relative Bioavailability and Effect of Food on TAK-831 Tablet Formulations in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Celerion
mi
from
Lincoln, NE
A Study to Evaluate the Relative Bioavailability (BA) and Effect of Food on TAK-831 Tablet Formulations in Healthy Participants
A Phase 1, Open-Label, Randomized, Single Dose, 5-Period, 5-Treatment Study to Evaluate the Relative Bioavailability and Effect of Food on TAK-831 Tablet Formulations in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Lincoln, NE
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Prenatal Interventions to Promote Exclusive Breastfeeding
Assessing the Feasibility of a Breastfeeding Champion Intervention and a Positive Messaging Module During the Prenatal Period - a Pilot
Status: Enrolling
Updated:  12/31/1969
University Hospital MacDonald Women's Hospital
mi
from
Cleveland, OH
Prenatal Interventions to Promote Exclusive Breastfeeding
Assessing the Feasibility of a Breastfeeding Champion Intervention and a Positive Messaging Module During the Prenatal Period - a Pilot
Status: Enrolling
Updated: 12/31/1969
University Hospital MacDonald Women's Hospital
mi
from
Cleveland, OH
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SpO2 Validation of Noninvasive Red Diamond Disposable Pulse Oximeter Sensor
SpO2 Validation of Noninvasive Red Diamond Disposable Pulse Oximeter Sensor
Status: Enrolling
Updated:  12/31/1969
Masimo Corporation
mi
from
Irvine, CA
SpO2 Validation of Noninvasive Red Diamond Disposable Pulse Oximeter Sensor
SpO2 Validation of Noninvasive Red Diamond Disposable Pulse Oximeter Sensor
Status: Enrolling
Updated: 12/31/1969
Masimo Corporation
mi
from
Irvine, CA
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Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System
Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System: A Pilot Study
Status: Enrolling
Updated:  12/31/1969
Integrated Therapy Practice PC
mi
from
Hobart, IN
Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System
Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System: A Pilot Study
Status: Enrolling
Updated: 12/31/1969
Integrated Therapy Practice PC
mi
from
Hobart, IN
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Expanded Game Squad for Neurodiverse Youth
Engaging Children With Mental Health and Developmental Disabilities and Their Parents to Adopt a Healthy Lifestyle: Piloting the Game Squad Home Exergaming & Virtual Health Coaching Intervention
Status: Enrolling
Updated:  12/31/1969
Marblehead Public Schools
mi
from
Marblehead, MA
Expanded Game Squad for Neurodiverse Youth
Engaging Children With Mental Health and Developmental Disabilities and Their Parents to Adopt a Healthy Lifestyle: Piloting the Game Squad Home Exergaming & Virtual Health Coaching Intervention
Status: Enrolling
Updated: 12/31/1969
Marblehead Public Schools
mi
from
Marblehead, MA
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Expanded Game Squad for Neurodiverse Youth
Engaging Children With Mental Health and Developmental Disabilities and Their Parents to Adopt a Healthy Lifestyle: Piloting the Game Squad Home Exergaming & Virtual Health Coaching Intervention
Status: Enrolling
Updated:  12/31/1969
Boston Medical Center Developmental and Behavioral Pediatrics Clinic
mi
from
Boston, MA
Expanded Game Squad for Neurodiverse Youth
Engaging Children With Mental Health and Developmental Disabilities and Their Parents to Adopt a Healthy Lifestyle: Piloting the Game Squad Home Exergaming & Virtual Health Coaching Intervention
Status: Enrolling
Updated: 12/31/1969
Boston Medical Center Developmental and Behavioral Pediatrics Clinic
mi
from
Boston, MA
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A Study of LY3090106 in Japanese and Caucasian Healthy Participants
A Single-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3090106 in Japanese and Caucasian Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
A Study of LY3090106 in Japanese and Caucasian Healthy Participants
A Single-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3090106 in Japanese and Caucasian Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Anaheim Clinical Trials, LLC
mi
from
Anaheim, CA
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Pharmacogenetics of Warfarin Induction and Inhibition
Pharmacogenetics of Warfarin Induction and Inhibition
Status: Enrolling
Updated:  12/31/1969
Clinical and Translational Science Institute
mi
from
Minneapolis, MN
Pharmacogenetics of Warfarin Induction and Inhibition
Pharmacogenetics of Warfarin Induction and Inhibition
Status: Enrolling
Updated: 12/31/1969
Clinical and Translational Science Institute
mi
from
Minneapolis, MN
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The Bioavailability of a Spray Dried Dispersion Solid Dose Formulation of PF-06260414 Relative to a Suspension Formulation
A Phase 1 Single-dose Open Label 3-way Crossover Study To Evaluate The Bioavailability Of A Spray Dried Dispersion Solid Dose Formulation Of Pf-06260414 Relative To A Suspension Formulation Under Fasted Conditions And The Effect Of Food On The Bioavailability Of The Pf-06260414 Spray Dried Dispersion Solid Formulation In Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
The Bioavailability of a Spray Dried Dispersion Solid Dose Formulation of PF-06260414 Relative to a Suspension Formulation
A Phase 1 Single-dose Open Label 3-way Crossover Study To Evaluate The Bioavailability Of A Spray Dried Dispersion Solid Dose Formulation Of Pf-06260414 Relative To A Suspension Formulation Under Fasted Conditions And The Effect Of Food On The Bioavailability Of The Pf-06260414 Spray Dried Dispersion Solid Formulation In Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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A Food Effect Study in Healthy Volunteers With PT2977 Tablets
A Single-Dose, Open-Label, Randomized, Food Effect Study in Healthy Volunteers With PT2977 Tablets
Status: Enrolling
Updated:  12/31/1969
Spaulding Clinical
mi
from
West Bend, WI
A Food Effect Study in Healthy Volunteers With PT2977 Tablets
A Single-Dose, Open-Label, Randomized, Food Effect Study in Healthy Volunteers With PT2977 Tablets
Status: Enrolling
Updated: 12/31/1969
Spaulding Clinical
mi
from
West Bend, WI
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A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants
An Open-Label, Multicenter, Randomized, Parallel-Group, 3-Arm, Single-Dose Bioequivalence Study of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-Injector in Adult Healthy Participants
Status: Enrolling
Updated:  12/31/1969
Up0033 002
mi
from
Baltimore, MD
A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants
An Open-Label, Multicenter, Randomized, Parallel-Group, 3-Arm, Single-Dose Bioequivalence Study of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-Injector in Adult Healthy Participants
Status: Enrolling
Updated: 12/31/1969
Up0033 002
mi
from
Baltimore, MD
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A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants
An Open-Label, Multicenter, Randomized, Parallel-Group, 3-Arm, Single-Dose Bioequivalence Study of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-Injector in Adult Healthy Participants
Status: Enrolling
Updated:  12/31/1969
Up0033 001
mi
from
Berlin,
A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants
An Open-Label, Multicenter, Randomized, Parallel-Group, 3-Arm, Single-Dose Bioequivalence Study of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-Injector in Adult Healthy Participants
Status: Enrolling
Updated: 12/31/1969
Up0033 001
mi
from
Berlin,
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Safety, Tolerability and Pharmacokinetics of 14-day Multiple Dose Titrations of TS-134 in Healthy Volunteers
A Randomized, Double-blind, Placebo-controlled, Multiple Ascending Dose Titration Study to Evaluate the Safety, Tolerability and Pharmacokinetics of TS-134 Administered Orally to Healthy Male and Female Subjects
Status: Enrolling
Updated:  12/31/1969
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
Safety, Tolerability and Pharmacokinetics of 14-day Multiple Dose Titrations of TS-134 in Healthy Volunteers
A Randomized, Double-blind, Placebo-controlled, Multiple Ascending Dose Titration Study to Evaluate the Safety, Tolerability and Pharmacokinetics of TS-134 Administered Orally to Healthy Male and Female Subjects
Status: Enrolling
Updated: 12/31/1969
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
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Safety, Tolerability and Pharmacokinetics of Single Doses of TS-134 in Healthy Volunteers
A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Effects of Food on the Absorption of TS-134 Administered Orally to Healthy Male and Female Subjects
Status: Enrolling
Updated:  12/31/1969
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
Safety, Tolerability and Pharmacokinetics of Single Doses of TS-134 in Healthy Volunteers
A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Effects of Food on the Absorption of TS-134 Administered Orally to Healthy Male and Female Subjects
Status: Enrolling
Updated: 12/31/1969
PAREXEL, Early Phase Clinical Unit-Los Angeles
mi
from
Glendale, CA
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An Open Label Study to Evaluate the Pharmacokinetic Exposure of Apremilast in Healthy Subjects
A Phase 1, Open Label, Randomized, Two Part Study to Evaluate the Pharmacokinetic Exposure of a Once-Daily (QD) Apremilast Formulation Relative to the Twice-Daily (BID) Reference Immediate Release (IR) Tablet and the Effect of Food on the QD Apremilast Formulation in Healthy Subjects.
Status: Enrolling
Updated:  12/31/1969
Covance-Daytona Beach
mi
from
Daytona Beach, FL
An Open Label Study to Evaluate the Pharmacokinetic Exposure of Apremilast in Healthy Subjects
A Phase 1, Open Label, Randomized, Two Part Study to Evaluate the Pharmacokinetic Exposure of a Once-Daily (QD) Apremilast Formulation Relative to the Twice-Daily (BID) Reference Immediate Release (IR) Tablet and the Effect of Food on the QD Apremilast Formulation in Healthy Subjects.
Status: Enrolling
Updated: 12/31/1969
Covance-Daytona Beach
mi
from
Daytona Beach, FL
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An Open Label Study to Evaluate the Pharmacokinetic Exposure of Apremilast in Healthy Subjects
A Phase 1, Open Label, Randomized, Two Part Study to Evaluate the Pharmacokinetic Exposure of a Once-Daily (QD) Apremilast Formulation Relative to the Twice-Daily (BID) Reference Immediate Release (IR) Tablet and the Effect of Food on the QD Apremilast Formulation in Healthy Subjects.
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
An Open Label Study to Evaluate the Pharmacokinetic Exposure of Apremilast in Healthy Subjects
A Phase 1, Open Label, Randomized, Two Part Study to Evaluate the Pharmacokinetic Exposure of a Once-Daily (QD) Apremilast Formulation Relative to the Twice-Daily (BID) Reference Immediate Release (IR) Tablet and the Effect of Food on the QD Apremilast Formulation in Healthy Subjects.
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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A Study of the Absorption, Metabolism, and Excretion of Tucatinib in Healthy Participants
A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [¹⁴C]-Tucatinib Following a Single Oral Dose in Healthy Male and Female Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
A Study of the Absorption, Metabolism, and Excretion of Tucatinib in Healthy Participants
A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [¹⁴C]-Tucatinib Following a Single Oral Dose in Healthy Male and Female Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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A Study To Evaluate The Effect Of Food On The Behavior Of Tofacitinib Modified Release 11 Milligram Tablets In Healthy Western And Japanese Volunteers
A Phase 1, Randomized, Open Label, Single Dose, 2-Period Crossover Study To Evaluate The Effect Of Food On The Pharmacokinetics Of Tofacitinib Modified Release (MR) 11 Mg Tablets In Healthy Western And Japanese Volunteers
Status: Enrolling
Updated:  12/31/1969
Glendale Adventist Medical Center
mi
from
Glendale, CA
A Study To Evaluate The Effect Of Food On The Behavior Of Tofacitinib Modified Release 11 Milligram Tablets In Healthy Western And Japanese Volunteers
A Phase 1, Randomized, Open Label, Single Dose, 2-Period Crossover Study To Evaluate The Effect Of Food On The Pharmacokinetics Of Tofacitinib Modified Release (MR) 11 Mg Tablets In Healthy Western And Japanese Volunteers
Status: Enrolling
Updated: 12/31/1969
Glendale Adventist Medical Center
mi
from
Glendale, CA
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Study In Healthy Subjects To Evaluate The Changes In The Protein sAPP-Alpha In Cerebrospinal Fluid Following A Single Oral Dose Of PF-04995274
A Phase 1 Investigator And Subject-Blind Study In Healthy Subjects To Evaluate The Pharmacodynamic Effects Of Single Doses Of PF-04995274 On Sapp-Alpha Concentrations In Cerebrospinal Fluid Using Serial Sampling Methodology
Status: Enrolling
Updated:  12/31/1969
Pfizer Investigational Site
mi
from
New Haven, CT
Study In Healthy Subjects To Evaluate The Changes In The Protein sAPP-Alpha In Cerebrospinal Fluid Following A Single Oral Dose Of PF-04995274
A Phase 1 Investigator And Subject-Blind Study In Healthy Subjects To Evaluate The Pharmacodynamic Effects Of Single Doses Of PF-04995274 On Sapp-Alpha Concentrations In Cerebrospinal Fluid Using Serial Sampling Methodology
Status: Enrolling
Updated: 12/31/1969
Pfizer Investigational Site
mi
from
New Haven, CT
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First In Human Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of PF-04427429 Administered Intravenously To Healthy Adult Volunteers
A Randomized, Placebo Controlled, Double-Blind, Third Party Open, Parallel Group, First In Human Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of PF-04427429 Administered Intravenously To Healthy Adult Volunteers
Status: Enrolling
Updated:  12/31/1969
Pfizer Investigational Site
mi
from
Phoenix, AZ
First In Human Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of PF-04427429 Administered Intravenously To Healthy Adult Volunteers
A Randomized, Placebo Controlled, Double-Blind, Third Party Open, Parallel Group, First In Human Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of PF-04427429 Administered Intravenously To Healthy Adult Volunteers
Status: Enrolling
Updated: 12/31/1969
Pfizer Investigational Site
mi
from
Phoenix, AZ
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Study To Establish The Effects Of PF-04457845 On Sleep In Healthy Volunteers
Double-Blind, Randomized, Multiple-Dose, Placebo-Controlled, 2-Way Crossover Study To Study Effects of PF-04457845 On Polysomnographic Endpoints In Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Pfizer Investigational Site
mi
from
New York, NY
Study To Establish The Effects Of PF-04457845 On Sleep In Healthy Volunteers
Double-Blind, Randomized, Multiple-Dose, Placebo-Controlled, 2-Way Crossover Study To Study Effects of PF-04457845 On Polysomnographic Endpoints In Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Pfizer Investigational Site
mi
from
New York, NY
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ESTIMATION OF THE EFFECT OF MULTIPLE DOSE PF-06651600 ON THE PHARMACOKINETICS OF SINGLE DOSE MIDAZOLAM AND EFAVIRENZ
A PHASE 1, RANDOMIZED, OPEN LABEL, 2-WAY CROSSOVER STUDY TO ESTIMATE THE EFFECT OF MULTIPLE DOSE PF-06651600 ON THE PHARMACOKINETICS OF SINGLE DOSE MIDAZOLAM AND EFAVIRENZ IN HEALTHY PARTICIPANTS
Status: Enrolling
Updated:  12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
ESTIMATION OF THE EFFECT OF MULTIPLE DOSE PF-06651600 ON THE PHARMACOKINETICS OF SINGLE DOSE MIDAZOLAM AND EFAVIRENZ
A PHASE 1, RANDOMIZED, OPEN LABEL, 2-WAY CROSSOVER STUDY TO ESTIMATE THE EFFECT OF MULTIPLE DOSE PF-06651600 ON THE PHARMACOKINETICS OF SINGLE DOSE MIDAZOLAM AND EFAVIRENZ IN HEALTHY PARTICIPANTS
Status: Enrolling
Updated: 12/31/1969
Pfizer New Haven Clinical Research Unit
mi
from
New Haven, CT
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A Study Comparing User Experience of Different Delivery Devices for Glucagon
A Simulation Study Comparing Successful Administration, Time to Administer, and User Experience of Ready-to-Use Nasal Glucagon With Reconstitutable Injectable Glucagon
Status: Enrolling
Updated:  12/31/1969
High Point Clinical Trials Center
mi
from
High Point, NC
A Study Comparing User Experience of Different Delivery Devices for Glucagon
A Simulation Study Comparing Successful Administration, Time to Administer, and User Experience of Ready-to-Use Nasal Glucagon With Reconstitutable Injectable Glucagon
Status: Enrolling
Updated: 12/31/1969
High Point Clinical Trials Center
mi
from
High Point, NC
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Effect of tACS Stimulation on Alpha Oscillations
Rational Optimization of tACS for Targeting Thalamo-Cortical Oscillations (Experiment 2)
Status: Enrolling
Updated:  12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
Effect of tACS Stimulation on Alpha Oscillations
Rational Optimization of tACS for Targeting Thalamo-Cortical Oscillations (Experiment 2)
Status: Enrolling
Updated: 12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
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Levoketoconazole Food Effect Study in Healthy Subjects
A Phase I Randomized, Open-Label, Two-Period, Two-Sequence Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of Levoketoconazole in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Clinical Pharmacology of Miami
mi
from
Miami, FL
Levoketoconazole Food Effect Study in Healthy Subjects
A Phase I Randomized, Open-Label, Two-Period, Two-Sequence Crossover Study to Evaluate the Effect of Food on the Pharmacokinetics of Levoketoconazole in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Clinical Pharmacology of Miami
mi
from
Miami, FL
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A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects
A Phase 1, Double-blind, Placebo-controlled Crossover Study of SAGE-718 Using a Ketamine Challenge, to Evaluate the Electrophysiology, Safety, Tolerability, and Pharmacokinetics in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Long Beach, CA
A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects
A Phase 1, Double-blind, Placebo-controlled Crossover Study of SAGE-718 Using a Ketamine Challenge, to Evaluate the Electrophysiology, Safety, Tolerability, and Pharmacokinetics in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Long Beach, CA
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A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects
A Phase 1, Double-blind, Placebo-controlled Crossover Study of SAGE-718 Using a Ketamine Challenge, to Evaluate the Electrophysiology, Safety, Tolerability, and Pharmacokinetics in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Berlin, NJ
A Study to Assess the Electrophysiology, Safety, Tolerability, and Pharmacokinetics of SAGE-718 Using a Ketamine Challenge in Healthy Subjects
A Phase 1, Double-blind, Placebo-controlled Crossover Study of SAGE-718 Using a Ketamine Challenge, to Evaluate the Electrophysiology, Safety, Tolerability, and Pharmacokinetics in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Berlin, NJ
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Single Dose Mass Balance Study With C14 - Labeled AAI101 in Healthy Male Volunteers
A Phase 1, Open-Label, Single-Dose Study to Assess the Mass Balance, Pharmacokinetics and Metabolism of Intravenously Administered 14C-AAI101 in Healthy Male Subjects
Status: Enrolling
Updated:  12/31/1969
Pharmaron Clinical Pharmacology Center
mi
from
Baltimore, MD
Single Dose Mass Balance Study With C14 - Labeled AAI101 in Healthy Male Volunteers
A Phase 1, Open-Label, Single-Dose Study to Assess the Mass Balance, Pharmacokinetics and Metabolism of Intravenously Administered 14C-AAI101 in Healthy Male Subjects
Status: Enrolling
Updated: 12/31/1969
Pharmaron Clinical Pharmacology Center
mi
from
Baltimore, MD
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Engaging School and Family in Navajo Gardening for Health
Engaging School and Family in Navajo Gardening for Health
Status: Enrolling
Updated:  12/31/1969
Fred Hutch/University of Washington Cancer Consortium
mi
from
Seattle, WA
Engaging School and Family in Navajo Gardening for Health
Engaging School and Family in Navajo Gardening for Health
Status: Enrolling
Updated: 12/31/1969
Fred Hutch/University of Washington Cancer Consortium
mi
from
Seattle, WA
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Effects of Tucatinib on Cardiac Repolarization in Healthy Participants
A Phase 1, Randomized, Partially Double-Blind, Placebo- and Positive-controlled Study to Evaluate the Effect of Tucatinib on Cardiac Repolarization in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit Dallas
mi
from
Dallas, TX
Effects of Tucatinib on Cardiac Repolarization in Healthy Participants
A Phase 1, Randomized, Partially Double-Blind, Placebo- and Positive-controlled Study to Evaluate the Effect of Tucatinib on Cardiac Repolarization in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit Dallas
mi
from
Dallas, TX
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Multiple Risk Behavior Intervention in Health Care Settings
Multiple Risk Behavior Intervention in Health Care Settings
Status: Enrolling
Updated:  12/31/1969
Harvard Vanguard Medical Associates
mi
from
Boston, MA
Multiple Risk Behavior Intervention in Health Care Settings
Multiple Risk Behavior Intervention in Health Care Settings
Status: Enrolling
Updated: 12/31/1969
Harvard Vanguard Medical Associates
mi
from
Boston, MA
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Reverse Cholesterol Transport (RCT) Study
A Pilot Study To Evaluate The Use Of 3H Particulate Cholesterol As A Method To Study Reverse Cholesterol Transport In Humans Followed By A Study On The Effect Of HDL-C On RCT Measured By This Method
Status: Enrolling
Updated:  12/31/1969
Univ of Pennsylvania
mi
from
Philadelphia, PA
Reverse Cholesterol Transport (RCT) Study
A Pilot Study To Evaluate The Use Of 3H Particulate Cholesterol As A Method To Study Reverse Cholesterol Transport In Humans Followed By A Study On The Effect Of HDL-C On RCT Measured By This Method
Status: Enrolling
Updated: 12/31/1969
Univ of Pennsylvania
mi
from
Philadelphia, PA
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Effects of CS-8080 in Healthy Volunteers
A Randomized, Placebo-Controlled, Single Ascending Dose Study To Assess The Safety, Tolerability and Pharmacokinetics Of CS-8080 In Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Mds Pharma Services
mi
from
Neptune, NJ
Effects of CS-8080 in Healthy Volunteers
A Randomized, Placebo-Controlled, Single Ascending Dose Study To Assess The Safety, Tolerability and Pharmacokinetics Of CS-8080 In Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Mds Pharma Services
mi
from
Neptune, NJ
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Effects of Multiple Doses of CS-8080 in Healthy Volunteers
A Randomized, Placebo-Controlled, Multiple Ascending Dose Study To Assess The Safety, Pharmacokinetics and Pharmacodynamics Of CS-8080 In Healthy Volunteers
Status: Enrolling
Updated:  12/31/1969
Mds Pharma Services
mi
from
Neptune, NJ
Effects of Multiple Doses of CS-8080 in Healthy Volunteers
A Randomized, Placebo-Controlled, Multiple Ascending Dose Study To Assess The Safety, Pharmacokinetics and Pharmacodynamics Of CS-8080 In Healthy Volunteers
Status: Enrolling
Updated: 12/31/1969
Mds Pharma Services
mi
from
Neptune, NJ
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An Interaction Study of LY3200882 in Healthy Participants
Effects of CYP3A4 Inhibition by Itraconazole on the Pharmacokinetics of LY3200882 in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Inc
mi
from
Daytona Beach, FL
An Interaction Study of LY3200882 in Healthy Participants
Effects of CYP3A4 Inhibition by Itraconazole on the Pharmacokinetics of LY3200882 in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Inc
mi
from
Daytona Beach, FL
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A Study to Investigate the Bioequivalence of Two Different Forms of Entrectinib (Forms A and C) Under Fasted Conditions in Healthy Subjects
A Randomized, Open-Label, Two-Treatment, Two-Period, Two-Way Crossover Study to Investigate the Bioequivalence of Entrectinib Polymorph Forms A and C Under Fasted Conditions in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Research Unit - Dallas
mi
from
Dallas, TX
A Study to Investigate the Bioequivalence of Two Different Forms of Entrectinib (Forms A and C) Under Fasted Conditions in Healthy Subjects
A Randomized, Open-Label, Two-Treatment, Two-Period, Two-Way Crossover Study to Investigate the Bioequivalence of Entrectinib Polymorph Forms A and C Under Fasted Conditions in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Research Unit - Dallas
mi
from
Dallas, TX
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Effects of a Valgus Unloader Brace on Medial Femoral Cartilage
Effects of a Valgus Unloader Brace on Medial Femoral Cartilage Changes Following Walking Protocol
Status: Enrolling
Updated:  12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
Effects of a Valgus Unloader Brace on Medial Femoral Cartilage
Effects of a Valgus Unloader Brace on Medial Femoral Cartilage Changes Following Walking Protocol
Status: Enrolling
Updated: 12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
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Prevention of HIV/AIDS and STDs in Women Over Fifty
Prevention of HIV/AIDS and STDs in Women Over Fifty
Status: Enrolling
Updated:  12/31/1969
Environment and Health Group
mi
from
Cambridge, MA
Prevention of HIV/AIDS and STDs in Women Over Fifty
Prevention of HIV/AIDS and STDs in Women Over Fifty
Status: Enrolling
Updated: 12/31/1969
Environment and Health Group
mi
from
Cambridge, MA
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A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated:  12/31/1969
Clinical Research Unit
mi
from
Pasadena, CA
A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated: 12/31/1969
Clinical Research Unit
mi
from
Pasadena, CA
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A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated:  12/31/1969
Clinical Research Unit
mi
from
San Antonio, TX
A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated: 12/31/1969
Clinical Research Unit
mi
from
San Antonio, TX
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A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated:  12/31/1969
Clinical Research Unit
mi
from
Salt Lake City, UT
A Multiple Dose Study of TD-1211 in Healthy Volunteers and Patients With Opioid-Induced Constipation
A Phase 1/Phase 2, Randomized, Double-Blind, Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, and Effect on Opioid Analgesia of TD-1211 Administered Orally to Healthy Volunteers and to Assess the Safety, Pharmacokinetics, and Effect on Bowel Movements in Subjects With Opioid-Induced Constipation
Status: Enrolling
Updated: 12/31/1969
Clinical Research Unit
mi
from
Salt Lake City, UT
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A Trial to Study the Absorption, Metabolism, and Excretion of [14C]-Olinciguat in Healthy Male Volunteers
A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-Olinciguat ([14C]-IW-1701) Following a Single Oral Dose in Healthy Male Subjects
Status: Enrolling
Updated:  12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
A Trial to Study the Absorption, Metabolism, and Excretion of [14C]-Olinciguat in Healthy Male Volunteers
A Phase 1, Open-label Study of the Absorption, Metabolism, and Excretion of [14C]-Olinciguat ([14C]-IW-1701) Following a Single Oral Dose in Healthy Male Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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A Study to Compare the Bioavailability (BA) of Dexlansoprazole Delayed-release Capsules
A Phase 1, Randomized, Open-Label, Single-Dose, Two-Period Crossover Study to Compare the Bioavailability of Dexlansoprazole Capsules Manufactured by Takeda GmbH Relative to Dexlansoprazole Capsules Manufactured by Takeda Osaka Following a High-Fat Meal
Status: Enrolling
Updated:  12/31/1969
Celerion
mi
from
Tempe, AZ
A Study to Compare the Bioavailability (BA) of Dexlansoprazole Delayed-release Capsules
A Phase 1, Randomized, Open-Label, Single-Dose, Two-Period Crossover Study to Compare the Bioavailability of Dexlansoprazole Capsules Manufactured by Takeda GmbH Relative to Dexlansoprazole Capsules Manufactured by Takeda Osaka Following a High-Fat Meal
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Tempe, AZ
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A Study to Assess Absolute Bioavailability (ABA) of TAK-788 and to Characterize Mass Balance, Pharmacokinetics (PK), Metabolism, and Excretion of Carbon-14 ([14C])-TAK-788 in Male Healthy Participants
A Phase 1 Study to Assess Absolute Bioavailability of TAK-788 and to Characterize Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]-TAK-788 in Male Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
Celerion
mi
from
Lincoln, NE
A Study to Assess Absolute Bioavailability (ABA) of TAK-788 and to Characterize Mass Balance, Pharmacokinetics (PK), Metabolism, and Excretion of Carbon-14 ([14C])-TAK-788 in Male Healthy Participants
A Phase 1 Study to Assess Absolute Bioavailability of TAK-788 and to Characterize Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]-TAK-788 in Male Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Celerion
mi
from
Lincoln, NE
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A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated:  12/31/1969
Sleep Disorders Center of Alabama
mi
from
Birmingham, AL
A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated: 12/31/1969
Sleep Disorders Center of Alabama
mi
from
Birmingham, AL
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A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated:  12/31/1969
Arkansas Center for Sleep Medicine
mi
from
Little Rock, AR
A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated: 12/31/1969
Arkansas Center for Sleep Medicine
mi
from
Little Rock, AR
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A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated:  12/31/1969
Florida Lung & Sleep Associates
mi
from
Lehigh Acres, FL
A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated: 12/31/1969
Florida Lung & Sleep Associates
mi
from
Lehigh Acres, FL
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A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated:  12/31/1969
Neurotrials Research, Inc.
mi
from
Atlanta, GA
A Study of the Effectiveness and Efficacy of the PowerSleep Device
A Double-Blind Placebo-Controlled Multi-Site Randomized Cross-Over Study of the Effectiveness and Efficacy of the PowerSleep Device
Status: Enrolling
Updated: 12/31/1969
Neurotrials Research, Inc.
mi
from
Atlanta, GA
Click here to add this to my saved trials