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
20,707
archived clinical trials in
Gastrointestinal

A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
574
mi
from
Fort Sam Houston, TX
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Brooke Army Medical Center
574
mi
from
Fort Sam Houston, TX
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A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
575
mi
from
San Antonio, TX
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Texas Liver Institute
575
mi
from
San Antonio, TX
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A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
1186
mi
from
Norfolk, VA
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Digestive and Liver Disease Specialists
1186
mi
from
Norfolk, VA
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A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
1113
mi
from
Richmond, VA
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Virginia Commonwealth University
1113
mi
from
Richmond, VA
Click here to add this to my saved trials
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
1044
mi
from
Chapel Hill, NC
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Unc Hospitals And Clinics
1044
mi
from
Chapel Hill, NC
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A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
569
mi
from
Houston, TX
A Study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
St. Luke'S Episcopal Hospital - Baylor College Of Medicine
569
mi
from
Houston, TX
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Per-Oral Endoscopic Myotomy for Esophageal Swallowing Disorders
Prospective Evaluation of Per-Oral Endoscopic Myotomy (POEM) of the Lower Esophageal Sphincter for the Treatment of Esophageal Swallowing Disorders
Status: Enrolling
Updated:  1/17/2018
347
mi
from
Dallas, TX
Per-Oral Endoscopic Myotomy for Esophageal Swallowing Disorders
Prospective Evaluation of Per-Oral Endoscopic Myotomy (POEM) of the Lower Esophageal Sphincter for the Treatment of Esophageal Swallowing Disorders
Status: Enrolling
Updated: 1/17/2018
Baylor University Medical Center
347
mi
from
Dallas, TX
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Prevention of Amputation in Diabetic Foot Ulcers Using Amniotic Tissue
Prevention of Amputation in a High Risk Population With Comprehensive Care and Amniotic Tissue
Status: Enrolling
Updated:  1/17/2018
1041
mi
from
Boise, ID
Prevention of Amputation in Diabetic Foot Ulcers Using Amniotic Tissue
Prevention of Amputation in a High Risk Population With Comprehensive Care and Amniotic Tissue
Status: Enrolling
Updated: 1/17/2018
Boise VAMC
1041
mi
from
Boise, ID
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A Sub-study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Sub-study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
1225
mi
from
Philadelphia, PA
A Sub-study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Sub-study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Thomas Jefferson University Hospital
1225
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Sub-study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Sub-study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated:  1/17/2018
575
mi
from
San Antonio, TX
A Sub-study of BMS-986036 in Subjects With Non-Alcoholic Steatohepatitis (NASH)
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple Dose Sub-study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Adults With Non-alcoholic Steatohepatitis
Status: Enrolling
Updated: 1/17/2018
Texas Liver Institute
575
mi
from
San Antonio, TX
Click here to add this to my saved trials
Evaluation of Performance Characteristics of Capsule Endoscopy With PillCam UGI Capsule Compared to Standard Endoscopy
Evaluation of Performance Characteristics of Capsule Endoscopy With PillCam UGI Capsule Compared to Standard Endoscopy for Screening of Barrett's Esophagus: A Prospective Tandem Study
Status: Enrolling
Updated:  1/17/2018
199
mi
from
Kansas City, MO
Evaluation of Performance Characteristics of Capsule Endoscopy With PillCam UGI Capsule Compared to Standard Endoscopy
Evaluation of Performance Characteristics of Capsule Endoscopy With PillCam UGI Capsule Compared to Standard Endoscopy for Screening of Barrett's Esophagus: A Prospective Tandem Study
Status: Enrolling
Updated: 1/17/2018
Kansas City VA Medical Center
199
mi
from
Kansas City, MO
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Efficacy of Vitamin D Supplementation in Bariatric Surgery Patients
Preoperative Vitamin D Status and Efficacy of Therapeutic Vitamin D Supplementation Postoperatively in Bariatric Surgery Patients
Status: Enrolling
Updated:  1/18/2018
572
mi
from
Houston, TX
Efficacy of Vitamin D Supplementation in Bariatric Surgery Patients
Preoperative Vitamin D Status and Efficacy of Therapeutic Vitamin D Supplementation Postoperatively in Bariatric Surgery Patients
Status: Enrolling
Updated: 1/18/2018
Methodist Hospital
572
mi
from
Houston, TX
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Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated:  1/18/2018
1068
mi
from
Jacksonville, FL
Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated: 1/18/2018
Mayo Clinic Department of Surgery
1068
mi
from
Jacksonville, FL
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Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated:  1/18/2018
1135
mi
from
Lakeland, FL
Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated: 1/18/2018
Watson Clinic Center for Research
1135
mi
from
Lakeland, FL
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Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated:  1/18/2018
801
mi
from
Atlanta, GA
Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated: 1/18/2018
Atlanta Colon & Rectal Surgery, P.A.
801
mi
from
Atlanta, GA
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Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated:  1/18/2018
1102
mi
from
Fredericksburg, VA
Veritas in Non-Bridging Ventral Hernia Repair
Veritas in Non-Bridging Ventral Hernia Repair
Status: Enrolling
Updated: 1/18/2018
Pratt Medical Center
1102
mi
from
Fredericksburg, VA
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Once-Daily Oral Avatrombopag Tablets Used in Subjects With Chronic Liver Diseases and Thrombocytopenia Prior to Elective Surgical or Diagnostic Procedures
A Phase 2, Randomized, Multicenter, Placebo-Controlled, Double-Blind, Parallel-Group Study to Evaluate the Efficacy, Safety, and Population Pharmacokinetics of Once-Daily Oral E5501 Tablets Used Up to 7 Days in Subjects With Chronic Liver Diseases and Thrombocytopenia Prior to Elective Surgical or Diagnostic Procedures
Status: Enrolling
Updated:  1/19/2018
694
mi
from
New Orleans, LA
Once-Daily Oral Avatrombopag Tablets Used in Subjects With Chronic Liver Diseases and Thrombocytopenia Prior to Elective Surgical or Diagnostic Procedures
A Phase 2, Randomized, Multicenter, Placebo-Controlled, Double-Blind, Parallel-Group Study to Evaluate the Efficacy, Safety, and Population Pharmacokinetics of Once-Daily Oral E5501 Tablets Used Up to 7 Days in Subjects With Chronic Liver Diseases and Thrombocytopenia Prior to Elective Surgical or Diagnostic Procedures
Status: Enrolling
Updated: 1/19/2018
Ochsner Clinic Foundation
694
mi
from
New Orleans, LA
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Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated:  1/19/2018
1443
mi
from
Boston, MA
Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated: 1/19/2018
Massachusetts General Hospital
1443
mi
from
Boston, MA
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Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated:  1/19/2018
mi
from
New York, NY
Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated: 1/19/2018
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
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Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated:  1/19/2018
517
mi
from
Austin, TX
Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated: 1/19/2018
Texas Cardiac Arrhythmia Institute
517
mi
from
Austin, TX
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Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated:  1/19/2018
1142
mi
from
Orlando, FL
Deviating the Esophagus in Atrial Fibrillation Ablation
Esophageal Deviation in Atrial Fibrillation Ablation: A Randomized Control Trial
Status: Enrolling
Updated: 1/19/2018
Florida Hospital
1142
mi
from
Orlando, FL
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Probability Ramp Control of Propofol for EGD
A Prospective, Randomized Comparison of Depth of Sedation With Propofol Titrated by Probability Ramp Control to Control by Anesthesia Providers During Esophagogastroduodenoscopy (EGD)
Status: Enrolling
Updated:  1/19/2018
1223
mi
from
Philadelphia, PA
Probability Ramp Control of Propofol for EGD
A Prospective, Randomized Comparison of Depth of Sedation With Propofol Titrated by Probability Ramp Control to Control by Anesthesia Providers During Esophagogastroduodenoscopy (EGD)
Status: Enrolling
Updated: 1/19/2018
Endoscopy Center, Perelman Center for Advanced Medicine
1223
mi
from
Philadelphia, PA
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A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Balsalazide Disodium 750 mg Capsules Under Fasting Conditions
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Balsalazide Disodium 750 mg Capsules Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
569
mi
from
Houston, TX
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Balsalazide Disodium 750 mg Capsules Under Fasting Conditions
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Balsalazide Disodium 750 mg Capsules Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
Novum Pharmaceutical Research Services
569
mi
from
Houston, TX
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Bioequivalency Study of Balsalazide Capsules Under Fasting Conditions
A Single Dose, Two-Period, Two-Treatment, Randomized Crossover Bioequivalency Study of 750 mg Balsalazide Capsules Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
569
mi
from
Houston, TX
Bioequivalency Study of Balsalazide Capsules Under Fasting Conditions
A Single Dose, Two-Period, Two-Treatment, Randomized Crossover Bioequivalency Study of 750 mg Balsalazide Capsules Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
Novum Pharmaceuticals Research Services
569
mi
from
Houston, TX
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Bioequivalency Study of Buprenorphine Hydrochloride 8 mg Tablet Under Fasted Conditions
A Single Dose, Two-Period, Two-Treatment, Two-Way Crossover Bioequivalency Study of Buprenorphine HCl (Sublingual) 8 mg Tablets With a Naltrexone Block Under Fasting Conditions
Status: Enrolling
Updated:  1/19/2018
517
mi
from
Austin, TX
Bioequivalency Study of Buprenorphine Hydrochloride 8 mg Tablet Under Fasted Conditions
A Single Dose, Two-Period, Two-Treatment, Two-Way Crossover Bioequivalency Study of Buprenorphine HCl (Sublingual) 8 mg Tablets With a Naltrexone Block Under Fasting Conditions
Status: Enrolling
Updated: 1/19/2018
CEDRA Clinical Research, LLC
517
mi
from
Austin, TX
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Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated:  1/23/2018
1166
mi
from
Los Angeles, CA
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated: 1/23/2018
University of Southern California
1166
mi
from
Los Angeles, CA
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Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated:  1/23/2018
1121
mi
from
Rochester, NY
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated: 1/23/2018
University of Rochester
1121
mi
from
Rochester, NY
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Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated:  1/23/2018
973
mi
from
Pittsburgh, PA
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated: 1/23/2018
University of Pittsburgh
973
mi
from
Pittsburgh, PA
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Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated:  1/23/2018
AMC
4686
mi
from
Amsterdam,
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium
Status: Enrolling
Updated: 1/23/2018
AMC
4686
mi
from
Amsterdam,
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Safety of Lactobacillus Reuteri (L. Reuteri) in Healthy Adults
Phase I Safety and Tolerance of Lactobacillus Reuteri in Adults
Status: Enrolling
Updated:  1/23/2018
563
mi
from
Houston, TX
Safety of Lactobacillus Reuteri (L. Reuteri) in Healthy Adults
Phase I Safety and Tolerance of Lactobacillus Reuteri in Adults
Status: Enrolling
Updated: 1/23/2018
University of Texas Health Science Center at Houston
563
mi
from
Houston, TX
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Comparison of Bowel Ultrasound & MR Enterography in the Follow-up of Previously Diagnosed Pediatric Small Bowel Crohn Disease
Comparison of Bowel Ultrasound & MR Enterography in the Follow-up of Previously Diagnosed Pediatric Sm. Bowel Crohn Disease.
Status: Enrolling
Updated:  1/23/2018
810
mi
from
Ann Arbor, MI
Comparison of Bowel Ultrasound & MR Enterography in the Follow-up of Previously Diagnosed Pediatric Small Bowel Crohn Disease
Comparison of Bowel Ultrasound & MR Enterography in the Follow-up of Previously Diagnosed Pediatric Sm. Bowel Crohn Disease.
Status: Enrolling
Updated: 1/23/2018
University of Michigan Hospital
810
mi
from
Ann Arbor, MI
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Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated:  1/24/2018
1223
mi
from
Philadelphia, PA
Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated: 1/24/2018
The Children's Hospital of Philadelphia, University of Pennsylvania
1223
mi
from
Philadelphia, PA
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Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated:  1/24/2018
569
mi
from
Houston, TX
Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated: 1/24/2018
Baylor College of Medicine
569
mi
from
Houston, TX
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Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated:  1/24/2018
572
mi
from
Houston, TX
Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated: 1/24/2018
Harris County Hospital District Outpatient Clinics
572
mi
from
Houston, TX
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Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated:  1/24/2018
572
mi
from
Houston, TX
Understanding Patient's Knowledge and Use of Acetaminophen
Understanding Patient's Knowledge and Use of Acetaminophen
Status: Enrolling
Updated: 1/24/2018
Kelsey Seybold
572
mi
from
Houston, TX
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An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
403
mi
from
Aurora, CO
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
403
mi
from
Aurora, CO
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An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1344
mi
from
New Haven, CT
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1344
mi
from
New Haven, CT
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1058
mi
from
Jacksonville, FL
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1058
mi
from
Jacksonville, FL
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An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1444
mi
from
Boston, MA
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1444
mi
from
Boston, MA
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
515
mi
from
Rochester, MN
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
515
mi
from
Rochester, MN
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
515
mi
from
Austin, TX
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
515
mi
from
Austin, TX
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An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1113
mi
from
Richmond, VA
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1113
mi
from
Richmond, VA
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
mi
from
Little Rock, AZ
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
mi
from
Little Rock, AZ
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
833
mi
from
Tucson, AZ
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
833
mi
from
Tucson, AZ
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1142
mi
from
La Jolla, CA
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1142
mi
from
La Jolla, CA
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
407
mi
from
Denver, CO
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
407
mi
from
Denver, CO
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
408
mi
from
Littleton, CO
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
408
mi
from
Littleton, CO
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1345
mi
from
Hamden, CT
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1345
mi
from
Hamden, CT
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1127
mi
from
Washington,
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1127
mi
from
Washington,
Click here to add this to my saved trials
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated:  1/25/2018
1133
mi
from
Port Orange, FL
An Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Crohn's Disease
A Randomised, Double-blind, Active Treatment Study to Induce Clinical Response and/or Remission With GSK1605786A in Subjects With Moderately-to-Severely Active Crohn's Disease
Status: Enrolling
Updated: 1/25/2018
GSK Investigational Site
1133
mi
from
Port Orange, FL
Click here to add this to my saved trials