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

Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Hurst, TX
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Texas Familicare Clinical Research
mi
from
Hurst, TX
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Longview, TX
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
DCOL Center for Clinical Research
mi
from
Longview, TX
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Richardson, TX
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Bexar Clinical Trials, LLC
mi
from
Richardson, TX
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Ogden, UT
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Advance Research Institute
mi
from
Ogden, UT
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Salt Lake City, UT
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Highland Clinical Research
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Salt Lake City, UT
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
University of Utah
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Christianburg, VA
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
New River Valley Research Institute
mi
from
Christianburg, VA
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Portsmouth, VA
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Hampton Roads Institute for Performance and Sports Medicine (HIPS)
mi
from
Portsmouth, VA
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Richmond, VA
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
McGuire Research Institute
mi
from
Richmond, VA
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Bellevue, WA
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Northwest Gastroenterology Associates
mi
from
Bellevue, WA
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Spokane, WA
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Daniel R. Coulston
mi
from
Spokane, WA
Click here to add this to my saved trials
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated:  11/2/2015
mi
from
Edmonton,
Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone
A Multi-center, Randomized, Double-Blinded Study of the Efficacy and Safety of Lubiprostone in Patients With Opioid-induced Bowel Dysfunction (OBD)
Status: Enrolling
Updated: 11/2/2015
Hermitage Medicentre
mi
from
Edmonton,
Click here to add this to my saved trials
Transcutaneous Electroacupuncture for Gastroparesis
Transcutaneous Electroacupuncture for Gastroparesis
Status: Enrolling
Updated:  11/3/2015
mi
from
Jackson, MS
Transcutaneous Electroacupuncture for Gastroparesis
Transcutaneous Electroacupuncture for Gastroparesis
Status: Enrolling
Updated: 11/3/2015
University of Mississippi
mi
from
Jackson, MS
Click here to add this to my saved trials
Transcutaneous Electroacupuncture for Gastroparesis
Transcutaneous Electroacupuncture for Gastroparesis
Status: Enrolling
Updated:  11/3/2015
mi
from
El Paso, TX
Transcutaneous Electroacupuncture for Gastroparesis
Transcutaneous Electroacupuncture for Gastroparesis
Status: Enrolling
Updated: 11/3/2015
Texas tech university health science center
mi
from
El Paso, TX
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Phoenix, AZ
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Phoenix Children's Hospital
mi
from
Phoenix, AZ
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Orange, CA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children's Hospital of Orange County
mi
from
Orange, CA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
San Diego, CA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
UCSD/Rady Childrens Hospital
mi
from
San Diego, CA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Aurora, CO
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children'S Hospital
mi
from
Aurora, CO
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Atlanta, GA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children's Center for Digestive Healthcare
mi
from
Atlanta, GA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Chicago, IL
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Northwestern Scool of Medicine
mi
from
Chicago, IL
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Park Ridge, IL
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Center for Children's Digestive Health
mi
from
Park Ridge, IL
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Indianapolis, IN
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Riley Hospital for Children
mi
from
Indianapolis, IN
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Indianapolis, IN
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Indiana University Health - University Hospital
mi
from
Indianapolis, IN
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Iowa City, IA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Boston, MA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Tufts Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Chapel Hill, NC
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Cincinnati, OH
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
The Cincinnati Center for Eosinophilic Disorders
mi
from
Cincinnati, OH
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Mentor, OH
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Great Lakes Gastroenterology
mi
from
Mentor, OH
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Philadelphia, PA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Univ of Pennsylvania
mi
from
Philadelphia, PA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Providence, RI
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Rhode Island Hospital
mi
from
Providence, RI
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Greenville, SC
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children's Center for Digestive Health
mi
from
Greenville, SC
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Nashville, TN
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Salt Lake City, UT
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
University of Utah Healthcare
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Roanoke, VA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Carilion Pediatric Gastroenterology
mi
from
Roanoke, VA
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OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Chicago, IL
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children's Memorial Hospital
mi
from
Chicago, IL
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OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Boston, MA
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
Children's Hospital Boston
mi
from
Boston, MA
Click here to add this to my saved trials
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated:  11/3/2015
mi
from
Rochester, MN
OBS in Adolescent and Adults With EOE: A Phase II, Randomized, Double-Blind, Placebo Controlled, Study With an Open Label Extension
Oral Budesonide Suspension (OBS) in Adolescent and Adult Subjects (11-40 Years of Age)With Eosinophilic Esophagitis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study With an Open Label Extension
Status: Enrolling
Updated: 11/3/2015
The Mayo Clinic
mi
from
Rochester, MN
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Glycerin Suppositories to Reduce Jaundice in Premature Infants
The Use of Glycerin Suppositories to Reduce Hyperbilirubinemia in Premature Infants Requiring Phototherapy
Status: Enrolling
Updated:  11/4/2015
mi
from
Rochester, NY
Glycerin Suppositories to Reduce Jaundice in Premature Infants
The Use of Glycerin Suppositories to Reduce Hyperbilirubinemia in Premature Infants Requiring Phototherapy
Status: Enrolling
Updated: 11/4/2015
University of Rochester Medical Center NICU
mi
from
Rochester, NY
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A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Scottsdale, AZ
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Mayo Clinic Arizona
mi
from
Scottsdale, AZ
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A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
La Jolla, CA
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Clinical and Translational Research Institute
mi
from
La Jolla, CA
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A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
La Jolla, CA
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Perlman Medical Offices
mi
from
La Jolla, CA
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
La Jolla, CA
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Thornton Hospital
mi
from
La Jolla, CA
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Orange, CA
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Community Clinical Trials
mi
from
Orange, CA
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Orange, CA
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
GastroDiagnostics - Community Clinical Trials Drug
mi
from
Orange, CA
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
LaFayette, CO
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Clinical Research of the Rockies
mi
from
LaFayette, CO
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Guilford, CT
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Endoscopy Center of Connecticut, LLC
mi
from
Guilford, CT
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Hamden, CT
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Endoscopy Center of Connecticut, LLC
mi
from
Hamden, CT
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Hamden, CT
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Gastroenterology Center of Connecticut
mi
from
Hamden, CT
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Hamden, CT
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Medical Research Center of CT Drug
mi
from
Hamden, CT
Click here to add this to my saved trials
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated:  11/5/2015
mi
from
Hamden, CT
A Study Of PF-00547659 In Patients With Moderate To Severe Ulcerative Colitis
A Double-blind, Randomized, Placebo-controlled, Parallel, Dose-ranging Study To Evaluate The Efficacy And Safety Of Pf-00547659 In Subjects With Moderate To Severe Ulcerative Colitis (Turandot)
Status: Enrolling
Updated: 11/5/2015
Medical Research Network of Connecticut
mi
from
Hamden, CT
Click here to add this to my saved trials