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
8,177
archived clinical trials in
Orthopedic

Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated:  12/31/1969
University of Tennessee
1587
mi
from 91732
Memphis, TN
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated: 12/31/1969
University of Tennessee
1587
mi
from 91732
Memphis, TN
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Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated:  12/31/1969
Alberta Children's Hospital
1190
mi
from 91732
Calgary,
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated: 12/31/1969
Alberta Children's Hospital
1190
mi
from 91732
Calgary,
Click here to add this to my saved trials
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated:  12/31/1969
Washington University
1568
mi
from 91732
Saint Louis, MO
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated: 12/31/1969
Washington University
1568
mi
from 91732
Saint Louis, MO
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Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated:  12/31/1969
U.T. Southwestern Medical Center
1225
mi
from 91732
Dallas, TX
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
PITT0112: Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping
Status: Enrolling
Updated: 12/31/1969
U.T. Southwestern Medical Center
1225
mi
from 91732
Dallas, TX
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Infants With Spinal Muscular Atrophy Type I
A Pilot Study of the Natural History of Infants With Spinal Muscular Atrophy (SMA) Type 1
Status: Enrolling
Updated:  12/31/1969
National Institute of Neurological Disorders and Stroke (NINDS), 9000 Rockville
2277
mi
from 91732
Bethesda, MD
Infants With Spinal Muscular Atrophy Type I
A Pilot Study of the Natural History of Infants With Spinal Muscular Atrophy (SMA) Type 1
Status: Enrolling
Updated: 12/31/1969
National Institute of Neurological Disorders and Stroke (NINDS), 9000 Rockville
2277
mi
from 91732
Bethesda, MD
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Shriners Hospital for Children
363
mi
from 91732
Sacramento, CA
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Shriners Hospital for Children
363
mi
from 91732
Sacramento, CA
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Nemours Children's Hospital
2184
mi
from 91732
Orlando, FL
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Nemours Children's Hospital
2184
mi
from 91732
Orlando, FL
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Shriners Hospital for Children
1881
mi
from 91732
Lexington, KY
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Shriners Hospital for Children
1881
mi
from 91732
Lexington, KY
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Shriners Hospital for Children
826
mi
from 91732
Portland, OR
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Shriners Hospital for Children
826
mi
from 91732
Portland, OR
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Seattle Children's Hospital
964
mi
from 91732
Seattle, WA
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Seattle Children's Hospital
964
mi
from 91732
Seattle, WA
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Washington University School of Medicine
1569
mi
from 91732
Saint Louis, MO
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Washington University School of Medicine
1569
mi
from 91732
Saint Louis, MO
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Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated:  12/31/1969
Shriners Hospital For Children
1561
mi
from 91732
Saint Louis, MO
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trial
Duration of Brace Wear in Clubfoot Treatment - A Prospective Randomized Trail
Status: Enrolling
Updated: 12/31/1969
Shriners Hospital For Children
1561
mi
from 91732
Saint Louis, MO
Click here to add this to my saved trials
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated:  12/31/1969
St. Joseph's Hospital and Medical Center
342
mi
from 91732
Phoenix, AZ
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated: 12/31/1969
St. Joseph's Hospital and Medical Center
342
mi
from 91732
Phoenix, AZ
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Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated:  12/31/1969
Community Orthopedic Medical Group
36
mi
from 91732
Mission Viejo, CA
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated: 12/31/1969
Community Orthopedic Medical Group
36
mi
from 91732
Mission Viejo, CA
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Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated:  12/31/1969
Goodman Campbell Brian and Spine
1793
mi
from 91732
Indianapolis, IN
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated: 12/31/1969
Goodman Campbell Brian and Spine
1793
mi
from 91732
Indianapolis, IN
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Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated:  12/31/1969
Buffalo Spine Surgery
2191
mi
from 91732
Lockport, NY
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated: 12/31/1969
Buffalo Spine Surgery
2191
mi
from 91732
Lockport, NY
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Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated:  12/31/1969
Pacific Spine Specialists
820
mi
from 91732
Tualatin, OR
Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis
A Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
Status: Enrolling
Updated: 12/31/1969
Pacific Spine Specialists
820
mi
from 91732
Tualatin, OR
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Yale-New Haven Hospital
2486
mi
from 91732
New Haven, CT
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Yale-New Haven Hospital
2486
mi
from 91732
New Haven, CT
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Tampa General Hospital
2136
mi
from 91732
Tampa, FL
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Tampa General Hospital
2136
mi
from 91732
Tampa, FL
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Piedmont Heart Institute
1918
mi
from 91732
Atlanta, GA
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Piedmont Heart Institute
1918
mi
from 91732
Atlanta, GA
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
University of Chicago Medical Center
1730
mi
from 91732
Chicago, IL
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
University of Chicago Medical Center
1730
mi
from 91732
Chicago, IL
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Advocate Christ Medical Center
1721
mi
from 91732
Oak Lawn, IL
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Advocate Christ Medical Center
1721
mi
from 91732
Oak Lawn, IL
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
St.Vincent's Hospital and Health Services
1793
mi
from 91732
Indianapolis, IN
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
St.Vincent's Hospital and Health Services
1793
mi
from 91732
Indianapolis, IN
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
University of Iowa Hospital
1528
mi
from 91732
Iowa City, IA
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospital
1528
mi
from 91732
Iowa City, IA
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Henry Ford Hospital
1965
mi
from 91732
Detroit, MI
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Henry Ford Hospital
1965
mi
from 91732
Detroit, MI
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Abbott Northwestern
1509
mi
from 91732
Minneapolis, MN
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Abbott Northwestern
1509
mi
from 91732
Minneapolis, MN
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Univ of North Carolina
2194
mi
from 91732
Chapel Hill, NC
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Univ of North Carolina
2194
mi
from 91732
Chapel Hill, NC
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Baylor Medical Ctr
1224
mi
from 91732
Dallas, TX
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Baylor Medical Ctr
1224
mi
from 91732
Dallas, TX
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Intermountain Medical Center
565
mi
from 91732
Murray, UT
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Intermountain Medical Center
565
mi
from 91732
Murray, UT
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Virginia Commonwealth University
2269
mi
from 91732
Richmond, VA
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Virginia Commonwealth University
2269
mi
from 91732
Richmond, VA
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Sacred Heart Medical Center
938
mi
from 91732
Spokane, WA
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Sacred Heart Medical Center
938
mi
from 91732
Spokane, WA
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Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated:  12/31/1969
Washington University/ Barnes-Jewish Hospital
1568
mi
from 91732
Saint Louis, MO
Driveline Silicone Skin Interface Registry
Driveline Silicone Skin Interface (SSI) Registry
Status: Enrolling
Updated: 12/31/1969
Washington University/ Barnes-Jewish Hospital
1568
mi
from 91732
Saint Louis, MO
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Validating a New Writer s Cramp Scale
Validating a New Writer's Cramp Scale
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
2277
mi
from 91732
Bethesda, MD
Validating a New Writer s Cramp Scale
Validating a New Writer's Cramp Scale
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
2277
mi
from 91732
Bethesda, MD
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Sun Valley Arthritis Center, Ltd
333
mi
from 91732
Peoria, AZ
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Sun Valley Arthritis Center, Ltd
333
mi
from 91732
Peoria, AZ
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
UCSD - Thornton Hospital
95
mi
from 91732
La Jolla, CA
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
UCSD - Thornton Hospital
95
mi
from 91732
La Jolla, CA
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Tampa Medical Group, PA
2132
mi
from 91732
Tampa, FL
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Tampa Medical Group, PA
2132
mi
from 91732
Tampa, FL
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Saint Paul Rheumatology
1512
mi
from 91732
Eagan, MN
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Saint Paul Rheumatology
1512
mi
from 91732
Eagan, MN
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
STAT Research, Inc.
1894
mi
from 91732
Dayton, OH
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
STAT Research, Inc.
1894
mi
from 91732
Dayton, OH
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Ramesh C. Gupta, M.D.
1586
mi
from 91732
Memphis, TN
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Ramesh C. Gupta, M.D.
1586
mi
from 91732
Memphis, TN
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
University of Utah
572
mi
from 91732
Salt Lake City, UT
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
University of Utah
572
mi
from 91732
Salt Lake City, UT
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Desert Medical Advances
96
mi
from 91732
Palm Desert, CA
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Desert Medical Advances
96
mi
from 91732
Palm Desert, CA
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
University of California at San Francisco
356
mi
from 91732
San Francisco, CA
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
University of California at San Francisco
356
mi
from 91732
San Francisco, CA
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Advent Clinical Research
2125
mi
from 91732
Pinellas Park, FL
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Advent Clinical Research
2125
mi
from 91732
Pinellas Park, FL
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Alastair Kennedy, MD Research
2261
mi
from 91732
Vero Beach, FL
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Alastair Kennedy, MD Research
2261
mi
from 91732
Vero Beach, FL
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Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Northwestern Center for Clinical Research
1728
mi
from 91732
Chicago, IL
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Northwestern Center for Clinical Research
1728
mi
from 91732
Chicago, IL
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Klein & Associates MD, PA.
2241
mi
from 91732
Hagerstown, MD
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Klein & Associates MD, PA.
2241
mi
from 91732
Hagerstown, MD
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Clinical Pharmacology Study Group
2540
mi
from 91732
Worcester, MA
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Clinical Pharmacology Study Group
2540
mi
from 91732
Worcester, MA
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
MetroHealth Medical Systems
2032
mi
from 91732
Cleveland, OH
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
MetroHealth Medical Systems
2032
mi
from 91732
Cleveland, OH
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
Altoona Center for Clinical Research
2201
mi
from 91732
Duncansville, PA
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
Altoona Center for Clinical Research
2201
mi
from 91732
Duncansville, PA
Click here to add this to my saved trials
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated:  12/31/1969
The Arthritis Clinic
1653
mi
from 91732
Jackson, TN
Study of Apremilast to Treat Subjects With Active Ankylosing Spondylitis
A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF APREMILAST (CC-10004) IN THE TREATMENT OF ACTIVE ANKYLOSING SPONDYLITIS
Status: Enrolling
Updated: 12/31/1969
The Arthritis Clinic
1653
mi
from 91732
Jackson, TN
Click here to add this to my saved trials