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We've found
184,457
clinical trials

Dermatology / Plastic Surgery, Otolaryngology Clinical Trial
Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Prurigo Nodularis
Status: Enrolling, Phase III
Updated: 12/31/1969
Study Site 16017
mi
from
Philadelphia, PA
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Fox Valley Clinical Research Center, LLC
mi
from
Aurora, IL
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Grace Research, LLC
mi
from
Bossier City, LA
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Phillips Medical Services, Pllc
mi
from
Jackson, MS
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Research Integrity, Llc
mi
from
Owensboro, KY
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Chronic Heart Failure With Preserved Ejection Fraction Clinical Trial
Patient-reported Outcomes in Vericiguat-treated Patients With HFpEF
Status: Enrolling, Phase II
Updated: 12/31/1969
Clinical Advancement Center, PLLC
mi
from
San Antonio, TX
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Immunology / Infectious Diseases Clinical Trial
Microbial Restoration for Individuals With One or More Recurrences of Clostridium Difficile Associated Disease (CDAD)
Status: Enrolling, Phase I, II
Updated: 12/31/1969
Emory Vaccine Center - The Hope Clinic
mi
from
Decatur, GA
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Musculoskeletal, Neurology, Orthopedics / Podiatry Clinical Trial
Neurophysiology of Weakness and Exercise in Rotator Cuff Tendinopathy
Status: Enrolling
Updated: 12/31/1969
University of Oregon
mi
from
Eugene, OR
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Oncology Clinical Trial
A Phase 2 Study of NIR178 in Combination With PDR001 in Patients With Solid Tumors and Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 12/31/1969
Novartis
mi
from
Baltimore, MD
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Oncology Clinical Trial
A Phase 2 Study of NIR178 in Combination With PDR001 in Patients With Solid Tumors and Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Columbus, OH
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Cardiology / Vascular Diseases Clinical Trial
International BPA Registry
Status: Enrolling, Phase
Updated: 12/31/1969
The University of California, San Diego
mi
from
La Jolla, CA
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Hematology, Oncology Clinical Trial
DEPLETHINK - LymphoDEPLEtion and THerapeutic Immunotherapy With NKR-2
Status: Enrolling, Phase I
Updated: 12/31/1969
New York School of Medicine
mi
from
New York, NY
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Sedentary Lifestyle Clinical Trial
Sedentary Behavior Interrupted Randomized Controlled Trial (P2)
Status: Enrolling
Updated: 12/31/1969
UC San Diego
mi
from
La Jolla, CA
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PTSD Clinical Trial
A 40-week Study to Evaluate TNX-102 SL 5.6 mg Taken Daily at Bedtime in Patients With PTSD
Status: Enrolling, Phase III
Updated: 12/31/1969
Investigational Site - Atlanta
mi
from
Atlanta, GA
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PTSD Clinical Trial
A 40-week Study to Evaluate TNX-102 SL 5.6 mg Taken Daily at Bedtime in Patients With PTSD
Status: Enrolling, Phase III
Updated: 12/31/1969
Investigator Site - Little Rock
mi
from
Little Rock, AR
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Atopic Dermatitis Clinical Trial
Phase 2B Study to Evaluate ASN002 in Subjects With Moderate to Severe Atopic Dermatitis (RADIANT)
Status: Enrolling, Phase II
Updated: 12/31/1969
Center for Dermatology Clinical Research
mi
from
Fremont, CA
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Atopic Dermatitis Clinical Trial
Phase 2B Study to Evaluate ASN002 in Subjects With Moderate to Severe Atopic Dermatitis (RADIANT)
Status: Enrolling, Phase II
Updated: 12/31/1969
Dermatology Specialists Research
mi
from
Louisville, KY
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RHEUMATOID ARTHRITIS Clinical Trial
Measurement of the Structural Efficacy in Active RA Patients Treated With Sarilumab in Combination With MTX and Naive to Biologics
Status: Enrolling, Phase III
Updated: 12/31/1969
AARDS Research, Inc
mi
from
Aventura, FL
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Multiple Myeloma Clinical Trial
A Study of JNJ-68284528, a Chimeric Antigen Receptor T Cell (CAR-T) Therapy Directed Against B-Cell Maturation Antigen (BCMA) in Participants With Relapsed or Refractory Multiple Myeloma
Status: Enrolling, Phase I, II
Updated: 12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
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Clinical Trial
A Study to Evaluate Efficacy and Safety of AG-348 in Not Regularly Transfused Adult Participants With Pyruvate Kinase Deficiency (PKD)
Status: Enrolling, Phase III
Updated: 12/31/1969
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
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Clinical Trial
A Study to Evaluate Efficacy and Safety of AG-348 in Not Regularly Transfused Adult Participants With Pyruvate Kinase Deficiency (PKD)
Status: Enrolling, Phase III
Updated: 12/31/1969
Wayne State University School of Medicine - Children's Hospital of Michigan
mi
from
Detroit, MI
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Lehigh Center for Clinical Research
mi
from
Allentown, PA
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Neurology Center of North Orange County
mi
from
Fullerton, CA
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Maxblue Institute
mi
from
Hialeah, FL
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Axis Clinical Trials
mi
from
Los Angeles, CA
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Bio Behavioral Health
mi
from
Toms River, NJ
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Neurology Clinical Trial
A Trial to Evaluate the Safety, Efficacy, and Tolerability of Brexpiprazole in Treating Agitation Associated With Dementia of the Alzheimer's Type
Status: Enrolling, Phase III
Updated: 12/31/1969
Territory Neurology & Research Institute
mi
from
Tucson, AZ
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ALS Clinical Trial
Genomic Translation for Amyotrophic Lateral Sclerosis Care
Status: Enrolling, Phase
Updated: 12/31/1969
University of Utah
mi
from
Salt Lake City, UT
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ALS Clinical Trial
Genomic Translation for Amyotrophic Lateral Sclerosis Care
Status: Enrolling, Phase
Updated: 12/31/1969
Oregon Health and Sciences University
mi
from
Portland, OR
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Shoulder Arthritis Clinical Trial
Reverse Shoulder Replacement: Age 60 or Younger Outcomes
Status: Enrolling, Phase
Updated: 12/31/1969
Washington University School of Medicine
mi
from
Saint Louis, MO
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Carcinoma, Hepatocellular Clinical Trial
Regorafenib Plus Pembrolizumab in First Line Systemic Treatment of HCC
Status: Enrolling, Phase I
Updated: 12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
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Hepatocellular Carcinoma (HCC) Clinical Trial
Study of BGB-A317 in Patients With Previously Treated Unresectable HCC
Status: Enrolling, Phase II
Updated: 12/31/1969
Rutgers New Jersey Medical School
mi
from
Newark, NJ
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Oncology Clinical Trial
Efficacy and Safety Study of Tisotumab Vedotin for Patients With Solid Tumors
Status: Enrolling, Phase II
Updated: 12/31/1969
Shands Cancer Center / University of Florida
mi
from
Gainesville, FL
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Multiple Myeloma Clinical Trial
Up-front CART-BCMA With or Without huCART19 in High-risk Multiple Myeloma
Status: Enrolling, Phase I
Updated: 12/31/1969
Univ of Pennsylvania
mi
from
Philadelphia, PA
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Autism Spectrum Disorder Clinical Trial
Fatty Acid Supplementation in Children With ASD
Status: Enrolling, Phase II
Updated: 12/31/1969
Nationwide Children's Hospital
mi
from
Columbus, OH
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
University of Texas Medical Branch
mi
from
Galveston, TX
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
Advanced Research Center, Inc.
mi
from
Anaheim, CA
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
Marshall Health
mi
from
Huntington, WV
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
Acevedo Clinical Research Associates
mi
from
Miami, FL
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
Center for Clinical Trials, LLC.
mi
from
Paramount, CA
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Pneumococcal Infections Clinical Trial
Study to Evaluate the Safety and Immunogenicity of a Multivalent Pneumococcal Vaccine Given With Prevnar 13 in Healthy Infants
Status: Enrolling, Phase II
Updated: 12/31/1969
Sanford Children's Specialty Clinic
mi
from
Sioux Falls, SD
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
University of Chicago
mi
from
Chicago, IL
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
University of Miami Miller School of Medicine
mi
from
Miami, FL
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
Northwestern Medical Faculty Foundation
mi
from
Chicago, IL
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
Kentuckiana Pulmonary Associates
mi
from
Louisville, KY
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
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Pulmonary Hypertension Clinical Trial
Extended Access Program to Assess Long-term Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension RANGER
Status: Enrolling, Phase III
Updated: 12/31/1969
University of Rochester - University of Rochester Medical Center
mi
from
Rochester, NY
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Oncology Clinical Trial
Self-Management Program and Survivorship Care Plan in Improving the Health of Cancer Survivors After Stem Cell Transplant
Status: Enrolling
Updated: 12/31/1969
UNC Lineberger Comprehensive Cancer Center
mi
from
Chapel Hill, NC
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Oncology Clinical Trial
Self-Management Program and Survivorship Care Plan in Improving the Health of Cancer Survivors After Stem Cell Transplant
Status: Enrolling
Updated: 12/31/1969
Wayne State University/Karmanos Cancer Institute
mi
from
Detroit, MI
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Oncology Clinical Trial
Self-Management Program and Survivorship Care Plan in Improving the Health of Cancer Survivors After Stem Cell Transplant
Status: Enrolling
Updated: 12/31/1969
University of Kansas Cancer Center
mi
from
Kansas City, KS
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Oncology Clinical Trial
Self-Management Program and Survivorship Care Plan in Improving the Health of Cancer Survivors After Stem Cell Transplant
Status: Enrolling
Updated: 12/31/1969
University of Pennsylvania:Abramson Cancer Center
mi
from
Philadelphia, PA
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Musculoskeletal, Rheumatology Clinical Trial
Biologic Mechanisms for Pain Variation After Physical Activity in Osteoarthritis
Status: Enrolling
Updated: 12/31/1969
University of Maryland, Baltimore
mi
from
Baltimore, MD
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ALK-positive Advanced NSCLC Clinical Trial
A Study of Brigatinib in Participants With Anaplastic Lymphoma Kinase-Positive (ALK+), Advanced Non-Small-Cell Lung Cancer (NSCLC) Progressed on Alectinib or Ceritinib
Status: Enrolling, Phase II
Updated: 12/31/1969
University of Utah Medical Center
mi
from
Salt Lake City, UT
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Rotator Cuff Tear Clinical Trial
LifeNet: Extracellular Matrix Graft in Rotator Cuff Repair
Status: Enrolling, Phase IV
Updated: 12/31/1969
Cleveland Clinic Florida
mi
from
Weston, FL
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Cardiology / Vascular Diseases, Oncology Clinical Trial
Sulfur Colloid SPECT/CT in Measuring Liver Function in Patients With Primary or Metastatic Liver Cancer Undergoing Radiation Therapy or Surgery
Status: Enrolling
Updated: 12/31/1969
Fred Hutch/University of Washington Cancer Consortium
mi
from
Seattle, WA
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Endocrinology, Reproductive Clinical Trial
Medical Optimization of Management of Type 2 Diabetes Complicating Pregnancy (MOMPOD)
Status: Enrolling, Phase III
Updated: 12/31/1969
University of California, San Diego
mi
from
San Diego, CA
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Neurology, Orthopedics / Podiatry Clinical Trial
Can Prophylactic Foraminotomy Prevent C5 Palsy
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic Foundation
mi
from
Cleveland, OH
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HIV-1/HBV Co-Infection Clinical Trial
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment Naive, HIV-1 and Hepatitis B Co-Infected Adults
Status: Enrolling, Phase III
Updated: 12/31/1969
North Texas Infectious Diseases Consultants, PA
mi
from
Dallas, TX
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HIV-1/HBV Co-Infection Clinical Trial
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment Naive, HIV-1 and Hepatitis B Co-Infected Adults
Status: Enrolling, Phase III
Updated: 12/31/1969
Henry Ford Health System
mi
from
Detroit, MI
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HIV-1/HBV Co-Infection Clinical Trial
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment Naive, HIV-1 and Hepatitis B Co-Infected Adults
Status: Enrolling, Phase III
Updated: 12/31/1969
Spectrum Medical Group
mi
from
Phoenix, AZ
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HIV-1/HBV Co-Infection Clinical Trial
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment Naive, HIV-1 and Hepatitis B Co-Infected Adults
Status: Enrolling, Phase III
Updated: 12/31/1969
Southampton Healthcare, Inc.
mi
from
Saint Louis, MO
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Borland-Groover Clinic
mi
from
Jacksonville, FL
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Cotton-O'Neil Clinical Research Center
mi
from
Topeka, KS
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Chase Medical Research, LLC
mi
from
Waterbury, CT
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Gastroenterology Associates of Fairfield County
mi
from
Bridgeport, CT
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
GW Research Inc,
mi
from
Chula Vista, CA
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Gastro One
mi
from
Germantown, TN
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Loyola University Medical Center
mi
from
Maywood, IL
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Facey Medical Foundation
mi
from
Mission Hills, CA
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Manhattan Medical Research Practice PLLC
mi
from
New York, NY
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Advanced Research Institute
mi
from
Ogden, UT
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Elite Clinical Studies
mi
from
Phoenix, AZ
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
A Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Texas Digestive Disease Consultants
mi
from
Southlake, TX
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Oncology Clinical Trial
A Study of Therapeutic Iobenguane (131-I) for Relapsed, High-Risk Neuroblastoma Subjects
Status: Enrolling, Phase II
Updated: 12/31/1969
Seattle Children's Hospital
mi
from
Seattle, WA
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Primary Sclerosing Cholangitis Clinical Trial
Sulfasalazine for the Treatment of Primary Sclerosing Cholangitis
Status: Enrolling, Phase II
Updated: 12/31/1969
University of California Davis
mi
from
Davis, CA
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
AppleMed Research Inc.
mi
from
Miami, FL
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
MetroHealth Med Ctr
mi
from
Cleveland, OH
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Remington Davis Inc.
mi
from
Columbus, OH
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Dayton Gastroenterology, Inc.
mi
from
Dayton, OH
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Texas Tech University Health Sciences Center
mi
from
El Paso, TX
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Prestige Clinical Research
mi
from
Franklin, OH
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Holland Center for Family Health
mi
from
Peoria, AZ
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Research Protocol Management Specialists
mi
from
Pittsburgh, PA
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Gastroesophageal Reflux Disease (GERD) Clinical Trial
Trial of IW-3718 for 8 Weeks in Patients With Persistent Gastroesophageal Reflux Disease (GERD) Receiving Proton Pump Inhibitors
Status: Enrolling, Phase III
Updated: 12/31/1969
Kansas Medical Clinic, PA
mi
from
Topeka, KS
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Iron Deficiency Anemia Clinical Trial
Daily vs Alternate Day Iron Supplementation for Pregnant Women With Iron Deficiency Anemia
Status: Enrolling
Updated: 12/31/1969
Mount Sinai-West
mi
from
New York, NY
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Orthopedics / Podiatry Clinical Trial
Early Advanced Weight Bearing for Peri-articular Knee and Pilon Injuries
Status: Enrolling
Updated: 12/31/1969
University of Virginia
mi
from
Charlottesville, VA
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Triple Negative Breast Cancer Clinical Trial
Study of Adagloxad Simolenin (OBI-822) and OBI-821 Versus Placebo Treatment for High Risk Early Stage Triple Negative Breast Cancer Patients (TNBC) Following Neoadjuvant or Adjuvant Chemotherapy.
Status: Enrolling, Phase III
Updated: 12/31/1969
University of Texas Health Science Center at San Antonio
mi
from
San Antonio, TX
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Triple Negative Breast Cancer Clinical Trial
Study of Adagloxad Simolenin (OBI-822) and OBI-821 Versus Placebo Treatment for High Risk Early Stage Triple Negative Breast Cancer Patients (TNBC) Following Neoadjuvant or Adjuvant Chemotherapy.
Status: Enrolling, Phase III
Updated: 12/31/1969
Advanced Research Institute, Inc
mi
from
New Port Richey, FL
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Triple Negative Breast Cancer Clinical Trial
Study of Adagloxad Simolenin (OBI-822) and OBI-821 Versus Placebo Treatment for High Risk Early Stage Triple Negative Breast Cancer Patients (TNBC) Following Neoadjuvant or Adjuvant Chemotherapy.
Status: Enrolling, Phase III
Updated: 12/31/1969
Summit Cancer Care
mi
from
Savannah, GA
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Triple Negative Breast Cancer Clinical Trial
Study of Adagloxad Simolenin (OBI-822) and OBI-821 Versus Placebo Treatment for High Risk Early Stage Triple Negative Breast Cancer Patients (TNBC) Following Neoadjuvant or Adjuvant Chemotherapy.
Status: Enrolling, Phase III
Updated: 12/31/1969
Cotton-O'Neil Clinical Research Center, Hematology & Oncology
mi
from
Topeka, KS
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Gastroenterology, Other Clinical Trial
Comparing Speedlyte and IV Rehydration Treating Children With Gastroenteritis in a Pediatric Emergency Department (ED)
Status: Enrolling
Updated: 12/31/1969
Nicklaus Children's Hospital f/k/a Miami Children's Hospital
mi
from
Miami, FL
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Heart Failure Clinical Trial
Stimulation Of the Left Ventricular Endocardium for Cardiac Resynchronization Therapy in Non-Responders and Previously Untreatable Patients (SOLVE CRT)
Status: Enrolling, Phase III
Updated: 12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
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Heart Failure Clinical Trial
Stimulation Of the Left Ventricular Endocardium for Cardiac Resynchronization Therapy in Non-Responders and Previously Untreatable Patients (SOLVE CRT)
Status: Enrolling, Phase III
Updated: 12/31/1969
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Heart Failure Clinical Trial
Stimulation Of the Left Ventricular Endocardium for Cardiac Resynchronization Therapy in Non-Responders and Previously Untreatable Patients (SOLVE CRT)
Status: Enrolling, Phase III
Updated: 12/31/1969
The Heart Hospital Baylor Plano
mi
from
Plano, TX
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Heart Failure Clinical Trial
Stimulation Of the Left Ventricular Endocardium for Cardiac Resynchronization Therapy in Non-Responders and Previously Untreatable Patients (SOLVE CRT)
Status: Enrolling, Phase III
Updated: 12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
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Endocrinology, Oncology, Reproductive Clinical Trial
Copanlisib, Letrozole, and Palbociclib in Treating Patients With Hormone Receptor Positive HER2 Negative Stage I-IV Breast Cancer
Status: Enrolling, Phase I, II
Updated: 12/31/1969
UCLA Jonsson Comprehensive Cancer Center
mi
from
Los Angeles, CA
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Anxiety Clinical Trial
Attention Training to Modify Error-related Negativity and Risk for Anxiety in Adolescence
Status: Enrolling
Updated: 12/31/1969
Florida State University
mi
from
Tallahassee, FL
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