Search clinical trials for: genetic: CXCR3 polymorphism rs2280964

Total 17884 results

University Women's Hospital Tübingen

Unknown

Clinical Value of Molecular Genetic Analyzes in Gynecological Malignomas (MAGynMA)

Gynecologic Cancer

Germany
Assiut University

Unknown

Clinical Characteristic and MEFV Gene Mutations in Patient With Juvenile Onest Systemic Lupus Erythematosus

SLE (Systemic Lupus)
UNC Lineberger Comprehensive Cancer Center

Completed

Development of a Tumor Molecular Analyses Program and Its Use to Support Treatment Decisions

Neoplasm

United States
University Hospital, Strasbourg, France

Completed

Virulence of Staphylococcus Lugdunensis in Severe Infections (VISLISI)

Bacteremia | Endocarditis | Staphylococcus Lugdunensis | Virulence Factors

France
Weill Medical College of Cornell University
National Heart, Lung, and Blood Institute (NHLBI)

Terminated

Alternate Nicotine Delivery Systems and Airway Epithelial Biology

Smoking | Smoking Cessation

United States
Applied Genetic Technologies Corp

Active, not recruiting

Safety and Efficacy Trial of AAV Gene Therapy in Patients With CNGA3 Achromatopsia (A Clarity Clinical Trial)

Achromatopsia

United States, Israel
Myriad Genetic Laboratories, Inc.

Terminated

Long-term Study to Evaluate and Clinical Outcomes in Patients With Favorable Intermediate Risk Localized Prostate Cancer

Prostate Cancer

United States
Myriad Genetic Laboratories, Inc.

Terminated

EndoPredict® Extended Endocrine Trial (EXET)

Primary Invasive Breast Cancer

United States
Esoterix Genetic Laboratories, LLC

Unknown

Validation of Saliva in the Esoterix Genetic Laboratories Fragile X Assay

Fragile X Syndrome

United States
Esoterix Genetic Laboratories, LLC

Unknown

Preterm Delivery Risk Prediction by Measurement of Prenatal Serum Screening Markers

Preterm Delivery

United States
National Institute of Cancerología

Recruiting

Validation of the Genetic Signature 354849 as a Prognostic Method

Cervix Cancer

Mexico
Nationwide Children's Hospital
Parent Project Muscular Dystrophy

Recruiting

Characterization of Clinical Skeletal and Cardiac Impairment in Carriers of DMD and BMD

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
Samsung Medical Center

Recruiting

Personalized Sequence for Thoracic, Esophageal, and H&N Cancer

Lung Cancer

Korea, Republic of
CENTOGENE GmbH Rostock

Active, not recruiting

Epidemiological Study in FRONtoTemporal Dementia (EFRONT)

Frontotemporal Dementia

Italy, Spain, Belgium, Turkey, Portugal, Germany, Greece
Mayo Clinic

Completed

Comprehensive Genetic Assessment, Risk and Education in a Mammography Pilot

Women Age 35+ Qualifies if >15% Lifetime Risk of Breast Cancer as Defined by IBIS Version 8

United States
University of Chicago

Completed

Parkinson's Disease in African American and Caucasian Patients

Parkinson Disease

United States
Fudan University

Completed

Health-promoting Lifestyle in a Genetic Counseling Clinic

Breast Cancer | Genetic Testing

China
Erasmus Medical Center

Completed

Young Pectus Excavatum Patients and Genetic Defects

Genetic Disease | Children, Adult | Pectus Excavatum

Netherlands
Hospitales Universitarios Virgen del Rocío

Completed

Genetic Profile in Patients With Aortic Syndrome (GEN-AOR)

Acute Aortic Syndrome | Gene Abnormality

Spain
Mayo Clinic
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Completed

Dent Disease Mutation Genotyping

Dent Disease

United States
University of Pennsylvania
Lancaster General Hospital; The Familial Hypercholesterolemia Foundation

Completed

IN-TANDEM Familial Hypercholesterolemia Pilot Study

Familial Hypercholesterolemia

United States
Hospices Civils de Lyon

Unknown

Dependence Receptors and Leukemia

Acute Lymphoblastic Leukemia | Acute Leukemia

France
Centre Hospitalier Universitaire de Nice

Completed

Study of the Involvement of 15q11 - q13 Chromosome Region and CYFIP1 Gene in Autism. Attempt a Genotype-phenotype Correlation

Autistic Disorder

France
Mayo Clinic
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Oxalosis...

Completed

Primary Hyperoxaluria Mutation Genotyping

Primary Hyperoxaluria

United States
Igenomix

Unknown

Somatic Stem Cells in Endometriosis

Endometriosis

Spain
Rabin Medical Center
Charite University, Berlin, Germany; National Institute on Aging (NIA)

Unknown

Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases (NGS)

Neurological Diseases

Israel
Hillel Yaffe Medical Center
Technion, Israel Institute of Technology

Unknown

Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases

Retinitis Pigmentosa
National Center for Research Resources (NCRR)
Medical University of South Carolina

Completed

Genetic Study of Sitosterolemia

Lipid Metabolism, Inborn Errors | Sitosterolemia

United States
University of North Carolina, Chapel Hill
The Hospital for Sick Children; Washington University School of Medicine; McGill... and other collaborators

Recruiting

Defining the Genetic Etiology of Suppurative Lung Disease in Children and Adults

Primary Ciliary Dyskinesia | Kartagener Syndrome | Primary Immune Deficiency

United States, Canada
University of Florida

Completed

Pharmacotoxicology of Trichloroethylene Metabolites

Congenital Lactic Acidosis

United States
Myriad Genetic Laboratories, Inc.

Recruiting

Long-Term Prospective Registry in Prostate Cancer Patients From Diverse Urology Practice Settings Following Prolaris® Testing

Prostate Cancer

United States
Myriad Genetic Laboratories, Inc.

Terminated

Study Comparing Optimized 5-FU Dosing and Standard Dosing in Metastatic Colorectal Cancer Patients Treated With mFOLFOX6 (PROFUSE)

Colorectal Cancer, Metastatic

United States
Applied Genetic Technologies Corp

Completed

Clinical Evaluation of Patients With X-linked Retinitis Pigmentosa (XLRP)

X-Linked Retinitis Pigmentosa

United States
Myriad Genetic Laboratories, Inc.

Completed

Clinical Outcomes in Men With Prostate Cancer Who Selected Active Surveillance Using Prolaris® Testing (URO-009Low)

Prostate Cancer

United States
Myriad Genetic Laboratories, Inc.

Terminated

Registry Measuring Impact of RNA Expression Testing on Treatment Decisions in Early Stage Lung Cancer and Assessing the Disease-free Survival With Long-term Follow-up (ONC006) (ONC006)

NSCLC | Lung Cancer | NSCLC Adenocarcinoma

United States
Myriad Genetic Laboratories, Inc.

Withdrawn

Endometriosis Biomarker Discovery Study (EMBARK)

Endometriosis | Chronic Pelvic Pain
Myriad Genetic Laboratories, Inc.

Completed

Open Registry Measuring Impact of Genomic Testing on Treatment Decision After Biopsy in Newly Diagnosed Prostate Cancer Patients (PROCEDE-2000)

Prostate Cancer

United States
Interleukin Genetics, Inc.
Duke University; Kaiser Permanente

Withdrawn

Dental Engagement Study Behavior Modification

PERIODONTAL DISEASE
Applied Genetic Technologies Corp

Completed

Safety and Efficacy of rAAV-hRS1 in Patients With X-linked Retinoschisis (XLRS)

X-linked Retinoschisis

United States
Myriad Genetic Laboratories, Inc.

Completed

Combined Breast Cancer Risk Study

Hereditary Cancer

United States
Myriad Genetic Laboratories, Inc.

Terminated

Registry Measuring the Impact of Adding RNA Expression Testing on Referral Decisions in Early Stage Lung Cancer Patients and Assessing the Disease-free Survival With Long-term Follow-up (ONC003)

NSCLC | Lung Cancer | Lung Adenocarcinoma

United States
Iverson Genetic Diagnostics, Inc.

Suspended

Warfarin Adverse Event Reduction For Adults Receiving Genetic Testing at Therapy INitiation (WARFARIN) (WARFARIN)

Atrial Fibrillation | Pulmonary Embolism | DVT | Prosthetic Replacement of Mitral Valve | Anti-coagulation Therapy | Joint Surgery Multiple

United States
Myriad Genetic Laboratories, Inc.

Completed

Open Registry Measuring Impact of Genomic Testing on Treatment of Prostate Cancer Patients

Prostate Cancer

United States
Federico II University
San Raffaele University Hospital, Italy; San Giuseppe Moscati Hospital

Recruiting

Creation of a Multicenter National Registry for Peripartum Cardiomyopathy. (PPCMREGISTRY)

Peripartum Cardiomyopathy

Italy
Centre Hospitalier Universitaire Dijon

Recruiting

Diagnostic Research in Patients With Rare Diseases -Solving the Unsolved Rare Diseases (AnDDI-Solve-RD)

Rare Diseases

France
Scripps Translational Science Institute

Recruiting

MyGeneRank: A Digital Platform for Next-Generation Genetic Studies

Heart Diseases

United States
Centre Hospitalier Universitaire, Amiens

Recruiting

Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing (GENEPIC)

Cleft Lip and Palate

France
Boston Children's Hospital

Active, not recruiting

Genetics of Differences of Sex Development and Hypospadias

Disorders of Sex Development | Hypospadias

United States
Institut Curie

Completed

Use of Specific Genetic Alteration s of Tumoral Cells Identified by the Next Generation Sequencing Techniques (NGS) to Follow Peripheral Samples of Children With Metastatic and/or High Risk Solid Tumor - NGSKids (NGSKids)

Metastatic and/or High Risk Solid Tumor of Children

France
Fondation Ophtalmologique Adolphe de Rothschild

Completed

Genetic Analysis and Multimodal Retinal Imaging of Asymptomatic Fovea Plana Cases in the General Population (APOGEE)

Albinism | Fovea Plana

France

Search clinical trials for: genetic: CXCR3 polymorphism rs2280964

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Russia

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations