Search clinical trials for: Mutation

Total 1181 results

Assistance Publique - Hôpitaux de Paris

Completed

Study of Factors of Genetic Susceptibility Associated to Severe Caries Phenotype (Cariogene)

Dental Caries

France
Seoul National University Bundang Hospital

Completed

Prognostic Value of Each Codon-specific KRAS Mutation in Colorectal Cancer

Colorectal Cancer

Korea, Republic of
Fondazione IRCCS Ca' Granda, Ospedale Maggiore...

Completed

Clinical Determinants of Disease Progression in Patients With Limb Girdle Muscular Distrophy Type 2E (NeuroLGMD2E)

LGMD2E

Italy
Sun Yat-sen University

Enrolling by invitation

Mutation Detection for VRL

Uveitis | Vitreoretinal Lymphoma

China
Centre Hospitalier Universitaire de Besancon

Completed

IMpact of Breast cAncer Gene Status on Survival in Adjuvant Breast Cancer (IMBASSA) (IMBASSA)

Breast Cancer | BRCA1 Mutation | BRCA2 Mutation

France
DermTech

Recruiting

Sample Collection Study to Assess Prevalence of Gene Mutations: Establishing Population Norms

Photoaging

United States
State University of New York at Buffalo
Hadley Jo Foundation

Completed

Natural History Study of SLC25A46 Mutation-related Mitochondriopathy

Mitochondrial Diseases | Optic Atrophy | Neurodegenerative Disease, Hereditary

United States
Centre Hospitalier Universitaire de la Réunion

Completed

Prevalence of EGFR Mutations in epidermoïd Bronchopulmonary Cancers in Réunion Island (EPIMURE)

Squamous Cell Lung Cancer

Réunion
TRPHARM
Klinar CRO; Damagen Genetic Diagnostic Center

Enrolling by invitation

A Study on the Prevalence of Mutation of Cerebrotendinous Xanthomatosis (CTX) (F-GENE)

Xanthomatosis, Cerebrotendinous

Turkey
Fudan University

Unknown

Mutation of BRCA1/2 and Other Potential Genes in Triple-negative Breast Cancer

Breast Cancer

China
National Institutes of Health Clinical Center (CC)
National Cancer Institute (NCI)

Completed

Genetic Study to Identify Gene Mutations in Participants Previously Enrolled in Clinical Trial NCI-99-C-0053 Who Have Von Hippel-Lindau Syndrome or Are at Risk for Von Hippel-Lindau Syndrome

Kidney Cancer | Von Hippel-lindau Syndrome

United States
AstraZeneca

Completed

Asia Pacific and Russia Diagnostic Study for EGFR Testing (IGNITE)

EGFR Mutation Status in aNSCLC Patients

Korea, Republic of, Russian Federation, Malaysia, China, Australia, Taiwan, Thailand, Indonesia, Singapore
Qilu Hospital of Shandong University

Recruiting

Biomarkers to Predict Acute Respiratory Distress Syndrome(ARDS) in Patients With Sepsis

Sepsis

China
Maxima Medical Center

Recruiting

Sodium Channel Mutations in Patient With the Anterior Cutaneous Nerve Entrapment Syndrome (ACNES) (Nav-ACNES)

Chronic Pain Syndrome | Nerve Entrapment Syndrome | Anterior Cutaneous Nerve Entrapment Syndrome

Netherlands
Centre Henri Becquerel

Unknown

Detection of Recurrent Mutations in Waldenström's Disease (DigiWAL)

Waldenstrom's Disease

France
Dr Cipto Mangunkusumo General Hospital

Completed

Patogenic Mutation in 5 Genes

Colorectal Cancer | APC Gene Mutation | TP53 Gene Mutation | PIK3CA Gene Mutation | KRAS Mutation-Related Tumors | MLH1 Gene Mutation

Indonesia
Shanghai Zhongshan Hospital

Unknown

Gastroesophageal Varices in Cavernoma

Portal Hypertension | Myeloproliferative Neoplasm | Gastroesophageal Varices | Portal Caver Cavernoma

China
Pediatrix

Completed

Demographic, Metabolic, and Genomic Description of Neonates With Severe Hyperbilirubinemia

Jaundice | Hyperbilirubinemia

United States
Universitaire Ziekenhuizen KU Leuven

Completed

HbA2 Leuven and Its Impact on HbA1c Results (HbA2 Leuven)

Family Study HbA2 Leuven Mutation.

Belgium
University Hospital Center of Martinique

Recruiting

Prevalence of the c.853delT Mutation of the HOXB13 Gene in Prostate Cancer in Martinique (HOXB13_Mart)

Prostate Cancer

Martinique
Chinese PLA General Hospital

Unknown

Liquid Biopsy for Detection of Driver Mutation in NSCLC

Non Small Cell Lung Cancer

China
National Institute of Nursing Research (NINR)

Completed

Family Health After Predictive Huntington Disease (HD) Testing

Huntington Disease

United States
Anthony Magliocco

Recruiting

Idylla EGFR Lung Trial

Lung Cancer | Oncology | Technology

United States
Changi General Hospital

Completed

A Comprehensive Evaluation of Circulating Tumor DNA and Circulating Tumor Cells as a Predictive Marker in Lung Cancer

Lung Cancer
NYU Langone Health
Genzyme, a Sanofi Company

Completed

Genzyme Osteopenia/Osteoporosis Study

Gaucher Disease

United States
Institut Paoli-Calmettes

Unknown

Triple Negative Breast Cancer: Study of Molecular and Genetic Factors

Breast Cancer

France
Rigshospitalet, Denmark
Odense University Hospital; Zealand University Hospital; Aarhus University Hospital and other collaborators

Recruiting

Danish Elder Lymphoma Patient Hematopoietic Investigation (DELPHI)

Lymphoma | Chemotherapeutic Toxicity | Chemotherapy-induced Neutropenia | Chemotherapy-Related Leukemia

Denmark
Biocartis NV
AstraZeneca

Withdrawn

EGFR_IUO 3.20 Clinical Study Protocol

NSCLC
M.D. Anderson Cancer Center
European Commission

Completed

Rational Therapeutics Based on Matched Tumor and Normal Tissue

Advanced Cancers

United States, Spain, France, Israel
Hellenic Cooperative Oncology Group

Completed

Germline Mutations in Pancreatic Adenocarcinoma (PaMPA)

Pancreatic Cancer | Hereditary Cancer | Predisposition, Genetic | Germline Mutation Abnormality

Greece
Centre Hospitalier Universitaire de la Réunion

Not yet recruiting

Contribution of Oncogenetics in Breast Cancer in Reunion Epidemiology of Breast Cancer in Reunion: Study of the Reunion Mutation on BRCA2 (CanSeR-OGen)

Breast Cancer | BRCA2 Mutation | Genetic Disease
Jinsong Wu

Completed

Molecular Pathology Research Project of Glioma

Glioma, Malignant

China
Centre Hospitalier Universitaire de Nice

Unknown

Detection of Plasmatic Cell-free BRAF and NRAS Mutations : a New Tool for Monitoring Patients With Metastatic Malignant Melanoma Treated With Targeted Therapies or Immunotherapy ( MALT ) (MALT)

Malignant Melanoma Stage III | Malignant Melanoma Stage IV
Hospital General de Mexico

Unknown

IDH1/IDH2 Mutation Frequency in Acute Myeloblastic Patients

Acute Myeloid Leukemia (AML)

Mexico
University Hospital, Caen
Thong DAO; Annie BOREL-DERLON; Nathalie GANNE-CARRIE; Pierre NAHON; Sylvie Chevret

Completed

Influence of ABO Blood Group on the Risk of Complications in Alcoholic or Viral C Cirrhosis? (ABOCIRRALVIR)

Alcoholic or Viral C Compensated Cirrhosis

France
Corporacion Parc Tauli

Completed

APPLICATION OF MOLECULAR TECHNIQUES FOR IMPROVING THE DIAGNOSIS AND TREATMENT OF NODULAR THYROID LESIONS.

Papillary Thyroid Carcinoma

Spain
Shanghai Chest Hospital

Recruiting

NGS-based Comprehensive Genomic ctDNA Panel in NSCLC With Immunotherapy

Lung Cancer

China
ECOG-ACRIN Cancer Research Group
National Cancer Institute (NCI)

Completed

DNA Analysis of Tissue From Patients With T-Cell Acute Lymphoblastic Leukemia

Leukemia
Shanghai Chest Hospital

Unknown

NGS-based Large-panel in Targeted Drug Delivery and Immunotherapy of Lung Cancer

Lung Neoplasms

China
University of Pennsylvania

Completed

Factor V Leiden Mutation and Implantation Failure

Infertility

United States
Leeds Cancer Centre at St. James's University Hospital

Unknown

Study of Families With Melanoma

Melanoma (Skin)

United Kingdom
Institut Bergonié
AstraZeneca

Recruiting

Implementing Circulating Tumor DNA Analysis at Initial Diagnosis to Improve Management of Advanced NSCLC Patients (CIRCULAR)

Non Small Cell Lung Cancer | Advanced Solid Tumor

France
State University of New York at Buffalo
The Callum McKeefery and Nikki Albano McKeefery Pediatric Division of Genetics...

Completed

Natural History Study of FDXR Mutation-related Mitochondriopathy

Mitochondrial Diseases | Optic Atrophy | Neurodegenerative Disease, Hereditary

United States
Chang Gung Memorial Hospital
Sanofi

Unknown

Fabry Disease in Cerebrovascular Disease

Fabry Disease

Taiwan
Children's Oncology Group
National Cancer Institute (NCI)

Completed

Molecular Genetic Lesions and Clinical Outcomes in Children With Acute Lymphoblastic Leukemia

Leukemia

Australia
Alliance for Clinical Trials in Oncology
National Cancer Institute (NCI)

Completed

Study of Tumor Samples in Patients Undergoing Treatment for Gastrointestinal Stromal Tumors on Clinical Trial ACOSOG-Z9001

Gastrointestinal Stromal Tumor

United States
Leeds Cancer Centre at St. James's University Hospital

Unknown

Identifying Gene Mutations in Patients With Melanoma and in Families With a History of Hereditary Melanoma

Melanoma (Skin) | Hereditary Multiple Melanoma

United Kingdom
Grupo Cooperativo de Hemopatías Malignas

Recruiting

Myeloid Mutations Register in R/R CML

Chronic Myeloid Leukaemia Recurrent | Chronic Myeloid Leukemia, in Relapse

Mexico
Universitair Ziekenhuis Brussel

Recruiting

Sub-type Specific Genomic Mutations in sBOTs

Ovarian Neoplasm Epithelial

Belgium
National Cancer Institute (NCI)

Completed

Genetic Study of Patients Previously Treated With Flavopiridol on Clinical Trial NCI-97-C-0171C

Unspecified Adult Solid Tumor, Protocol Specific

United States

Search clinical trials for: Mutation

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