Identifying Novel Variants in the DPYD Gene in Patients of Non-Western Descent
NCT04300361 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 600
Last updated 2020-03-09
Summary
This is a observational, multicenter study to identify novel variants of the DPYD gene which are possible deleterious in patients of non-Western descent.
Conditions
- Neoplasms
Interventions
- GENETIC
-
Sequencing of DPYD gene
The DPYD gene of non-Western patients will be sequenced to identify DPYD variants that are possibly associated with an increased risk of developing severe fluoropyrimidine-related toxicity.
Sponsors & Collaborators
-
The Netherlands Cancer Institute
collaborator OTHER - collaborator OTHER
-
Haga Hospital
collaborator OTHER -
Medical Center Haaglanden
collaborator OTHER -
Leiden University Medical Center
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-03-01
- Primary Completion
- 2022-03-01
- Completion
- 2022-08-01
- FDA Drug
- Yes
More Related Trials
-
Inter-regional Project of the Great Western Exploration Approach for Exome Molecular Causes Severe Intellectual Disability Isolated or Syndromic
NCT02136849 ·Status: COMPLETED
-
Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset
NCT06475651 ·Status: RECRUITING
-
Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plain Community
NCT02927158 ·Status: RECRUITING
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Prenatal Molecular Characterisation by CGH+SNP-ARRAY of Supernumerary Marker Chromosomes and de Novo Apparently Balanced Reciprocal Translocations
NCT01907425 ·Status: TERMINATED ·Phase: NA
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Rare and Undiagnosed Disease Research Biorepository
NCT04703179 ·Status: ENROLLING_BY_INVITATION
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Discovering the Gene(s) Causing Developmental Dysplasia of the Hip (DDH)
NCT01193673 ·Status: COMPLETED
-
Genetic Variation in Platelet Aggregation
NCT01576536 ·Status: COMPLETED
-
Genetics in the Progression of Nephropathies
NCT06416761 ·Status: RECRUITING
-
Genetics of Middle Ear Disease
NCT00422136 ·Status: COMPLETED
-
Risk of Recurrence of de Novo Mutations: Research and Quantification of Paternal Germinal Mosaicism by the Combined Use of Genomic Tools
NCT04564235 ·Status: COMPLETED ·Phase: NA
-
Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN
NCT05499091 ·Status: RECRUITING ·Phase: NA
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings
NCT04315727 ·Status: RECRUITING ·Phase: NA
-
An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene
NCT06435000 ·Status: RECRUITING
-
Screening for Genes in Patients With Congenital Neutropenia
NCT02866162 ·Status: COMPLETED
-
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia
NCT02175264 ·Status: COMPLETED
-
Drivers of Hypoxia-induced Angiogenesis in Tumor Development
NCT03979833 ·Status: UNKNOWN
-
Do Patients With Early Post Operative Recurrence of Pelvic Organ Prolapse Have a Genetic Predisposition?
NCT01614587 ·Status: COMPLETED
-
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study
NCT02862808 ·Status: COMPLETED
-
Psychosocial Impact of Disclosing Cancer Predisposition Genetic Testing Results During Childhood
NCT04848142 ·Status: COMPLETED
-
Genetic Study of Families Affected by Paget's Disease of Bone
NCT00747994 ·Status: COMPLETED
-
Study for Characterisation of Predictive Parameters of Clonal Evolution in Subjects With GATA2 Germline Mutation
NCT05983991 ·Status: RECRUITING ·Phase: NA