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Spots Global Cancer Trial Database for Advanced GC Multi-omic Characterization in EU and CELAC Populations

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Trial Identification

Brief Title: Advanced GC Multi-omic Characterization in EU and CELAC Populations

Official Title: Advanced GC Multi-omic Characterization in EU and CELAC Populations

Study ID: NCT04015466

Conditions

Gastric Cancer

Interventions

Study Description

Brief Summary: Observational study (cohort type) of advanced GC patients that will be recruited prospectively to study biological factors associated with the disease and relevant clinical outcomes.

Detailed Description: Despite of multiple attempts to improve treatment in recent decades, none strategies has improved prognosis in locally advanced stage III and IV GC. A therapeutic approach to GC based on current histological and image criteria (Tumour Node Metastasis -TNM- stage) is insufficient. Although multiple targeted agents are currently under investigation, so far, only trastuzumab and ramucirumab have demonstrated efficacy in advanced GC and have a regulatory approval. For this reason, the identification of specific targets that could be susceptible for drug inhibition, is an urgent requirement. Moreover, most studies and current international databases on late-stage/advanced GC are largely based on Asian populations, in sharp contrast tumour biology and genome of EU or CELAC populations remain poorly known. The primary objective of this study are to: 1. Characterize a multi-centric cohort including EU and CELAC populations diagnosed with advanced GC through a multi-omic approach including proteomics, genomics, transcriptomics, microbiome and exposome analysis due to study the determinants of GC. 2. Identify the regional differences in EU and CELAC populations recruiting patients for this study for each omic characterization due to identify the high-risk group populations. 3. Identify and select from the multi-omic approach those biomarkers useful for the development of an algorithm to guide the therapeutic approach for advanced GC.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Instituto Alexander Fleming, Buenos Aires, , Argentina

Pontificia Universidad Católica de Chile, Santiago, , Chile

Instituto Nacional de Cancerología de México, Mexico, , Mexico

VU Medical Centre, Amsterdam, , Netherlands

GenPat, Asunción, , Paraguay

Institute of Pathology and Immunology of University of Porto, Porto, , Portugal

Vall d'Hebron Institut d'Oncologia, Barcelona, , Spain

Hospital Clínico Univeristario de Valencia, Valencia, , Spain

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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