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RecruitingNCT04991922

BostonGene-Integrated Genomic Registry (BIGR)

BostonGene-Integrated Genomic Registry Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
100,000 (estimated)
Sponsor
BostonGene · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this project is to develop a comprehensive database of genomic, transcriptomic, molecular, and clinical characteristics of oncology patients to discover, define, and develop genomic and transcriptomic markers to improve future clinical outcomes across cancer types

Detailed description

Immuno- and targeted therapies have shown promising results for many types of cancer (1). However, the effectiveness of these treatments is not optimal for many patients (2). Therefore, further research is needed to discover, define, and develop genomic, transcriptomic, and integrated molecular markers that can improve clinical outcomes across cancer types (3). Unfortunately, current research is restricted by the limited availability of genomic and transcriptomic results linked to clinical outcomes (3). This study will allow for the collection of key clinical data, including longitudinal follow-up, linked with individual genetic and molecular findings in a single comprehensive registry-based databank. Analysis of these data may lead to advances across cancer subtypes through the identification of transcriptomic and genomic associations with therapies. Clinical and pathological information, including detailed genetic information from a participant's tumor biopsy, will be obtained by the research staff for each participant enrolled in the BIGR Study. Clinical information will include relevant details about the patient's diagnosis and treatment and will be stored in a secure electronic registry database. No extra scans or procedures for this study will be collected as part of this study. Information will be collected regarding a participant's initial diagnosis, treatment, and outcome. To obtain this information, study staff will contact participants or a participant's doctor at regular time intervals for up to 15 years.

Conditions

Timeline

Start date
2021-07-01
Primary completion
2031-07-01
Completion
2036-07-01
First posted
2021-08-05
Last updated
2024-02-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04991922. Inclusion in this directory is not an endorsement.