The future of cancer immunotherapy: microenvironment-targeting combinations.
Yonina R Murciano-Goroff, Allison Betof Warner, Jedd D Wolchok
https://pubmed.ncbi.nlm.nih.gov/32467593Actively Recruiting
Led by BostonGene · Updated on 2024-02-07
100000
Participants Needed
1
Research Sites
261 weeks
Total Duration
This research aims to create a detailed database combining genetic, molecular, and clinical information from patients with various cancers. The goal is to identify genetic and molecular markers that could help improve future treatments and outcomes across different cancer types. The study recognizes that current research is limited by the lack of linked genetic and clinical data and seeks to address this gap through a comprehensive registry. Participants will have their clinical and pathological data collected, including detailed genetic information from their tumor biopsies. This data will be securely stored in an electronic registry. The study does not require additional scans or procedures; instead, it gathers existing diagnostic and treatment information. Follow-up data will be collected over time by contacting participants or their doctors periodically for up to 15 years. Throughout the study, researchers will review the associations between genetic findings and patient outcomes at intervals up to five years. They will also assess predictive probabilities and how patients may match to clinical trials. Participants can expect regular data collection about their cancer diagnosis, treatments, and outcomes without undergoing extra procedures, with their information securely maintained for long-term study.
CONDITIONS
BostonGene-Integrated Genomic Registry (BIGR)
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - Up to 1 month
Clinical and pathological information, including detailed genetic and molecular data from a participant's tumor biopsy, is collected and recorded.
1 visit (in-person or remote) to collect existing clinical and genomic data
Duration - Up to 15 years
Participants are followed over time with periodic collection of clinical outcomes and treatment information through contact with participants or their doctors.
Regular contact at specified intervals over 15 years (remote or in-person)
Total: 1 location
1
BostonGene
Waltham, Massachusetts, United States, 02453
Actively Recruiting
N
Nathan Fowler
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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