Actively Recruiting
New York Cancer and Blood Specialists Clinical Biospecimen Collection for Research Use
Led by North Shore Hematology Oncology Associates P.C dba New York Cancer and Blood Specialists · Updated on 2026-04-24
900000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to collect and store biological samples and health information from thousands of individuals, including cancer patients, high-risk groups, survivors, and healthy donors. This research aims to support the development of new diagnostic tools and treatments for various diseases such as cancer, infectious diseases, autoimmune disorders, and endocrine conditions. The study contributes to understanding how diseases affect the body over time, with a goal to improve patient care and outcomes. Participants will provide biological samples that may be used for genetic research, including RNA and DNA analysis, gene and protein expression studies, and the development of biomarkers and diagnostic devices. These samples will be stored in a centralized biorepository alongside detailed health data. The study plans to collect samples from individuals with benign or diagnosed conditions, as well as from healthy normal donors. During the study, participants may be asked to provide biological specimens and share health information over an extended period of up to 10 years. Researchers will use this information to develop and test new medical assays, diagnostics, and treatments aimed at improving quality and length of life for people with various diseases. The study involves ongoing collection and analysis, with no interventional treatments administered as part of the protocol.
CONDITIONS
Brief Title
Clinical Biospecimen Collection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be at least 18 years old
- Able to provide legally documented informed consent
- May have or not have active disease at enrollment
- Include individuals with benign conditions, diagnosed or suspected oncological, infectious, autoimmune, or endocrine diseases, and healthy donors
You will not qualify if you...
- Not meeting the inclusion criteria
- Additional criteria may apply depending on specific project plans, such as genetic mutation status, disease progression, or prior treatments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single time point
Participants provide biological specimens such as blood, tissue, or other samples for research purposes.
1 visit (in-person)
Duration - Up to 10 years
Participants' biospecimens and data are used for ongoing genetic research and development of new diagnostics and treatments.
Trial Site Locations
Total: 1 location
1
NYCBS
Shirley, New York, United States, 11967
Actively Recruiting
Research Team
A
Andrew Lee, MHA
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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